A population-based study of familial coaggregation and shared genetic etiology of psychiatric and gastrointestinal disorders

被引:0
|
作者
Pan, Yi-Jiun [1 ]
Lin, Mei-Chen [2 ]
Liou, Jyh-Ming [3 ,4 ,5 ]
Fan, Chun-Chieh [6 ,7 ]
Su, Mei-Hsin [8 ,9 ]
Chen, Cheng-Yun [8 ]
Wu, Chi-Shin [2 ,10 ]
Chen, Pei-Chun [2 ]
Huang, Yen-Tsung [11 ]
Wang, Shi-Heng [2 ,12 ]
机构
[1] China Med Univ, Coll Med, Sch Med, Dept Microbiol & Immunol, Taichung, Taiwan
[2] Natl Hlth Res Inst, Natl Ctr Geriatr & Welf Res, Zhunan, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Internal Med, Div Gastroenterol & Hepatol, Taipei, Taiwan
[4] Natl Taiwan Univ Coll Med, Dept Internal Med, Taipei, Taiwan
[5] Natl Taiwan Univ Canc Ctr, Dept Med, Taipei, Taiwan
[6] Laureate Inst Brain Res, Ctr Populat Neurosci & Genet, Tulsa, OK USA
[7] Univ Calif San Diego, Sch Med, Dept Radiol, La Jolla, CA USA
[8] China Med Univ, Coll Publ Hlth, Dept Publ Hlth, Taichung, Taiwan
[9] Virginia Commonwealth Univ, Virginia Inst Psychiat Behav Genet, Dept Psychiat, Richmond, VA USA
[10] Natl Taiwan Univ Hosp, Dept Psychiat, Yunlin branch, Touliu, Taiwan
[11] Acad Sinica, Inst Stat Sci, Taipei, Taiwan
[12] China Med Univ, China Med Univ Hosp, Dept Med Res, Taichung, Taiwan
来源
COMMUNICATIONS MEDICINE | 2024年 / 4卷 / 01期
关键词
IRRITABLE-BOWEL-SYNDROME; GENOME-WIDE ASSOCIATION; MENDELIAN RANDOMIZATION; IDENTIFIES; DISEASE; ANXIETY; IMMUNE; STRESS; RISK; STRATIFICATION;
D O I
10.1038/s43856-024-00607-7
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundIt has been proposed that having a psychiatric disorder could increase the risk of developing a gastrointestinal disorder, and vice versa. The role of familial coaggregation and shared genetic loading between psychiatric and gastrointestinal disorders remains unclear.MethodsThis study used the Taiwan National Health Insurance Research Database; 4,504,612 individuals born 1970-1999 with parental information, 51,664 same-sex twins, and 3,322,959 persons with full-sibling(s) were enrolled. Genotyping was available for 106,796 unrelated participants from the Taiwan Biobank. A logistic regression model was used to examine the associations of individual history, affected relatives, and polygenic risk scores (PRS) for schizophrenia (SCZ), bipolar disorder (BPD), major depressive disorder (MDD), and obsessive-compulsive disorder (OCD), with the risk of peptic ulcer disease (PUD), gastroesophageal reflux disease (GERD), irritable bowel syndrome (IBS), and inflammatory bowel disease (IBD), and vice versa.ResultsHere we show that parental psychiatric disorders are associated with gastrointestinal disorders. Full-siblings of psychiatric cases have an increased risk of gastrointestinal disorders except for SCZ/BPD and IBD; the magnitude of coaggregation is higher in same-sex twins than in full-siblings. The results of bidirectional analyses mostly remain unchanged. PRS for SCZ, MDD, and OCD are associated with IBS, PUD/GERD/IBS/IBD, and PUD/GERD/IBS, respectively. PRS for PUD, GERD, IBS, and IBD are associated with MDD, BPD/MDD, SCZ/BPD/MDD, and BPD, respectively.ConclusionsThere is familial coaggregation and shared genetic etiology between psychiatric and gastrointestinal comorbidity. Individuals with psychiatric disorder-affected relatives or with higher genetic risk for psychiatric disorders should be monitored for gastrointestinal disorders, and vice versa. It has been proposed that people with psychiatric disorders such as depression could have an increased chance of developing gastrointestinal disorders such as irritable bowel syndrome. We looked at whether this was the case in a large number of people from Taiwan. We found that people with a psychiatric disorder, or with relatives having a psychiatric disorder, were more likely to have gastrointestinal disorders, and vice versa. These findings suggest that people who have psychiatric disorders or have psychiatric disorder-affected relatives should be monitored for gastrointestinal disorders, and vice versa, to enable them to benefit from all the treatments they might need to improve their health. Pan et al. examine whether there is a shared pathophysiological mechanism underlying brain-gut comorbidity. This population-based cohort and biobank study demonstrates that there is familial coaggregation and shared genetic etiology between psychiatric and gastrointestinal comorbidity.
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页数:11
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