Genetic Modification of Huntington Disease Acts Early in the Prediagnosis Phase

• Published in: American journal of human genetics Vol. 103; no. 3; pp. 349 - 357
• Main Authors: Long, Jeffrey D., Lee, Jong-Min, Aylward, Elizabeth H., Gillis, Tammy, Mysore, Jayalakshmi Srinidhi, Abu Elneel, Kawther, Chao, Michael J., Paulsen, Jane S., MacDonald, Marcy E., Gusella, James F.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 06.09.2018; Elsevier
• Subjects: Adult; age at onset; Alleles; CAG expansion; Chromosomes, Human, Pair 15 - genetics; Chromosomes, Human, Pair 8 - genetics; FAN1; Female; genetic modifier; Genotype; HTT; Humans; Huntingtin Protein - genetics; Huntington disease; Huntington Disease - genetics; Male; Mutation - genetics; Phenotype; RRM2B; symbol digits modalities test; total motor score; trinucleotide repeat; Trinucleotide Repeat Expansion - genetics; total motor score; RRM2B; Huntington disease; HTT; CAG expansion; trinucleotide repeat; symbol digits modalities test; age at onset; genetic modifier; FAN1
• DOI: 10.1016/j.ajhg.2018.07.017
• ISSN: 0002-9297; 1537-6605

Age at onset of Huntington disease, an inherited neurodegenerative disorder, is influenced by the size of the disease-causing CAG trinucleotide repeat expansion in HTT and by genetic modifier loci on chromosomes 8 and 15. Stratifying by modifier genotype, we have examined putamen volume, total motor score (TMS), and symbol digit modalities test (SDMT) scores, both at study entry and longitudinally, in normal controls and CAG-expansion carriers who were enrolled prior to the emergence of manifest HD in the PREDICT-HD study. The modifiers, which included onset-hastening and onset-delaying alleles on chromosome 15 and an onset-hastening allele on chromosome 8, revealed no major effect in controls but distinct patterns of modification in prediagnosis HD subjects. Putamen volume at study entry showed evidence of reciprocal modification by the chromosome 15 alleles, but the rate of loss of putamen volume was modified only by the deleterious chromosome 15 allele. By contrast, both alleles modified the rate of change of the SDMT score, but neither had an effect on the TMS. The influence of the chromosome 8 modifier was evident only in the rate of TMS increase. The data indicate that (1) modification of pathogenesis can occur early in the prediagnosis phase, (2) the modifier loci act in genetic interaction with the HD mutation rather than through independent additive effects, and (3) HD subclinical phenotypes are differentially influenced by each modifier, implying distinct effects in different cells or tissues. Together, these findings indicate the potential benefit of using genetic modifier strategies for dissecting the prediagnosis pathogenic process in HD.