Academic Journal
Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease.
| Title: | Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease. |
|---|---|
| Authors: | Cavin K Ward-Caviness, Paul S de Vries, Kerri L Wiggins, Jennifer E Huffman, Lisa R Yanek, Lawrence F Bielak, Franco Giulianini, Xiuqing Guo, Marcus E Kleber, Tim Kacprowski, Stefan Groß, Astrid Petersman, George Davey Smith, Fernando P Hartwig, Jack Bowden, Gibran Hemani, Martina Müller-Nuraysid, Konstantin Strauch, Wolfgang Koenig, Melanie Waldenberger, Thomas Meitinger, Nathan Pankratz, Eric Boerwinkle, Weihong Tang, Yi-Ping Fu, Andrew D Johnson, Ci Song, Moniek P M de Maat, André G Uitterlinden, Oscar H Franco, Jennifer A Brody, Barbara McKnight, Yii-Der Ida Chen, Bruce M Psaty, Rasika A Mathias, Diane M Becker, Patricia A Peyser, Jennifer A Smith, Suzette J Bielinski, Paul M Ridker, Kent D Taylor, Jie Yao, Russell Tracy, Graciela Delgado, Stella Trompet, Naveed Sattar, J Wouter Jukema, Lewis C Becker, Sharon L R Kardia, Jerome I Rotter, Winfried März, Marcus Dörr, Daniel I Chasman, Abbas Dehghan, Christopher J O'Donnell, Nicholas L Smith, Annette Peters, Alanna C Morrison |
| Source: | PLoS ONE, Vol 14, Iss 5, p e0216222 (2019) |
| Publisher Information: | Public Library of Science (PLoS), 2019. |
| Publication Year: | 2019 |
| Collection: | LCC:Medicine LCC:Science |
| Subject Terms: | Medicine, Science |
| More Details: | BackgroundFibrinogen is an essential hemostatic factor and cardiovascular disease risk factor. Early attempts at evaluating the causal effect of fibrinogen on coronary heart disease (CHD) and myocardial infraction (MI) using Mendelian randomization (MR) used single variant approaches, and did not take advantage of recent genome-wide association studies (GWAS) or multi-variant, pleiotropy robust MR methodologies.Methods and findingsWe evaluated evidence for a causal effect of fibrinogen on both CHD and MI using MR. We used both an allele score approach and pleiotropy robust MR models. The allele score was composed of 38 fibrinogen-associated variants from recent GWAS. Initial analyses using the allele score used a meta-analysis of 11 European-ancestry prospective cohorts, free of CHD and MI at baseline, to examine incidence CHD and MI. We also applied 2 sample MR methods with data from a prevalent CHD and MI GWAS. Results are given in terms of the hazard ratio (HR) or odds ratio (OR), depending on the study design, and associated 95% confidence interval (CI). In single variant analyses no causal effect of fibrinogen on CHD or MI was observed. In multi-variant analyses using incidence CHD cases and the allele score approach, the estimated causal effect (HR) of a 1 g/L higher fibrinogen concentration was 1.62 (CI = 1.12, 2.36) when using incident cases and the allele score approach. In 2 sample MR analyses that accounted for pleiotropy, the causal estimate (OR) was reduced to 1.18 (CI = 0.98, 1.42) and 1.09 (CI = 0.89, 1.33) in the 2 most precise (smallest CI) models, out of 4 models evaluated. In the 2 sample MR analyses for MI, there was only very weak evidence of a causal effect in only 1 out of 4 models.ConclusionsA small causal effect of fibrinogen on CHD is observed using multi-variant MR approaches which account for pleiotropy, but not single variant MR approaches. Taken together, results indicate that even with large sample sizes and multi-variant approaches MR analyses still cannot exclude the null when estimating the causal effect of fibrinogen on CHD, but that any potential causal effect is likely to be much smaller than observed in epidemiological studies. |
| Document Type: | article |
| File Description: | electronic resource |
| Language: | English |
| ISSN: | 1932-6203 |
| Relation: | https://doaj.org/toc/1932-6203 |
| DOI: | 10.1371/journal.pone.0216222 |
| Access URL: | https://doaj.org/article/138107b510a249878e58480e248bba04 |
| Accession Number: | edsdoj.138107b510a249878e58480e248bba04 |
| Database: | Directory of Open Access Journals |
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| FullText | Links: – Type: pdflink Url: https://content.ebscohost.com/cds/retrieve?content=AQICAHjPtM4BHU3ZchRwgzYmadcigk49r9CVlbU7V5F6lgH7WwGGhxm5tv1I75ykWc2Dh45nAAAA4jCB3wYJKoZIhvcNAQcGoIHRMIHOAgEAMIHIBgkqhkiG9w0BBwEwHgYJYIZIAWUDBAEuMBEEDGuP8TeaBYaATbra8AIBEICBmgzIcdYZN-0zO7PTeHAsxeEbhL2S6_vHdsNsZ4w69hUgwLtO4TMPiNqpkhRJS6o7-kiefsHIuZLqOYguo0FSronxwBnpS7TxHxxsQbM5tlE09VafRSF-p90pYPHa3T8xX7oRH7QxVNxhmzQXIjRLNuGCRr2rtLlUF_LFR2b-AZJznE4K9Irvx_OVblRmgEp2PhZVS-zqEiYw_lg= Text: Availability: 1 Value: <anid>AN0136395773;[78be]10may.19;2019May13.14:14;v2.2.500</anid> <title id="AN0136395773-1">Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease </title> <p>Background: Fibrinogen is an essential hemostatic factor and cardiovascular disease risk factor. Early attempts at evaluating the causal effect of fibrinogen on coronary heart disease (CHD) and myocardial infraction (MI) using Mendelian randomization (MR) used single variant approaches, and did not take advantage of recent genome-wide association studies (GWAS) or multi-variant, pleiotropy robust MR methodologies. Methods and findings: We evaluated evidence for a causal effect of fibrinogen on both CHD and MI using MR. We used both an allele score approach and pleiotropy robust MR models. The allele score was composed of 38 fibrinogen-associated variants from recent GWAS. Initial analyses using the allele score used a meta-analysis of 11 European-ancestry prospective cohorts, free of CHD and MI at baseline, to examine incidence CHD and MI. We also applied 2 sample MR methods with data from a prevalent CHD and MI GWAS. Results are given in terms of the hazard ratio (HR) or odds ratio (OR), depending on the study design, and associated 95% confidence interval (CI). In single variant analyses no causal effect of fibrinogen on CHD or MI was observed. In multi-variant analyses using incidence CHD cases and the allele score approach, the estimated causal effect (HR) of a 1 g/L higher fibrinogen concentration was 1.62 (CI = 1.12, 2.36) when using incident cases and the allele score approach. In 2 sample MR analyses that accounted for pleiotropy, the causal estimate (OR) was reduced to 1.18 (CI = 0.98, 1.42) and 1.09 (CI = 0.89, 1.33) in the 2 most precise (smallest CI) models, out of 4 models evaluated. In the 2 sample MR analyses for MI, there was only very weak evidence of a causal effect in only 1 out of 4 models. Conclusions: A small causal effect of fibrinogen on CHD is observed using multi-variant MR approaches which account for pleiotropy, but not single variant MR approaches. Taken together, results indicate that even with large sample sizes and multi-variant approaches MR analyses still cannot exclude the null when estimating the causal effect of fibrinogen on CHD, but that any potential causal effect is likely to be much smaller than observed in epidemiological studies.</p> <p>Keywords: Research Article; Biology and life sciences; Biochemistry; Glycobiology; Glycoproteins; Fibrinogen; Medicine and health sciences; Cardiology; Myocardial infarction; Vascular medicine; Coronary heart disease; Computational biology; Genome analysis; Genome-wide association studies; Genetics; Genomics; Human genetics; Research and analysis methods; Mathematical and statistical techniques; Statistical methods; Metaanalysis; Physical sciences; Mathematics; Statistics; Genetic loci; Alleles; Epidemiology; Medical risk factors; Genetic epidemiology</p> <hd id="AN0136395773-2">Introduction</hd> <p>Fibrinogen is an essential component of the clotting and hemostasis system with a strong genetic basis [[<reflink idref="bib1" id="ref1">1</reflink>]–[<reflink idref="bib3" id="ref2">3</reflink>]]. Although it primarily serves as the precursor to fibrin, it also carries out several other functions, including enhancing platelet aggregation and mediating inflammation [[<reflink idref="bib4" id="ref3">4</reflink>], [<reflink idref="bib5" id="ref4">5</reflink>]]. In epidemiologic studies, fibrinogen levels are associated with coronary heart disease (CHD) [[<reflink idref="bib6" id="ref5">6</reflink>]–[<reflink idref="bib8" id="ref6">8</reflink>]], myocardial infarction (MI) [[<reflink idref="bib9" id="ref7">9</reflink>], [<reflink idref="bib10" id="ref8">10</reflink>]], ischemic stroke [[<reflink idref="bib11" id="ref9">11</reflink>], [<reflink idref="bib12" id="ref10">12</reflink>]], and abdominal aortic aneurysm [[<reflink idref="bib13" id="ref11">13</reflink>], [<reflink idref="bib14" id="ref12">14</reflink>]].