Urinary N-terminal titin fragment ascertained as biomarker in a small cohort of limb-girdle muscular dystrophy LGMDR1-calpain 3 related.

IF 3.2 4区 医学 Q2 CLINICAL NEUROLOGY
Andrea Valls, Cristina Ruiz-Roldán, Jenita Immanuel, Pilar Camaño, Juan José Poza, Roberto Fernández-Torrón, Adolfo López de Munain, Amets Sáenz
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引用次数: 0

Abstract

We aimed to investigate the validity of urinary N-terminal titin (TTN) fragment as a biomarker for limb-girdle muscular dystrophy LGMDR1-calpain 3 related. Thirteen LGMDR1 patients and eleven healthy controls were enrolled for the study. LGMDR1 patients had significantly increased urinary N-terminal titin fragment concentrations than age-matched controls. Even if urinary level of titin decreased with aging, it was still high in wheelchair bound patients. Thus, our findings indicate that urinary N-terminal titin fragment is a non-invasive measure of muscle damage in LGMDR1, which could be used in disease monitoring in clinical trials even in wheelchair-bound patients.

尿n -末端titin片段被确定为LGMDR1-calpain 3相关肢带肌营养不良小队列的生物标志物。
我们旨在研究尿n -末端titin (TTN)片段作为LGMDR1-calpain 3相关肢带肌营养不良生物标志物的有效性。13名LGMDR1患者和11名健康对照者参加了这项研究。LGMDR1患者的尿n -末端titin片段浓度明显高于同龄对照组。尽管尿titin水平随着年龄的增长而下降,但在轮椅患者中仍然很高。因此,我们的研究结果表明,尿n端titin片段是LGMDR1中肌肉损伤的非侵入性测量,甚至可以用于轮椅束缚患者的临床试验疾病监测。
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来源期刊
Journal of neuromuscular diseases
Journal of neuromuscular diseases Medicine-Neurology (clinical)
CiteScore
5.10
自引率
6.10%
发文量
102
期刊介绍: The Journal of Neuromuscular Diseases aims to facilitate progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias and myositis). The journal publishes research reports, reviews, short communications, letters-to-the-editor, and will consider research that has negative findings. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases.
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