Inserm U1061, Montpellier, France.
Drugs. 2012 Sep 10;72(13):1725-38. doi: 10.2165/11635960-000000000-00000.
Accumulating evidence suggests the involvement of estrogen in depression. Estrogen can modulate neurotransmitter turnover, enhancing the levels of serotonin and noradrenaline (norepinephrine), and it is involved in the regulation of serotonin receptor number and function. Across the female reproductive life, fluctuating estrogen levels and low levels have been associated with depressed mood and there is strong support for a beneficial effect of estrogen-containing hormone treatment in depressed peri-menopausal women. Estrogen exerts its biological effects in large part through intracellular activation of its principal receptors, estrogen receptor α (ESR1) and estrogen receptor β (ESR2). Genetic variation in the estrogen receptors may therefore modify estrogen signalling, thus influencing a woman's susceptibility to developing depression. This review provides a synthesis of studies that have examined the association between estrogen receptor polymorphisms and depression-related mood disorders across the lifetime. Studies were identified through a search of the literature from January 1980 until March 2012 using MEDLINE, Web of Knowledge, Cochrane Library and PsycINFO databases. The studies conducted to date have produced inconsistent findings, which likely relates to the large heterogeneity in terms of the populations, study design and depression measures used. It appears unlikely that the common ESR1 variants rs2234693 and rs9340799 are associated with moderate depressive symptoms in women; however, there is some evidence that indicates a significant association with more severe depressive symptoms, major depressive disorder and anxiety. There are too few studies of ESR2 polymorphisms to draw any definite conclusions; however, preliminary evidence suggests that specific variants may modify the risk of depression associated with the use of hormone treatment in women. Few studies have investigated associations in men, and they have focused almost exclusively on ESR1, but all report non-significant findings. Much work is therefore still needed in this field. If it is confirmed that specific estrogen receptor polymorphisms are associated with the risk of depression, this could have important preventive and therapeutic implications, with the potential to develop targeted estrogen receptor agonists and antagonists. Furthermore, it is possible that such therapies may be more effective in treating particular people with depression based on their genetic profile, which is an exciting prospect given that many people do not respond to current antidepressant treatments.
越来越多的证据表明雌激素与抑郁症有关。雌激素可以调节神经递质的代谢,增加 5-羟色胺和去甲肾上腺素(去甲肾上腺素)的水平,并且参与调节 5-羟色胺受体的数量和功能。在女性生殖生命周期中,波动的雌激素水平和低水平与情绪低落有关,并且有强有力的证据支持含有雌激素的激素治疗对绝经前患有抑郁症的女性有益。雌激素主要通过其主要受体雌激素受体 α(ESR1)和雌激素受体 β(ESR2)的细胞内激活来发挥其生物学作用。因此,雌激素受体的遗传变异可能会改变雌激素信号转导,从而影响女性患抑郁症的易感性。这篇综述提供了一个综合研究,研究了整个生命周期中雌激素受体多态性与与抑郁相关的心境障碍之间的关系。通过在 MEDLINE、Web of Knowledge、Cochrane Library 和 PsycINFO 数据库中从 1980 年 1 月到 2012 年 3 月进行文献检索,确定了研究。迄今为止进行的研究得出的结果不一致,这可能与人群、研究设计和使用的抑郁措施方面的巨大异质性有关。似乎不太可能常见的 ESR1 变体 rs2234693 和 rs9340799 与女性中度抑郁症状有关;然而,有一些证据表明,它们与更严重的抑郁症状、重度抑郁症和焦虑症有显著关联。关于 ESR2 多态性的研究太少,无法得出任何明确的结论;然而,初步证据表明,特定的变体可能会改变与女性使用激素治疗相关的抑郁风险。很少有研究调查男性的关联,而且几乎只关注 ESR1,但所有报告都没有发现显著的关联。因此,在这一领域仍有许多工作要做。如果证实特定的雌激素受体多态性与患抑郁症的风险有关,这可能具有重要的预防和治疗意义,并有可能开发靶向雌激素受体激动剂和拮抗剂。此外,根据患者的遗传特征,这种疗法可能对某些患有抑郁症的人更有效,这是一个令人兴奋的前景,因为许多人对目前的抗抑郁治疗没有反应。