</p> <p>Mendelian randomization (MR) is an instrumental variable analysis method which uses genetic variants as instruments to uncover evidence for a causal relationship between a modifiable risk factor and outcome.[[<reflink idref="bib15" id="ref13">15</reflink>]] MR studies utilizing a limited number of genetic variants in the <emph>FGB</emph> promoter have yielded little evidence of a causal effect of fibrinogen on CHD or MI [[<reflink idref="bib16" id="ref14">16</reflink>]–[<reflink idref="bib18" id="ref15">18</reflink>]]. In a genome-wide association study (GWAS) for fibrinogen, each fibrinogen-associated variant was individually evaluated for association with CHD, but no associations provided substantial evidence of a causal effect [[<reflink idref="bib19" id="ref16">19</reflink>]]. To date MR studies of fibrinogen have been limited to single variant approaches which have not taken into account recent GWAS findings or modern, multi-variant MR methodologies. Here we re-examine the potential for fibrinogen to be a causal biomarker for CHD and MI, taking into account these improved approaches.</p> <hd id="AN0136395773-3">Results</hd> <p>For incident CHD there were 3,147 incident events observed in 15,427 participants in the discovery analyses, and 1,482 incident events among the 34,209 participants in the replication analyses. Of the 18,798 participants in the incident MI discovery analyses, 1,711 had an incident MI. For the replication analyses, there were 687 incident MI events out of the 33,288 participants. Table 1 contains the distributions of clinical covariates and fibrinogen. The FGB variant rs1800790 (commonly used in previous fibrinogen MR analyses) had a weaker association (by effect size) than the allele score (Table A in S1 File). In single variant analyses of rs1800790 the estimated causal effect appeared to be centered around the null with little evidence of a causal effect of fibrinogen on CHD or MI (Table B in S1 File), consistent with published literature. In multi-variant MR using the 2SC model, we observed evidence of a causal association of fibrinogen on incident CHD in the discovery and replication analyses which remained in a combined analysis of all cohorts (HR = 1.75; CI = 1.22–2.51; P = 0.002; Fig 1). For incident MI, we observed an elevated HR that included the null, even in the combined analysis (HR = 1.45; CI = 0.85–2.49; P = 0.17; Fig 2).</p> <p>Table 1: Clinical covariates.</p> <p> <ephtml> &lt;table&gt;&lt;tr&gt;&lt;th align="center" /&gt;&lt;th align="center" colspan="7"&gt;Discovery&lt;/th&gt;&lt;th align="center" colspan="4" style="background-color:#BFBFBF"&gt;Replication&lt;/th&gt;&lt;/tr&gt;&lt;tr&gt;&lt;th align="center" /&gt;&lt;th align="center"&gt;KORA&lt;/th&gt;&lt;th align="center"&gt;GENOA&lt;/th&gt;&lt;th align="center"&gt;ARIC&lt;/th&gt;&lt;th align="center"&gt;CHS&lt;/th&gt;&lt;th align="center"&gt;GeneSTAR&lt;/th&gt;&lt;th align="center"&gt;FHS&lt;/th&gt;&lt;th align="center"&gt;RS&lt;/th&gt;&lt;th align="center"&gt;MESA&lt;/th&gt;&lt;th align="center"&gt;WGHS&lt;/th&gt;&lt;th align="center"&gt;LURIC&lt;/th&gt;&lt;th align="center"&gt;SHIP&lt;/th&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;N&lt;/td&gt;&lt;td align="center"&gt;3,788&lt;/td&gt;&lt;td align="center"&gt;417&lt;/td&gt;&lt;td align="center"&gt;8,815&lt;/td&gt;&lt;td align="center"&gt;2,939&lt;/td&gt;&lt;td align="center"&gt;594&lt;/td&gt;&lt;td align="center"&gt;1,828&lt;/td&gt;&lt;td align="center"&gt;834&lt;/td&gt;&lt;td align="center"&gt;2,506&lt;/td&gt;&lt;td align="center"&gt;27,553&lt;/td&gt;&lt;td align="center"&gt;921&lt;/td&gt;&lt;td align="center"&gt;3,229&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;Mean &amp;#177; SD&amp;#8224;&lt;/td&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;MI follow-up time (y)&lt;/td&gt;&lt;td align="center"&gt;8.44 &amp;#177; 1.5&lt;/td&gt;&lt;td align="center"&gt;-&lt;/td&gt;&lt;td align="center"&gt;20.8 &amp;#177; 6.0&lt;/td&gt;&lt;td align="center"&gt;10.3 &amp;#177; 6.0&lt;/td&gt;&lt;td align="center"&gt;6.72 &amp;#177; 3.6&lt;/td&gt;&lt;td align="center"&gt;17.9 &amp;#177; 5.3&lt;/td&gt;&lt;td align="center"&gt;9.32 &amp;#177; 3.2&lt;/td&gt;&lt;td align="center"&gt;6.25 &amp;#177; 1.1&lt;/td&gt;&lt;td align="center"&gt;17.5 &amp;#177; 3.8&lt;/td&gt;&lt;td align="center"&gt;-&lt;/td&gt;&lt;td align="center"&gt;11.1 &amp;#177; 0.8**&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;CHD follow-up time (y)&lt;/td&gt;&lt;td align="center"&gt;-&lt;/td&gt;&lt;td align="center"&gt;10.4 &amp;#177; 3.6&lt;/td&gt;&lt;td align="center"&gt;20.0 &amp;#177; 6.5&lt;/td&gt;&lt;td align="center"&gt;10.3 &amp;#177; 5.9&lt;/td&gt;&lt;td align="center"&gt;6.07 &amp;#177; 3.2&lt;/td&gt;&lt;td align="center"&gt;17.9 &amp;#177; 5.3&lt;/td&gt;&lt;td align="center"&gt;9.18 &amp;#177; 3.2&lt;/td&gt;&lt;td align="center"&gt;6.18 &amp;#177; 1.2&lt;/td&gt;&lt;td align="center"&gt;17.4 &amp;#177; 4.0&lt;/td&gt;&lt;td align="center"&gt;9.43 &amp;#177; 2.6&lt;/td&gt;&lt;td align="center"&gt;11.1 &amp;#177; 0.8**&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;Age (y)&lt;/td&gt;&lt;td align="center"&gt;49.2 &amp;#177; 13.9&lt;/td&gt;&lt;td align="center"&gt;58.6 &amp;#177; 10.0&lt;/td&gt;&lt;td align="center"&gt;54.2 &amp;#177; 5.68&lt;/td&gt;&lt;td align="center"&gt;72.4 &amp;#177; 5.4&lt;/td&gt;&lt;td align="center"&gt;51.1 &amp;#177; 11.3&lt;/td&gt;&lt;td align="center"&gt;53.8 &amp;#177; 10.0&lt;/td&gt;&lt;td align="center"&gt;72.2 &amp;#177; 6.8&lt;/td&gt;&lt;td align="center"&gt;62.7 &amp;#177; 10.2&lt;/td&gt;&lt;td align="center"&gt;54.6 &amp;#177; 7.1&lt;/td&gt;&lt;td align="center"&gt;60.1 &amp;#177; 11.5&lt;/td&gt;&lt;td align="center"&gt;46.4 &amp;#177; 15.1&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;BMI (kg/m&lt;sup&gt;2&lt;/sup&gt;)&lt;/td&gt;&lt;td align="center"&gt;27.2 &amp;#177; 4.7&lt;/td&gt;&lt;td align="center"&gt;30.6 &amp;#177; 6.3&lt;/td&gt;&lt;td align="center"&gt;27.0 &amp;#177; 4.9&lt;/td&gt;&lt;td align="center"&gt;26.2 &amp;#177; 4.4&lt;/td&gt;&lt;td align="center"&gt;29.3 &amp;#177; 6.3&lt;/td&gt;&lt;td align="center"&gt;27.4 &amp;#177; 4.93&lt;/td&gt;&lt;td align="center"&gt;26.7 &amp;#177; 3.8&lt;/td&gt;&lt;td align="center"&gt;27.7 &amp;#177; 5.1&lt;/td&gt;&lt;td align="center"&gt;25.1 &amp;#177; 6.8&lt;/td&gt;&lt;td align="center"&gt;27.5 &amp;#177; 4.4&lt;/td&gt;&lt;td align="center"&gt;27.0 &amp;#177; 4.8&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;Fibrinogen (g/L)&lt;/td&gt;&lt;td align="center"&gt;2.60 &amp;#177; 0.6&lt;/td&gt;&lt;td align="center"&gt;3.19 &amp;#177; 0.8&lt;/td&gt;&lt;td align="center"&gt;2.95 &amp;#177; 0.61&lt;/td&gt;&lt;td align="center"&gt;3.14 &amp;#177; 0.61&lt;/td&gt;&lt;td align="center"&gt;3.83 &amp;#177; 1.1&lt;/td&gt;&lt;td align="center"&gt;3.14 &amp;#177; 0.61&lt;/td&gt;&lt;td align="center"&gt;3.95 &amp;#177; 0.87&lt;/td&gt;&lt;td align="center"&gt;3.35 &amp;#177; 0.70&lt;/td&gt;&lt;td align="center"&gt;3.59 &amp;#177; 0.78&lt;/td&gt;&lt;td align="center"&gt;3.69 &amp;#177; 0.90&lt;/td&gt;&lt;td align="center"&gt;2.95 &amp;#177; 0.68&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;log(Fibrinogen)&lt;/td&gt;&lt;td align="center"&gt;0.94 &amp;#177; 0.22&lt;/td&gt;&lt;td align="center"&gt;1.11 &amp;#177; 0.36&lt;/td&gt;&lt;td align="center"&gt;3.97 &amp;#177; 0.11&lt;/td&gt;&lt;td align="center"&gt;1.13 &amp;#177; 0.19&lt;/td&gt;&lt;td align="center"&gt;1.30 &amp;#177; 0.27&lt;/td&gt;&lt;td align="center"&gt;1.12 &amp;#177; 0.19&lt;/td&gt;&lt;td align="center"&gt;1.35 &amp;#177; 0.21&lt;/td&gt;&lt;td align="center"&gt;1.19 &amp;#177; 0.20&lt;/td&gt;&lt;td align="center"&gt;1.25 &amp;#177; 0.22&lt;/td&gt;&lt;td align="center"&gt;1.28 &amp;#177; 0.26&lt;/td&gt;&lt;td align="center"&gt;1.06 &amp;#177; 0.22&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;HDL (mg/dL)&lt;/td&gt;&lt;td align="center"&gt;57.9 &amp;#177; 17.0&lt;/td&gt;&lt;td align="center"&gt;52.5 &amp;#177; 14.3&lt;/td&gt;&lt;td align="center"&gt;51.1 &amp;#177; 16.7&lt;/td&gt;&lt;td align="center"&gt;55.8 &amp;#177; 15.9&lt;/td&gt;&lt;td align="center"&gt;52.1 &amp;#177; 15.8&lt;/td&gt;&lt;td align="center"&gt;51.3 &amp;#177; 15.3&lt;/td&gt;&lt;td align="center"&gt;204 &amp;#177; 24.5&lt;/td&gt;&lt;td align="center"&gt;52.4 &amp;#177; 15.7&lt;/td&gt;&lt;td align="center"&gt;53.1 &amp;#177; 16.6&lt;/td&gt;&lt;td align="center"&gt;41.8 &amp;#177; 11.7&lt;/td&gt;&lt;td align="center"&gt;57.0 &amp;#177; 17.1&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;LDL (mg/dL)&lt;/td&gt;&lt;td align="center"&gt;137 &amp;#177; 41.4&lt;/td&gt;&lt;td align="center"&gt;117 &amp;#177; 31.0&lt;/td&gt;&lt;td align="center"&gt;137 &amp;#177; 37.6&lt;/td&gt;&lt;td align="center"&gt;134 &amp;#177; 35.8&lt;/td&gt;&lt;td align="center"&gt;130 &amp;#177; 41.6&lt;/td&gt;&lt;td align="center"&gt;126 &amp;#177; 33.0&lt;/td&gt;&lt;td align="center"&gt;104 &amp;#177; 12.5&lt;/td&gt;&lt;td align="center"&gt;117 &amp;#177; 30.3&lt;/td&gt;&lt;td align="center"&gt;122 &amp;#177; 37.3&lt;/td&gt;&lt;td align="center"&gt;121 &amp;#177; 33.7&lt;/td&gt;&lt;td align="center"&gt;137.3 &amp;#177; 44.2&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;N (%)&lt;/td&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;td align="center" /&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;MI&lt;/td&gt;&lt;td align="center"&gt;109 (2.88)&lt;/td&gt;&lt;td align="center"&gt;-&lt;/td&gt;&lt;td align="center"&gt;859 (9.74)&lt;/td&gt;&lt;td align="center"&gt;498 (16.9)&lt;/td&gt;&lt;td align="center"&gt;30 (5.05)&lt;/td&gt;&lt;td align="center"&gt;158 (8.64)&lt;/td&gt;&lt;td align="center"&gt;57 (6.83)&lt;/td&gt;&lt;td align="center"&gt;62 (2.50)&lt;/td&gt;&lt;td align="center"&gt;413 (1.50)&lt;/td&gt;&lt;td align="center"&gt;-&lt;/td&gt;&lt;td align="center"&gt;212 (6.5)&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;CHD&lt;/td&gt;&lt;td align="center"&gt;-&lt;/td&gt;&lt;td align="center"&gt;77 (18.5)&lt;/td&gt;&lt;td align="center"&gt;1,625 (18.4)&lt;/td&gt;&lt;td align="center"&gt;942 (32.1)&lt;/td&gt;&lt;td align="center"&gt;85 (14.31)&lt;/td&gt;&lt;td align="center"&gt;305 (16.7)&lt;/td&gt;&lt;td align="center"&gt;113 (13.6)&lt;/td&gt;&lt;td align="center"&gt;128 (5.10)&lt;/td&gt;&lt;td align="center"&gt;1,035 (3.76)&lt;/td&gt;&lt;td align="center"&gt;59 (6.41)&lt;/td&gt;&lt;td align="center"&gt;260 (8.0)&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;Sex (male)&lt;/td&gt;&lt;td align="center"&gt;1,854 (48.9)&lt;/td&gt;&lt;td align="center"&gt;156 (37.4)&lt;/td&gt;&lt;td align="center"&gt;3,983 (45.2)&lt;/td&gt;&lt;td align="center"&gt;1,792 (61.0)&lt;/td&gt;&lt;td align="center"&gt;321 (54.0)&lt;/td&gt;&lt;td align="center"&gt;829 (45.0)&lt;/td&gt;&lt;td align="center"&gt;421 (50.5)&lt;/td&gt;&lt;td align="center"&gt;1,308 (52.2)&lt;/td&gt;&lt;td align="center"&gt;0 (0.00)&lt;/td&gt;&lt;td align="center"&gt;499 (54.2)&lt;/td&gt;&lt;td align="center"&gt;1,537 (47.6)&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;Current Smokers&lt;/td&gt;&lt;td align="center"&gt;962 (25.4)&lt;/td&gt;&lt;td align="center"&gt;47 (11.3)&lt;/td&gt;&lt;td align="center"&gt;2,633 (29.9)&lt;/td&gt;&lt;td align="center"&gt;322 (11.0)&lt;/td&gt;&lt;td align="center"&gt;135 (22.8)&lt;/td&gt;&lt;td align="center"&gt;341 (18.7)&lt;/td&gt;&lt;td align="center"&gt;144 (17.3)&lt;/td&gt;&lt;td align="center"&gt;286 (11.4)&lt;/td&gt;&lt;td align="center"&gt;3200 (11.6)&lt;/td&gt;&lt;td align="center"&gt;197 (21.4)&lt;/td&gt;&lt;td align="center"&gt;1,096 (33.9)&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;Former Smokers&lt;/td&gt;&lt;td align="center"&gt;1,262 (33.3)&lt;/td&gt;&lt;td align="center"&gt;157 (37.6)&lt;/td&gt;&lt;td align="center"&gt;2,050 (23.3)&lt;/td&gt;&lt;td align="center"&gt;1,216 (41.4)&lt;/td&gt;&lt;td align="center"&gt;202 (34.0)&lt;/td&gt;&lt;td align="center"&gt;404*&lt;/td&gt;&lt;td align="center"&gt;429 (51.4)&lt;/td&gt;&lt;td align="center"&gt;1,109 (44.4)&lt;/td&gt;&lt;td align="center"&gt;10,096 (36.6)&lt;/td&gt;&lt;td align="center"&gt;273 (29.6)&lt;/td&gt;&lt;td align="center"&gt;1,004 (31.1)&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;Never Smokers&lt;/td&gt;&lt;td align="center"&gt;1,560 (41.2)&lt;/td&gt;&lt;td align="center"&gt;213 (51.0)&lt;/td&gt;&lt;td align="center"&gt;4,109 (46.6)&lt;/td&gt;&lt;td align="center"&gt;1401 (47.7)&lt;/td&gt;&lt;td align="center"&gt;257 (43.3)&lt;/td&gt;&lt;td align="center"&gt;911*&lt;/td&gt;&lt;td align="center"&gt;261 (31.3)&lt;/td&gt;&lt;td align="center"&gt;1,104 (44.2)&lt;/td&gt;&lt;td align="center"&gt;14,233 (51.7)&lt;/td&gt;&lt;td align="center"&gt;451 (49.0)&lt;/td&gt;&lt;td align="center"&gt;1,129 (35.0)&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;Hypertension&lt;/td&gt;&lt;td align="center"&gt;1,079 (28.5)&lt;/td&gt;&lt;td align="center"&gt;310 (74.3)&lt;/td&gt;&lt;td align="center"&gt;2,272 (25.8)&lt;/td&gt;&lt;td align="center"&gt;1549 (52.7)&lt;/td&gt;&lt;td align="center"&gt;261 (43.94)&lt;/td&gt;&lt;td align="center"&gt;563 (30.8)&lt;/td&gt;&lt;td align="center"&gt;204 (24.5)&lt;/td&gt;&lt;td align="center"&gt;1,097 (43.8)&lt;/td&gt;&lt;td align="center"&gt;6,654 (24.2)&lt;/td&gt;&lt;td align="center"&gt;625 (67.5)&lt;/td&gt;&lt;td align="center"&gt;671 (20.8)&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="center"&gt;Type 2 Diabetes&lt;/td&gt;&lt;td align="center"&gt;565 (14.9)&lt;/td&gt;&lt;td align="center"&gt;52 (12.5)&lt;/td&gt;&lt;td align="center"&gt;1,659 (18.8)&lt;/td&gt;&lt;td align="center"&gt;349 (11.9)&lt;/td&gt;&lt;td align="center"&gt;59 (9.93)&lt;/td&gt;&lt;td align="center"&gt;129 (7.10)&lt;/td&gt;&lt;td align="center"&gt;104 (12.5)&lt;/td&gt;&lt;td align="center"&gt;150 (6.70)&lt;/td&gt;&lt;td align="center"&gt;0 (0.00)&lt;/td&gt;&lt;td align="center"&gt;283 (30.7)&lt;/td&gt;&lt;td align="center"&gt;174 (5.4)&lt;/td&gt;&lt;/tr&gt;&lt;/table&gt; </ephtml> </p> <ulist> <item>4 Clinical covariates for all participating cohorts. KORA did not have incident CHD data and thus did not participate in these analyses. GENOA and LURIC had too few incident MI cases for analysis. ANOVA and Chi-squared tests showed significant differences across cohorts for all clinical covariates with P &lt; 0.001 for all tests. BMI = body mass index; CHD = coronary heart disease; HDL = high-density lipoprotein cholesterol; LDL = low-density lipoprotein cholesterol; MI = myocardial infarction; NA = not available</item> <item>3 * For FHS 172 individuals were not current smokers but were not distinguished as former vs never smokers thus percentages were not computed for these categories and the N for those with information is given.</item> <item>2 ** For SHIP only interval censored data was available. Follow-up time represents the time from initial exam to final exam.</item> </ulist> <p>1 † Continuous variables are summarized as the mean ± standard deviation while binary variables are summarized as the sample size "N" and percentage of samples for a given level of the variable</p> <hd id="AN0136395773-4">Pleiotropy robust models</hd> <p>In sensitivity analyses four MR methods were used each of which is at least partially robust to horizontal pleiotropy under differing assumptions. Sensitivity analyses were performed using summary statistics from the CARDIoGRAMplusC4D consortium [[<reflink idref="bib34" id="ref17">34</reflink>]] which used prevalent cases, but had a larger sample size than the CHARGE cohorts (60,801 prevalent cases and 123,504 controls). For CHD, three of the four models showed a positive effect, albeit smaller than the effect observed in the 2SC model, with the MR PRESSO method having the largest causal OR (OR = 1.18; CI = 0.98, 1.42; Table 2). For MI only the MR PRESSO method showed a causal OR &gt; 1 (OR = 1.16; CI = 0.98, 1.38; Table 2), again substantially reduced from that observed in the 2SC model. All other models for MI showed little evidence of a causal effect of fibrinogen on MI.</p> <p>Table 2: Multi-variant, pleiotropy robust MR methods.</p> <p> <ephtml> &lt;table&gt;&lt;tr&gt;&lt;th align="left"&gt;Method&lt;/th&gt;&lt;th align="left"&gt;Robust to pleiotropy by ...