Plasma thrombin-activatable fibrinolysis inhibitor and the 1040C/T polymorphism are risk factors for diabetic kidney disease in Chinese patients with type 2 diabetes

Bibliographic Details
Title: Plasma thrombin-activatable fibrinolysis inhibitor and the 1040C/T polymorphism are risk factors for diabetic kidney disease in Chinese patients with type 2 diabetes
Authors: Qinghua Huang, Dujin Feng, Lianlian Pan, Huan Wang, Yan Wu, Bin Zhong, Jianguang Gong, Huijun Lin, Xianming Fei
Source: PeerJ, Vol 11, p e16352 (2023)
Publisher Information: PeerJ Inc., 2023.
Publication Year: 2023
Collection: LCC:Medicine
LCC:Biology (General)
Subject Terms: Diabetic microangiopathy, Diabetic kidney disease, Thrombin-activatable fibrinolysis inhibitor, 1040C/T polymorphism, Risk factor, Medicine, Biology (General), QH301-705.5
More Details: Background Inflammatory and hemostatic disorders in diabetic microangiopathy (DMA) can be linked to thrombin-activatable fibrinolysis inhibitor (TAFI) and its own gene polymorphisms. Thus, the study aimed to investigate the associations of plasma TAFI and gene polymorphisms with DMA in Chinese patients with type 2 diabetes (T2D). Methods Plasma TAFI of 223 patients with T2D was measured, and the genotypes and alleles of the 1040C/T, 438G/A, and 505G/A polymorphisms of the TAFI gene were analyzed. A ROC curve was constructed to evaluate the identifying power of TAFI between patients with T2D and DMA, and logistic regression analysis was used to observe the correlation of plasma TAFI and gene polymorphisms with the risk for DMA. Results Plasma TAFI was higher in patients with DMA than in patients with only T2D (p < 0.05). TAFI exhibited the largest area under ROC in identifying diabetic kidney disease (DKD) from only T2D (0.763, 95% CI [0.674–0.853], p < 0.01), and adjusted multivariate analysis showed a high odds ratio (OR: 15.72, 95% CI [4.573–53.987], p < 0.001) for DKD. Higher frequencies of the CT genotype and T allele of the 1040C/T polymorphism were found in DKD compared with only T2D (respectively p < 0.05), and the CT genotype exhibited a high OR (1.623, 95% CI [1.173–2.710], p < 0.05) for DKD. DKD patients with the CT genotype had higher plasma TAFI levels, while T2D and DKD patients with CC/TT genotypes had lower plasma TAFI levels. Conclusion Plasma TAFI and the CT genotype and T allele of the 1040C/T polymorphism are independent risk factors for DKD in Chinese T2D patients.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2167-8359
Relation: https://peerj.com/articles/16352.pdf; https://peerj.com/articles/16352/; https://doaj.org/toc/2167-8359
DOI: 10.7717/peerj.16352
Access URL: https://doaj.org/article/c6e755321c5849c89509d9f629ac08ea
Accession Number: edsdoj.6e755321c5849c89509d9f629ac08ea
Database: Directory of Open Access Journals
More Details
ISSN:21678359
DOI:10.7717/peerj.16352
Published in:PeerJ
Language:English