Department of Psychiatry, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.
J Clin Endocrinol Metab. 2011 Jan;96(1):E40-7. doi: 10.1210/jc.2010-0978. Epub 2010 Oct 13.
Perinatal depression has a prevalence of 10% with devastating consequences for mother and baby. The prospective identification of those at risk for postpartum (PPD) or prenatal (PND) depression has led to biomarker searches in pregnancy. There are conflicting reports of associations between midpregnancy placental CRH (pCRH) and PPD or PND.
The objective of the study was to quantify the association of maternal pCRH with PPD and PND.
This was a prospective cohort study (the Pregnancy, Infection, and Nutrition Study).
The study was conducted at a prenatal clinics at the University of North Carolina at Chapel Hill.
Patients included 1230 pregnant women.
The relationship between pCRH at less than 20 wk and 24-29 wk and maternal depression assessed in pregnancy [Center for Epidemiologic Studies Depression Scale (CES-D)] and postpartum (12 wk and 1 yr) with the Edinburgh Postnatal Depression Scale (EPDS).
At 24-29 wk, 24.8% of women had CES-D score of 17 or greater, and 9.7% had a CES-D score of 25 or greater. At 12 wk postpartum, 18.2% of women had an EPDS score of 10 or greater and 7.6% had an EPDS score of 13 or greater. CRH measures at less than 20 wk and 24-29 wk were inversely correlated with a CES-D score at 24-29 wk (n = 1080, P < 0.05 and P < 0.01, respectively). Pregnancy pCRH was not correlated with the EPDS score at 12 wk (n = 484) or 1 yr postpartum (n = 391). In covariate-adjusted models, higher pCRH was not associated with a CES-D of 17 or greater at 24-29 wk (odds ratio 0.88 per sd change in pCRH at 24-29 wk, 95% confidence interval 0.76-1.03). There was no association between log CRH at 24-29 wk and PPD (covariate-adjusted odds ratio per sd 0.99, 95% confidence interval 0.69-1.42).
Higher midpregnancy pCRH was not associated with an increased risk of PND or PPD.
围产期抑郁症的患病率为 10%,对母婴都有毁灭性的影响。对产后(PPD)或产前(PND)抑郁症高危人群的前瞻性识别导致了妊娠期间生物标志物的搜索。在妊娠中期胎盘 CRH(pCRH)与 PPD 或 PND 之间的关联存在相互矛盾的报告。
本研究的目的是量化母亲 pCRH 与 PPD 和 PND 的相关性。
这是一项前瞻性队列研究(怀孕、感染和营养研究)。
该研究在北卡罗来纳大学教堂山分校的产前诊所进行。
患者包括 1230 名孕妇。
在妊娠(中心流行病学研究抑郁量表(CES-D))和产后(12 周和 1 年)时,妊娠中期(小于 20 周和 24-29 周) pCRH 与产妇抑郁的关系,采用爱丁堡产后抑郁量表(EPDS)。
在 24-29 周时,24.8%的女性 CES-D 评分≥17,9.7%的女性 CES-D 评分≥25。产后 12 周时,18.2%的女性 EPDS 评分≥10,7.6%的女性 EPDS 评分≥13。小于 20 周和 24-29 周的 CRH 测量值与 24-29 周时的 CES-D 评分呈负相关(n=1080,分别为 P<0.05 和 P<0.01)。妊娠 pCRH 与 12 周时的 EPDS 评分(n=484)或产后 1 年时的 EPDS 评分(n=391)均无相关性。在调整协变量的模型中,较高的 pCRH 与 24-29 周时 CES-D 评分≥17 无关(24-29 周时 pCRH 每标准差变化的优势比为 0.88,95%置信区间为 0.76-1.03)。24-29 周时 log CRH 与 PPD 之间无关联(调整后的协变量比值比每标准差为 0.99,95%置信区间为 0.69-1.42)。
妊娠中期较高的 pCRH 与 PND 或 PPD 风险增加无关。