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Research article summary (published 30 Oct 2002):

Neuropsychological manifestations of the genetic mutation for Huntington's disease in presymptomatic individuals.

Full Abstract

A triplet repeat (CAG) expansion mutation in the huntingtin gene on chromosome 4 is responsible for Huntington's disease (HD). Presymptomatic genetic testing for this mutation has identified clinically normal persons who are virtually certain to develop this dementing illness if they live a normal lifespan. The present study sought to determine whether these "mutation-positive" persons have impairments in cognitive functioning. Seventy-five mutation-positive persons did not differ from 128 mutation-negative persons on tests selected for their sensitivity to early-stage HD. Interestingly, however, those with the mutation viewed themselves as more likely to develop HD than did those without the mutation. Among mutation-positive subjects, having a longer CAG repeat mutation was likewise not associated with cognitive impairment. However, being closer to estimated disease onset (a product of repeat length and parent's age at onset) was associated with selected cognitive impairments. When viewed in light of previous studies showing atrophy of the caudate nucleus and putamen in mutation-carriers who are close to onset but not those far from onset, these results suggest that subtle changes in brain and behavior may be detected shortly before subjects with the HD mutation develop sufficient signs and symptoms for diagnosis. Conceptual and methodological problems associated with the search for presymptomatic cognitive and behavioral indicators of dementing illness are discussed.

 

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Author information

Author/s: Brandt, Jason (J); Shpritz, Barnett (B); Codori, Ann Marie (AM); Margolis, Russell (R); Rosenblatt, Adam (A);

Affiliation: Baltimore Huntington's Disease Research Center, Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, MD, USA. jbrandt(-atsign-)jhmi.edu

Grants: MH46034 (Agency:United States NIMH) ; NS16375 (Agency:United States NINDS)

Journal and publication information

Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.

Journal: Journal of the International Neuropsychological Society : JINS (J Int Neuropsychol Soc), published in England. (Language: eng)

Reference: 2002-Nov; vol 8 (issue 7) : pp 918-24

Dates: Created 2002/10/30; Completed 2002/11/26; Revised 2007/11/14;

PMID: 12405543, status: MEDLINE (last retrieval date: 11/6/2008)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Associated Chemicals: HD protein, human (0) ; Nerve Tissue Proteins (0) ; Nuclear Proteins (0)

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