Krysko Kristen M, Anderson Annika, Singh Jessica, McPolin Kira, Rutatangwa Alice, Rowles William, Sadovnick A Dessa, Houtchens Maria K, Bove Riley
Department of Neurology, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA/ Division of Neurology, Department of Medicine, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada/Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, ON, Canada.
Department of Neurology, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA.
Mult Scler. 2022 May;28(6):970-979. doi: 10.1177/13524585211041108. Epub 2021 Sep 9.
Peripartum depression (PPD) is underexplored in multiple sclerosis (MS).
To evaluate prevalence of and risk factors for PPD in women with MS.
Retrospective single-center analysis of women with MS with a live birth. Prevalence of PPD was estimated with logistic regression with generalized estimating equations (GEE). GEE evaluated predictors of PPD (e.g. age, marital status, parity, pre-pregnancy depression/anxiety, antidepressant discontinuation, sleep disturbance, breastfeeding, relapses, gadolinium-enhancing lesions, and disability). Factors significant in univariable analyses were included in multivariable analysis.
We identified 143 live births in 111 women (mean age 33.1 ± 4.7 years). PPD was found in 18/143 pregnancies (12.6%, 95% CI = 7.3-17.8). Factors associated with PPD included older age (OR 1.16, 95% CI = 1.03-1.32 for 1-year increase), primiparity (OR 4.02, CI = 1.14-14.23), pre-pregnancy depression (OR 3.70, CI = 1.27-10.01), sleep disturbance (OR 3.23, CI = 1.17-8.91), and breastfeeding difficulty (OR 3.58, CI = 1.27-10.08). Maternal age (OR 1.17, CI = 1.02-1.34), primiparity (OR 8.10, CI = 1.38-47.40), and pre-pregnancy depression (OR 3.89, CI = 1.04-14.60) remained significant in multivariable analyses. Relapses, MRI activity, and disability were not associated with PPD.
The prevalence of PPD in MS appeared similar to the general population, but was likely underestimated due to lack of screening. PPD can affect MS self-management and offspring development, and prospective studies are needed.
围产期抑郁症(PPD)在多发性硬化症(MS)中的研究较少。
评估MS女性中PPD的患病率及危险因素。
对有活产史的MS女性进行回顾性单中心分析。采用广义估计方程(GEE)的逻辑回归估计PPD的患病率。GEE评估PPD的预测因素(如年龄、婚姻状况、产次、孕前抑郁/焦虑、停用抗抑郁药、睡眠障碍、母乳喂养、复发、钆增强病变和残疾)。单变量分析中有显著意义的因素纳入多变量分析。
我们确定了111名女性的143次活产(平均年龄33.1±4.7岁)。143例妊娠中有18例发生PPD(12.6%,95%CI=7.3-17.8)。与PPD相关的因素包括年龄较大(每增加1岁,OR 1.16,95%CI=1.03-1.32)、初产(OR 4.02,CI=1.14-14.23)、孕前抑郁(OR 3.70,CI=1.27-10.01)、睡眠障碍(OR 3.23,CI=1.17-8.91)和母乳喂养困难(OR 3.58,CI=1.27-10.08)。多变量分析中,产妇年龄(OR 1.17,CI=1.02-1.34)、初产(OR 8.10,CI=1.38-47.40)和孕前抑郁(OR 3.89,CI=1.04-14.60)仍然具有显著意义。复发、MRI活动和残疾与PPD无关。
MS中PPD的患病率似乎与一般人群相似,但由于缺乏筛查可能被低估。PPD会影响MS的自我管理和后代发育,需要进行前瞻性研究。