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应用生存分析估计古巴脊髓小脑共济失调 2 型患者的发病年龄。

Estimation of the age at onset in spinocerebellar ataxia type 2 Cuban patients by survival analysis.

机构信息

Center for Investigation and Rehabilitation of Hereditary Ataxias (CIRAH), Holguín Province, Cuba.

出版信息

Clin Genet. 2010 Aug;78(2):169-74. doi: 10.1111/j.1399-0004.2009.01358.x. Epub 2009 Dec 2.

Abstract

Previous studies have investigated the close association that exists between CAG repeat number and the age at onset in SCA2 = spinocerebellar ataxia type 2. These studies have focused on affected individuals. To further characterize this association and estimate the risk of a carrier developing SCA2 at a particular age as a function of a specific CAG repeat size, we have analyzed a large group of 924 individuals, including 394 presymptomatic and 530 affected individuals with a CAG repeat length of 32-79 units. Using a Kaplan-Meier survival analysis, we obtained cumulative probability curves for disease manifestation at a particular age for each CAG repeat length in the 34-45 range. These curves were significantly different (p < 0.001) and showed small overlap. All these information may be very valuable in predictive-testing programs, in the planning of studies for the identification of other genetic and environmental factors as modifiers of age at onset, and in the design of clinical trials for people at enlarged risk for SCA2.

摘要

先前的研究已经探讨了 CAG 重复数与 SCA2(脊髓小脑性共济失调 2 型)发病年龄之间的密切关联。这些研究主要集中在受影响的个体上。为了进一步描述这种关联,并根据特定的 CAG 重复大小估计特定年龄携带者发展 SCA2 的风险,我们分析了一个由 924 个人组成的大型群组,其中包括 394 名无症状前和 530 名 CAG 重复长度为 32-79 个单位的受影响个体。使用 Kaplan-Meier 生存分析,我们获得了每个 CAG 重复长度在 34-45 范围内特定年龄发病的累积概率曲线。这些曲线差异显著(p<0.001),并且几乎没有重叠。所有这些信息在预测测试计划、鉴定其他遗传和环境因素作为发病年龄修饰因子的研究计划以及针对 SCA2 风险增加人群的临床试验设计中可能非常有价值。

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