Nielsen Sebastian Werngreen, Ljungdalh Perniller Møller, Nielsen Jan, Nørgård Bente Mertz, Qvist Niels
Department of Surgical Gastroenterology A, Odense University Hospital, and Research Unit of Surgery, Institute of Clinical Research, University of Southern Denmark, 5000, Odense C, DK, Denmark.
, Engelshøjgade 26 1TH, 6400, Sønderborg, Denmark.
Orphanet J Rare Dis. 2017 Jun 20;12(1):116. doi: 10.1186/s13023-017-0667-4.
Hirschsprung's disease is a rare condition caused by congenital malformation of the gastrointestinal tract affecting 1:5000 children. Not much is known about risk factors for development of Hirschsprung's disease. Two clinical cases of hirschsprung's disease led to an investigation of the association between maternal use of selective serotonin reuptake inhibitors (SSRIs) during pregnancy and development of Hirschsprung's Disease in the newborn child. The study examined a nationwide, unselected cohort of children born in Denmark from 1 January 1996 until 12 March 2016 (n = 1,256,317). We applied multivariate models to register-based data to estimate the odds ratio of Hirschsprung's disease, adjusting for possible confounders. The studied exposure period for SSRIs were 30 days prior to conception to the end of the first trimester.
In the main exposed cohort the prevalence of Hirschsprung's disease was 16/19.807 (0.08%) compared to 584/1.236.510 (0.05%) in the unexposed cohort. In women who redeemed a minimum of one prescription of selective serotonin reuptake inhibitors, the adjusted odds ratio for development of Hirschsprung's disease was 1.76 (95%CI: 1.07-2.92). In women who redeemed a minimum of two prescriptions, the adjusted odds ratio for Hirschsprung's disease was 2.34 (95% CI: 1.21-4.55).
Our data suggest that early maternal use of selective serotonin reuptake inhibitors is significantly associated with the development of Hirschsprung's disease in the newborn child. Treatment of depression during pregnancy always has to be weighed against the risks posed by untreated maternal depression. Our results have to be confirmed in other studies.
先天性巨结肠症是一种由胃肠道先天性畸形引起的罕见疾病,发病率约为1/5000。目前对先天性巨结肠症的发病风险因素了解不多。两例先天性巨结肠症临床病例促使人们对孕期母亲使用选择性5-羟色胺再摄取抑制剂(SSRI)与新生儿先天性巨结肠症发病之间的关联展开调查。该研究调查了1996年1月1日至2016年3月12日在丹麦出生的全国性、未经筛选的队列儿童(n = 1,256,317)。我们将多变量模型应用于基于登记的数据,以估计先天性巨结肠症的比值比,并对可能的混杂因素进行调整。SSRI的研究暴露期为受孕前30天至孕早期结束。
在主要暴露队列中,先天性巨结肠症的患病率为16/19,807(0.08%),而未暴露队列中的患病率为584/1,236,510(0.05%)。在至少兑换过一次选择性5-羟色胺再摄取抑制剂处方的女性中,先天性巨结肠症发病的调整比值比为1.76(95%置信区间:1.07 - 2.92)。在至少兑换过两次处方的女性中,先天性巨结肠症的调整比值比为2.34(95%置信区间:1.21 - 4.55)。
我们的数据表明,母亲早期使用选择性5-羟色胺再摄取抑制剂与新生儿先天性巨结肠症的发病显著相关。孕期抑郁症的治疗始终需要权衡未治疗的母亲抑郁症所带来的风险。我们的结果有待其他研究证实。