| Title: |
Shared genetic basis connects smoking behaviors and bone health: insights from a genome-wide cross-trait analysis. |
| Authors: |
Qin, Chenjiarui, Zhang, Wenqiang, Xiao, Changfeng, Qu, Yang, Xiao, Jinyu, Wu, Xueyao, Zhang, Li, Wang, Yutong, He, Lin, Zhu, Jingwei, Wang, Wenzhi, Li, Yun, Sun, Lei, Jiang, Xia |
| Source: |
Journal of Bone & Mineral Research; Jul2024, Vol. 39 Issue 7, p918-928, 11p |
| Abstract: |
Although the negative association of tobacco smoking with osteoporosis is well-documented, little is known regarding the shared genetic basis underlying these conditions. In this study, we aim to investigate a shared genetic architecture between smoking and heel estimated bone mineral density (eBMD), a reliable proxy for osteoporosis. We conducted a comprehensive genome-wide cross-trait analysis to identify genetic correlation, pleiotropic loci and causal relationship of smoking with eBMD, leveraging summary statistics of the hitherto largest genome-wide association studies conducted in European ancestry for smoking initiation (Nsmoker = 1 175 108, Nnonsmoker = 1 493 921), heaviness (cigarettes per day, N = 618 489), cessation (Ncurrent smoker = 304 244, Nformer smoker = 843 028), and eBMD (N = 426 824). A significant negative global genetic correlation was found for smoking cessation and eBMD (${r}_g$ = −0.051, P = 0.01), while we failed to identify a significant global genetic correlation of smoking initiation or heaviness with eBMD. Partitioning the whole genome into independent blocks, we observed 6 significant shared local signals for smoking and eBMD, with 22q13.1 showing the strongest regional genetic correlation. Such a genetic overlap was further supported by 71 pleiotropic loci identified in the cross-trait meta-analysis. Mendelian randomization identified no causal effect of smoking initiation (beta = −0.003 g/cm2, 95% CI = −0.033 to 0.027) or heaviness (beta = −0.017 g/cm2, 95% CI = −0.072 to 0.038) on eBMD, but a putative causal effect of genetic predisposition to being a current smoker was associated with a lower eBMD compared to former smokers (beta = −0.100 g/cm2, 95% CI = −0.181 to −0.018). Our study demonstrates a pronounced biological pleiotropy as well as a putative causal link between current smoking status and eBMD, providing novel insights into the primary prevention and modifiable intervention of osteoporosis by advocating individuals to avoid, reduce or quit smoking as early as possible. Lay Summary: We conducted a comprehensive genome-wide cross-trait analysis to investigate the shared genetic basis and causal relationship underlying smoking and osteoporosis. Our findings revealed that smoking and eBMD are inherently linked through biological pleiotropy. Importantly, our study discovered that quitting smoking significantly reduced the risk of lower eBMD. We recommend individuals to avoid, reduce, or quit smoking as early as possible to protect bone health. [ABSTRACT FROM AUTHOR] |
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| Database: |
Complementary Index |
