A scoping review of functional genomics in perinatal depression☆

被引:0
作者
Bruzzone, Silvia Elisabetta Portis [1 ,2 ]
Garre, Victoria Frederikke S. [1 ]
Hogh, Stinne [1 ]
Frokjaer, Vibe G. [1 ,2 ,5 ]
O'Donnell, Kieran J. [3 ,4 ]
Eid, Rand S. [6 ]
机构
[1] Rigshosp, Neurobiol Res Unit, Copenhagen, Denmark
[2] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[3] Yale Sch Med, Yale Child Study Ctr, New Haven, CT USA
[4] Yale Sch Med, Dept Obstet Gynecol & Reprod Sci, New Haven, CT USA
[5] Psychiat Ctr Copenhagen, Mental Hlth Serv Capital Reg Denmark, Copenhagen, Denmark
[6] McGill Univ, Dept Psychol, Montreal, PQ, Canada
基金
欧盟地平线“2020”;
关键词
Depression; Perinatal; Postpartum; Gene expression; DNA methylation; Biomarkers; POSTPARTUM DEPRESSION; INFLAMMATORY MARKERS; DNA METHYLATION; ASSOCIATION; DISORDERS; PREGNANCY; RECEPTOR; ANXIETY; WOMEN; MOOD;
D O I
10.1016/j.yfrne.2025.101202
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Perinatal depression (PD) is a major public mental health problem affecting 10-20% of pregnant women. Women undergo profound biological and psychosocial adaptations during pregnancy and the postpartum period. Measures of genomic function can reveal pregnancy-associated adaptations, and may also illuminate mechanisms underlying PD, offering potential for clinically useful biomarkers. A systematic overview of functional genomic signatures of PD is currently lacking. We conducted a scoping review of the current literature on two aspects of genomic function: DNA methylation and gene expression. Literature was reviewed through May 2024. Thirtythree studies met inclusion criteria. Altered genomic function related to estrogen signaling and immune function were most consistently associated with PD. However, the reviewed studies used heterogeneous molecular profiling methods, were based on small sample sizes, largely used candidate-gene approaches, and reported mixed findings. The lack of replicated signatures underscores the need for a more comprehensive assessment of genomic function in PD.
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页数:13
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