TY - JOUR
T1 - An adapted clinical global Impression of improvement for use in Angelman syndrome
T2 - Validation analyses utilizing data from the NEPTUNE study
AU - Ventola, Pamela
AU - Jaeger, Judith
AU - Keary, Christopher J.
AU - Kolevzon, Alexander
AU - Adams, Maxwell
AU - Keshavan, Bina
AU - Zinger-Salmun, Celia
AU - Ochoa-Lubinoff, Cesar
N1 - Publisher Copyright:
© 2023 European Paediatric Neurology Society
PY - 2023/11
Y1 - 2023/11
N2 - Purpose: Angelman Syndrome (AS) is a rare, severe neurogenetic disorder that causes symptoms such as intellectual disability and motor impairments and is typically diagnosed in early childhood. The complexity and heterogeneity of AS confound characterization of disease severity and pose unique challenges when determining an individual's response to treatment. There is therefore a substantial unmet need for rating scales specifically designed for complex conditions such as AS. To address this, the Clinical Global Impressions (CGI) scale, which has components for both symptom severity (CGI-S) and improvement (CGI-I) was specifically adapted to measure severity (CGI-S-AS) and improvement (CGI-I-AS) in AS. Methods: The modified CGI-S/I-AS was used in the NEPTUNE trial of gaboxadol for the treatment of AS. Here we report on the validation of the CGI-I-AS using data from NEPTUNE and discuss insights for its potential use in future trials. Results: Improvements in the CGI-I-AS rating tended to be consistent with changes on other relevant rating scales. Sleep-related symptoms were particularly well represented, while communication-related symptoms were not. Conclusions: Our validation analysis of the CGI-I-AS demonstrates its usefulness along with possible areas of improvement. The CGI-I-AS is a potential tool for use in other trials of AS drug candidates, and the process for its development can serve as a road map for the development of assessment tools for other neuropsychiatric disorders with similar complexities and heterogeneity.
AB - Purpose: Angelman Syndrome (AS) is a rare, severe neurogenetic disorder that causes symptoms such as intellectual disability and motor impairments and is typically diagnosed in early childhood. The complexity and heterogeneity of AS confound characterization of disease severity and pose unique challenges when determining an individual's response to treatment. There is therefore a substantial unmet need for rating scales specifically designed for complex conditions such as AS. To address this, the Clinical Global Impressions (CGI) scale, which has components for both symptom severity (CGI-S) and improvement (CGI-I) was specifically adapted to measure severity (CGI-S-AS) and improvement (CGI-I-AS) in AS. Methods: The modified CGI-S/I-AS was used in the NEPTUNE trial of gaboxadol for the treatment of AS. Here we report on the validation of the CGI-I-AS using data from NEPTUNE and discuss insights for its potential use in future trials. Results: Improvements in the CGI-I-AS rating tended to be consistent with changes on other relevant rating scales. Sleep-related symptoms were particularly well represented, while communication-related symptoms were not. Conclusions: Our validation analysis of the CGI-I-AS demonstrates its usefulness along with possible areas of improvement. The CGI-I-AS is a potential tool for use in other trials of AS drug candidates, and the process for its development can serve as a road map for the development of assessment tools for other neuropsychiatric disorders with similar complexities and heterogeneity.
KW - Angelman syndrome (AS)
KW - Clinical global impressions (CGI) scale
KW - Disease-specific rating scale
KW - Gaboxadol
UR - https://www.scopus.com/pages/publications/85169897423
U2 - 10.1016/j.ejpn.2023.08.003
DO - 10.1016/j.ejpn.2023.08.003
M3 - Article
C2 - 37688937
AN - SCOPUS:85169897423
SN - 1090-3798
VL - 47
SP - 35
EP - 40
JO - European Journal of Paediatric Neurology
JF - European Journal of Paediatric Neurology
ER -