&lt;/th&gt;&lt;th align="left"&gt;CHD Causal OR (95% CI)&lt;/th&gt;&lt;th align="left"&gt;MI Causal OR (95% CI)&lt;/th&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="left"&gt;MR Egger&lt;/td&gt;&lt;td align="left"&gt;Intercept-based adjustment for global effect of pleiotropy&lt;/td&gt;&lt;td align="left"&gt;0.98 (0.70, 1.39)&lt;/td&gt;&lt;td align="left"&gt;0.89 (0.63, 1.26)&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="left"&gt;Weighted MBE (phi = 1)&lt;/td&gt;&lt;td align="left"&gt;Assuming causal effect is most common shared effect across variants&lt;/td&gt;&lt;td align="left"&gt;1.09 (0.89, 1.33)&lt;/td&gt;&lt;td align="left"&gt;0.98 (0.79, 1.21)&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="left"&gt;Weighted Median&lt;/td&gt;&lt;td align="left"&gt;Assuming most (&amp;#8805; 50%) genetic instruments are unaffected by pleiotropy&lt;/td&gt;&lt;td align="left"&gt;1.12 (0.91, 1.37)&lt;/td&gt;&lt;td align="left"&gt;1.03 (0.82, 1.29)&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td align="left"&gt;MR PRESSO&lt;/td&gt;&lt;td align="left"&gt;Assuming &amp;#60;50% of genetic instruments have horizontal pleiotropy&lt;/td&gt;&lt;td align="left"&gt;1.18 (0.98, 1.42)&lt;/td&gt;&lt;td align="left"&gt;1.17 (0.98, 1.40)&lt;/td&gt;&lt;/tr&gt;&lt;/table&gt; </ephtml> </p> <p>5 To further examine potential effects of pleiotropy we ran several multi-variant, pleiotropy robust models including MR Egger, Weighted Mode Based Estimator (MBE), Weighted Median, and MR PRESSO. Each uses a different means to account for pleiotropy and has different assumptions used to estimate the causal effect in the presence of pleiotropy. Odds ratios are per 1 g/L increase in genetically determined fibrinogen. CHD = coronary heart disease; CI = confidence interval; MI = myocardial infarction; MR = mendelian randomization</p> <p>We also examined MR associations of fibrinogen on metabolic CHD risk factors using published data available in MR-base as described in the methods. While fibrinogen showed a positive causal effect estimate for some of the CHD risk factors, none provided substantial evidence for excluding the null after accounting for the number of tests performed (Table C S1 File).</p> <hd id="AN0136395773-5">Discussion</hd> <p>The attractiveness of fibrinogen as a causal factor in CHD comes from its roles in both thrombosis and inflammation. Fibrinogen is the precursor to fibrin, which interlinks into a mesh that acts as the scaffold of blood clots. Additionally, fibrinogen also has an active role in platelet aggregation,[[<reflink idref="bib20" id="ref18">20</reflink>]] thus contributing to the formation of platelet plugs. By binding the CD11b/CD18 integrin receptor fibrinogen activates the NF-κB pathway [[<reflink idref="bib5" id="ref19">5</reflink>]], an important pathway in inflammation as well as the formation, destabilization, and rupture of atherosclerotic plaques [[<reflink idref="bib21" id="ref20">21</reflink>], [<reflink idref="bib22" id="ref21">22</reflink>]]. As a modifiable risk factor [[<reflink idref="bib23" id="ref22">23</reflink>]] even a small causal effect of fibrinogen on CHD could have substantial public health implications.</p> <p>Using the allele score approach, a 1 g/L higher fibrinogen concentration was causally associated with a HR of 1.75 (CI = 1.22–2.51) in the combined cohort analysis for CHD. However, sensitivity analysis using methods robust to pleiotropy arising from independent effects of SNPs on exposure and outcome (which could invalidate MR analyses) suggested a substantially weaker causal effect on CHD even for the model with the strongest effect estimate (OR = 1.18 per 1 g/L higher fibrinogen; CI = 0.98, 1.42), and the MR Egger model showed virtually no evidence of a causal effect–though the wide 95% confidence interval encompassed effects from all other models. Overall, when accounting for potential horizontal pleiotropy, the accumulated evidence points to a substantially weaker casual effect of fibrinogen on CHD than the observational risk ratio of 1.8 (CI = 1.6, 2.0) previously reported [[<reflink idref="bib6" id="ref23">6</reflink>]]. Using rs1800790 in a single variant MR analysis, there was limited evidence of any causal effect, though the 95% confidence interval could not exclude positive estimated causal effects seen in multi-variant analyses. In combination these analyses suggest that after accounting for horizontal pleiotropy the effect of fibrinogen on CHD is likely to be small, if any at all, and that current MR estimates of the potential causal effect remain unable to exclude the null, despite large sample sizes and the latest methodologies. Discrepancies in the estimates of the causal effect of fibrinogen on CHD obtained by different MR approaches are likely to be due to differences in their approach to accounting for horizontal pleiotropy, given the clear influence of such pleiotropy on estimates from observations studies.</p> <hd id="AN0136395773-6">Comparison with previous MR analyses</hd> <p>Previous MR studies assessing the causal effect of fibrinogen on CHD or MI focused exclusively on rs1800790 [[<reflink idref="bib24" id="ref24">24</reflink>], [<reflink idref="bib25" id="ref25">25</reflink>]]. In a few studies one additional variant also in the <emph>FGB</emph> promoter region was examined, however this variant is in nearly complete LD with rs1800790, particularly in Europeans [[<reflink idref="bib16" id="ref26">16</reflink>], [<reflink idref="bib18" id="ref27">18</reflink>]]. The allele score was a better predictor of fibrinogen than rs1800790 alone (Table A in S1 File). Though the allele score estimated a causal effect of fibrinogen on CHD similar to observational studies, much of this appeared to be driven by pleiotropy as estimated effects decreased in models more robust to pleiotropy (Table 2). This highlights the need to balance increased power from multi-variant approaches with the potential for increased pleiotropy in these instruments.</p> <p>For the CHARGE cohorts we used exclusively incident cases whereas previous studies utilized populations composed entirely or primarily of prevalent cases. In some instances, the use of prevalent cases may bias MR studies such as if the disease subsequently what is perceived as a disease risk factor, e.g. if CHD leads to higher fibrinogen as opposed to the reverse, then reverse confounding can still occur even in an MR setting [[<reflink idref="bib26" id="ref28">26</reflink>]]. Additionally, if the risk factor were to affect severity of an event, e.g. the fatality of MI, then use of prevalent cases may dilute the MR-estimated causal effect as the most severe cases may not be observed due to being too ill to participate or suffering a fatal event. This type of prevalence-incidence bias is not exclusive to MR analyses [[<reflink idref="bib27" id="ref29">27</reflink>]–[<reflink idref="bib29" id="ref30">29</reflink>]]. However, care must still be taken when interpreting results from incident case MR studies as the exclusion of prevalent cases is equivalent to conditioning on disease status at baseline. This has the potential to introduce bias in the form of an exclusion restriction violation.[[<reflink idref="bib30" id="ref31">30</reflink>]] Whether bias is introduced and the degree of confounding are dependent on the actual biological processes that account for the relationship between the genetic instrument(s) chosen, the modifiable risk factor, and outcome in the MR analysis. When performing incident case MR it is best to combine the efforts with MR analyses including prevalent cases and interpret results for both with careful consideration towards their underlying assumptions, strengths, and weaknesses.</p> <p>In general, our results are compatible with previous MR studies, however we use more modern methods, including multi-variant, pleiotropy robust methods, able to produce smaller confidence intervals and which indicate that after accounting for pleiotropy there may be a small positive effect of fibrinogen on CHD. This is particularly true for the methods producing the most precise estimates. However, these results warrant further investigations as confidence intervals for some models were still wide and with results for the single variant and MR Egger analyses possibly more consistent with no causal effect than even a small causal effect.