Shared genetic basis connects smoking behaviors and bone health: insights from a genome-wide cross-trait analysis

Author:

Qin Chenjiarui12ORCID,Zhang Wenqiang32,Xiao Changfeng32,Qu Yang32,Xiao Jinyu32,Wu Xueyao324,Zhang Li32,Wang Yutong32,He Lin32,Zhu Jingwei32,Wang Wenzhi52,Li Yun12,Sun Lei52,Jiang Xia123267

Affiliation:

1. Department of Nutrition and Food Hygiene , West China School of Public Health and West China Fourth Hospital, , Chengdu, Sichuan, 610041 , China

2. Sichuan University , West China School of Public Health and West China Fourth Hospital, , Chengdu, Sichuan, 610041 , China

3. Department of Epidemiology and Biostatistics , West China School of Public Health and West China Fourth Hospital, , Chengdu, Sichuan, 610041 , China

4. National Cancer Institute , Rockville, MD 610041 , United States

5. Department of Osteoporosis/Rheumatology , West China School of Public Health and West China Fourth Hospital, , Chengdu, Sichuan, 610041 , China

6. Department of Clinical Neuroscience , Center for Molecular Medicine, , Solna, Stockholm, 17177 , Sweden

7. Karolinska Institute , Center for Molecular Medicine, , Solna, Stockholm, 17177 , Sweden

Abstract

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.

Funder

Karolinska Institute

Science Fund for Creative Research Groups of Science and Technology Bureau of Sichuan Province

Publisher

Oxford University Press (OUP)

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