Maternal stress in the early postpartum period is associated with alterations in human milk microbiome composition.

IF 8.8 2区 医学 Q1 IMMUNOLOGY Brain, Behavior, and Immunity Pub Date : 2024-11-21 DOI:10.1016/j.bbi.2024.11.020
Hannah G Juncker, Rasmus R Jakobsen, Eva F G Naninck, Mark Davids, Hilde Herrema, Johannes B van Goudoever, Susanne R de Rooij, Aniko Korosi
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Abstract

Background: Maternal stress is associated with negative early-life development and (mental)health outcomes. There is recent evidence that maternal stress in the postpartum period impacts the nutrient composition of human milk (HM). However, it is currently not known whether maternal stress is associated with changes in the HM microbiome during the critical early postpartum period.

Methods: In this prospective observational cohort study, lactating women were recruited into a high-stress (HS, n = 23) and control (CTL, n = 69) group. The HS group included mothers with infants hospitalized for at least two days. Maternal stress was assessed using validated questionnaires and cortisol concentrations in hair, saliva and HM. HM was collected at days 10 and 24 and its microbiome was analyzed using 16 s rRNA sequencing. HM bacterial composition was compared between study groups and their correlation with maternal stress levels, maternal characteristics and infant outcomes was determined.

Results: HM microbiome β-diversity differed significantly between study groups, with HS mothers displaying decreased abundance of Streptococcus, Gemella, and Veillonella, and increased levels of Staphylococcus, Corynebacterium and Acinetobacter compared to the control group. While the strongest correlation of β-diversity was with stress, HM microbiome β-diversity also correlated significantly with maternal education level and infant sex. No correlation between HM microbiome composition and HM cortisol concentrations was found.

Conclusions: This study demonstrates stress-associated alterations in the early HM microbiome that could potentially contribute to early gut colonization and subsequent (mental)health outcomes. Future research is needed to elucidate the physiological significance of these changes for infant development and health.

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产后早期的母体压力与母乳微生物组组成的改变有关。
背景:孕产妇压力与早期生命发育和(心理)健康的负面结果有关。最近有证据表明,产妇在产后的压力会影响母乳(HM)的营养成分。然而,目前尚不清楚在关键的产后早期,产妇压力是否与母乳微生物组的变化有关:在这项前瞻性观察队列研究中,哺乳期妇女被分为高压力组(HS,n = 23)和对照组(CTL,n = 69)。高压力组包括婴儿住院至少两天的母亲。采用经过验证的问卷以及头发、唾液和血液中的皮质醇浓度对产妇的压力进行评估。在第 10 天和第 24 天收集 HM,并使用 16 s rRNA 测序分析其微生物组。比较了不同研究组的 HM 细菌组成,并确定了它们与产妇压力水平、产妇特征和婴儿结局的相关性:与对照组相比,HS 母亲体内链球菌、Gemella 和 Veillonella 的数量减少,而葡萄球菌、Corynebacterium 和 Acinetobacter 的数量增加。虽然 β 多样性与压力的相关性最强,但 HM 微生物组 β 多样性与母亲教育水平和婴儿性别也有显著相关性。HM微生物组的组成与HM皮质醇浓度之间没有相关性:这项研究表明,早期 HM 微生物组中与压力相关的改变可能会导致早期肠道定植和随后的(心理)健康结果。未来的研究需要阐明这些变化对婴儿发育和健康的生理意义。
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来源期刊
CiteScore
29.60
自引率
2.00%
发文量
290
审稿时长
28 days
期刊介绍: Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals. As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.
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