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Genetic Variation Underlying Psychosis-inducing Effects of Cannabis: Critical Review and Future Directions

机译:大麻引起精神病的遗传变异:严格审查和未来方向。

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Cannabis use is associated with an increased risk for psychotic disorder, yet most cannabis users do not develop psychosis, suggesting that other factors are also involved. This paper reviews the available evidence suggesting that differential sensitivity to the psychosis-inducing effects of cannabis may be related to underlying genetic liability. There is robust evidence that persons at psychometric risk for psychosis are most vulnerable to display psychotic symptoms subsequent to the use of cannabis. Multiple studies have also found that persons at familial risk for psychosis have an increased sensitivity to the effects of cannabis. Together, these findings support the concept of a biological interaction between cannabis use and one's underlying genetic vulnerability. At the molecular-genetic level, however, few (if any) interactions have been consistently replicated, although a reported interaction with variation in AKT1 is promising and deserves further follow-up. The apparent lack of consistent replication can be ascribed to problems of initial gene selection, statistical power, a bias towards positive results and insufficient attempts at true replication, leading to the conclusion that increased sample sizes, greater density of genetic markers and a stronger focus on true replication are necessary. The major challenge for molecular-genetic gene-environment interaction research will be to combine the agnostic detection of disorder-associated genetic variants from genome-wide studies with the hypothesis-based approach from epidemiological and neurobiological studies. Possible strategies for future cannabis interaction studies are discussed.
机译:大麻的使用与精神病性疾病的风险增加有关,但大多数大麻使用者并未发展为精神病,这表明还涉及其他因素。本文回顾了现有证据,这些证据表明对大麻引起的精神病的不同敏感性可能与潜在的遗传易感性有关。有确凿的证据表明,处于精神病风险心理状态的人在使用大麻后最容易出现精神病症状。多项研究还发现,患有家族性精神病风险的人对大麻影响的敏感性增加。总之,这些发现支持了大麻使用与潜在的遗传易感性之间的生物学相互作用的概念。然而,在分子遗传学水平上,很少(如果有的话)相互作用被一致地复制,尽管报道的与AKT1变异的相互作用是有前途的,值得进一步跟踪。明显缺乏一致的复制可归因于最初的基因选择,统计能力,对阳性结果的偏见以及对真实复制的尝试不足等问题,从而得出结论,即样本数量增加,遗传标记物密度更高以及对基因的关注程度更高。真正的复制是必要的。分子-遗传基因-环境相互作用研究的主要挑战是将来自全基因组研究的与疾病相关的遗传变异的不可知检测与来自流行病学和神经生物学研究的基于假设的方法相结合。讨论了未来大麻相互作用研究的可能策略。

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