5-HTTLPR polymorphism and depression risk in Parkinson's disease: an updated meta-analysis.

Published
March 29, 2020
Journal
Acta neurologica Belgica
PICOID
56c174c4
DOI
Citations
7
Keywords
5-HTTLPR, 5-Hydroxytryptamine transporter, Depression, Gene, Parkinson's disease
Copyright
© 2020. Belgian Neurological Society.
Patients/Population/Participants

PD patients

Intervention

5-HTTLPR genotype (S/S-Allele)

Comparison

PD patients without depression

Outcome

Depression risk

Abstract

P
I
C
O

The relationship between the 5-hydroxytryptamine transporter gene-linked polymorphic region (5-HTTLPR) and depression in Parkinson's disease (PD) has remained controversial. Therefore, we conducted this meta-analysis to evaluate the relationship between 5-HTTLPR polymorphisms and depression in PD. Relevant online databases were searched for cross-sectional, case-control or cohort studies examining relations between 5-HTTLPR polymorphisms (S/L) and the risk of developing depression of PD using a meta-analysis. Odd ratios (ORs) of 5-HTTLPR polymorphisms (S/L allele genotype) were calculated between depression in PD and PD for each study. Five observational studies were identified. Overall ORs for 5-HTTLPR S-Allele genotype was 1.98 (95% CI 0.92-4.26) in the dominant model, 1.43 (95% CI 1.08-1.90) in the recessive model, 2.64 (95% CI 1.01-6.88) in the additive model, independently. The overall ORs of S-Allele genotype was 1.51 (95% CI 0.63-3.64) for the Caucasian subgroup, and 1.44 (95% CI 1.05-1.98) for the non-Caucasian subgroup in the recessive model. This meta-analysis indicates that the 5-HTTLPR genotype (S/S-Allele) is correlated with an increased depression risk in PD, and this highlights the needs for these people to take some effective approaches (if any) in prevention of depression of PD before its onset.

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