Val158Met polymorphism of COMT gene and Parkinson’s disease risk in Asians

In previous study, we have found the catechol- O -methyltransferase ( COMT ) Val158Met polymorphism as an associated risk factor for Parkinson’s disease (PD) in Asian rather than Caucasian populations. The aim of this study was to further evaluate the associations of PD risk with COMT polymorphisms...

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Veröffentlicht in:Neurological sciences 2015-01, Vol.36 (1), p.109-115
Hauptverfasser: Chuan, Lixue, Gao, Jie, Lei, Yuying, Wang, Raoxiang, Lu, Lechun, Zhang, Xianyu
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Sprache:eng
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Zusammenfassung:In previous study, we have found the catechol- O -methyltransferase ( COMT ) Val158Met polymorphism as an associated risk factor for Parkinson’s disease (PD) in Asian rather than Caucasian populations. The aim of this study was to further evaluate the associations of PD risk with COMT polymorphisms in different Asian populations. We carried out a retrieval of studies that investigated associations between COMT Val158Met polymorphism and PD risk in Asians, and included the study if it met the eligibility criteria. Stata version 12.0 was used to analyze the data. A total of 13 studies including 1,834 patients and 2,298 controls were included. The overall result indicated that COMT Val158Met polymorphism was significantly associated with the risk of PD in Asians (AA vs others: OR = 1.58, 95 % CI 1.26–1.97, p  
ISSN:1590-1874
1590-3478
DOI:10.1007/s10072-014-1896-0