Application of longitudinal item response theory models to modeling Parkinson's disease progression.


Journal

CPT: pharmacometrics & systems pharmacology
ISSN: 2163-8306
Titre abrégé: CPT Pharmacometrics Syst Pharmacol
Pays: United States
ID NLM: 101580011

Informations de publication

Date de publication:
10 2022
Historique:
revised: 27 06 2022
received: 04 05 2022
accepted: 19 07 2022
pubmed: 28 7 2022
medline: 19 10 2022
entrez: 27 7 2022
Statut: ppublish

Résumé

The Movement Disorder Society revised version of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS) parts 2 and 3 reflect patient-reported functional impact and clinician-reported severity of motor signs of Parkinson's disease (PD), respectively. Total scores are common clinical outcomes but may obscure important time-based changes in items. We aim to analyze longitudinal disease progression based on MDS-UPRDS parts 2 and 3 item-level responses over time and as functions of Hoehn & Yahr (H&Y) stages 1 and 2 for subjects with early PD. The longitudinal item response theory (IRT) modeling is a novel statistical method addressing limitations in traditional linear regression approaches, such as ignoring varying item sensitivities and the sum score balancing out improvements and declines. We utilized a harmonized dataset consisting of six studies with 3573 subjects with early PD and 14,904 visits, and mean follow-up time of 2.5 years (±1.57). We applied both a unidimensional (each part separately) and multidimensional (both parts combined) longitudinal IRT models. We assessed the progression rates for both parts, anchored to baseline H&Y stages 1 and 2. Both the uni- and multidimensional longitudinal IRT models indicate significant worsening time effects in both parts 2 and 3. Baseline H&Y stage 2 was associated with significantly higher baseline severities, but slower progression rates in both parts, as compared with stage 1. Patients with baseline H&Y stage 1 demonstrated slower progression in part 2 severity compared to part 3, whereas patients with baseline H&Y stage 2 progressed faster in part 2 than part 3. The multidimensional model had a superior fit compared to the unidimensional models and it had excellent model performance.

Identifiants

pubmed: 35895005
doi: 10.1002/psp4.12853
pmc: PMC9574723
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1382-1392

Subventions

Organisme : NIA NIH HHS
ID : P30 AG028716
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG072958
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG064803
Pays : United States
Organisme : NIA NIH HHS
ID : P30AG072958
Pays : United States

Informations de copyright

© 2022 The Authors. CPT: Pharmacometrics & Systems Pharmacology published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

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Auteurs

Haotian Zou (H)

University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Varun Aggarwal (V)

Critical Path Institute, Tucson, Arizona, USA.

Glenn T Stebbins (GT)

Rush University Medical Center, Chicago, Illinois, USA.

Martijn L T M Müller (MLTM)

Critical Path Institute, Tucson, Arizona, USA.

Jesse M Cedarbaum (JM)

Coeruleus Clinical Sciences LLC, Woodbridge, Connecticut, USA.

Anne Pedata (A)

Critical Path Institute, Tucson, Arizona, USA.

Diane Stephenson (D)

Critical Path Institute, Tucson, Arizona, USA.

Tanya Simuni (T)

Northwestern University Medical Center, Chicago, Illinois, USA.

Sheng Luo (S)

Duke University, Durham, North Carolina, USA.

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Classifications MeSH