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Metrics of progression and prognosis in untreated adults with thymidine kinase 2 deficiency: An observational study.
Domínguez-González, Cristina; Hernández-Voth, Ana; de Fuenmayor-Fernández de la Hoz, Carlos Pablo; Guerrero, Laura Bermejo; Morís, Germán; García-García, Jorge; Muelas, Nuria; León Hernández, Juan Carlos; Rabasa, Maria; Lora, David; Blázquez, Alberto; Arenas, Joaquín; Martin, Miguel Ángel.
Afiliação
  • Domínguez-González C; Neuromuscular Disorders Unit, Neurology Department, Hospital 12 de Octubre, Madrid, Spain; Center for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain; Instituto de Investigación imas12, Hospital 12 de Octubre, Madrid, Spain. Electronic address: cd
  • Hernández-Voth A; Pneumology Department, Mechanical Ventilation Unit, Hospital 12 de Octubre, Madrid, Spain.
  • de Fuenmayor-Fernández de la Hoz CP; Neuromuscular Disorders Unit, Neurology Department, Hospital 12 de Octubre, Madrid, Spain.
  • Guerrero LB; Neuromuscular Disorders Unit, Neurology Department, Hospital 12 de Octubre, Madrid, Spain.
  • Morís G; Neuromuscular Disorders Unit, Neurology Department, Hospital Universitario Central de Asturias, Asturias, Spain.
  • García-García J; Department of Neurology, Hospital Universitario de Albacete, Albacete, Spain.
  • Muelas N; Center for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain; Neurology Department, Neuromuscular Diseases Unit. Hospital Universitari i Politecnic La Fe, Neuromuscular and Ataxias Research Group, Instituto de Investigación Sanitaria La Fe, Valencia
  • León Hernández JC; Neurology Department, Hospital Universitario Nuestra Señora de Candelaria, Tenerife, Spain.
  • Rabasa M; Neurology Department, Hospital de Fuenlabrada, Madrid, Spain.
  • Lora D; Clinical Research Unit, Hospital 12 de Octubre Research Institute (imas12), 28041 Madrid, Spain; Departamento de Estadística y Ciencia de los Datos, Facultad de Estudios Estadísticos, Universidad Complutense de Madrid, 28040 Madrid, Spain; Centro de Investigación Biomédica en Red de Epidemiología y
  • Blázquez A; Center for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain; Research Institute imas12, Mitochondrial Disorders Laboratory, Clinical Biochemistry Department, Hospital Universitario 12 de Octubre, Madrid, Spain.
  • Arenas J; Research Institute imas12, Mitochondrial Disorders Laboratory, Clinical Biochemistry Department, Hospital Universitario 12 de Octubre, Madrid, Spain.
  • Martin MÁ; Center for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain; Research Institute imas12, Mitochondrial Disorders Laboratory, Clinical Biochemistry Department, Hospital Universitario 12 de Octubre, Madrid, Spain.
Neuromuscul Disord ; 32(9): 728-735, 2022 09.
Article em En | MEDLINE | ID: mdl-35907766
ABSTRACT
This historical cohort study evaluated clinical characteristics of progression and prognosis in adults with thymidine kinase 2 deficiency (TK2d). Records were available for 17 untreated adults with TK2d (mean age of onset, 32 years), including longitudinal data from 6 patients (mean follow-up duration, 26.5 months). Pearson's correlation assessed associations between standard motor and respiratory assessments, clinical characteristics, and laboratory values. Longitudinal data were assessed by linear regression mixed models. Respiratory involvement progressed at an annual rate of 8.16% decrement in forced vital capacity (FVC). Most patients under noninvasive ventilation (NIV) remained ambulant (12/14, 86%), reduced FVC was not associated with concomitant decline in 6-minute walk test (6MWT), and 6MWT results were not correlated with FVC. Disease severity, assessed by age at NIV onset, correlated most strongly at diagnosis with creatinine levels (r = 0.8036; P = 0.0009), followed by FVC (r = 0.7265; P = 0.0033), mtDNA levels in muscle (r = 0.7933; P = 0.0188), and age at disease onset (r = 0.7128; P = 0.0042). This population of adults with TK2d demonstrates rapid deterioration of respiratory muscles, which progresses independently of motor impairment. The results support FVC at diagnosis, mtDNA levels in muscle, and age at disease onset as prognostic indicators. Creatinine levels may also be potentially prognostic, as previously reported in other neuromuscular disorders.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article