Sex- and Substance-Specific Associations of Circadian-Related Genes with Addiction in the UK Biobank Cohort Implicate Neuroplasticity Pathways

Background/Objectives: The circadian clockwork is implicated in the etiology of addiction, with circadian rhythm disruptions bidirectionally linked to substance abuse, but the molecular mechanisms that underlie this connection are not well known. Methods: Here, we use machine learning to reveal sex-...

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Main Authors: Ayub Khan, Mete Minbay, Ziad Attia, Ahmet Ali Ay, Krista K. Ingram
Format: Article
Language:English
Published: MDPI AG 2024-12-01
Series:Brain Sciences
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Online Access:https://www.mdpi.com/2076-3425/14/12/1282
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author Ayub Khan
Mete Minbay
Ziad Attia
Ahmet Ali Ay
Krista K. Ingram
author_facet Ayub Khan
Mete Minbay
Ziad Attia
Ahmet Ali Ay
Krista K. Ingram
author_sort Ayub Khan
collection DOAJ
description Background/Objectives: The circadian clockwork is implicated in the etiology of addiction, with circadian rhythm disruptions bidirectionally linked to substance abuse, but the molecular mechanisms that underlie this connection are not well known. Methods: Here, we use machine learning to reveal sex- and substance-specific associations with addiction in variants from 51 circadian-related genes (156,702 SNPs) in 98,800 participants from a UK Biobank cohort. We further analyze SNP associations in a subset of the cohort for substance-specific addictions (alcohol, illicit drugs (narcotics), and prescription drugs (opioids)). Results: We find robust (OR > 10) and novel sex-specific and substance-specific associations with variants in synaptic transcription factors (ZBTB20, CHRNB3) and hormone receptors (RORA), particularly in individuals addicted to narcotics and opioids. Circadian-related gene variants associated with male and female addiction were non-overlapping; variants in males primarily involve dopaminergic pathways, while variants in females factor in metabolic and inflammation pathways, with a novel gene association of female addiction with DELEC1, a gene of unknown function. Conclusions: Our findings underscore the complexity of genetic pathways associated with addiction, involving core clock genes and circadian-regulated pathways, and reveal novel circadian-related gene associations that will aid the development of targeted, sex-specific therapeutic interventions for substance abuse.
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spelling doaj-art-fb5bd62a2b9f4d86be90c0ce1d6f6c082024-12-27T14:15:00ZengMDPI AGBrain Sciences2076-34252024-12-011412128210.3390/brainsci14121282Sex- and Substance-Specific Associations of Circadian-Related Genes with Addiction in the UK Biobank Cohort Implicate Neuroplasticity PathwaysAyub Khan0Mete Minbay1Ziad Attia2Ahmet Ali Ay3Krista K. Ingram4Department of Biology, Colgate University, Hamilton, NY 13346, USADepartment of Computer Science, Colgate University, Hamilton, NY 13346, USADepartment of Computer Science, Colgate University, Hamilton, NY 13346, USADepartment of Biology, Colgate University, Hamilton, NY 13346, USADepartment of Biology, Colgate University, Hamilton, NY 13346, USABackground/Objectives: The circadian clockwork is implicated in the etiology of addiction, with circadian rhythm disruptions bidirectionally linked to substance abuse, but the molecular mechanisms that underlie this connection are not well known. Methods: Here, we use machine learning to reveal sex- and substance-specific associations with addiction in variants from 51 circadian-related genes (156,702 SNPs) in 98,800 participants from a UK Biobank cohort. We further analyze SNP associations in a subset of the cohort for substance-specific addictions (alcohol, illicit drugs (narcotics), and prescription drugs (opioids)). Results: We find robust (OR > 10) and novel sex-specific and substance-specific associations with variants in synaptic transcription factors (ZBTB20, CHRNB3) and hormone receptors (RORA), particularly in individuals addicted to narcotics and opioids. Circadian-related gene variants associated with male and female addiction were non-overlapping; variants in males primarily involve dopaminergic pathways, while variants in females factor in metabolic and inflammation pathways, with a novel gene association of female addiction with DELEC1, a gene of unknown function. Conclusions: Our findings underscore the complexity of genetic pathways associated with addiction, involving core clock genes and circadian-regulated pathways, and reveal novel circadian-related gene associations that will aid the development of targeted, sex-specific therapeutic interventions for substance abuse.https://www.mdpi.com/2076-3425/14/12/1282circadian clockaddictionneuroplasticitysex-specific associationssubstance abuse
spellingShingle Ayub Khan
Mete Minbay
Ziad Attia
Ahmet Ali Ay
Krista K. Ingram
Sex- and Substance-Specific Associations of Circadian-Related Genes with Addiction in the UK Biobank Cohort Implicate Neuroplasticity Pathways
Brain Sciences
circadian clock
addiction
neuroplasticity
sex-specific associations
substance abuse
title Sex- and Substance-Specific Associations of Circadian-Related Genes with Addiction in the UK Biobank Cohort Implicate Neuroplasticity Pathways
title_full Sex- and Substance-Specific Associations of Circadian-Related Genes with Addiction in the UK Biobank Cohort Implicate Neuroplasticity Pathways
title_fullStr Sex- and Substance-Specific Associations of Circadian-Related Genes with Addiction in the UK Biobank Cohort Implicate Neuroplasticity Pathways
title_full_unstemmed Sex- and Substance-Specific Associations of Circadian-Related Genes with Addiction in the UK Biobank Cohort Implicate Neuroplasticity Pathways
title_short Sex- and Substance-Specific Associations of Circadian-Related Genes with Addiction in the UK Biobank Cohort Implicate Neuroplasticity Pathways
title_sort sex and substance specific associations of circadian related genes with addiction in the uk biobank cohort implicate neuroplasticity pathways
topic circadian clock
addiction
neuroplasticity
sex-specific associations
substance abuse
url https://www.mdpi.com/2076-3425/14/12/1282
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