Literature DB >> 23466833

The COMT Val158Met polymorphism as an associated risk factor for Parkinson's disease in Asian rather than Caucasian populations.

Lu Lechun1, Su Yu, Hou Pengling, Huang Changqi.   

Abstract

BACKGROUND: Catechol-O-methyltransferase (COMT) gene has been reported to be associated with the risk of Parkinson's disease (PD). AIMS: To evaluate the associations of PD risk with COMT polymorphisms.
MATERIALS AND METHODS: A retrieval of studies that investigated associations between COMT polymorphisms and PD was carried out. Studies were included if they met the eligibility criteria. STATISTICAL ANALYSIS: Data were analyzed using Stata version 12.0.
RESULTS: A total of 18 studies including 2926 PD cases and 3151 controls were included. The results showed no significant association with all genotypes and alleles in Caucasians. However in Asians, the homozygote A/A (Odds ratio [OR] =1.51, 95% confidence interval [CI] =1.16-1.98, P =0.002) tends to increase risk of PD, however, the homozygote G/A (OR =0.85, 95% CI =0.74-0.98, P =0.03) may be a slightly protective effect against PD.
CONCLUSIONS: This study showed that the COMT polymorphisms may be associated with PD in Asians rather than Caucasians. But further studies are needed to confirm our results.

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Year:  2013        PMID: 23466833     DOI: 10.4103/0028-3886.108121

Source DB:  PubMed          Journal:  Neurol India        ISSN: 0028-3886            Impact factor:   2.117


  7 in total

1.  Association of COMT Val158Met polymorphism with wearing-off susceptibility in Parkinson's disease.

Authors:  Jianxing Liu; Pan Chen; Meihua Guo; Lechun Lu; Lihua Li
Journal:  Neurol Sci       Date:  2014-11-04       Impact factor: 3.307

2.  Sexual dimorphism in xenobiotic genetic variants-mediated risk for Parkinson's disease.

Authors:  Nadella Kumudini; Addepally Uma; Shaik Mohammad Naushad; Rukmini Mridula; Rupam Borgohain; Vijay Kumar Kutala
Journal:  Neurol Sci       Date:  2014-01-04       Impact factor: 3.307

3.  Val158Met polymorphism of COMT gene and Parkinson's disease risk in Asians.

Authors:  Lixue Chuan; Jie Gao; Yuying Lei; Raoxiang Wang; Lechun Lu; Xianyu Zhang
Journal:  Neurol Sci       Date:  2014-07-25       Impact factor: 3.307

4.  Polymorphisms of the dopamine metabolic and signaling pathways are associated with susceptibility to motor levodopa-induced complications (MLIC) in Parkinson's disease: a systematic review and meta-analysis.

Authors:  Gita Vita Soraya; Zulvikar Syambani Ulhaq; Syifaus Shodry; Muhammad A'raaf Sirojan Kusuma; Sarah Herawangsa; Maharani Oryza Sativa; Aridin Gustaf; Dzakky Avecienna Nur Faridwazdi; Shinta Wulandari Florentia; Neila Raisa; Andi Kurnia Bintang; Muhammad Akbar
Journal:  Neurol Sci       Date:  2022-01-25       Impact factor: 3.307

Review 5.  COMT Val158Met and PPARγ Pro12Ala polymorphisms and susceptibility to Alzheimer's disease: a meta-analysis.

Authors:  Young Ho Lee; Gwan Gyu Song
Journal:  Neurol Sci       Date:  2014-01-30       Impact factor: 3.307

6.  Roles of functional catechol-O-methyltransferase genotypes in Chinese patients with Parkinson's disease.

Authors:  Qin Xiao; Yiwei Qian; Jiujiang Liu; Shaoqing Xu; Xiaodong Yang
Journal:  Transl Neurodegener       Date:  2017-04-26       Impact factor: 8.014

7.  Gene polymorphisms and motor levodopa-induced complications in Parkinson's disease.

Authors:  Małgorzata Michałowska; Małgorzata Chalimoniuk; Ewa Jówko; Iwona Przybylska; Józef Langfort; Beata Toczylowska; Anna Krygowska-Wajs; Urszula Fiszer
Journal:  Brain Behav       Date:  2020-02-05       Impact factor: 2.708

  7 in total

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