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体重指数与 SCA3/MJD 患者扩展的 CAG 重复长度呈负相关。

Body mass index is inversely correlated with the expanded CAG repeat length in SCA3/MJD patients.

机构信息

Postgraduate Program in Medical Sciences, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil.

出版信息

Cerebellum. 2012 Sep;11(3):771-4. doi: 10.1007/s12311-011-0326-6.

Abstract

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.

摘要

脊髓小脑性共济失调 3 型,又称 Machado-Joseph 病(SCA3/MJD),是一种常染色体显性遗传的神经退行性疾病,目前尚无治疗方法。我们旨在评估 SCA3/MJD 患者的体重指数(BMI),并评估其与临床、分子、生化和神经影像学发现的相关性。对 46 例 SCA3/MJD 患者和 42 例年龄和性别相匹配的健康非相关对照个体进行了病例对照研究。采用共济失调量表 SARA 和 NESSCA 进行临床评估。还评估了血清胰岛素、胰岛素样生长因子 1(IGF-1)和磁共振成像校正的小脑和脑干容积。与对照组相比,SCA3/MJD 患者的 BMI 较低(p=0.01)。BMI 与 NESSCA、扩展 CAG 重复数(CAG)n、发病年龄、年龄、疾病持续时间和血清胰岛素水平相关;然而,在线性回归模型中,(CAG)n 是唯一与 BMI 呈负相关的变量(R=-0.396,p=0.015)。在本报告中,我们提供了证据表明,低 BMI 不仅存在于 SCA3/MJD 中,而且与扩展的 CAG 重复长度直接相关,这是疾病的致病突变。这种相关性表明,体重减轻可能是 SCA3/MJD 的主要障碍,尽管需要进一步详细分析以更好地理解营养不足及其在 SCA3/MJD 病理生理学中的作用。

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