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

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

Beteiligte Einrichtungen

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.

Bibliografische Daten

OriginalspracheEnglisch
ISSN0340-5354
DOIs
StatusVeröffentlicht - 02.2024

Anmerkungen des Dekanats

© 2023. The Author(s).

PubMed 37803149