</p> <hd id="AN0136395773-7">Strengths and limitations</hd> <p>As with all MR studies the causal effects estimated here are based on regression estimates for genetic variants and are only valid, causal estimates under the assumptions of MR. Additionally, causal estimates generated via MR methodologies are for lifelong, genetically determined increases in the exposure, e.g. fibrinogen, which means that caution should be exercised when applying clinical interpretations or attempting to translate results into estimates of an intervention [[<reflink idref="bib31" id="ref32">31</reflink>], [<reflink idref="bib32" id="ref33">32</reflink>]]. In the initial analysis a meta-analysis was performed across studies which were heterogeneous in their distribution of underlying clinical covariates (Table 1). Though there was heterogeneity in the clinical covariate distribution, the allele score variants were evaluated for associations with these clinical covariates. Additionally, in the two sample MR we used approaches robust to confounding from pleiotropy due to associations between SNPs and other clinical covariates, such as body mass index, which might lie outside any causal pathway linking fibrinogen and CHD. This study had some overlap between studies involved in the GWAS used to select fibrinogen variants and those used in the MR analyses. Our approach to mitigate this was to replicate the allele score analysis in an independent set of cohorts. For the pleiotropy robust 2-sample MR approaches this overlap was unavoidable, however there was no overlap for the cases which means that unbiased estimates should be obtained [[<reflink idref="bib33" id="ref34">33</reflink>]]. A strength of the study is the use of incident cases for the allele score model approach which reduces the potential for bias from reverse confounding (which can still affect MR studies) and prevalence-incidence bias. Additionally, even though the allele score approach was sensitive to horizontal pleiotropy we used an array of additional approaches that were each partially robust to horizontal pleiotropy through different assumptions about the nature of the pleiotropy. These models often have lower power than other approaches, which motivated our use of a previously published GWAS which had 60,801 prevalent cases and 123,504 controls [[<reflink idref="bib34" id="ref35">34</reflink>]]. However, to prevent potential bias and more closely align with our initial analyses, a large sample size of incident cases independent of those used to evaluate associations between genetic variants and fibrinogen would have been preferable.</p> <hd id="AN0136395773-8">Conclusion</hd> <p>Fibrinogen represents an important role in thrombosis, platelet aggregation, and inflammation making it a promising risk factor for CHD. Despite the epidemiological evidence, MR studies using prevalent cases and single variant approaches have consistently shown no causal effect of fibrinogen on CHD. Out results indicate that epidemiologic studies may substantially over-estimate any causal effect of fibrinogen on CHD. While some MR models which accounted for pleiotropy did show a modest causal effect, the 95% confidence intervals still contained the null indicating that researchers should exercise caution in interpreting these results. Though, it may be tempting to relate these results to the utility of fibrinogen in clinical testing, caution is urged in this endeavor. Causal estimates, null or not, are at best imperfect proxies for the potential utility of a biomarker in a clinical setting, and other estimates, e.g. receiver operating characteristic, positive/negative predictive value, are important to consider. Our results suggest any causal effect of fibrinogen on CHD is likely to be small, and resolving any causal effect will require further analyses using larger sample sizes and more precise methods.</p> <hd id="AN0136395773-9">Methods</hd> <p>This study was conducted within the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium [[<reflink idref="bib35" id="ref36">35</reflink>]] using 11 European-ancestry cohorts. For incident CHD, six cohorts participated in the initial (discovery) analyses (N = 15,427), and four cohorts (N = 34,209) contributed data for replication. For incident MI, six cohorts participated in the discovery (N = 18,798), and three cohorts participated in the replication (N = 33,288) analyses. Details on all cohorts are given in the Supplemental Materials and the clinical covariates in Table 1, and Fig 3 outlines all analyses. Data collection analysis for all cohorts was approved by their respective Institutional Review Boards and/or ethical committees, and all cohorts obtained written, informed consent from participants.</p> <hd id="AN0136395773-10">Assessment of CHD and MI</hd> <p>We defined incident CHD as validated, incident fatal or non-fatal CHD events which included: validated hospitalized MI, CHD-related hospitalizations, definite CHD deaths, likely CHD deaths, and CHD-related revascularization procedures, e.g. percutaneous coronary intervention and coronary artery bypass grafting. Incident MI was defined as a validated fatal or non-fatal MI and included definite MI hospitalizations. For cohorts that used questionnaires as a component of the follow-up procedures, all events were corroborated with medical records and/or review by trained medical personnel. Cohort specific details are given in the Supplemental Online Methods.</p> <hd id="AN0136395773-11">Fibrinogen assessment</hd> <p>Fibrinogen was assessed by multiple methods, with seven cohorts using the Clauss method [[<reflink idref="bib36" id="ref37">36</reflink>]]. Of the remaining four cohorts, RS used a clotting time-derived method to assess fibrinogen concentrations, while KORA, MESA, and WGHS used immunological assays to assess total fibrinogen. Comparisons of these three methods have shown that the Class and clotting-time derived methods have very similar means, while the immunological assays can have slightly lower means [[<reflink idref="bib37" id="ref38">37</reflink>]]. However, the correlations between the methods have been reported to be high, with Pearson correlations &gt; 0.95 [[<reflink idref="bib38" id="ref39">38</reflink>]]. Previous studies have also found that effect estimates obtained using the different fibrinogen assessment methods are comparable [[<reflink idref="bib1" id="ref40">1</reflink>], [<reflink idref="bib39" id="ref41">39</reflink>], [<reflink idref="bib40" id="ref42">40</reflink>]]. We also did not observe heterogeneity in effect estimates by fibrinogen assessment method.</p> <hd id="AN0136395773-12">Genotyping and imputation</hd> <p>Genotyping and imputation were performed separately in all cohorts, per published methods [[<reflink idref="bib41" id="ref43">41</reflink>]]. All participating studies used either the HapMap build 36 [[<reflink idref="bib42" id="ref44">42</reflink>]], 1000 Genomes phase I version 3, or 1000 Genomes phase I version 2 reference panel for imputation [[<reflink idref="bib43" id="ref45">43</reflink>]]. Imputation was performed via MACH[[<reflink idref="bib44" id="ref46">44</reflink>]] or IMPUTE [[<reflink idref="bib45" id="ref47">45</reflink>]]. Low quality variants were excluded in line with previously published approaches: MACH imputation quality &lt; 0.3 or IMPUTE imputation quality &lt; 0.4 [[<reflink idref="bib41" id="ref48">41</reflink>]].