We aim to explore the mechanism of relationship between insomnia and liver metabolism by examining the gene × insomnia interactions.
Individual level genotypic and phenotypic data were obtained from the UK Biobank cohort. Regression analysis was first conducted to test the association of insomnia with plasma total bilirubin (TBil; n = 186,793), direct bilirubin (DBil; n = 159,854) and total protein (TP; n = 171,574) in UK Biobank cohort. Second, genome-wide gene-environment interaction study (GWGEIS) was conducted by PLINK 2.0, and FUMA platform was used to identify enriched pathway terms.
In UK Biobank cohort, we found that TP (P < 2.00 × 10), DBil (P = 1.72 × 10) and TBil (P = 3.38 × 10) were significantly associated with insomnia. GWGEIS of both DBil and TBil observed significant G × INSOMNIA effects between insomnia and UDP Glucuronosyltransferase Family 1 (rs6431558, P = 6.26 × 10) gene. GWGEIS of TP also detected several significant genes interacting with insomnia, such as KLF15, (rs70940816, P = 6.77 × 10) and DOK7, (rs2344205, P = 1.37 × 10). Multiple gene ontology (GO) terms were identified for bilirubin, such as GO_URONIC_ACID_METABOLIC_PROCESS (adjusted P = 4.15 × 10).
Our study results suggested negative associations between insomnia and DBil and TBil; and a positive association between insomnia and TP.
Copyright © 2021 Elsevier B.V. All rights reserved.
About The Expert
Xiaomeng Chu
Li Liu
Jing Ye
Yan Wen
Ping Li
Bolun Cheng
Shiqiang Cheng
Lu Zhang
Xin Qi
Mei Ma
Chujun Liang
Om Prakash Kafle
Cuiyan Wu
Sen Wang
Xi Wang
Yujie Ning
Feng Zhang
References
PubMed