Mixed effects models but not t-tests or linear regression detect progression of apathy in Parkinson’s disease over seven years in a cohort: a comparative analysis

Anne Marie Hanff*, Rejko Krüger, Geeta Acharya, Gloria Aguayo, Myriam Alexandre, Wim Ammerlaan, Roxane Batutu, Katy Beaumont, Sibylle Béchet, Guy Berchem, Ibrahim Boussaad, Gessica Contesotto, Nancy de Bremaeker, Angelo Ferrari, Joëlle Fritz, Carlos Gamio, Manon Gantenbein, Laura georges, Marijus Giraitis, Jérôme GraasEstelle Henry, Margaux Henry, Alexander Hundt, Sonja Jónsdóttir, Jochen Klucken, Olga Kofanova, Pauline Lambert, Zied Landoulsi, Ana Festas Lopes, Victoria Lorentz, Tainá M. Marques, Guilherme Marques, Deborah Mcintyre, Chouaib Mediouni, Alexia Mendibide, Myriam Menster, Michel Mittelbronn, Saïda Mtimet, Maeva Munsch, Ulf Nehrbass, Sarah Nickels, Fozia Noor, Claire Pauly, Laure Pauly, Lukas Pavelka, Magali Perquin, Achilleas Pexaras, Armin Rauschenberger, Lucie Remark, Ilsé Richard, Olivia Roland, Stefano Sapienza, Amir Sharify, Kate Sokolowska, Maud Theresine, Hermann Thien, Johanna Trouet, Michel Vaillant, Carlos Vega, Gelani Zelimkhanov, on behalf of NCER-PD

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

1 Citation (Scopus)

Abstract

Introduction: While there is an interest in defining longitudinal change in people with chronic illness like Parkinson’s disease (PD), statistical analysis of longitudinal data is not straightforward for clinical researchers. Here, we aim to demonstrate how the choice of statistical method may influence research outcomes, (e.g., progression in apathy), specifically the size of longitudinal effect estimates, in a cohort. Methods: In this retrospective longitudinal analysis of 802 people with typical Parkinson’s disease in the Luxembourg Parkinson's study, we compared the mean apathy scores at visit 1 and visit 8 by means of the paired two-sided t-test. Additionally, we analysed the relationship between the visit numbers and the apathy score using linear regression and longitudinal two-level mixed effects models. Results: Mixed effects models were the only method able to detect progression of apathy over time. While the effects estimated for the group comparison and the linear regression were smaller with high p-values (+ 1.016/ 7 years, p = 0.107, -0.056/ 7 years, p = 0.897, respectively), effect estimates for the mixed effects models were positive with a very small p-value, indicating a significant increase in apathy symptoms by + 2.345/ 7 years (p < 0.001). Conclusion: The inappropriate use of paired t-tests and linear regression to analyse longitudinal data can lead to underpowered analyses and an underestimation of longitudinal change. While mixed effects models are not without limitations and need to be altered to model the time sequence between the exposure and the outcome, they are worth considering for longitudinal data analyses. In case this is not possible, limitations of the analytical approach need to be discussed and taken into account in the interpretation.

Original languageEnglish
Article number183
JournalBMC Medical Research Methodology
Volume24
Issue number1
DOIs
Publication statusPublished - 24 Aug 2024

Keywords

  • Cohort studies
  • Disease progression
  • Epidemiology
  • Lost to follow-up
  • Parkinson
  • Statistical model

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