Yao Ziqin, Jiang Feiyu, Luo Hongbin, Zhou Jiahui, Shi Wanting, Xu Shoufang, Zhang Yingying, Dai Feng, Li Xinran, Liu Zhiwei, Wang Xinhui
Department of Blood Transfusion, Sir Run Run Shaw Hospital, School of Public Health, Zhejiang University School of Medicine, Hangzhou 310058, China.
Metabolites. 2023 Jun 7;13(6):730. doi: 10.3390/metabo13060730.
Inflammatory bowel diseases (IBDs), including Crohn's disease (CD) and ulcerative colitis (UC), have become a global health problem with a rapid growth of incidence in newly industrialized countries. Observational studies have recognized associations between blood lipid traits and IBDs, but the causality still remains unclear. To determine the causal effects of blood lipid traits, including triglycerides (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C) on IBDs, two-sample Mendelian randomization (MR) analyses were conducted using the summary-level genome-wide association study (GWAS) statistics of blood lipid traits and IBDs. Our univariable MR using multiplicative random-effect inverse-variance weight (IVW) method identified TC (OR: 0.674; 95% CI: 0.554, 0.820; < 0.00625) and LDL-C (OR: 0.685; 95% CI: 0.546, 0.858; < 0.00625) as protective factors of UC. The result of our multivariable MR analysis further provided suggestive evidence of the protective effect of TC on UC risk (OR: 0.147; 95% CI: 0.025, 0.883; < 0.05). Finally, our MR-BMA analysis prioritized TG (MIP: 0.336; θ^: -0.025; PP: 0.31; θ^: -0.072) and HDL-C (MIP: 0.254; θ^: -0.011; PP: 0.232; θ^: -0.04) for CD and TC (MIP: 0.721; θ^: -0.257; PP: 0.648; θ^: -0.356) and LDL-C (MIP: 0.31; θ^: -0.095; PP: 0.256; θ^: -0.344) for UC as the top-ranked protective factors. In conclusion, the causal effect of TC for UC prevention was robust across all of our MR approaches, which provide the first evidence that genetically determined TC is causally associated with reduced risk of UC. The finding of this study provides important insights into the metabolic regulation of IBDs and potential metabolites targeting strategies for IBDs intervention.
炎症性肠病(IBDs),包括克罗恩病(CD)和溃疡性结肠炎(UC),在新兴工业化国家发病率迅速增长,已成为一个全球性的健康问题。观察性研究已认识到血脂特征与IBDs之间的关联,但因果关系仍不明确。为了确定甘油三酯(TG)、总胆固醇(TC)、高密度脂蛋白胆固醇(HDL-C)和低密度脂蛋白胆固醇(LDL-C)等血脂特征对IBDs的因果效应,我们使用血脂特征和IBDs的汇总水平全基因组关联研究(GWAS)统计数据进行了两样本孟德尔随机化(MR)分析。我们使用乘性随机效应逆方差权重(IVW)方法进行的单变量MR分析确定TC(比值比:0.674;95%置信区间:0.554,0.820;P<0.00625)和LDL-C(比值比:0.685;95%置信区间:0.546,0.858;P<0.00625)是UC的保护因素。我们的多变量MR分析结果进一步提供了TC对UC风险具有保护作用的提示性证据(比值比:0.147;95%置信区间:0.025,0.883;P<0.05)。最后,我们的MR-BMA分析将TG(最大后验概率:0.336;效应估计值:-0.025;P值:0.31;效应估计值:-0.072)和HDL-C(最大后验概率:0.254;效应估计值:-0.011;P值:0.232;效应估计值:-0.04)列为CD的首要保护因素,将TC(最大后验概率:0.721;效应估计值:-0.257;P值:0.648;效应估计值:-0.356)和LDL-C(最大后验概率:0.31;效应估计值:-0.095;P值:0.256;效应估计值:-0.344)列为UC的首要保护因素。总之,在我们所有的MR方法中,TC预防UC的因果效应都是稳健的,这首次证明了基因决定的TC与UC风险降低存在因果关联。本研究结果为IBDs的代谢调节以及IBDs干预的潜在代谢物靶向策略提供了重要见解。