McCormick Ashley, Farmer Jennifer, Perlman Susan, Delatycki Martin, Wilmot George, Matthews Katherine, Yoon Grace, Hoyle Chad, Subramony Sub H, Zesiewicz Theresa, Lynch David R, McCormack Shana E
Division of Neurology Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104.
Department of Neurology Perelman School of Medicine at the University of Pennsylvania Philadelphia Pennsylvania 19104.
Ann Clin Transl Neurol. 2017 Jul 26;4(9):622-631. doi: 10.1002/acn3.439. eCollection 2017 Sep.
Friedreich ataxia (FA) is a progressive neuromuscular disorder caused by GAA triplet repeat expansions or point mutations in the gene. FA is associated with increased risk of diabetes mellitus (DM). This study assessed the age-specific prevalence of FA-associated DM and its impact on neurologic outcomes.
Participants were 811 individuals with FA from 12 international sites in a prospective natural history study (FA Clinical Outcome Measures Study, FACOMS). Physical function was assessed, using validated instruments. Multivariable regression analyses examined the independent association of DM with outcomes.
Mean age of participants was 30.1 years (SD 15.3, range: 7-82), 50% were female, and 94% were non-Hispanic white. 9% (42/459) of adults and 3% (10/352) of children had DM. Individuals with FA-associated DM were older ( < 0.001), had longer GAA repeat length on the least affected allele ( = 0.037), and more severe FA ( = 0.0001). Of individuals with DM, 65% (34/52) were taking insulin. Even after accounting statistically for both age and GAA repeat length, DM was independently associated with greater FA symptom burden ( = 0.010), reduced capacity to perform activities of daily living ( = 0.021), and a decrease of 0.33 SDs on a composite performance measure (95% CI: -0.56-0.11, = 0.004); the relative impact of DM was most apparent in younger individuals.
DM-associated FA has an independent adverse impact on well-being in affected individuals, particularly at younger ages. In future, evidence-based approaches for identification and management of FA-related DM may improve both health and function.
弗里德赖希共济失调(FA)是一种由该基因中GAA三联体重复扩增或点突变引起的进行性神经肌肉疾病。FA与糖尿病(DM)风险增加相关。本研究评估了FA相关DM的年龄特异性患病率及其对神经学结局的影响。
在一项前瞻性自然史研究(FA临床结局测量研究,FACOMS)中,参与者为来自12个国际地点的811名FA患者。使用经过验证的工具评估身体功能。多变量回归分析检验了DM与结局的独立关联。
参与者的平均年龄为30.1岁(标准差15.3,范围:7 - 82岁),50%为女性,94%为非西班牙裔白人。9%(42/459)的成年人和3%(10/352)的儿童患有DM。FA相关DM患者年龄更大(<0.001),在受影响最小的等位基因上GAA重复长度更长(=0.037),且FA更严重(=0.0001)。在患有DM的个体中,65%(34/52)正在使用胰岛素。即使在对年龄和GAA重复长度进行统计学校正后,DM仍与更大的FA症状负担独立相关(=0.010),进行日常生活活动的能力降低(=0.021),并且在综合性能测量上下降0.33标准差(95%CI:-0.56 - 0.11,=0.004);DM的相对影响在较年轻个体中最为明显。
DM相关的FA对受影响个体的健康有独立的不利影响,尤其是在较年轻的年龄段。未来,基于证据的FA相关DM识别和管理方法可能会改善健康和功能。