Johan Marinus1, Jorine F van der Heeden2, Jacobus J van Hilten2. 1. Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands. Electronic address: j.marinus@lumc.nl. 2. Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Abstract
INTRODUCTION: Disease progression in Parkinson's disease is often calculated in data from cross-sectional studies, where a severity score (e.g. UPDRS-motor score) is divided by disease duration. While this intuitively may seem a plausible approach, it is uncertain if these rates are similar to those calculated from longitudinal data. The aim of this study is to examine if progression rates calculated according to both methods yield the same results. METHODS: We calculated two progression rates in data from the PROPARK study: one where last follow-up SPES/SCOPA motor and activities-of-daily-living scores were divided by disease duration, and one in which baseline motor and activities-of-daily-living scores were subtracted from data collected at last follow-up, and where the difference was divided by the time that passed between both assessments. We subsequently calculated the rank order correlation between both approaches. RESULTS: We found that progression rates calculated from cross-sectional data are 1.5-2 times higher than those calculated from longitudinal data, and that the correlation between both methods is <0.50. CONCLUSION: Progression rates calculated from cross-sectional data not only overestimate actual progression, but also yield a different rank order. We also discuss potential explanations for the discrepancy between both methods and argue that the method of calculating progression rates in data from cross-sectional studies in PD should not be used.
INTRODUCTION: Disease progression in Parkinson's disease is often calculated in data from cross-sectional studies, where a severity score (e.g. UPDRS-motor score) is divided by disease duration. While this intuitively may seem a plausible approach, it is uncertain if these rates are similar to those calculated from longitudinal data. The aim of this study is to examine if progression rates calculated according to both methods yield the same results. METHODS: We calculated two progression rates in data from the PROPARK study: one where last follow-up SPES/SCOPA motor and activities-of-daily-living scores were divided by disease duration, and one in which baseline motor and activities-of-daily-living scores were subtracted from data collected at last follow-up, and where the difference was divided by the time that passed between both assessments. We subsequently calculated the rank order correlation between both approaches. RESULTS: We found that progression rates calculated from cross-sectional data are 1.5-2 times higher than those calculated from longitudinal data, and that the correlation between both methods is <0.50. CONCLUSION: Progression rates calculated from cross-sectional data not only overestimate actual progression, but also yield a different rank order. We also discuss potential explanations for the discrepancy between both methods and argue that the method of calculating progression rates in data from cross-sectional studies in PD should not be used.
Authors: Danielle S Abraham; Ann L Gruber-Baldini; Laurence S Magder; Patrick F McArdle; Sarah E Tom; Erik Barr; Katrina Schrader; Lisa M Shulman Journal: Parkinsonism Relat Disord Date: 2019-10-23 Impact factor: 4.891
Authors: Carmen Rodríguez-Blázquez; Maria João Forjaz; Monica M Kurtis; Roberta Balestrino; Pablo Martinez-Martin Journal: Front Neurol Date: 2018-06-07 Impact factor: 4.003