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The Unified Batten Disease Rating Scale (UBDRS): Validation and reliability in an independent CLN3 disease sample.
Wibbeler, Eva; Nickel, Miriam; Schwering, Christoph; Schulz, Angela; Mink, Jonathan W.
Afiliación
  • Wibbeler E; University Medical Center Hamburg Eppendorf (UKE), Hamburg, Germany. Electronic address: e.wibbeler@uke.de.
  • Nickel M; University Medical Center Hamburg Eppendorf (UKE), Hamburg, Germany.
  • Schwering C; University Medical Center Hamburg Eppendorf (UKE), Hamburg, Germany.
  • Schulz A; University Medical Center Hamburg Eppendorf (UKE), Hamburg, Germany.
  • Mink JW; Department of Neurology, University of Rochester, 601 Elmwood Avenue, Rochester, NY, 14642, USA.
Eur J Paediatr Neurol ; 38: 62-65, 2022 May.
Article en En | MEDLINE | ID: mdl-35427884
BACKGROUND: The neuronal ceroid lipofuscinoses (NCLs) are a group of disorders characterized by neurodegeneration and intracellular accumulation of an auto-fluorescent lipopigment. Together, NCLs represent the most common cause of cerebral neurodegenerative disease in children. CLN3 disease, the classic juvenile-onset form (JNCL) due to mutations in CLN3, is characterized by progressive vision loss, epilepsy, dementia, behavioral difficulties, and motor impairment. The Unified Batten Disease Rating Scale (UBDRS) is a disease-specific rating scale that was developed to assess disease severity in 4 domains: physical, behavior, seizures, and functional capability. Validity and reliability of the UBDRS has been established in a large North American cohort of over 130 individuals. The purpose of this study was to determine whether the UBDRS is valid and reliable when tested in an independent sample. METHODS: Over the course of one week, 13 individuals with genetically confirmed CLN3 disease were evaluated with the UBDRS by 5 examiners at the University Medical Center Hamburg Eppendorf (UKE). One rater (JWM), one of the developers of the UBDRS, served as the reference standard. The other 4 raters were physicians with expertise in various forms of Batten Disease. After a formal training session, 13 individuals (age 16.5 ± 5.6 yrs) were evaluated simultaneous in parallel by the 5 raters. Inter-rater reliability of the Physical subscale was assessed with Intra-class Correlation (ICC) analysis. The relationship between age and severity was assessed and compared to previously published data from the North American cohort. FINDINGS: The ICC among the 5 independent raters was 0.92, demonstrating excellent inter-rater reliability. The individual correlations of each UKE rater compared to the reference standard rater were all >0.95. The average UBDRS Physical Subscale score in this sample was 28 ± 21 (mean ± SD) with a range from 1 to 61. When evaluated as a function of participant age, the slope was 3.06 points/year (R2 = 0.66). INTERPRETATION: We have shown excellent interrater reliability for the UBDRS as a clinical rating scale for CLN3 disease in a sample independent from previous work. The results of this study are comparable to those published by Kwon et al., 2011 in a North American cohort showing a slope of 2.86 points per year with a 95% CI of 2.27-3.45 (N = 82). Our results demonstrate excellence inter-rater reliability after training a new group of raters and provide additional evidence for construct validity of the UBDRS. The UBDRS is a valid and reliable rating scale that can used by trained raters to assess the severity and rate of progression of CLN3 disease.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Lipofuscinosis Ceroideas Neuronales Tipo de estudio: Diagnostic_studies Límite: Adolescent / Adult / Child / Humans Idioma: En Revista: Eur J Paediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Lipofuscinosis Ceroideas Neuronales Tipo de estudio: Diagnostic_studies Límite: Adolescent / Adult / Child / Humans Idioma: En Revista: Eur J Paediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article Pais de publicación: Reino Unido