Department of Biomedical Science, Faculty of Medicine, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Department of Neurology, National Neuroscience Institute, Singapore General Hospital, Singapore, Singapore.
Neurol Sci. 2021 Oct;42(10):4203-4207. doi: 10.1007/s10072-021-05056-x. Epub 2021 Feb 8.
Genome-wide association studies (GWAS) have shown that variants in the 3-methylcrotonyl-CoA carboxylase (MCCC1)/lysosome-associated membrane protein 3 (LAMP3) loci (rs10513789, rs12637471, rs12493050) reduce the risk of Parkinson's disease (PD) in Caucasians, Chinese and Ashkenazi-Jews while the rs11248060 variant in the diacylglycerol kinase theta (DGKQ) gene increases the risk of PD in Caucasian and Han Chinese cohorts. However, their roles in Malays are unknown. Therefore, this study aims to investigate the association of these variants with the risk of PD in individuals of Malay ancestry.
A total of 1114 subjects comprising of 536 PD patients and 578 healthy controls of Malay ancestry were recruited and genotyped using Taqman® allelic discrimination assays.
The G allele of rs10513789 (OR = 0.83, p = 0.001) and A allele of rs12637471 (OR = 0.79, p = 0.007) in the MCCC1/LAMP3 locus were associated with a protective effect against developing PD in the Malay population. A recessive model of penetrance showed a protective effect of the GG genotype for rs10513789 and the AA genotype for rs12637471. No association with PD was found with the other MCCC1/LAMP3 rs12493050 variant or with the DGKQ (rs11248060) variant. No significant associations were found between the four variants with the age at PD diagnosis.
MCCC1/LAMP3 variants rs10513789 and rs12637471 protect against PD in the Malay population.
全基因组关联研究(GWAS)表明,3-甲基戊二酰辅酶 A 羧化酶(MCCC1)/溶酶体相关膜蛋白 3(LAMP3)基因座中的变体(rs10513789、rs12637471、rs12493050)降低了白种人、中国人和阿什肯纳兹犹太人患帕金森病(PD)的风险,而二酰基甘油激酶θ(DGKQ)基因中的 rs11248060 变体增加了白种人和汉族人群患 PD 的风险。然而,它们在马来人中的作用尚不清楚。因此,本研究旨在探讨这些变体与马来人患 PD 风险的关系。
共纳入 1114 名研究对象,包括 536 名 PD 患者和 578 名马来裔健康对照者,采用 Taqman®等位基因鉴别分析进行基因分型。
MCCC1/LAMP3 基因座中的 rs10513789 的 G 等位基因(OR=0.83,p=0.001)和 rs12637471 的 A 等位基因(OR=0.79,p=0.007)与马来人群 PD 的发病风险呈负相关。显性模型的穿透性显示,rs10513789 的 GG 基因型和 rs12637471 的 AA 基因型具有保护作用。其他 MCCC1/LAMP3 rs12493050 变体或 DGKQ(rs11248060)变体与 PD 无关联。四个变体与 PD 诊断年龄之间也没有显著关联。
MCCC1/LAMP3 变体 rs10513789 和 rs12637471 可保护马来人群免受 PD 的侵害。