Related Experiment Video
Updated: May 7, 2026

Rating L-DOPA-Induced Dyskinesias in the Unilaterally 6-OHDA-Lesioned Rat Model of Parkinson's Disease
Published on: October 4, 2021
The unified Huntington's Disease Rating Scale for advanced patients: validation and follow-up study
Katia Youssov1, Guillaume Dolbeau, Patrick Maison
1Centre de Référence Maladie de Huntington, Assistance Publique Hôpitaux de Paris (AP-HP), Groupe Hospitalier Henri Mondor-Albert Chenevier, Créteil, France; Unité INSERM U955, Equipe 01 Neuropsychologie Interventionnelle, Créteil, France; Institut d'Etudes Cognitives, Ecole Normale Supérieure, Paris, France; Faculté de Médecine, Université Paris Est, Créteil, France.
Insights
The new UHDRS-FAP scale effectively tracks Huntington's disease (HD) progression in advanced stages. This tool offers improved sensitivity for motor and cognitive decline compared to the standard UHDRS.
Area of Science:
- Neurology
- Clinical Assessment
- Neurodegenerative Diseases
Background:
- The Unified Huntington's Disease Rating Scale (UHDRS) is limited in assessing advanced Huntington's disease (HD) due to floor effects.
- A need exists for a more sensitive scale to evaluate disease progression in late-stage HD patients.
Purpose of the Study:
- To develop and validate the UHDRS-For Advanced Patients (UHDRS-FAP) for improved longitudinal assessment of advanced HD.
- To compare the sensitivity to decline of the UHDRS-FAP against the standard UHDRS.
Main Methods:
- Sixty-nine patients with advanced HD (Total Functional Capacity score ≤5) were recruited.
- Forty-five patients underwent longitudinal assessment with UHDRS-FAP (1.6 ± 1.2 years), with 30 also assessed using UHDRS.
- Psychometric properties, inter-rater reliability, and longitudinal sensitivity to decline were evaluated.
Main Results:
- UHDRS-FAP demonstrated higher internal consistency for motor (0.84) and cognitive (0.91) domains.
- Inter-rater reliability was high (≥0.88) across all UHDRS-FAP scores.
- UHDRS-FAP showed greater sensitivity to decline in motor and cognitive function, particularly in patients with severe impairment (TFC ≤1).
Conclusions:
- The UHDRS-FAP is a reliable and more sensitive tool than the UHDRS for assessing motor and cognitive decline in advanced HD.
- The scale includes relevant items for daily care and shows promise for tracking disease progression.
- Further research is needed to understand the decline in behavioral scores, potentially related to communication deficits.
Abstract:
The Unified Huntington's Disease Rating Scale (UHDRS) adequately measures decline in patients at early and moderate stages of Huntington's disease (HD). In patients with advanced HD, floor effects hamper the evaluation, thus calling for an adjusted scale. We designed the UHDRS-For Advanced Patients (UHDRS-FAP) to improve longitudinal assessment of patients at the advanced disease stage. Sixty-nine patients with a Total Functional Capacity score ≤ 5 were recruited in France and the Netherlands. Among them, 45 patients were followed longitudinally (mean ± standard deviation, 1.6 ± 1.2 years) with the UHDRS-FAP; 30 patients also were assessed with the UHDRS. In cross-sectional analyses, the psychometric properties and inter-rater reliability of the scale were evaluated. Longitudinal analyses were used to evaluate the sensitivity to decline of the UHDRS-FAP compared with the UHDRS. Internal consistency was higher for motor (0.84) and cognitive (0.91) scores than for somatic (0.70) and behavioral (0.49) scores. Inter-rater reliability was ≥ 0.88 for all scores. The somatic score, which was specific to the UHDRS-FAP, declined over time along with motor and cognitive performance on both scales. Although performance with the two scales was correlated, the UHDRS-FAP appeared to be more sensitive to change and was the only scale that detected decline in patients with a Total Functional Capacity score ≤ 1. Neither scale detected a significant decline in behavioral scores. The results indicate that the UHDRS-FAP is reliable and more sensitive to change than the original UHDRS for cognitive and motor domains. It offers items that are relevant for daily care. Behavioral scores tended to decline, but this may reflect the decline in patients' communicative abilities.
More Related Videos
09:18Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
Published on: January 12, 2019
09:06Whole-brain Segmentation and Change-point Analysis of Anatomical Brain MRI—Application in Premanifest Huntington's Disease
Published on: June 9, 2018