Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease.

ABSTRACT: As a Mendelian neurodegenerative disorder, the genetic risk of Huntington's disease (HD) is conferred entirely by an HTT CAG repeat expansion whose length is the primary determinant of the rate of pathogenesis leading to disease onset. To investigate the pathogenic process that precedes disease, we used genome-wide association (GWA) analysis to identify loci harboring genetic variations that alter the age at neurological onset of HD. A chromosome 15 locus displays two independent effects that accelerate or delay onset by 6.1 years and 1.4 years, respectively, whereas a chromosome 8 locus hastens onset by 1.6 years. Association at MLH1 and pathway analysis of the full GWA results support a role for DNA handling and repair mechanisms in altering the course of HD. Our findings demonstrate tha

SUBMITTER: Genetic Modifiers of Huntington’s Disease (GeM-HD) Consortium 

PROVIDER: S-EPMC4524551 | biostudies-literature | 2015 Jul

REPOSITORIES: biostudies-literature