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Investigating the shared genetic architecture and causal relationship between pain and neuropsychiatric disorders.

Mengya Chen, Si Li, Ziwei Zhu, Chengguqiu Dai, Xingjie Hao
Other Human genetics 2023 17 citations

Study Design

Study Type
Mendelian randomization and GWAS analysis
Sample Size
482730
Population
European-ancestry population; GWAS cohorts for 26 pain and neuropsychiatric disorders; sample sizes 17,310 to 482,730
Intervention
Investigating the shared genetic architecture and causal relationship between pain and neuropsychiatric disorders. None
Comparator
reference GWAS populations; European-ancestry cohorts
Primary Outcome
genetic correlation and causal relationships between pain and neuropsychiatric disorders (insomnia, neuroticism, MDD, ADHD, multisite chronic pain)
Effect Direction
Mixed
Risk of Bias
Unclear

Abstract

Pain often occurs in parallel with neuropsychiatric disorders. However, the underlying mechanisms and potential causality have not been well studied. We collected the genome-wide association study (GWAS) summary statistics of 26 common pain and neuropsychiatric disorders with sample size ranging from 17,310 to 482,730 in European population. The genetic correlation between pair of pain and neuropsychiatric disorders, as well as the relevant cell types were investigated by linkage disequilibrium (LD) score regression analyses. Then, transcriptome-wide association study (TWAS) was applied to identify the potential shared genes by integrating the gene expression information and GWAS. In addition, Mendelian randomization (MR) analyses were conducted to infer the potential causality between pain and neuropsychiatric disorders. Among the 169 pairwise pain and neuropsychiatric disorders, 55 pairs showed positive correlations (median rg = 0.43) and 9 pairs showed negative correlations (median rg =  -0.31). Using MR analyses, 26 likely causal associations were identified, including that neuroticism and insomnia were risk factors for most of short-term pain, and multisite chronic pain was risk factor for neuroticism, insomnia, major depressive disorder and attention deficit/hyperactivity disorder, and vice versa. The signals of pain and neuropsychiatric disorders tended to be enriched in the functional regions of cell types from central nervous system (CNS). A total of 19 genes shared in at least one pain and neuropsychiatric disorder pair were identified by TWAS, including AMT, NCOA6, and UNC45A, which involved in glycine degradation, insulin secretion, and cell proliferation, respectively. Our findings provided the evidence of shared genetic structure, causality and potential shared pathogenic mechanisms between pain and neuropsychiatric disorders, and enhanced our understanding of the comorbidities of pain and neuropsychiatric disorders.

TL;DR

The findings provided the evidence of shared genetic structure, causality and potential shared pathogenic mechanisms between pain and neuropsychiatric disorders, and enhanced the understanding of the comorbidities of pain and neuropsychiatric disorders.

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