RT Journal Article
SR Electronic
T1 Humanistic Burden of Huntington Disease: Evidence From the Huntington Disease Burden of Illness Study
JF Neurology: Clinical Practice
FD Lippincott Williams & Wilkins
SP 10.1212/CPJ.0000000000200095
DO 10.1212/CPJ.0000000000200095
A1 Santana, Idaira Rodriguez
A1 Frank, Samuel
A1 Doherty, Maria
A1 Willock, Rosa
A1 Hamilton, Jamie
A1 Hubberstey, Hayley
A1 Stanley, Cath
A1 Vetter, Louise
A1 Winkelmann, Michaela
A1 Dolmetsch, Ricardo E
A1 Li, Nanxin
A1 Ratsch, Sarah
A1 Ali, Talaha M
YR 2022
UL http://cp.neurology.org/content/early/2022/10/12/CPJ.0000000000200095.abstract
AB Background and Objectives: Huntington’s Disease (HD) is a rare, inherited and highly complex neuro-degenerative disorder with no currently approved disease modifying treatments. We investigated the impact of HD on health-related quality of life (HRQoL) and other patient-reported outcomes in the Huntington’s Disease Burden of Illness (HDBOI) study.Methods: The HDBOI study is a retrospective, cross-sectional study conducted between September 2020 and May 2021 in France, Germany, Italy, Spain, the United Kingdom and the United States. People with symptomatic onset HD (PwHD) were recruited by their HD-treating physicians and categorized as early (ES), mid (MS) or advanced stage (AS) HD. Physicians provided sociodemographic and clinical information from the participant’s medical records in electronic case report forms (eCRF); participants or their proxies completed online Patient Public Involvement Engagement questionnaires (PPIE-P). Patient-reported outcomes included the EQ-5D-5L, SF-36 v2 (and SF-6D utility), Huntington Quality of Life Instrument (H-QoL-I), and the Work Productivity and Activity Impairment Specific Health Problem (WPAI-SHP). All outcomes were summarized using descriptive statistics, differences between disease stages were assessed by Kruskal-Wallis tests.Results: A total of 2,094 PwHD were enrolled with completed eCRFs (100%) and PPIE-P forms (n=482, 23%). Participants mean age was 47.3 years, they were generally evenly distributed across countries, with the majority being ES (40%) followed by MS (33%) and LS (26%). Mean EQ-5D-5L (n=336) utility scores was 0.59 (SD, 0.27), with the highest mean utility scores [SD] in ES (0.72 [0.22]) followed by MS (0.62 [0.18]) and AS (0.37 [0.30]), p<0.001. Mean SF-6D score (n=482) was 0.57 (SD, 0.10), with mean values decreasing with advanced disease (ES, 0.61; MS, 0.56; AS, 0.50, p<0.001). H-QoL-I mean scores (n=482) also worsened with more advanced disease, from 0.58 for ES to 0.49 for MS and 0.37 for AS, p<0.001. Impairment in daily activities and in work productivity. Overall proxy-respondents reported on average worse outcomes than PwHD (self-reported) across all outcomes and disease stages suggesting a possible unawareness of deficits by PwHD.Conclusion: The HDBOI study provides new insights into the characteristics and humanistic burden of PwHD, and offers a meaningful contribution to this underserved research area.