Abstract
奚玉娥,高文静,吕筠,余灿清,王胜锋,黄涛,孙点剑一,廖春晓,逄增昌,俞敏,汪华,吴先萍,董忠,吴凡,江国虹,王晓节,刘彧,邓健,陆林,曹卫华,李立明.基于中国双生子人群的冠心病遗传-BMI交互作用研究[J].Chinese journal of Epidemiology,2021,42(9):1573-1579
基于中国双生子人群的冠心病遗传-BMI交互作用研究
Gene-body mass index interaction on coronary heart disease in Chinese adult twins
Received:November 30, 2020  
DOI:10.3760/cma.j.cn112338-20201130-01362
KeyWord: 冠心病  体质指数  遗传-环境交互作用  双生子研究
English Key Word: Coronary heart disease  Body mass index  Gene-environment interaction  Twin study
FundProject:公益性行业科研专项(201502006,201002007);国家自然科学基金(81711530051)
Author NameAffiliationE-mail
Xi Yu'e Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Gao Wenjing Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Lyu Jun Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Yu Canqing Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Wang Shengfeng Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Huang Tao Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Sun Dianjianyi Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Liao Chunxiao Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Pang Zengchang Qingdao Municipal Center for Disease Control and Prevention, Qingdao 266033, China  
Yu Min Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou 310051, China  
Wang Hua Jiangsu Provincial Center for Disease Control and Prevention, Nanjing 210009, China  
Wu Xianping Sichuan Center for Disease Control and Prevention, Chengdu 610041, China  
Dong Zhong Beijing Center for Disease Prevention and Control, Beijing 100013, China  
Wu Fan Shanghai Municipal Center for Disease Control and Prevention, Shanghai 200336, China  
Jiang Guohong Tianjin Centers for Disease Control and Prevention, Tianjin 300011, China  
Wang Xiaojie Qinghai Center for Diseases Prevention and Control, Xining 810007, China  
Liu Yu Heilongjiang Provincial Center for Disease Control and Prevention, Harbin 150030, China  
Deng Jian Handan Center for Disease Control and Prevention, Handan 056001, China  
Lu Lin Yunnan Center for Disease Control and Prevention, Kunming 650034, China  
Cao Weihua Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China caoweihua60@163.com 
Li Liming Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
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Abstract:
      目的 分析冠心病患病的遗传-BMI交互作用。方法 利用中国双生子登记系统募集的20 340对≥ 25岁的同性别双生子,构建单变量遗传-环境交互作用模型,通过评估BMI对冠心病遗传效应的修饰作用反映冠心病的遗传-BMI交互作用。结果 调整年龄后,在男性中发现BMI对冠心病患病受到的遗传效应有负向修饰作用,遗传效应修饰系数(βa)及95% CI为-0.14(-0.22~-0.04),说明log-BMI每增加1个标准差,冠心病的遗传通径系数减小0.14,从而导致冠心病的遗传效应减小。而且低BMI(<24.0 kg/m2)男性冠心病患病的遗传度为0.77(0.65~0.86),而高BMI(≥ 24.0 kg/m2)组对应模型中的遗传度为0.56(0.33~0.74)。在女性中未观察到冠心病的遗传-BMI交互作用。结论 中国成年男性双生子人群中发现冠心病患病的遗传-BMI交互作用,且遗传因素在低BMI组冠心病患病中发挥更重要的作用。
English Abstract:
      Objective To explore the gene-body mass index (BMI) interaction on coronary heart disease (CHD) in the Chinese adult twins. Methods A total of 20 340 same-sex twin pairs registered in the Chinese National Twin Registry (CNTR) were enrolled in this study. Classical twin structure equation model was used to estimate the gene-BMI interaction on CHD. Results After adjusting for age, we found that genetic variance of CHD differed as the function of BMI in male twins, which indicated the presence of a gene-BMI interaction on CHD (P=0.008).The genetic moderating effect (βa) was -0.14 (95%CI:-0.22--0.04), indicating that for each logarithmic transformation value of BMI increase, genetic path parameters would decrease by 0.14, which would result in the decrease of genetic variance of CHD. And the heritability of CHD was 0.77 (95%CI:0.65-0.86) among the male twins with lower BMI (<24.0 kg/m2), but 0.56 (95%CI:0.33-0.74) among the male twins with high BMI (≥ 24.0 kg/m2). However, there was no evidence suggesting that BMI could moderate genetic variants of CHD in female. Conclusion We found a significant gene-BMI interaction on CHD in the Chinese male adult twins in China, and the heritability of CHD was higher among the twins whose BMI was <24.0 kg/m2.
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