</p> <hd id="AN0136395773-13">Creation of the allele score</hd> <p>We evaluated 69 variants associated with fibrinogen in at least one of three recent genome/exome-wide association studies [[<reflink idref="bib2" id="ref49">2</reflink>], [<reflink idref="bib19" id="ref50">19</reflink>], [<reflink idref="bib41" id="ref51">41</reflink>]] for inclusion into the allele score [[<reflink idref="bib46" id="ref52">46</reflink>]]. We applied four criteria to each variant to improve the plausibility that each meets the MR assumptions. First, to ensure that the variants were not correlated with known risk factors for cardiovascular disease (CVD), the Spearman correlation between each of the variants and body mass index (BMI), low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, type 2 diabetes mellitus (binary), hypertension (binary), and smoking (ever, never, current) was tested within each cohort and any variants with a Spearman correlation greater than 0.10 in any cohort for any of these outcomes were removed. Second, the variants were tested for linkage disequilibrium (LD) with known CHD loci [[<reflink idref="bib34" id="ref53">34</reflink>], [<reflink idref="bib47" id="ref54">47</reflink>]–[<reflink idref="bib56" id="ref55">56</reflink>]] using SNAP from the Broad Institute with LD patterns coming from European ancestry individuals [[<reflink idref="bib57" id="ref56">57</reflink>]]. As no variant had r<sups>2</sups> &gt; 0.20 with a CHD locus, they were considered independent of known CHD loci. Next, we reduced pairs of variants in high LD (r<sups>2</sups> &gt; 0.70) by preferentially retaining those variants that were found in the largest genome-wide scan [[<reflink idref="bib41" id="ref57">41</reflink>]]. Finally, we eliminated any variants that were missing across any of the discovery cohorts, leaving 38 variants that composed the allele score (Table D in S1 File). We tested the allele score for association with each of the aforementioned CHD risk factors in each cohort as well as in a meta-analysis of all cohorts. The allele score was not associated with any CHD risk factor in the meta-analysis after a Bonferroni correction for the six tests performed (P &gt; 0.008; Table E in S1 File). Six variants from the allele score which were unavailable in one or more replication cohorts were removed from the allele score in the replication phase to ensure a consistent allele score in the replication meta-analysis (Table D in S1 File). In a sensitivity analysis these variants were also removed from the discovery cohorts and the causal effect evaluated in a combined meta-analysis.</p> <p>Each genotype was aligned prior to summing to create the score so that the designated effect allele corresponded to a positive association with fibrinogen according to the direction of effect in the largest and most recent fibrinogen GWAS [[<reflink idref="bib19" id="ref58">19</reflink>]].</p> <hd id="AN0136395773-14">Mendelian randomization</hd> <p>MR is a powerful framework that uses genetic variants as instrumental variables to infer causal relationships between a defined exposure and outcome. The causal effect estimated by MR is the alteration in exposure due to genetic variation and is thus assumed to be over the entire life course. There are three assumptions for a genetic variant to be a valid instrument for MR [[<reflink idref="bib58" id="ref59">58</reflink>]]</p> <p></p> <ulist> <item> The genetic variant is independent of confounders of exposure and outcome under examination</item> <p></p> <item> The genetic variant is associated with the exposure</item> <p></p> <item> The genetic variant is independent of the outcome conditional on the exposure and any confounders</item> </ulist> <p>In addition to these three conditions, valid estimates from MR are dependent on any parametric assumptions of the model being used to estimate relevant coefficients and standard errors.</p> <p>Our initial MR analyses used a two-stage procedure employing a Cox regression model (2SC). To improve power, we regressed fibrinogen on age and sex and used the resulting residuals as input to the 2SC analyses. In the first stage of the 2SC procedure the fibrinogen residuals were regressed on the allele score. In the second stage the predicted values from the first stage regression were associated with incident MI or CHD via a Cox proportional hazards model. This approach is similar to the two-stage predictor-substitution MR approach [[<reflink idref="bib59" id="ref60">59</reflink>]–[<reflink idref="bib61" id="ref61">61</reflink>]], and results from the 2SC model are given per unit (g/L) increase in the fibrinogen residuals. We used a fixed effects model for all meta-analyses since we observed little heterogeneity according to the Q-statistics [[<reflink idref="bib62" id="ref62">62</reflink>]] (P(Q) &gt; 0.05 for all analyses). We also compared associations with our allele score to those obtained using a single variant, FGB -455G&gt;A (rs1800790), which is a commonly used variant for fibrinogen MR analyses [[<reflink idref="bib16" id="ref63">16</reflink>], [<reflink idref="bib18" id="ref64">18</reflink>]]. We tested the allele score in the discovery cohorts and replication cohorts separately as well as in a combined meta-analysis. We separated the discovery and replication cohorts to evaluate any evidence for bias produced by selecting the variants for the allele score and testing the association of the allele score with incident CHD and MI both in the discovery cohort. As the replication cohort was not used to select variants for the allele score it would not suffer from such bias.</p> <p>We performed sensitivity analyses using four pleiotropy robust methods each of which uses a different approach to partially relax the no horizontal pleiotropy assumption of MR analyses:[[<reflink idref="bib63" id="ref65">63</reflink>]] MR-Egger [[<reflink idref="bib58" id="ref66">58</reflink>]], MR mode based estimate (MBE),[[<reflink idref="bib64" id="ref67">64</reflink>]] MR PRESSO [[<reflink idref="bib65" id="ref68">65</reflink>]], and Weighted median [[<reflink idref="bib66" id="ref69">66</reflink>]]. For these sensitivity analyses, we used the prevalent CHD and MI GWAS results from CARDIoGRAMplusC4D consortium [[<reflink idref="bib34" id="ref70">34</reflink>]] as it had a larger sample size (60,801 prevalent cases and 123,504 controls) and these methods often have lower power to detect effects. For estimates of variant effects on fibrinogen we used fixed-effects meta-analysis estimates from the 11 cohorts in these analyses. Since an individual cannot be both a prevalent and incident CHD or MI case at the same sampling, there was no overlap amongst the cases between our incident analyses and the prevalent cases used in the CARDIoGRAMplusC4D GWAS. There would still be some overlap amongst the non-cases/controls which could bias estimates towards the null.</p> <p>We also examined whether fibrinogen showed evidence for a causal effect on 7 metabolic CHD risk factors using MR-base (<ulink href="http://www.mrbase.org/">http://www.mrbase.org/</ulink>), a database of published GWAS available for MR [[<reflink idref="bib67" id="ref71">67</reflink>]]. We focused on metabolic CHD risk factors as initial results indicated that body mass index was the trait with which our allele score showed the strongest evidence for pleiotropy—potentially horizontal (i.e. SNPs affecting fibrinogen and CHD via independent pathways) and vertical (i.e. fibrinogen-associated SNPs also associated with risk factors downstream of fibrinogen) as the associations did not distinguish between the two. The CHD risk factors were body mass index [[<reflink idref="bib68" id="ref72">68</reflink>]], waist circumference [[<reflink idref="bib69" id="ref73">69</reflink>]], waist-to-hip ratio [[<reflink idref="bib69" id="ref74">69</reflink>]], low-density lipoprotein cholesterol [[<reflink idref="bib70" id="ref75">70</reflink>]], triglycerides [[<reflink idref="bib70" id="ref76">70</reflink>]], homeostatic model assessment insulin resistance (HOMA-IR) [[<reflink idref="bib71" id="ref77">71</reflink>]], and Type 2 diabetes [[<reflink idref="bib72" id="ref78">72</reflink>]]. As MR-base only contains published GWAS we used the most recently published GWAS for fibrinogen for our variant-fibrinogen associations [[<reflink idref="bib1" id="ref79">1</reflink>]] but limited to those variants present in our allele score. For the CHD risk factors we compared causal effect estimates obtained from the inverse variance weighted method (which assumes no unbalanced horizontal pleiotropy), to those from the pleiotropy robust MR Egger, and Weighted median methods. All three methodologies were implemented in MR-base.