HPA axis dysregulation and postpartum depression and anxiety symptoms in breastfeeding vs bottle-feeding parents.

IF 3.4 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Katharine E Bruce, Kathryn Wouk, Karen M Grewen, Brenda Pearson, Samantha Meltzer-Brody, Alison M Stuebe, Anna E Bauer
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引用次数: 0

Abstract

Objective: Hypothalamic-pituitary-adrenal (HPA) axis dysregulation has been implicated in the pathogenesis of perinatal mood disorders. Further, HPA axis response is known to be blunted during breastfeeding. We hypothesized that 1) postpartum depression/anxiety symptoms would be associated with HPA axis dysregulation, indexed by loss of expected adrenocorticotropic hormone (ACTH)-cortisol coupling, and 2) this association would vary by method of infant feeding.

Methods: Participants (N=222) intending to breastfeed were recruited in their 3rd trimester of pregnancy. During a lab visit at 2 months postpartum, depression and anxiety symptoms were assessed (Beck Depression Inventory score ≥14 and/or Speilberger State-Trait Anxiety Inventory score ≥40). Participants then breast or bottle-fed their infants as they would at home. After a 10-minute rest, participants completed the Trier Social Stress Test (TSST), a standardized stressor involving speech and math tasks. Blood ACTH and cortisol were measured 10 minutes after feeding, during each task, and at 10, 20, and 30 minutes of recovery. Multilevel models evaluated whether coupling of ACTH at time j with cortisol at time j+1 differed between those with and without depression/anxiety symptoms, and whether differences varied by feeding method.

Results: Of 205 participants who completed the TSST, 44 had depression/anxiety symptoms at 2-months postpartum. Depression/anxiety symptoms were associated with reduced ACTH-cortisol coupling (adjusted beta: -0.03; p-value: 0.03). Among those who breastfed, those with depression/anxiety showed greater blunting of ACTH-cortisol coupling than those without (adjusted beta: -0.04; p-value: 0.02), while those who bottle-fed had similar coupling patterns regardless of depression/anxiety symptoms (adjusted beta: -0.01; p-value: 0.87).

Conclusion: HPA axis response was blunted in those with postpartum depression/anxiety symptoms, and blunting varied by method of infant feeding. Findings support HPA axis dysregulation in perinatal mood and anxiety disorders. Future research should explore how method of infant feeding influences the relationship between perinatal mood disorders and HPA axis dysregulation. Elucidating the mechanistic pathways underlying perinatal mood disorders can aid in the development of better diagnostic and treatment strategies.

母乳喂养与奶瓶喂养父母的 HPA 轴失调以及产后抑郁和焦虑症状。
目的:下丘脑-垂体-肾上腺(HPA)轴失调与围产期情绪障碍的发病机制有关。此外,众所周知,母乳喂养期间 HPA 轴的反应会减弱。我们假设:1)产后抑郁/焦虑症状将与 HPA 轴失调有关,以预期促肾上腺皮质激素(ACTH)-皮质醇耦合的丧失为指标;2)这种关联将因婴儿喂养方式而异:方法:在怀孕三个月时招募打算母乳喂养的参与者(N=222)。在产后 2 个月的实验室访问期间,对抑郁和焦虑症状进行了评估(贝克抑郁量表得分≥14 和/或斯皮尔伯格状态-特质焦虑量表得分≥40)。然后,参与者像在家里一样用母乳或奶瓶喂养婴儿。休息10分钟后,参与者完成特里尔社会压力测试(TSST),这是一项标准化压力测试,包括语言和数学任务。在喂奶后 10 分钟、完成每项任务期间以及恢复后 10 分钟、20 分钟和 30 分钟分别测量了血液中的促肾上腺皮质激素和皮质醇。多层次模型评估了有抑郁/焦虑症状和无抑郁/焦虑症状的人在第j个时间的促肾上腺皮质激素与第j+1个时间的皮质醇的耦合是否存在差异,以及差异是否因喂食方法而异:在完成 TSST 的 205 名参与者中,有 44 人在产后 2 个月出现抑郁/焦虑症状。抑郁/焦虑症状与促肾上腺皮质激素-皮质醇耦合降低有关(调整后的β值:-0.03;P值:0.03)。在母乳喂养者中,有抑郁/焦虑症状者比无抑郁/焦虑症状者表现出更大的促肾上腺皮质激素-皮质醇耦合钝化(调整后的贝塔值:-0.04;P值:0.02),而奶瓶喂养者无论是否有抑郁/焦虑症状,其耦合模式相似(调整后的贝塔值:-0.01;P值:0.87):结论:产后抑郁/焦虑症状患者的 HPA 轴反应迟钝,且迟钝程度因婴儿喂养方式而异。研究结果支持围产期情绪和焦虑障碍中的 HPA 轴失调。未来的研究应探讨婴儿喂养方式如何影响围产期情绪障碍与 HPA 轴调节失调之间的关系。阐明围产期情绪障碍的机制途径有助于制定更好的诊断和治疗策略。
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来源期刊
Psychoneuroendocrinology
Psychoneuroendocrinology 医学-精神病学
CiteScore
7.40
自引率
8.10%
发文量
268
审稿时长
66 days
期刊介绍: Psychoneuroendocrinology publishes papers dealing with the interrelated disciplines of psychology, neurobiology, endocrinology, immunology, neurology, and psychiatry, with an emphasis on multidisciplinary studies aiming at integrating these disciplines in terms of either basic research or clinical implications. One of the main goals is to understand how a variety of psychobiological factors interact in the expression of the stress response as it relates to the development and/or maintenance of neuropsychiatric illnesses.
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