Abstract
BackgroundHuntington’s disease (HD) is a rare, genetic, neurodegenerative and ultimately fatal disease with no cure or progression-delaying treatment currently available. HD is characterized by a triad of cognitive, behavioural and motor symptoms. Evidence on epidemiology and management of HD is limited, especially for Germany. This study aims to estimate the incidence and prevalence of HD and analyze the current routine care based on German claims data.MethodsThe source of data was a sample of the Institute for Applied Health Research Berlin (InGef) Research Database, comprising data of approximately four million insured persons from approximately 70 German statutory health insurances. The study was conducted in a retrospective cross-sectional design using 2015 and 2016 as a two-year observation period. At least two outpatient or inpatient ICD-10 codes for HD (ICD-10: G10) during the study period were required for case identification. Patients were considered incident if no HD diagnoses in the 4 years prior to the year of case identification were documented. Information on outpatient drug dispensations, medical aids and remedies were considered to describe the current treatment situation of HD patients.ResultsA 2-year incidence of 1.8 per 100,000 persons (95%-Confidence interval (CI): 1.4–2.4) and a 2-year period prevalence of 9.3 per 100,000 persons (95%-CI: 8.3–10.4) was observed. The prevalence of HD increased with advancing age, peaking at 60–69 years (16.8 per 100,000 persons; 95%-CI: 13.4–21.0) and decreasing afterwards.The most frequently observed comorbidities and disease-associated symptoms in HD patients were depression (42.9%), dementia (37.7%), urinary incontinence (32.5%), extrapyramidal and movement disorders (30.5%), dysphagia (28.6%) and disorders of the lipoprotein metabolism (28.2%).The most common medications in HD patients were antipsychotics (66.9%), followed by antidepressants (45.1%). Anticonvulsants (16.6%), opioids (14.6%) and hypnotics (9.7%) were observed less frequently.Physical therapy was the most often used medical aid in HD patients (46.4%). Nursing services and speech therapy were used by 27.9 and 22.7% of HD patients, respectively, whereas use of psychotherapy was rare (3.2%).ConclusionsBased on a representative sample, this study provides new insights into the epidemiology and routine care of HD patients in Germany, and thus, may serve as a starting point for further research.
Highlights
Huntington’s disease (HD) is a rare, genetic, neurodegenerative and fatal disease with no cure or progression-delaying treatment currently available
HD patients present with a triad of cognitive, behavioral and motor symptoms [3,4,5], which lead to increasing disability, functional decline and loss of independence [2, 5]
Extrapyramidal and movement disorders were diagnosed in 30.5% of HD patients, and dysphagia was diagnosed in 28.6% of HD patients
Summary
Huntington’s disease (HD) is a rare, genetic, neurodegenerative and fatal disease with no cure or progression-delaying treatment currently available. This study aims to estimate the incidence and prevalence of HD and analyze the current routine care based on German claims data. HD patients present with a triad of cognitive, behavioral and motor symptoms [3,4,5], which lead to increasing disability, functional decline and loss of independence [2, 5]. This results in complex patient needs, which are best addressed with interdisciplinary teams consisting of general practitioners, specialists and other health care professionals, e. ‘gene silencing’ could be a potential therapeutic strategy in the future [9], HD is currently incurable, and therapeutic approaches focus on symptom management and maintaining the quality of life
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