Khan Ramisha, Turner Alyna, Berk Michael, Walder Ken, Rossell Susan, Guerin Alexandre A, Kim Jee Hyun
IMPACT, Institute for Innovation in Physical and Mental Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC 3220, Australia.
Centre for Mental Health, Swinburne University of Technology, Melbourne, VIC 3122, Australia.
Biomolecules. 2025 Feb 19;15(2):306. doi: 10.3390/biom15020306.
Methamphetamine use disorder is a pressing global health issue, often accompanied by significant cognitive deficits that impair daily functioning and quality of life and complicate treatment. Emerging evidence highlights the potential role of genetic factors in methamphetamine use disorder, particularly in association with cognitive function. This review examines the key genetic and cognitive dimensions and their interplay in methamphetamine use disorder. There is converging evidence from several studies that genetic polymorphisms in , , , and are associated with protection against or susceptibility to the disorder. In addition, people with methamphetamine use disorder consistently displayed impairments in cognitive flexibility and inhibitory control compared with people without the disorder. These cognitive domains were associated with reactivity to methamphetamine cues that were positively correlated with total years of methamphetamine use history. Emerging research also suggests that inhibitory control is negatively correlated with lower blood mRNA levels, while cognitive flexibility positively correlates with higher blood mRNA levels, highlighting how genetic and cognitive dimensions interact in methamphetamine use disorder. We also include some future directions, emphasizing potential personalized therapeutic strategies that integrate genetic and cognitive insights. By drawing attention to the interplay between genes and cognition, we hope to advance our understanding of methamphetamine use disorder and inform the development of targeted interventions.
甲基苯丙胺使用障碍是一个紧迫的全球健康问题,常常伴有显著的认知缺陷,这些缺陷会损害日常功能和生活质量,并使治疗复杂化。新出现的证据凸显了遗传因素在甲基苯丙胺使用障碍中的潜在作用,尤其是与认知功能的关联。本综述探讨了甲基苯丙胺使用障碍中的关键遗传和认知维度及其相互作用。多项研究有越来越多的证据表明,[此处原文未提及具体基因名称,无法准确翻译]、[此处原文未提及具体基因名称,无法准确翻译]、[此处原文未提及具体基因名称,无法准确翻译]和[此处原文未提及具体基因名称,无法准确翻译]的基因多态性与该障碍的易感性或抵御性有关。此外,与未患该障碍的人相比,甲基苯丙胺使用障碍患者在认知灵活性和抑制控制方面持续表现出受损。这些认知领域与对甲基苯丙胺线索的反应性相关,而这种反应性与甲基苯丙胺使用历史的总年数呈正相关。新出现的研究还表明,抑制控制与较低的血液[此处原文未提及具体物质,无法准确翻译]mRNA水平呈负相关,而认知灵活性与较高的血液[此处原文未提及具体物质,无法准确翻译]mRNA水平呈正相关,这凸显了遗传和认知维度在甲基苯丙胺使用障碍中是如何相互作用的。我们还纳入了一些未来的方向,强调整合遗传和认知见解的潜在个性化治疗策略。通过关注基因与认知之间的相互作用,我们希望增进对甲基苯丙胺使用障碍的理解,并为针对性干预措施的制定提供信息。