</p> <p>Statistical analyses were performed in R [[<reflink idref="bib73" id="ref80">73</reflink>]]. Meta-analyses were performed using the R package <emph>metaphor</emph> [[<reflink idref="bib74" id="ref81">74</reflink>]]. Cox models were estimated via the <emph>coxph</emph> function in the R package survival [[<reflink idref="bib75" id="ref82">75</reflink>]] with the exception of SHIP where the <emph>survreg</emph> function was used with an exponential distribution to account for the interval censored data. MR-Egger and weighted median results were performed using the R package <emph>MendelianRandomization</emph> and <emph>Two Sample MR</emph> [[<reflink idref="bib67" id="ref83">67</reflink>]]. MR MBE analyses were performed using the methods given by Hartwig <emph>et al</emph> [[<reflink idref="bib64" id="ref84">64</reflink>]]. The default bandwidth (φ = 1) was used for MR MBE as results did not show sensitivity to the choice of bandwidth. MR PRESSO analyses were performed using code available at the MR PRESSO GitHub repository (https://github.com/rondolab/MR-PRESSO) [[<reflink idref="bib65" id="ref85">65</reflink>]]. We used the robust MR estimates from MR PRESSO which are equivalent to performing an inverse-variance weighted MR analysis after removing outlying variants, which may be influenced by horizontal pleiotropy, as identified by MR PRESSO. Results from the 2SC model are reported in terms of the hazard ratio (HR), while all results that utilize the prevalent disease GWAS are reported in terms of the odds ratio (OR). All HR and OR are given per 1 g/L higher fibrinogen. All confidence intervals (CI) reported are 95% CI.</p> <hd id="AN0136395773-15">Supporting information</hd> <p>S1 File. Supplemental Methods and Tables v2. File containing the Supplemental Online Methods (including cohort specific information) as well as the Supplemental Tables (A-E). <bold>Table A. Association between allele score (AS) and fibrinogen as well as rs1800790 (FGB -455G&gt;A) and fibrinogen.</bold> Table contains association between AS and fibrinogen as well as the association between <emph>FGB</emph> variant rs1800790 with fibrinogen. Also given is the association between the AS and fibrinogen after rescaling (RS) the AS in each cohort so that a unit of 1 represented 50% of the range. This transformation allows the allele score associations to be more directly compared with those for rs1800790. Rs1800790 was unavailable in SHIP. The meta-analysis represents a fixed effects meta-analysis <bold>Table B. Comparison of allele score and rs1800790 as genetic instruments for CHD.</bold> Comparison of the allele score vs rs1800790 as a genetic instrument for CHD. 2SC = two-stage Cox (2SC) model; CI = 95% confidence interval; HR = Hazard Ratio; MR = Mendelian Randomization; OR = Odds Ratio; Q = Cochran's Q; SE = standard error. <bold>Table C. Estimates of causal effect of fibrinogen on metabolic CHD risk factors.</bold> As body mass index was the coronary heart disease (CHD) trait with the most evidence for pleiotropic effects from our allele score we used 3 Mendelian Randomization (MR) methods from as implemented in MR-base (<ulink href="http://www.mrbase.org/">http://www.mrbase.org/</ulink>)[[<reflink idref="bib4" id="ref86">4</reflink>]]. MR-base uses published genome-wide association studies (GWAS) to perform 2-sample MR. For the genetic variant-fibrinogen associations we used the most recently published fibrinogen GWAS.[[<reflink idref="bib5" id="ref87">5</reflink>]] References and sample sizes for each of the CHD risk factor outcomes appear in the table. Only variants that were a part of the allele score were used in the MR analyses, with each GWAS having between 23 and 32 of the 38 variants represented. HOMA-IR = homeostatic model assessment insulin resistance; LDL = low-density lipoprotein, OR = odds ratio; SD = standard deviation; SE = standard error; SNP = single nucleotide polymorphism. <bold>Table D. Allele Score Variants</bold>. Variants which composed the allele score along with their availability in each cohort as well as selection from either the 1000 Genomes imputation GWAS by de Vries et al,[[<reflink idref="bib1" id="ref88">1</reflink>]] the meta-analysis by Sabater-Lleal et al,[[<reflink idref="bib2" id="ref89">2</reflink>]] or the rare and low-frequency variant meta-analysis by Huffman et al,[[<reflink idref="bib3" id="ref90">3</reflink>]] and the published direction of association. NA indicates that the variant was not available. All variants were available for all discovery cohorts by design, thus only the replication cohorts (MESA, WGHS, LURIC, and SHIP) are listed where one or more variants may have been missing. Closest Gene = gene annotation based on location within a gene or the closest gene for intergenic variants; Locus = genomic location; Published Direction of Association = direction of association for the variant in the given study; Study = published study variant was taken from. <bold>Table E. Association of allele score with CHD risk factors</bold>. Fixed effects meta-analysis for association between fibrinogen and CHD risk factors. Fixed effects meta-analysis was used for all associations despite some evidence for heterogeneity for HDL P(Q) &lt; 0.05. The association was still not significant in the random effects meta-analysis. Hypertension and Type II Diabetes were binary variables. Smoking was a categorical outcome for current, former, or never smokers. Beta = meta-analysis effect estimate; SE = meta-analysis standard error; P = meta-analysis P; Q = Cochran's Q; P(Q) = P-value associated with Cochran's Q. (DOC)</p> <p>S2 File. PLoS One Fib MR PRISMA 2009 checklist. (DOC)</p> <p>DIAGRAM: Fig 1: CHD Forest plot. Forest plot of the CHD MR analysis for the discovery, replication, and combined sets of cohorts. Shown beside each cohort name is the sample size and number of incident CHD events given as (N events; N total). CHD = coronary heart disease; FE = fixed-effects; HR = hazard ratio; CI = confidence interval.</p> <p>DIAGRAM: Fig 2: MI Forest plot. Forest plot of the MI MR analysis for the discovery, replication, and combined sets of cohorts. Shown beside each cohort name is the sample size and number of incident MI events given as (N events; N total). MI = myocardial infarction, FE = fixed-effects, HR = hazard ratio, CI = confidence interval.</p> <p>DIAGRAM: Fig 3: Study outline. Outline of analyses using the allele score, rs1800790 and 2 Sample MR approaches including the analytic method used to estimate the causal effect, subject to valid MR assumptions, for all stages of the analysis. 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Hartwig, Methodology; Jack Bowden, Methodology; Gibran Hemani, Methodology; Martina Müller-Nuraysid, Resources; Konstantin Strauch, Supervision; Wolfgang Koenig, Writing – review &amp; editing; Melanie Waldenberger, Supervision; Thomas Meitinger, Resources; Nathan Pankratz, Writing – review &amp; editing; Eric Boerwinkle, Funding acquisition; Weihong Tang, Writing – review &amp; editing; Yi-Ping Fu, Supervision; Andrew D. Johnson, Writing – review &amp; editing; Ci Song, Writing – review &amp; editing; Moniek P. M. de Maat, Supervision; André G. Uitterlinden, Supervision; Oscar H. Franco, Supervision; Jennifer A. Brody, Writing – review &amp; editing; Barbara McKnight, Writing – review &amp; editing; Yii-Der Ida Chen, Supervision; Bruce M. Psaty, Writing – review &amp; editing; Rasika A. Mathias, Writing – review &amp; editing; Diane M. Becker, Supervision; Patricia A. Peyser, Supervision; Jennifer A. Smith, Supervision; Suzette J. Bielinski, Writing – review &amp; editing; Paul M. Ridker, Writing – review &amp; editing; Kent D. Taylor, Writing – review &amp; editing; Jie Yao, Supervision; Russell Tracy, Supervision; Graciela Delgado, Supervision; Stella Trompet, Supervision; Naveed Sattar, Writing – review &amp; editing; J. Wouter Jukema, Supervision; Lewis C. Becker, Supervision; Sharon L. R. Kardia, Supervision; Jerome I. Rotter, Supervision; Winfried März, Supervision; Marcus Dörr, Writing – review &amp; editing; Daniel I. Chasman, Supervision; Abbas Dehghan, Supervision; Christopher J. O’Donnell, Supervision; Nicholas L. Smith, Supervision; Annette Peters, Writing – review &amp; editing and Alanna C. 