Schiller Crystal Edler, Meltzer-Brody Samantha, Rubinow David R
Psychiatry Department,University of North Carolina at Chapel Hill,Chapel Hill,North Carolina,USA.
CNS Spectr. 2015 Feb;20(1):48-59. doi: 10.1017/S1092852914000480. Epub 2014 Sep 29.
Despite decades of research aimed at identifying the causes of postpartum depression (PPD), PPD remains common, and the causes are poorly understood. Many have attributed the onset of PPD to the rapid perinatal change in reproductive hormones. Although a number of human and nonhuman animal studies support the role of reproductive hormones in PPD, several studies have failed to detect an association between hormone concentrations and PPD. The purpose of this review is to examine the hypothesis that fluctuations in reproductive hormone levels during pregnancy and the postpartum period trigger PPD in susceptible women. We discuss and integrate the literature on animal models of PPD and human studies of reproductive hormones and PPD. We also discuss alternative biological models of PPD to demonstrate the potential for multiple PPD phenotypes and to describe the complex interplay of changing reproductive hormones and alterations in thyroid function, immune function, hypothalamic-pituitary-adrenal (HPA) axis function, lactogenic hormones, and genetic expression that may contribute to affective dysfunction. There are 3 primary lines of inquiry that have addressed the role of reproductive hormones in PPD: nonhuman animal studies, correlational studies of postpartum hormone levels and mood symptoms, and hormone manipulation studies. Reproductive hormones influence virtually every biological system implicated in PPD, and a subgroup of women seem to be particularly sensitive to the effects of perinatal changes in hormone levels. We propose that these women constitute a "hormone-sensitive" PPD phenotype, which should be studied independent of other PPD phenotypes to identify underlying pathophysiology and develop novel treatment targets.
尽管数十年来一直致力于确定产后抑郁症(PPD)的病因,但PPD仍然很常见,其病因也知之甚少。许多人将PPD的发病归因于围产期生殖激素的快速变化。虽然一些人类和非人类动物研究支持生殖激素在PPD中的作用,但也有几项研究未能检测到激素浓度与PPD之间的关联。本综述的目的是检验这样一种假设,即妊娠和产后期间生殖激素水平的波动会触发易感女性的PPD。我们讨论并整合了关于PPD动物模型以及生殖激素与PPD的人类研究的文献。我们还讨论了PPD的替代生物学模型,以展示多种PPD表型的可能性,并描述生殖激素变化与甲状腺功能、免疫功能、下丘脑 - 垂体 - 肾上腺(HPA)轴功能、催乳激素和基因表达改变之间复杂的相互作用,这些可能导致情感功能障碍。有三条主要的研究方向探讨了生殖激素在PPD中的作用:非人类动物研究、产后激素水平与情绪症状的相关性研究以及激素操纵研究。生殖激素几乎影响与PPD相关的每一个生物系统,并且有一部分女性似乎对围产期激素水平变化的影响特别敏感。我们认为这些女性构成了一种“激素敏感型”PPD表型,应该独立于其他PPD表型进行研究,以确定潜在的病理生理学机制并开发新的治疗靶点。