Velázquez-Pérez Luis, Seifried Carola, Santos-Falcón Nieves, Abele Michael, Ziemann Ulf, Almaguer Luis Enrique, Martínez-Góngora Edilberto, Sánchez-Cruz Gilberto, Canales Nalia, Pérez-González Ruth, Velázquez-Manresa Mercedes, Viebahn Bettina, von Stuckrad-Barre Sebastian, Fetter Michael, Klockgether Thomas, Auburger Georg
Clínica para la Investigación y Rehabilitación de las Ataxias Hereditarias, Holguín, Cuba.
Ann Neurol. 2004 Sep;56(3):444-7. doi: 10.1002/ana.20220.
We assessed maximal saccade velocity (MSV) in 82 spinocerebellar ataxia type 2 (SCA2) patients and 80 controls, correlating it to disease duration, polyglutamine expansion size, age at onset, ataxia score, age, and sex. Little overlap with normal values was found even at earliest stages. Stepwise linear regression analysis showed that 60-degree MSV was strongly influenced by polyglutamine size and less by disease duration, whereas the reverse was found for ataxia score. Saccade velocity thus is a sensitive, quite specific, and objective endophenotype, useful to search polyglutamine modifier genes.
我们评估了82例2型脊髓小脑共济失调(SCA2)患者和80名对照者的最大扫视速度(MSV),并将其与疾病持续时间、多聚谷氨酰胺扩展大小、发病年龄、共济失调评分、年龄和性别相关联。即使在疾病早期,与正常值的重叠也很少。逐步线性回归分析表明,60度MSV受多聚谷氨酰胺大小的影响较大,受疾病持续时间的影响较小,而共济失调评分的情况则相反。因此,扫视速度是一种敏感、相当特异且客观的内表型,有助于寻找多聚谷氨酰胺修饰基因。