https://scholars.lib.ntu.edu.tw/handle/123456789/463614
標題: | Analysis of GWAS-linked variants in multiple system atrophy | 作者: | Gu X Chen Y Zhou Q Lu Y.-C Cao B Zhang L MING-CHE KUO Wu Y.-R RUEY-MEEI WU Tan E.-K Shang H.-F Asian Multiple System Atrophy Consortium (AMSAC) |
關鍵字: | Association; Multiple system atrophy; Single nucleotide polymorphism | 公開日期: | 2018 | 卷: | 67 | 起(迄)頁: | 201 e.1-201 e.4 | 來源出版物: | Neurobiology of Aging | 摘要: | A recent genome-wide association study performed in European population identified 4 potentially interesting gene loci of multiple system atrophy (MSA), including the EDN1 rs16872704, MAPT rs9303521, FBXO47 rs78523330, and ELOVL7 rs7715147. Because of the genetic heterogeneity, we aimed to explore the possible genetic association between above 4 single nucleotide polymorphisms (SNPs) and MSA in Chinese Han population from Mainland China, Taiwan, and Singapore. A total of 1847 subjects comprising 906 MSA patients and 941 unrelated healthy controls were genotyped by directly sequencing for these SNPs. No significant differences in the genotype distributions, minor allele frequency of EDN1 rs16872704, MAPT rs9303521, FBXO47 rs78523330, and ELOVL7 rs7715147 between MSA patients and healthy controls, and between subtypes of MSA patients (MSA-C and MSA-P), were found. In conclusion, we demonstrated that genome-wide association study–linked SNPs in Caucasians do not confer a significant risk for MSA in the Chinese population. ? 2018 Elsevier Inc. |
URI: | https://scholars.lib.ntu.edu.tw/handle/123456789/463614 | ISSN: | 0197-4580 | DOI: | 10.1016/j.neurobiolaging.2018.03.018 | SDG/關鍵字: | adult; Article; China; controlled study; EDN1 gene; ELOVL7 gene; FBXO47 gene; female; gene; gene frequency; gene locus; gene sequence; genetic heterogeneity; genetic variability; genome-wide association study; genotyping technique; Han Chinese; human; major clinical study; male; MAPT gene; pathogenesis; priority journal; Shy Drager syndrome; Singapore; single nucleotide polymorphism; Taiwan; aged; Asian continental ancestry group; Caucasian; genetics; genotype; middle aged; Shy Drager syndrome; single nucleotide polymorphism; acyltransferase; endothelin 1; fatty acid elongases; FBXO47 protein, human; MAPT protein, human; tau protein; transcription factor; Acetyltransferases; Adult; Aged; Asian Continental Ancestry Group; Endothelin-1; European Continental Ancestry Group; Female; Genome-Wide Association Study; Genotype; Humans; Male; Middle Aged; Multiple System Atrophy; Polymorphism, Single Nucleotide; tau Proteins; Transcription Factors |
顯示於: | 醫學系 |
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