Unit of Cardiovascular and Nutritional Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, Nobelsväg 13, 17177, Stockholm, Sweden.
Centre for Global Health, Zhejiang University School of Medicine, Hangzhou, China.
Eur J Epidemiol. 2022 Jul;37(7):723-733. doi: 10.1007/s10654-022-00868-3. Epub 2022 Apr 30.
The risk factors for nonalcoholic fatty liver disease (NAFLD) have not been clearly identified. We conducted a Mendelian randomization (MR) study to explore this. Independent genetic variants strongly associated with 5 lifestyle and 9 metabolic factors were selected as instrumental variables from corresponding genome-wide association studies (GWASs). Summary-level data for NAFLD were obtained from a GWAS meta-analysis of 8434 cases and 770,180 non-cases (discovery dataset) and another GWAS meta-analysis of 1483 cases and 17,781 non-cases (replication dataset). Univariable and multivariable MR analyses were performed. There were associations with NAFLD for lifetime smoking index (odds ratio (OR) 1.59, 95% confidence interval (CI) 1.31-1.93 per SD-increase), body mass index (BMI, OR 1.33, 95% CI 1.23-1.43 per SD-increase), waist circumference (OR 1.82; 95% CI 1.48-2.24 per SD-increase), type 2 diabetes (OR 1.21, 95% CI 1.15-1.27 per unit increase in log-transformed odds), systolic blood pressure (OR 1.17; 95% CI 1.07-1.26 per 10 mmHg increase), high-density lipoprotein cholesterol (OR 0.84, 95% CI 0.77-0.90 per SD-increase), and triglycerides (OR 1.23, 95% CI 1.15-1.33 per SD-increase). The associations for type 2 diabetes, systolic blood pressure, triglycerides, but not for high-density lipoprotein cholesterol remained strong after adjusting for genetically-predicted BMI. Genetic liability to type 2 diabetes mediated 51.4% (95% CI 13.4-89.3%) of the BMI-effects on NAFLD risk. There were suggestive inverse associations of genetically-predicted alcohol, coffee, and caffeine consumption, and vigorous physical activity with NAFLD risk. This study identified several lifestyle and metabolic factors that may be causally implicated in NAFLD.
非酒精性脂肪性肝病(NAFLD)的风险因素尚未明确。我们进行了一项孟德尔随机化(MR)研究来对此进行探讨。从相应的全基因组关联研究(GWAS)中选择了与 5 种生活方式和 9 种代谢因素强烈相关的独立遗传变异作为工具变量。NAFLD 的汇总水平数据来自于对 8434 例病例和 770180 例非病例(发现数据集)的 GWAS 荟萃分析,以及对 1483 例病例和 17781 例非病例(复制数据集)的另一个 GWAS 荟萃分析。进行了单变量和多变量 MR 分析。终生吸烟指数(每标准差增加的优势比(OR)1.59,95%置信区间(CI)1.31-1.93)、体重指数(BMI,OR 1.33,95%CI 1.23-1.43 每 SD 增加)、腰围(OR 1.82;95%CI 1.48-2.24 每 SD 增加)、2 型糖尿病(OR 1.21,95%CI 1.15-1.27 每单位增加对数转换的几率)、收缩压(OR 1.17;95%CI 1.07-1.26 每 10mmHg 增加)、高密度脂蛋白胆固醇(OR 0.84,95%CI 0.77-0.90 每 SD 增加)和甘油三酯(OR 1.23,95%CI 1.15-1.33 每 SD 增加)与 NAFLD 相关。调整遗传预测 BMI 后,2 型糖尿病、收缩压、甘油三酯的相关性仍然很强,但高密度脂蛋白胆固醇的相关性则不然。2 型糖尿病的遗传易感性介导了 BMI 对 NAFLD 风险影响的 51.4%(95%CI 13.4-89.3%)。遗传预测的酒精、咖啡和咖啡因摄入以及剧烈的身体活动与 NAFLD 风险呈负相关。本研究确定了一些生活方式和代谢因素可能与 NAFLD 有因果关系。