主要精神疾病的遗传学和表观遗传学:困境、成就、应用和未来范围。

Hamid M Abdolmaleky, Sam Thiagalingam, Marsha Wilcox
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引用次数: 95

摘要

尽管有强有力的证据支持这些复杂和破坏性疾病的遗传基础,但尚未确定任何主要精神疾病(包括精神分裂症)的特定基因。这种失败可能有几个原因,从糟糕的研究设计和低统计能力到遗传机制,如多基因遗传、表观遗传相互作用和多效性。目前使用的大多数研究设计不足以揭示这些机制。然而,到目前为止,基因研究已经为精神疾病的病因和潜在治疗提供了一些有价值的见解。越来越多的证据表明,通过综合考虑遗传和表观遗传因素的方法,对包括精神分裂症在内的精神疾病的遗传病因的理解将更加成功。例如,通过荟萃分析和大型多中心研究,包括编码多巴胺受体(DRD2、DRD3和DRD4)、5 -羟色胺受体2A (HTR2A)和儿茶酚- o -甲基转移酶(COMT)在内的一些基因与精神分裂症和相关疾病的病因学有关。也有越来越多的证据表明,DRD1、NMDA受体基因(GRIN1、GRIN2A、GRIN2B)、脑源性神经营养因子(BDNF)和多巴胺转运蛋白(SLC6A3)在精神分裂症和双相情感障碍中的作用。最近的研究表明,reelin (RELN)、BDNF和DRD2启动子的表观遗传修饰与临床精神疾病的易感性有关。一旦分子发病机制被了解,精神疾病的药物治疗可能会更加有效。例如,DRD2的低活性等位基因和COMT的高活性等位基因(它们会降解突触间隙中的多巴胺)与精神分裂症有关。额叶多巴胺能传递不足可能在与这种疾病相关的阴性症状的发展中起作用。具有部分多巴胺D2受体激动剂作用的抗精神病治疗可能是目前治疗的一种可行的替代方案,并且对精神病患者的症状减轻有效。使用多巴胺D1/D2受体激动剂或COMT抑制剂的治疗也可能对精神分裂症和双相情感障碍的阴性症状患者有益。精神分裂症和其他精神疾病的病因复杂,需要考虑遗传和表观遗传系统,并仔细设计实验,以阐明导致这些疾病的遗传机制,以及现有和新疗法的益处。
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Genetics and epigenetics in major psychiatric disorders: dilemmas, achievements, applications, and future scope.

No specific gene has been identified for any major psychiatric disorder, including schizophrenia, in spite of strong evidence supporting a genetic basis for these complex and devastating disorders. There are several likely reasons for this failure, ranging from poor study design with low statistical power to genetic mechanisms such as polygenic inheritance, epigenetic interactions, and pleiotropy. Most study designs currently in use are inadequate to uncover these mechanisms. However, to date, genetic studies have provided some valuable insight into the causes and potential therapies for psychiatric disorders. There is a growing body of evidence suggesting that the understanding of the genetic etiology of psychiatric illnesses, including schizophrenia, will be more successful with integrative approaches considering both genetic and epigenetic factors. For example, several genes including those encoding dopamine receptors (DRD2, DRD3, and DRD4), serotonin receptor 2A (HTR2A) and catechol-O-methyltransferase (COMT) have been implicated in the etiology of schizophrenia and related disorders through meta-analyses and large, multicenter studies. There is also growing evidence for the role of DRD1, NMDA receptor genes (GRIN1, GRIN2A, GRIN2B), brain-derived neurotrophic factor (BDNF), and dopamine transporter (SLC6A3) in both schizophrenia and bipolar disorder. Recent studies have indicated that epigenetic modification of reelin (RELN), BDNF, and the DRD2 promoters confer susceptibility to clinical psychiatric conditions. Pharmacologic therapy of psychiatric disorders will likely be more effective once the molecular pathogenesis is known. For example, the hypoactive alleles of DRD2 and the hyperactive alleles of COMT, which degrade the dopamine in the synaptic cleft, are associated with schizophrenia. It is likely that insufficient dopaminergic transmission in the frontal lobe plays a role in the development of negative symptoms associated with this disorder. Antipsychotic therapies with a partial dopamine D2 receptor agonist effect may be a plausible alternative to current therapies, and would be effective in symptom reduction in psychotic individuals. It is also possible that therapies employing dopamine D1/D2 receptor agonists or COMT inhibitors will be beneficial for patients with negative symptoms in schizophrenia and bipolar disorder. The complex etiology of schizophrenia, and other psychiatric disorders, warrants the consideration of both genetic and epigenetic systems and the careful design of experiments to illumine the genetic mechanisms conferring liability for these disorders and the benefit of existing and new therapies.

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