Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Kapittelweg 29, 6525 EN, Nijmegen, The Netherlands.
Faculty of Earth and Life Sciences, Athena Institute, VU University, De Boelelaan 1085, 1081 HV, Amsterdam, The Netherlands.
Sci Rep. 2021 Feb 4;11(1):3051. doi: 10.1038/s41598-021-81204-9.
Probiotic use may be an efficacious treatment option to effectively manage symptoms of prenatal maternal anxiety and depression. Our primary aim was to test feasibility and acceptability for a probiotic randomized controlled trial (RCT) in pregnant women with pre-existing symptoms. This double-blind pilot RCT included 40 pregnant women with low-risk pregnancies and elevated depressive symptoms and/or anxiety. Once daily, participants orally consumed a probiotic (Ecologic Barrier) or a placebo, from 26 to 30 weeks gestation until delivery. A priori key progression criteria for primary outcomes were determined to decide whether or not a full RCT was feasible and acceptable. Secondary outcomes included depressive symptoms, anxiety, stress, and maternal bonding to offspring. In 19 months, 1573 women were screened; following screening, 155 women (10%) were invited for participation, of whom 135 (87%) received study information, and 40 women (30%) were included. Four out of six a priori determined criteria for success on feasibility and acceptability were met. After 8 weeks of intervention, there was no significant difference between the probiotic and placebo groups for secondary outcomes. The pilot trial was feasible and acceptable, but hampered by recruitment method and study design. Secondary endpoints did not reveal differences between the groups for improving maternal mood.
益生菌的使用可能是一种有效的治疗选择,可以有效地控制产前母婴焦虑和抑郁的症状。我们的主要目的是测试在有前期症状的孕妇中进行益生菌随机对照试验(RCT)的可行性和可接受性。这项双盲先导 RCT 纳入了 40 名低风险妊娠且抑郁症状和/或焦虑症状升高的孕妇。从 26 周到 30 周妊娠开始,参与者每天口服一次益生菌(Ecologic Barrier)或安慰剂,直至分娩。预先确定了主要结局的关键进展标准,以确定是否进行全面的 RCT 是可行和可接受的。次要结局包括抑郁症状、焦虑、压力和对后代的母性联系。在 19 个月内,对 1573 名妇女进行了筛查;在筛查后,邀请了 155 名妇女(10%)参加,其中 135 名(87%)收到了研究信息,40 名(30%)妇女入选。满足了可行性和可接受性的 6 个预先确定的成功标准中的 4 个。干预 8 周后,益生菌组和安慰剂组的次要结局无显著差异。初步试验是可行和可接受的,但受到招募方法和研究设计的限制。次要终点并未显示出两组在改善产妇情绪方面的差异。