Body Mass Index is Inversely Correlated with the Expanded CAG Repeat Length in SCA3/MJD Patients

被引:0
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作者
Jonas Alex Morales Saute
Andrew Chaves Feitosa da Silva
Gabriele Nunes Souza
Aline Dutra Russo
Karina Carvalho Donis
Leonardo Vedolin
Maria Luiza Saraiva-Pereira
Luis Valmor Cruz Portela
Laura Bannach Jardim
机构
[1] Universidade Federal do Rio Grande do Sul,Postgraduate Program in Medical Sciences
[2] Universidade Federal do Rio Grande do Sul,Department of Internal Medicine
[3] Universidade Federal do Rio Grande do Sul,Department of Biochemistry
[4] Hospital de Clínicas de Porto Alegre (HCPA),Neurology Service
[5] Hospital de Clínicas de Porto Alegre (HCPA),Medical Genetics Service
[6] Hospital Moinhos de Vento,Neuroradiology Service
[7] Universidade Federal do Rio Grande do Sul,Medical Genetics Service, Hospital de Clínicas de Porto Alegre (HCPA)
来源
The Cerebellum | 2012年 / 11卷
关键词
Spinocerebellar ataxia type 3; Machado–Joseph disease; Body mass index; Polyglutamine; Ataxia;
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中图分类号
学科分类号
摘要
Spinocerebellar ataxia type 3, also known as Machado–Joseph disease (SCA3/MJD), is an autosomal dominant neurodegenerative disorder with no current treatment. We aimed to evaluate the body mass index (BMI) of patients with SCA3/MJD and to assess the correlations with clinical, molecular, biochemical, and neuroimaging findings. A case–control study with 46 SCA3/MJD patients and 42 healthy, non-related control individuals with similar age and sex was performed. Clinical evaluation was done with the ataxia scales SARA and NESSCA. Serum insulin, insulin-like growth factor 1 (IGF-1) and magnetic resonance imaging normalized volumetries of cerebellum and brain stem were also assessed. BMI was lower in SCA3/MJD patients when compared to controls (p = 0.01). BMI was associated with NESSCA, expanded CAG repeat number (CAG)n, age of onset, age, disease duration, and serum insulin levels; however, in the linear regression model, (CAG)n was the only variable independently associated with BMI, in an inverse manner (R = −0.396, p = 0.015). In this report, we present evidence that low BMI is not only present in SCA3/MJD, but is also directly related to the length of the expanded CAG repeats, which is the causative mutation of the disease. This association points that weight loss might be a primary disturbance of SCA3/MJD, although further detailed analyses are necessary for a better understanding of the nutritional deficit and its role in the pathophysiology of SCA3/MJD.
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页码:771 / 774
页数:3
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