The comorbidity and co-medication profile of patients with progressive supranuclear palsy

Author:

Greten StephanORCID,Wegner Florian,Jensen Ida,Krey Lea,Rogozinski Sophia,Fehring Meret,Heine Johanne,Doll-Lee Johanna,Pötter-Nerger Monika,Zeitzschel Molly,Hagena Keno,Pedrosa David J.,Eggers Carsten,Bürk Katrin,Trenkwalder Claudia,Claus Inga,Warnecke Tobias,Süß Patrick,Winkler Jürgen,Gruber Doreen,Gandor Florin,Berg Daniela,Paschen Steffen,Classen Joseph,Pinkhardt Elmar H.,Kassubek Jan,Jost Wolfgang H.,Tönges Lars,Kühn Andrea A.,Schwarz Johannes,Peters Oliver,Dashti Eman,Priller Josef,Spruth Eike J.,Krause Patricia,Spottke Annika,Schneider Anja,Beyle Aline,Kimmich Okka,Donix Markus,Haussmann Robert,Brandt Moritz,Dinter Elisabeth,Wiltfang Jens,Schott Björn H.,Zerr Inga,Bähr Mathias,Buerger Katharina,Janowitz Daniel,Perneczky Robert,Rauchmann Boris-Stephan,Weidinger Endy,Levin Johannes,Katzdobler Sabrina,Düzel Emrah,Glanz Wenzel,Teipel Stefan,Kilimann Ingo,Prudlo Johannes,Gasser Thomas,Brockmann Kathrin,Hoffmann Daniel C.,Klockgether Thomas,Krause Olaf,Heck Johannes,Höglinger Günter U.,Klietz Martin

Abstract

Abstract Background Progressive supranuclear palsy (PSP) is usually diagnosed in elderly. Currently, little is known about comorbidities and the co-medication in these patients. Objectives To explore the pattern of comorbidities and co-medication in PSP patients according to the known different phenotypes and in comparison with patients without neurodegenerative disease. Methods Cross-sectional data of PSP and patients without neurodegenerative diseases (non-ND) were collected from three German multicenter observational studies (DescribePSP, ProPSP and DANCER). The prevalence of comorbidities according to WHO ICD-10 classification and the prevalence of drugs administered according to WHO ATC system were analyzed. Potential drug–drug interactions were evaluated using AiDKlinik®. Results In total, 335 PSP and 275 non-ND patients were included in this analysis. The prevalence of diseases of the circulatory and the nervous system was higher in PSP at first level of ICD-10. Dorsopathies, diabetes mellitus, other nutritional deficiencies and polyneuropathies were more frequent in PSP at second level of ICD-10. In particular, the summed prevalence of cardiovascular and cerebrovascular diseases was higher in PSP patients. More drugs were administered in the PSP group leading to a greater percentage of patients with polypharmacy. Accordingly, the prevalence of potential drug–drug interactions was higher in PSP patients, especially severe and moderate interactions. Conclusions PSP patients possess a characteristic profile of comorbidities, particularly diabetes and cardiovascular diseases. The eminent burden of comorbidities and resulting polypharmacy should be carefully considered when treating PSP patients.

Funder

Medizinische Hochschule Hannover (MHH)

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

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