Postpartum depression: association with genetic polymorphisms of noradrenaline metabolic enzymes and the risk factors.
10.12122/j.issn.1673-4254.2019.01.09
- Author:
Jiahui MA
1
;
Zhengdong HUANG
1
;
Saiying WANG
1
;
Shanshan ZHENG
1
;
Kaiming DUAN
1
Author Information
1. Department of Anesthesiology, Third Xiangya Hospital of Central South University, Changsha 410013, China.
- Publication Type:Journal Article
- Keywords:
catechol-O-methyltransferase;
genetic variants;
monoamine oxidase A;
noradrenaline;
postpartum depression
- MeSH:
Catechol O-Methyltransferase;
genetics;
Cesarean Section;
adverse effects;
Depression, Postpartum;
diagnosis;
enzymology;
genetics;
Domestic Violence;
psychology;
Female;
Gene-Environment Interaction;
Genotype;
Haplotypes;
Humans;
Linkage Disequilibrium;
Monoamine Oxidase;
genetics;
Norepinephrine;
metabolism;
Polymorphism, Single Nucleotide;
Postoperative Complications;
diagnosis;
enzymology;
genetics;
Pregnancy;
Pregnancy Complications;
etiology;
psychology;
Risk Factors;
Stress, Psychological
- From:
Journal of Southern Medical University
2019;39(1):57-62
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the association of genetic polymorphisms of norepinephrine metabolizing enzymes with postpartum depression and analyze the risk factors for postpartum depression in women following cesarean section.
METHODS:A total of 591 Chinese woman of Han Nationality undergoing caesarean section were enrolled in this study. The diagnosis of postpartum depression was established for an Edinburgh Postnatal Depression Scale (EPDS) score ≥9. For all the women without antepartum depression, the genotypes of catechol-O-methyltransferase (COMT; at 5 sites including rs2020917 and rs737865) and monoamine oxidase A (rs6323) were determined using Sequenom Mass Array single nucleotide polymorphism (SNP) analysis. We analyzed the contribution of the genetic factors (SNPs, linkage disequilibrium and haplotype) to postpartum depression and performed logistic regression analysis to identify all the potential risk factors for postpartum depression and define the interactions between the genetic and environmental factors.
RESULTS:The incidence of postpartum depression was 18.1% in this cohort. Univariate analysis suggested that COMT polymorphism at rs2020917 (TT genotype) and rs737865 (GG genotype) were significantly correlated with the occurrence of postpartum depression ( < 0.05). Logistic regression analysis showed that COMT polymorphism at rs2020917 (TT genotype) and rs737865 (GG genotype), severe stress during pregnancy, and domestic violence were the risk factors for postpartum depression ( < 0.05); no obvious interaction was found between the genetic polymorphisms and the environmental factors in the occurrence of postpartum depression.
CONCLUSIONS:The rs2020917TT and rs737865GG genotypes of COMT, stress in pregnancy, and domestic violence are the risk factors for postpartum depression.
