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Urinary titin in myotonic dystrophy type 1.
Varga, Dávid; Perecz, Brigitta; Fülöp, Krisztina; Sipos, Andrea; Janszky, József Vlagyimir; Hajdú, Nándor; Pál, Endre.
Afiliación
  • Varga D; Department of Neurology, University of Pécs, Medical School, Pécs, Hungary.
  • Perecz B; Department of Neurology, University of Pécs, Medical School, Pécs, Hungary.
  • Fülöp K; Department of Pathology, Neuropathology Unit, University of Pécs, Medical School, Pécs, Hungary.
  • Sipos A; Department of Neurology, University of Pécs, Medical School, Pécs, Hungary.
  • Janszky JV; Department of Neurology, University of Pécs, Medical School, Pécs, Hungary.
  • Hajdú N; Institute of Psychology, ELTE, Eötvös Loránd University, Budapest, Hungary.
  • Pál E; Department of Neurology, University of Pécs, Medical School, Pécs, Hungary.
Muscle Nerve ; 68(2): 215-218, 2023 08.
Article en En | MEDLINE | ID: mdl-37291994
INTRODUCTION/AIMS: Urinary titin, an easy-to-obtain marker, has been investigated in muscular dystrophies, but not in myotonic dystrophy type 1 (DM1). We investigated the role of titin as a biomarker of muscle injury in DM1. METHODS: We compared the urinary titin N-fragment/creatinine ratio in 29 patients with DM1 vs. 30 healthy controls. We also recorded clinical data such as muscle strength, serum creatine kinase, DM1-related outcome measures, and the 20-item DM1-activ questionnaire. The severity of the disease was graded using the Muscular Impairment Rating Scale (MIRS). RESULTS: The titin/creatinine ratio was significantly higher in the urine samples of DM1 patients than of healthy controls (median ± mean absolute deviation [MAD]: 39.313 ± 26.546 vs. 6.768 ± 5.245 pmol/mg creatinine; P < .001), and was related to muscle impairment graded by MIRS (τ = 0.503, P = .038). DISCUSSION: Urinary titin may be a biomarker for DM1. Long-term follow-up of DM1 patients is needed to investigate the potential role of titin as a biomarker for disease activity and progression.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Distrofia Miotónica Límite: Humans Idioma: En Revista: Muscle Nerve Año: 2023 Tipo del documento: Article País de afiliación: Hungria Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Distrofia Miotónica Límite: Humans Idioma: En Revista: Muscle Nerve Año: 2023 Tipo del documento: Article País de afiliación: Hungria Pais de publicación: Estados Unidos