Literature DB >> 21432905

What is the impact of education on Huntington's disease?

Jose Luis López-Sendón1, Ana Royuela, Patricia Trigo, Michael Orth, Herwig Lange, Ralf Reilmann, Jennifer Keylock, Hugh Rickards, Silvia Piacentini, Ferdinando Squitieri, Bernhard Landwehrmeyer, Marie-Noelle Witjes-Ane, Caroline K Jurgens, Raymund A C Roos, Victor Abraira, Justo G de Yébenes.   

Abstract

Huntington's disease (HD) is a neurodegenerative disease caused by a cytosine adenosine guanine (CAG) expansion in the huntingtin gene. The length of the triplet repeat is the most important factor in determining age of onset and the severity of the disease, but substantial variability of these parameters is attributed to other factors. To investigate the relationship between the years of education and the age at onset and the severity of the phenotype in patients with HD, we applied multiple linear regression analysis to examine the impact of education on the age at onset and the severity of the clinical scores assessed by the Unified Huntington's Disease Rating Scale (UHDRS) of 891 patients with HD from the multinational observational study "Registry" conducted by the European Huntintgton's Disease Network. The model was adjusted for CAG repeat length and age at the time of assessment. Patients with lengthier education exhibited earlier estimated age at onset but less severe clinical scores (motor = -3.6, P = 0.006; cognitive = 27.0, P < 0.001; behavioral = -3.0, P < 0.001; and functional capacity = 1.1 points, P < 0.001) than those with shorter education, after controlling for age and number of CAG repeats. These differences persisted throughout all quartiles of disease severity. An earlier recognition of symptoms and manifestations among the more educated patients could explain the earlier estimated age at onset in this group. The link between better clinical UHDRS scores and higher education might reflect a beneficial effect of education or its covariates on the course of HD.
Copyright © 2011 Movement Disorder Society.

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Year:  2011        PMID: 21432905     DOI: 10.1002/mds.23385

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  13 in total

1.  Selected health and lifestyle factors, cytosine-adenine-guanine status, and phenoconversion in Huntington's disease.

Authors:  Caroline Tanner; Karen Marder; Shirley Eberly; Kevin Biglan; David Oakes; Ira Shoulson
Journal:  Mov Disord       Date:  2018-01-03       Impact factor: 10.338

2.  Quantifying the bias due to observed individual confounders in causal treatment effect estimates.

Authors:  Layla Parast; Beth Ann Griffin
Journal:  Stat Med       Date:  2020-05-10       Impact factor: 2.373

Review 3.  Progress in Huntington's disease: the search for markers of disease onset and progression.

Authors:  Sarah Mason; Roger A Barker
Journal:  J Neurol       Date:  2015-03-21       Impact factor: 4.849

Review 4.  Association between sex and Huntington's disease: an updated review on symptomatology and prognosis of neurodegenerative disorders.

Authors:  Nimra Hasnain; Taha Bin Arif; Roha Shafaut; Faiza Zakaria; Syeda Zainab Fatima; Ibtehaj Ul Haque
Journal:  Wien Med Wochenschr       Date:  2022-06-20

5.  Cognitive reserve and brain reserve in prodromal Huntington's disease.

Authors:  Aaron Bonner-Jackson; Jeffrey D Long; Holly Westervelt; Geoffrey Tremont; Elizabeth Aylward; Jane S Paulsen
Journal:  J Int Neuropsychol Soc       Date:  2013-05-23       Impact factor: 2.892

6.  The Effect of Education on Symptom Onset and Severity of Huntington's Disease.

Authors:  Kristina K Cain; Joseph L Flanigan; William Alex Dalrymple; James Patrie; Madaline B Harrison; Matthew J Barrett
Journal:  Mov Disord Clin Pract       Date:  2021-03-30

7.  The effect of multidisciplinary rehabilitation on brain structure and cognition in Huntington's disease: an exploratory study.

Authors:  Travis M Cruickshank; Jennifer A Thompson; Juan F Domínguez D; Alvaro P Reyes; Mike Bynevelt; Nellie Georgiou-Karistianis; Roger A Barker; Mel R Ziman
Journal:  Brain Behav       Date:  2015-01-15       Impact factor: 2.708

8.  Is There an Association of Physical Activity with Brain Volume, Behavior, and Day-to-day Functioning? A Cross Sectional Design in Prodromal and Early Huntington Disease.

Authors:  McKenzie Wallace; Nancy Downing; Spencer Lourens; James Mills; Ji-In Kim; Jeffrey Long; Jane Paulsen
Journal:  PLoS Curr       Date:  2016-03-17

9.  Feasibility of computerized working memory training in individuals with Huntington disease.

Authors:  Mahsa Sadeghi; Emily Barlow-Krelina; Clare Gibbons; Komal T Shaikh; Wai Lun Alan Fung; Wendy S Meschino; Christine Till
Journal:  PLoS One       Date:  2017-04-28       Impact factor: 3.240

10.  Estimating the causal effects of modifiable, non-genetic factors on Huntington disease progression using propensity score weighting.

Authors:  Beth Ann Griffin; Marika Suttorp Booth; Monica Busse; Edward J Wild; Claude Setodji; John H Warner; Cristina Sampaio; Amrita Mohan
Journal:  Parkinsonism Relat Disord       Date:  2021-01-13       Impact factor: 4.891

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