Inflammatory Biomarkers and Postpartum Depression: A Systematic Review of Literature
被引:14
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作者:
Lambert, Mathilde
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机构:
Hop Bicetre, AP HP, Serv Psychiat, Interne DES Psychiat Ile France, Le Kremlin Bicetre, FranceHop Bicetre, AP HP, Serv Psychiat, Interne DES Psychiat Ile France, Le Kremlin Bicetre, France
Lambert, Mathilde
[1
]
Gressier, Florence
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机构:
Univ Paris Sud, Hop Bicetre, AP HP,CESP,Inserm UMR1178,Serv Psychiat, Responsable Unite Psychiat Perinatale CHU Bicetre, Le Kremlin Bicetre, FranceHop Bicetre, AP HP, Serv Psychiat, Interne DES Psychiat Ile France, Le Kremlin Bicetre, France
Gressier, Florence
[2
]
机构:
[1] Hop Bicetre, AP HP, Serv Psychiat, Interne DES Psychiat Ile France, Le Kremlin Bicetre, France
[2] Univ Paris Sud, Hop Bicetre, AP HP,CESP,Inserm UMR1178,Serv Psychiat, Responsable Unite Psychiat Perinatale CHU Bicetre, Le Kremlin Bicetre, France
Objective: Postpartum Depression (PPD) affects over 15% new mothers. Its etiology is multifactorial and still partly unknown. Some hypotheses suggest a link with inflammation. This review aims to explore the existence of inflammatory biomarkers associated with PPD. The possibility of potential adjunct treatments, linked with these biomarkers, will be discussed. Method: The systematic review of literature was performed using in PubMed, PsycInfo and Embase, and 25 articles were included. Various biomarkers were identified. The most often studied are C-reactive protein (CRP), interleukins 6 and 10, tumor necrosis factor-alpha and interferon-gamma. Results: Although few results appear as significant during the various testing times, the dosage of some inflammation biomarkers, including CRP, at the very end of pregnancy or immediately after delivery could predict PPD. Interactions between inflammation and the corticotropic axis could explain PPD onset. Epigenetic mechanisms could lead to pro-inflammatory state. Several therapeutics provide interest due to their anti-inflammatory property. Conclusions: Further studies are needed to assess these biomarkers value as predictive factors of PPD and to consider adjunct treatments to antidepressants. If this value is confirmed, the inflammatory marker dosage, in particular CRP, could help to provide early screening of women at risk of PPD, parallel of the clinical evaluation. A zinc supplementation could then be offered.