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A Study of the MTHFR Gene Prevalence in a Rural Tennessee Opioid Use Disorder Treatment Center Population

Bibliographic Data

ID15513233
AuthorsLeslie Cole (Pathways Behavioral Services), Alina Cernasev (0000-0001-9627-9541, University of Tennessee Health Science Center, corresponding author), K Webb (0000-0003-3230-102X, Pathways Behavioral Services), Santosh Kumar (0000-0002-8663-3006, University of Tennessee Health Science Center), A Shaun Rowe (University of Tennessee Health Science Center)
Year2022
Volume19
Issue6
Pages3255-3255
Publication date2022-03-10
Open AccessYes
TypeARTICLE
VenueInternational Journal of Environmental Research and Public Health (JOURNAL)
Journal identifiersISSN: 1661-7827 • E-ISSN: 1660-4601
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/ijerph19063255
PMID35328943
OpenAlexW4221052944
LanguageEN
References cited25

Background: Opioid Use Disorder (OUD) has been linked to dopamine and the neurological reward centers. Methylenetetrahydrofolate reductase (MTHFR) is an enzyme involved in the production of many neurotransmitters such as dopamine. As such, MTHFR variants that lead to decreased production of neurotransmitters may play a role in OUD. However, lacunae exist for characterizing the prevalence of the MTHFR mutations in an OUD population. The objective of this study was to determine prevalence of the MTHFR gene mutations in a rural Tennessean population with OUD. Methods: This study was a retrospective cohort of individuals with OUD that evaluated the prevalence of MTHFR variants. Patients were categorized as normal, homozygous C677T, heterozygous C677T, homozygous A1298C, or heterozygous A1298C. The primary outcome was a qualitative comparison of the prevalence of each of the MTHFR variants in our cohort to the publicly reported MTHR polymorphism prevalence. Secondary outcomes include race and ethnicity differences as well as stimulant use differences for each of the variants. Results: A total of 232 patients undergoing care for opioid use disorder were included in the study. Of those included, 30 patients had a normal MTHFR allele and 202 had a variant MTHFR allele. Overall, the prevalence of any MTHFR variant was 87.1% (95% CI 82.6-91.4%). When comparing those with a normal MTHFR allele to those with any MTHFR variant, there was no difference in age, sex, race and ethnicity, or stimulant use. Conclusion: The overall prevalence of MTHFR variants in patients with opioid use disorders is high

Allele · Biology · Cohort · Environmental health · Gene · Methylenetetrahydrofolate reductase · Population · Retrospective cohort study · Attention Deficit Hyperactivity Disorder · Medicine · Neurotransmitter Receptor Influence on Behavior · Prenatal Substance Exposure Effects · Genetics · Internal Medicine

  • Neurobiology of addiction

    Open Access•George F Koob, Nora D Volkow•The Lancet Psychiatry•2016

  • The MTHFR C677T Variant is Associated with Responsiveness to Disulfiram Treatment for Cocaine Dependency

    Open Access•Catherine J Spellicy, Thomas R Kosten et al.•Frontiers in Psychiatry•2013

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