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| Items | – Name: Title Label: Title Group: Ti Data: Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Cavin+K+Ward-Caviness%22">Cavin K Ward-Caviness</searchLink><br /><searchLink fieldCode="AR" term="%22Paul+S+de+Vries%22">Paul S de Vries</searchLink><br /><searchLink fieldCode="AR" term="%22Kerri+L+Wiggins%22">Kerri L Wiggins</searchLink><br /><searchLink fieldCode="AR" term="%22Jennifer+E+Huffman%22">Jennifer E Huffman</searchLink><br /><searchLink fieldCode="AR" term="%22Lisa+R+Yanek%22">Lisa R Yanek</searchLink><br /><searchLink fieldCode="AR" term="%22Lawrence+F+Bielak%22">Lawrence F Bielak</searchLink><br /><searchLink fieldCode="AR" term="%22Franco+Giulianini%22">Franco Giulianini</searchLink><br /><searchLink fieldCode="AR" term="%22Xiuqing+Guo%22">Xiuqing Guo</searchLink><br /><searchLink fieldCode="AR" term="%22Marcus+E+Kleber%22">Marcus E Kleber</searchLink><br /><searchLink fieldCode="AR" term="%22Tim+Kacprowski%22">Tim Kacprowski</searchLink><br /><searchLink fieldCode="AR" term="%22Stefan+Groß%22">Stefan Groß</searchLink><br /><searchLink fieldCode="AR" term="%22Astrid+Petersman%22">Astrid Petersman</searchLink><br /><searchLink fieldCode="AR" term="%22George+Davey+Smith%22">George Davey Smith</searchLink><br /><searchLink fieldCode="AR" term="%22Fernando+P+Hartwig%22">Fernando P Hartwig</searchLink><br /><searchLink fieldCode="AR" term="%22Jack+Bowden%22">Jack Bowden</searchLink><br /><searchLink fieldCode="AR" term="%22Gibran+Hemani%22">Gibran Hemani</searchLink><br /><searchLink fieldCode="AR" term="%22Martina+Müller-Nuraysid%22">Martina Müller-Nuraysid</searchLink><br /><searchLink fieldCode="AR" term="%22Konstantin+Strauch%22">Konstantin Strauch</searchLink><br /><searchLink fieldCode="AR" term="%22Wolfgang+Koenig%22">Wolfgang Koenig</searchLink><br /><searchLink fieldCode="AR" term="%22Melanie+Waldenberger%22">Melanie Waldenberger</searchLink><br /><searchLink fieldCode="AR" term="%22Thomas+Meitinger%22">Thomas Meitinger</searchLink><br /><searchLink fieldCode="AR" term="%22Nathan+Pankratz%22">Nathan Pankratz</searchLink><br /><searchLink fieldCode="AR" term="%22Eric+Boerwinkle%22">Eric Boerwinkle</searchLink><br /><searchLink fieldCode="AR" term="%22Weihong+Tang%22">Weihong Tang</searchLink><br /><searchLink fieldCode="AR" term="%22Yi-Ping+Fu%22">Yi-Ping Fu</searchLink><br /><searchLink fieldCode="AR" term="%22Andrew+D+Johnson%22">Andrew D Johnson</searchLink><br /><searchLink fieldCode="AR" term="%22Ci+Song%22">Ci Song</searchLink><br /><searchLink fieldCode="AR" term="%22Moniek+P+M+de+Maat%22">Moniek P M de Maat</searchLink><br /><searchLink fieldCode="AR" term="%22André+G+Uitterlinden%22">André G Uitterlinden</searchLink><br /><searchLink fieldCode="AR" term="%22Oscar+H+Franco%22">Oscar H Franco</searchLink><br /><searchLink fieldCode="AR" term="%22Jennifer+A+Brody%22">Jennifer A Brody</searchLink><br /><searchLink fieldCode="AR" term="%22Barbara+McKnight%22">Barbara McKnight</searchLink><br /><searchLink fieldCode="AR" term="%22Yii-Der+Ida+Chen%22">Yii-Der Ida Chen</searchLink><br /><searchLink fieldCode="AR" term="%22Bruce+M+Psaty%22">Bruce M Psaty</searchLink><br /><searchLink fieldCode="AR" term="%22Rasika+A+Mathias%22">Rasika A Mathias</searchLink><br /><searchLink fieldCode="AR" term="%22Diane+M+Becker%22">Diane M Becker</searchLink><br /><searchLink fieldCode="AR" term="%22Patricia+A+Peyser%22">Patricia A Peyser</searchLink><br /><searchLink fieldCode="AR" term="%22Jennifer+A+Smith%22">Jennifer A Smith</searchLink><br /><searchLink fieldCode="AR" term="%22Suzette+J+Bielinski%22">Suzette J Bielinski</searchLink><br /><searchLink fieldCode="AR" term="%22Paul+M+Ridker%22">Paul M Ridker</searchLink><br /><searchLink fieldCode="AR" term="%22Kent+D+Taylor%22">Kent D Taylor</searchLink><br /><searchLink fieldCode="AR" term="%22Jie+Yao%22">Jie Yao</searchLink><br /><searchLink fieldCode="AR" term="%22Russell+Tracy%22">Russell Tracy</searchLink><br /><searchLink fieldCode="AR" term="%22Graciela+Delgado%22">Graciela Delgado</searchLink><br /><searchLink fieldCode="AR" term="%22Stella+Trompet%22">Stella Trompet</searchLink><br /><searchLink fieldCode="AR" term="%22Naveed+Sattar%22">Naveed Sattar</searchLink><br /><searchLink fieldCode="AR" term="%22J+Wouter+Jukema%22">J Wouter Jukema</searchLink><br /><searchLink fieldCode="AR" term="%22Lewis+C+Becker%22">Lewis C Becker</searchLink><br /><searchLink fieldCode="AR" term="%22Sharon+L+R+Kardia%22">Sharon L R Kardia</searchLink><br /><searchLink fieldCode="AR" term="%22Jerome+I+Rotter%22">Jerome I Rotter</searchLink><br /><searchLink fieldCode="AR" term="%22Winfried+März%22">Winfried März</searchLink><br /><searchLink fieldCode="AR" term="%22Marcus+Dörr%22">Marcus Dörr</searchLink><br /><searchLink fieldCode="AR" term="%22Daniel+I+Chasman%22">Daniel I Chasman</searchLink><br /><searchLink fieldCode="AR" term="%22Abbas+Dehghan%22">Abbas Dehghan</searchLink><br /><searchLink fieldCode="AR" term="%22Christopher+J+O'Donnell%22">Christopher J O'Donnell</searchLink><br /><searchLink fieldCode="AR" term="%22Nicholas+L+Smith%22">Nicholas L Smith</searchLink><br /><searchLink fieldCode="AR" term="%22Annette+Peters%22">Annette Peters</searchLink><br /><searchLink fieldCode="AR" term="%22Alanna+C+Morrison%22">Alanna C Morrison</searchLink> – Name: TitleSource Label: Source Group: Src Data: PLoS ONE, Vol 14, Iss 5, p e0216222 (2019) – Name: Publisher Label: Publisher Information Group: PubInfo Data: Public Library of Science (PLoS), 2019. – Name: DatePubCY Label: Publication Year Group: Date Data: 2019 – Name: Subset Label: Collection Group: HoldingsInfo Data: LCC:Medicine<br />LCC:Science – Name: Subject Label: Subject Terms Group: Su Data: <searchLink fieldCode="DE" term="%22Medicine%22">Medicine</searchLink><br /><searchLink fieldCode="DE" term="%22Science%22">Science</searchLink> – Name: Abstract Label: Description Group: Ab Data: BackgroundFibrinogen is an essential hemostatic factor and cardiovascular disease risk factor. Early attempts at evaluating the causal effect of fibrinogen on coronary heart disease (CHD) and myocardial infraction (MI) using Mendelian randomization (MR) used single variant approaches, and did not take advantage of recent genome-wide association studies (GWAS) or multi-variant, pleiotropy robust MR methodologies.Methods and findingsWe evaluated evidence for a causal effect of fibrinogen on both CHD and MI using MR. We used both an allele score approach and pleiotropy robust MR models. The allele score was composed of 38 fibrinogen-associated variants from recent GWAS. Initial analyses using the allele score used a meta-analysis of 11 European-ancestry prospective cohorts, free of CHD and MI at baseline, to examine incidence CHD and MI. We also applied 2 sample MR methods with data from a prevalent CHD and MI GWAS. Results are given in terms of the hazard ratio (HR) or odds ratio (OR), depending on the study design, and associated 95% confidence interval (CI). In single variant analyses no causal effect of fibrinogen on CHD or MI was observed. In multi-variant analyses using incidence CHD cases and the allele score approach, the estimated causal effect (HR) of a 1 g/L higher fibrinogen concentration was 1.62 (CI = 1.12, 2.36) when using incident cases and the allele score approach. In 2 sample MR analyses that accounted for pleiotropy, the causal estimate (OR) was reduced to 1.18 (CI = 0.98, 1.42) and 1.09 (CI = 0.89, 1.33) in the 2 most precise (smallest CI) models, out of 4 models evaluated. In the 2 sample MR analyses for MI, there was only very weak evidence of a causal effect in only 1 out of 4 models.ConclusionsA small causal effect of fibrinogen on CHD is observed using multi-variant MR approaches which account for pleiotropy, but not single variant MR approaches. Taken together, results indicate that even with large sample sizes and multi-variant approaches MR analyses still cannot exclude the null when estimating the causal effect of fibrinogen on CHD, but that any potential causal effect is likely to be much smaller than observed in epidemiological studies. – Name: TypeDocument Label: Document Type Group: TypDoc Data: article – Name: Format Label: File Description Group: SrcInfo Data: electronic resource – Name: Language Label: Language Group: Lang Data: English – Name: ISSN Label: ISSN Group: ISSN Data: 1932-6203 – Name: NoteTitleSource Label: Relation Group: SrcInfo Data: https://doaj.org/toc/1932-6203 – Name: DOI Label: DOI Group: ID Data: 10.1371/journal.pone.0216222 – Name: URL Label: Access URL Group: URL Data: <link linkTarget="URL" linkTerm="https://doaj.org/article/138107b510a249878e58480e248bba04" linkWindow="_blank">https://doaj.org/article/138107b510a249878e58480e248bba04</link> – Name: AN Label: Accession Number Group: ID Data: edsdoj.138107b510a249878e58480e248bba04 |
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