Erlangen University Perinatal Center, Department of Gynaecology and Obstetrics, Erlangen University Hospital, Friedrich Alexander University of Erlangen-Nuremberg, Erlangen, Germany.
J Psychiatr Res. 2012 Sep;46(9):1109-17. doi: 10.1016/j.jpsychires.2012.05.011. Epub 2012 Jun 20.
A number of studies indicate that altered serotonergic transmission may be a risk factor for depression in the peripartum period. The aim of this study was to investigate whether genetic polymorphisms in the TPH2 gene, the gene product of which is the rate-limiting enzyme in the biosynthesis of serotonin in the central nervous system, are associated with depressive symptoms in pregnancy and the postpartum period.
In a cohort of 361 Caucasians, the severity of depression was assessed prospectively during pregnancy (third trimester) and the postpartum period (2-3 days and 6-8 months) using the Edinburgh Postnatal Depression Scale (EPDS). Tagging single nucleotide polymorphisms (SNPs) in TPH2 and SNPs that are known to be of functional relevance were genotyped. For each haplotype block or SNP, a multifactorial linear mixed model was performed to analyse the EPDS values over time.
The haplotype block in the promoter region of TPH2 showed significant associations with depression values during pregnancy and 6-8 months afterwards. Additionally, a haplotype block in intron 8 had an influence on depression values during pregnancy, but not after birth. There was a significant interaction between time and haplotypes and the severity of depression. The effect of TPH2 haplotypes on EPDS values was strongest during pregnancy and 6 months after birth, with a low depression rating in the first few days after delivery for all women.
In this cohort, TPH2 haplotypes known to be of functional relevance were found to be associated with different EPDS values during and after pregnancy. These haplotypes were associated with depressive symptoms both before and after delivery and were thus not specific for postpartum-onset depression. This underlines the relevance of these functional polymorphisms for depression in general and the importance of longitudinal assessments in research on postpartum depression.
多项研究表明,5-羟色胺能传递的改变可能是围产期抑郁的一个危险因素。本研究的目的是探讨中枢神经系统 5-羟色胺生物合成限速酶 TPH2 基因的遗传多态性是否与妊娠和产后期间的抑郁症状有关。
在一个由 361 名高加索人组成的队列中,使用爱丁堡产后抑郁量表(EPDS)前瞻性评估妊娠(孕晚期)和产后(产后 2-3 天和 6-8 个月)期间的抑郁严重程度。对 TPH2 中的标记单核苷酸多态性(SNP)和已知具有功能相关性的 SNP 进行基因分型。对于每个单倍型块或 SNP,采用多因素线性混合模型分析 EPDS 值随时间的变化。
TPH2 启动子区域的单倍型块与妊娠期间和产后 6-8 个月的抑郁值显著相关。此外,内含子 8 中的一个单倍型块对妊娠期间的抑郁值有影响,但对产后没有影响。TPH2 单倍型与抑郁严重程度之间存在显著的时间和单倍型相互作用。TPH2 单倍型对 EPDS 值的影响在妊娠期间和产后 6 个月最强,所有女性产后最初几天的抑郁评分都较低。
在本队列中,与功能相关的 TPH2 单倍型与妊娠期间和产后的不同 EPDS 值相关。这些单倍型与分娩前后的抑郁症状相关,因此不仅与产后发病的抑郁相关,而且强调了这些功能多态性对一般抑郁的相关性以及在产后抑郁研究中进行纵向评估的重要性。