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5HTTLPR polymorphism and postpartum depression risk
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AbstractObjective:Postpartum depression (PPD) is an episode of major depressive disorder that affecting women of childbearing age. 5-HTTLPR is 1 of the most extensively investigated polymorphisms in PPD. However, the previous results were inconsistent and inclusive. Hence, we performed a meta-analysis to precisely evaluate the association between 5-HTTLPR polymorphism and PPD susceptibility.Methods:The studies were retrieved through databases including PubMed, web of science, EMASE, and CNKI. The odd ratios (ORs) and 95% confidence interval (CIs) were applied for evaluating the genetic association between 5-HTTLPR (L/S) polymorphism and PPD risk.Results:Six studies with 519 cases and 737 controls were enrolled in the present study. The frequencies of allelic (OR = 0.72, 95%CI = 0.60–0.85,P = .0001) and dominant (OR = 0.57, 95%CI = 0.44–0.73,P = .004) models of 5-HTTLPR polymorphism significantly decreased in patients with PPD than those in the healthy controls. Subgroup analysis based on ethnicity revealed that the allelic (OR = 0.71, 95%CI = 0.60–0.85,P = .0001) and dominant (OR = 0.51, 95%CI = 0.32–0.79,P = .003) models of 5-HTTLPR polymorphism were significantly associated with PPD risk in Asian population (P > .05). No evidence was observed between the recessive model of 5-HTTLPR polymorphism and PPD risk (P > .05).Conclusions:The allelic and dominant models of 5-HTTLPR polymorphism might be protective factors for PPD. To confirm these results, larger number of association studies or multicenter case–control studies are necessary in the future.
Ovid Technologies (Wolters Kluwer Health)
Title: 5HTTLPR polymorphism and postpartum depression risk
Description:
AbstractObjective:Postpartum depression (PPD) is an episode of major depressive disorder that affecting women of childbearing age.
5-HTTLPR is 1 of the most extensively investigated polymorphisms in PPD.
However, the previous results were inconsistent and inclusive.
Hence, we performed a meta-analysis to precisely evaluate the association between 5-HTTLPR polymorphism and PPD susceptibility.
Methods:The studies were retrieved through databases including PubMed, web of science, EMASE, and CNKI.
The odd ratios (ORs) and 95% confidence interval (CIs) were applied for evaluating the genetic association between 5-HTTLPR (L/S) polymorphism and PPD risk.
Results:Six studies with 519 cases and 737 controls were enrolled in the present study.
The frequencies of allelic (OR = 0.
72, 95%CI = 0.
60–0.
85,P = .
0001) and dominant (OR = 0.
57, 95%CI = 0.
44–0.
73,P = .
004) models of 5-HTTLPR polymorphism significantly decreased in patients with PPD than those in the healthy controls.
Subgroup analysis based on ethnicity revealed that the allelic (OR = 0.
71, 95%CI = 0.
60–0.
85,P = .
0001) and dominant (OR = 0.
51, 95%CI = 0.
32–0.
79,P = .
003) models of 5-HTTLPR polymorphism were significantly associated with PPD risk in Asian population (P > .
05).
No evidence was observed between the recessive model of 5-HTTLPR polymorphism and PPD risk (P > .
05).
Conclusions:The allelic and dominant models of 5-HTTLPR polymorphism might be protective factors for PPD.
To confirm these results, larger number of association studies or multicenter case–control studies are necessary in the future.
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