Assessment of TREM2 rs75932628 variant's association with Parkinson's disease in a Greek population and Meta-analysis of current data.
Int J Neurosci
; 131(6): 544-548, 2021 Jun.
Article
em En
| MEDLINE
| ID: mdl-32250197
ABSTRACT
BACKGROUND:
Α number of genetic variants are considered to confer susceptibility to Parkinson's disease (PD). Rs75392628 (R47H), a rare variant of TREM2 gene, has been linked to PD, although its role on PD remains conflicting.OBJECTIVE:
Detection of a possible contribution of rs75392628 variant of TREM2 gene to PD risk.METHODS:
A total of 358 PD patients and 358 healthy controls genotyped for rs75392628. In addition, a meta-analysis was performed by merging our results with those from previous studies.RESULTS:
The rare variant of rs75932628 (47H) of TREM2 gene was not detected on cohort. Meta-analysis of a total of 9271 PD cases and 9777 controls across 14 independent PD data sets from 9 studies, including the present study, did not show any statistically significant effect of rs75392628 on PD risk (ORFE1.54 95% CI0.87-2.73. ORRE 1.54, 95%CI 0.71-3.32).CONCLUSIONS:
Rs75392628 TREM2 variant is rather unlikely to be a major genetic risk contributor of PD.Palavras-chave
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Doença de Parkinson
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Glicoproteínas de Membrana
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Receptores Imunológicos
Tipo de estudo:
Observational_studies
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Risk_factors_studies
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Systematic_reviews
Limite:
Aged
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Female
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Humans
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Male
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Middle aged
País como assunto:
Europa
Idioma:
En
Ano de publicação:
2021
Tipo de documento:
Article