Department of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
Department of Translational Medical Sciences, Federico II University, Naples, Italy.
Cerebellum. 2023 Oct;22(5):1034-1038. doi: 10.1007/s12311-022-01475-4. Epub 2022 Sep 6.
Friedreich's ataxia (FRDA) is the most common inherited recessive ataxia. Cardiomyopathy (CM) with myocardial hypertrophy is the predominant cause of death. The presence of CM is variable and the risk factors for cardiac involvement are not entirely clear. Markers of collagen degradation, such as C-terminal cross-linked telopeptide of type I collagen (CTX-I), seem to be associated with unfavorable cardiovascular outcomes. The aim of our study was to measure serum CTX-I as a marker of cardiac fibrosis in FRDA patients. We measured serum CTX value in twenty-five FRDA patients (mean age, 31.3 ± 14.7 years) and nineteen healthy controls (mean age, 34.0 ± 13.5 years). Patients underwent echocardiography and SARA scale evaluation. CTX values were significantly higher in the patients than in the control group (31.82 ± 2.27 vs 16.44 ± 1.6 μg/L; p = 0.006). CTX-I was inversely correlated with age (R = - 0,535; n = 44; p < 0.001). The regression model identified disease duration and TT3 levels to be independent predictors of CTX-I (model R = 0.938; intercept - 64.0, p = 0.071; disease duration coefficient = - 2.34, p = 0.005; TT3 coefficient = 127.17, p = 0.011). CTX-I, a biomarkers of collagen turnover, is elevated in FRDA and should provide complementary information to identify patients with high cardiological risk even if longitudinal studies are needed to define the role of this serologic marker of collagen metabolism in the natural history of cardiomyopathy in FRDA patients.
弗里德赖希共济失调(FRDA)是最常见的遗传性隐性共济失调。心肌肥厚性心肌病(CM)是主要的死亡原因。CM 的存在是可变的,心脏受累的危险因素尚不完全清楚。I 型胶原 C 端交联肽(CTX-I)等胶原降解标志物似乎与不良心血管结局相关。我们的研究目的是测量 FRDA 患者血清 CTX-I 作为心肌纤维化的标志物。我们测量了 25 名 FRDA 患者(平均年龄 31.3±14.7 岁)和 19 名健康对照者(平均年龄 34.0±13.5 岁)的血清 CTX 值。患者接受了超声心动图和 SARA 量表评估。患者的 CTX 值明显高于对照组(31.82±2.27 对 16.44±1.6μg/L;p=0.006)。CTX-I 与年龄呈负相关(R= - 0.535;n=44;p<0.001)。回归模型确定疾病持续时间和 TT3 水平是 CTX-I 的独立预测因子(模型 R=0.938;截距-64.0,p=0.071;疾病持续时间系数-2.34,p=0.005;TT3 系数 127.17,p=0.011)。CTX-I 是胶原转化的生物标志物,在 FRDA 中升高,即使需要进行纵向研究来确定这种胶原代谢的血清标志物在 FRDA 患者心肌病自然史中的作用,它也可以提供补充信息,以识别高心血管风险的患者。