Bridging Neurobiological Insights and Clinical Biomarkers in Postpartum Depression: A Narrative Review.
Keyi ZhangLingxuan HeZhuoen LiRuxuan DingXiaojiao HanBingqing ChenGuoxin CaoJiang-Hong YeTian LiRao FuPublished in: International journal of molecular sciences (2024)
Postpartum depression (PPD) affects 174 million women worldwide and is characterized by profound sadness, anxiety, irritability, and debilitating fatigue, which disrupt maternal caregiving and the mother-infant relationship. Limited pharmacological interventions are currently available. Our understanding of the neurobiological pathophysiology of PPD remains incomplete, potentially hindering the development of novel treatment strategies. Recent hypotheses suggest that PPD is driven by a complex interplay of hormonal changes, neurotransmitter imbalances, inflammation, genetic factors, psychosocial stressors, and hypothalamic-pituitary-adrenal (HPA) axis dysregulation. This narrative review examines recent clinical studies on PPD within the past 15 years, emphasizing advancements in neuroimaging findings and blood biomarker detection. Additionally, we summarize recent laboratory work using animal models to mimic PPD, focusing on hormone withdrawal, HPA axis dysfunction, and perinatal stress theories. We also revisit neurobiological results from several brain regions associated with negative emotions, such as the amygdala, prefrontal cortex, hippocampus, and striatum. These insights aim to improve our understanding of PPD's neurobiological mechanisms, guiding future research for better early detection, prevention, and personalized treatment strategies for women affected by PPD and their families.
Keyphrases
- prefrontal cortex
- polycystic ovary syndrome
- sleep quality
- pregnancy outcomes
- oxidative stress
- resting state
- functional connectivity
- type diabetes
- gene expression
- skeletal muscle
- multiple sclerosis
- genome wide
- autism spectrum disorder
- current status
- white matter
- brain injury
- stress induced
- cerebral ischemia
- loop mediated isothermal amplification
- weight gain
- subarachnoid hemorrhage
- label free