Sedentary and 21 gastrointestinal disorders: A Mendelian randomization study

被引:0
作者
Lin, Yunzhi [1 ]
He, Jun [1 ]
Ding, Zhen [1 ]
机构
[1] Anhui Med Univ, Dept Hepatobiliary Surg, Chaohu Hosp, Hefei, Anhui, Peoples R China
关键词
Gastrointestinal diseases; Mendelian randomization; sedentary; single nucleotide polymorphisms; watching television; COLORECTAL-CANCER RISK; BODY-MASS INDEX; PHYSICAL-ACTIVITY; GENETIC-VARIANTS; BEHAVIOR; OBESITY; HEALTH; INSTRUMENTS; DISEASE; DIET;
D O I
10.1097/MD.0000000000039813
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sedentary behavior (SB) has been linked in the past by observational studies to gastrointestinal illnesses, although the exact cause of the link is still unknown. To deal with this problem, we carried out a Mendelian randomization (MR) study to thoroughly examine the connection between SB and common gastrointestinal illnesses. We selected instrumental variables representing the SB from the UK Biobank study, including watching television viewing, playing computer, and driving. In addition, we obtained genetic associations of 21 common gastrointestinal disorders from the FinnGen research. After adjusting for common risk factors associated with gastrointestinal diseases, we analyzed the independent association between genetic. Furthermore, we used the inverse-variance weighted (IVW) method in conjunction with complementing techniques like MR-Egger (Mendelian randomization based on Egger Regression) and weighted median to assure the accuracy and dependability of the results. Our findings suggest that genetic susceptibility to prolonged television viewing is significantly associated with an increased risk of 9 out of 21 gastrointestinal disorders. Specifically, these disorders include gastroesophageal reflux disease, chronic gastritis, cholelithiasis, acute pancreatitis, chronic pancreatitis, gastroduodenal ulcer, fatty liver, irritable bowel syndrome, and acute appendicitis. These associations remained significant even after correcting for potential confounding factors. The replication analysis confirms the same conclusion. The results of this study demonstrate a causal relationship between cachexia and genetically predicted SB. To further understand the underlying pathogenic mechanisms at play, more study is required.
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