School of Public Health and the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China; Department of Gastroenterology, The Third Xiangya Hospital, Central South University, Changsha, China.
Department of Gastroenterology, The Third Xiangya Hospital, Central South University, Changsha, China.
EBioMedicine. 2024 May;103:105110. doi: 10.1016/j.ebiom.2024.105110. Epub 2024 Apr 6.
The causal associations of physical activity and sedentary behavior with the risk of gastrointestinal disease are unclear. We performed a Mendelian randomization analysis to examine these associations.
Genetic instruments associated with leisure screen time (LST, an indicator of a sedentary lifestyle) and moderate-to-vigorous intensity physical activity (MVPA) at the genome-wide significance (P < 5 × 10) level were selected from a genome-wide association study. Summary statistics for gastrointestinal diseases were obtained from the UK Biobank study, the FinnGen study, and large consortia. Multivariable MR analyses were conducted for genetically determined LST with adjustment for MVPA and vice versa. We also performed multivariable MR with adjustment for genetically proxied smoking, body mass index (BMI), waist-to-hip ratio, type 2 diabetes, and fasting insulin for both exposures.
Genetically proxied longer LST was associated with an increased risk of gastrointestinal reflux, gastric ulcer, duodenal ulcer, chronic gastritis, irritable bowel syndrome, diverticular disease, Crohn's disease, ulcerative colitis, non-alcoholic fatty liver disease, alcoholic liver disease, cholangitis, cholecystitis, cholelithiasis, acute pancreatitis, chronic pancreatitis, and acute appendicitis. Most associations remained after adjustment for genetic liability to MVPA. Genetic liability to MVPA was associated with decreased risk of gastroesophageal reflux, gastric ulcer, chronic gastritis, irritable bowel syndrome, cholecystitis, cholelithiasis, acute and chronic pancreatitis. The associations attenuated albeit directionally remained after adjusting for genetically predicted LST. Multivariable MR analysis found that BMI and type 2 diabetes mediated the associations of LST and MVPA with several gastrointestinal diseases.
The study suggests that a sedentary lifestyle may play a causal role in the development of many gastrointestinal diseases.
Natural Science Fund for Distinguished Young Scholars of Zhejiang Province (LR22H260001), Natural Science Foundation of Hunan Province (2021JJ30999), Swedish Heart-Lung Foundation (Hjärt-Lungfonden, 20210351), Swedish Research Council (Vetenskapsrådet, 2019-00977), Swedish Cancer Society (Cancerfonden), the Wellcome Trust (225790/7/22/Z), United Kingdom Research and Innovation Medical Research Council (MC_UU_00002/7) and National Institute for Health Research Cambridge Biomedical Research Centre (NHIR203312).
体力活动和久坐行为与胃肠道疾病风险之间的因果关系尚不清楚。我们进行了孟德尔随机化分析来研究这些关联。
从全基因组关联研究中选择与休闲屏幕时间(LST,久坐生活方式的指标)和中等到剧烈强度体力活动(MVPA)相关的全基因组显著水平(P<5×10)的遗传工具。从英国生物银行研究、芬兰遗传研究和大型联盟中获得胃肠道疾病的汇总统计数据。进行多变量 MR 分析,以调整 MVPA 后评估遗传决定的 LST,反之亦然。我们还针对两种暴露因素进行了多变量 MR 分析,调整了遗传上相近的吸烟、体重指数(BMI)、腰臀比、2 型糖尿病和空腹胰岛素。
遗传上较长的 LST 与胃食管反流、胃溃疡、十二指肠溃疡、慢性胃炎、肠易激综合征、憩室病、克罗恩病、溃疡性结肠炎、非酒精性脂肪性肝病、酒精性肝病、胆管炎、胆囊炎、胆结石、急性胰腺炎、慢性胰腺炎和急性阑尾炎的风险增加有关。大多数关联在调整 MVPA 的遗传易感性后仍然存在。MVPA 的遗传易感性与胃食管反流、胃溃疡、慢性胃炎、肠易激综合征、胆囊炎、胆结石、急性和慢性胰腺炎的风险降低有关。尽管方向保持不变,但在调整了遗传预测的 LST 后,关联减弱了。多变量 MR 分析发现,BMI 和 2 型糖尿病介导了 LST 和 MVPA 与多种胃肠道疾病的关联。
研究表明,久坐的生活方式可能在许多胃肠道疾病的发展中起因果作用。
浙江省杰出青年自然科学基金(LR22H260001)、湖南省自然科学基金(2021JJ30999)、瑞典心肺基金会(Hjärt-Lungfonden,20210351)、瑞典研究理事会(Vetenskapsrådet,2019-00977)、瑞典癌症协会(Cancerfonden)、惠康信托基金会(Wellcome Trust,225790/7/22/Z)、英国研究与创新医学研究理事会(Medical Research Council,MC_UU_00002/7)和英国国民健康保险制度剑桥生物医学研究中心(National Institute for Health Research Cambridge Biomedical Research Centre,NHIR203312)。