Open AccessMitochondrial NADH Dehydrogenase Subunit 3 Polymorphism Associated with an Earlier Age at Onset in Male Machado–Joseph disease Patients
Author(s) -
Chen Sheng,
Gan ShiRui,
Cai PingPing,
Ni Wang,
Zhou Qi,
Dong Yi,
Wang Ning,
Wu ZhiYing
Publication year - 2016
Publication title -
cns neuroscience and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 69
eISSN - 1755-5949
pISSN - 1755-5930
DOI - 10.1111/cns.12443
Subject(s) - machado–joseph disease , single nucleotide polymorphism , genetics , snp , sanger sequencing , biology , genotype , polymorphism (computer science) , candidate gene , gastroenterology , gene , medicine , dna sequencing , spinocerebellar ataxia
Summary Aims To investigate the potential effect of six previously reported candidate single nucleotide polymorphisms on age at onset ( AAO ) among Chinese patients with Machado–Joseph disease ( MJD ). Methods Three hundred and twenty‐four unrelated molecular‐confirmed MJD patients were recruited between January 2006 and December 2014. The screening of candidate polymorphisms was first performed in 173 subjects using the SN aPshot ® Multiplex System. The mitochondrial NADH dehydrogenase subunit 3 ( MT ‐ ND 3 ) polymorphism 10398A>G (rs2853826) was further verified with Sanger sequencing in additional 151 patients. Results An inverse correlation was found between expanded CAG repeat length and AAO . The expanded CAG repeat length can explain 63% of AAO variance. The 10398A polymorphism was significantly associated with a 3‐year earlier AAO in male patients with MJD ( P = 0.001). Stepwise multiple regressions revealed that the 10398A polymorphism could account for nearly 2% of AAO variance in male patients. Conclusion Six candidate SNP s have been screened in Chinese patients with MJD . A remarkable earlier AAO was noted in male Chinese MJD patients with MT ‐ ND 3 gene 10398A polymorphism.