Depression and Inflammatory Bowel Disease: A Bidirectional Two-sample Mendelian Randomization Study

被引:73
|
作者
Luo, Jiao [1 ,2 ]
Xu, Zhongwei [3 ]
Noordam, Raymond [2 ]
van Heemst, Diana [2 ]
Li-Gao, Ruifang [1 ,4 ,5 ]
机构
[1] Leiden Univ Med Ctr, Dept Clin Epidemiol, Leiden, Netherlands
[2] Leiden Univ Med Ctr, Dept Internal Med, Sect Gerontol & Geriatr, Leiden, Netherlands
[3] Karolinska Inst, Dept Med Biochem & Biophys, Sect Med Inflammat Res, Stockholm, Sweden
[4] Tilburg Univ, CoRPS Ctr Res Psychol Somat Dis, Tilburg, Netherlands
[5] Vrije Univ, Dept Biol Psychol, Amsterdam, Netherlands
来源
JOURNAL OF CROHNS & COLITIS | 2022年 / 16卷 / 04期
关键词
Depression; inflammatory bowel disease; Mendelian randomization; ASSOCIATION; SYMPTOMS; ANXIETY; MICROBIOME; PREVALENCE; LOCI; BIAS;
D O I
10.1093/ecco-jcc/jjab191
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims Observational studies have suggested a bidirectional association between depression and inflammatory bowel disease [IBD], including Crohn's disease [CD] and ulcerative colitis [UC]. However, it remains unclear whether the observed associations are causal due to the difficulties of determining sequential temporality. We investigated the association between depression and IBD by using bidirectional two-sample Mendelian randomization [MR]. Methods Independent genetic variants for depression and IBD were selected as instruments from published genome-wide association studies [GWAS] among individuals of predominantly European ancestry. Summary statistics for instrument-outcome associations were retrieved from three separate databases for both depression [Psychiatric Genomics Consortium, FinnGen and UK Biobank] and IBD [the largest GWAS meta-analysis, FinnGen and UK Biobank], respectively. MR analyses included the inverse-variance-weighted method, weighted-median estimator, MR-Egger regression, and sensitivity analyses of Steiger filtering and MR PRESSO. From either direction, analyses were performed per outcome database and were subsequently meta-analysed using a fixed-effect model. Results Genetically predicted depression [per log-odds ratio increase] was associated with a higher risk of IBD; odds ratios [95% confidence interval] for IBD, CD and UC were 1.20 [1.05, 1.36], 1.29 [1.07, 1.56] and 1.22 [1.01, 1.47] in a combined sample size of 693 183 [36 507 IBD cases], 212 172 [13 714 CD cases] and 219 686 [15 691 UC cases] individuals, respectively. In contrast, no association was observed between genetically influenced IBD and depression in 534 635 individuals [71 466 depression cases]. Conclusions Our findings corroborated a causal association of depression on IBD, which may impact the clinical decision on the management of depression in patients with IBD. Though our results did not support a causal effect of IBD on depression, further investigations are needed to clarify the effect of IBD activity on depression [with different symptomology].
引用
收藏
页码:633 / 642
页数:10
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