Validation of conversion between mini-mental state examination and montreal cognitive assessment

ABSTRACT Introduction Harmonizing data across cohorts is important for validating findings or combining data in meta‐analyses. We replicate and validate a previous conversion of MoCA to MMSE in PD. Methods We used five studies with 1,161 PD individuals and 2,091 observations measured with both the M...

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Published inMovement disorders Vol. 31; no. 4; pp. 593 - 596
Main Authors Lawton, Michael, Kasten, Meike, May, Margaret T., Mollenhauer, Brit, Schaumburg, Martina, Liepelt-Scarfone, Inga, Maetzler, Walter, Vollstedt, Eva-Juliane, Hu, Michele T.M., Berg, Daniela, Ben-Shlomo, Yoav
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.04.2016
Wiley Subscription Services, Inc
John Wiley and Sons Inc
Subjects
Online AccessGet full text
ISSN0885-3185
1531-8257
1531-8257
DOI10.1002/mds.26498

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Summary:ABSTRACT Introduction Harmonizing data across cohorts is important for validating findings or combining data in meta‐analyses. We replicate and validate a previous conversion of MoCA to MMSE in PD. Methods We used five studies with 1,161 PD individuals and 2,091 observations measured with both the MoCA and MMSE. We compared a previously published conversion table using equipercentile equating with log‐linear smoothing to our internally derived scores. Results Both conversions found good agreement within and across the studies when comparing true and converted MMSE (mean difference: 0.05; standard deviation: 1.84; median difference: 0; interquartile range: –1 to 1, using internal conversion). Conclusions These results show that one can get a reliable and valid conversion between two commonly used measures of cognition in PD studies. These approaches need to be applied to other scales and domains to enable large‐scale collaborative analyses across multiple PD cohorts. © 2016 International Parkinson and Movement Disorder Society
Bibliography:Monument Trust Discovery Award from Parkinson's UK
Dementias and Neurodegenerative Diseases Research Network (DeNDRoN)
TEVA Pharma GmbH
UCB Deutschland
GE Healthcare
Deutsche Parkinsonvereinigung
National Institute for Health Research (NIHR) Oxford Biomedical Research Center based at Oxford University Hospitals NHS Trust and University of Oxford
Abbott
Janssen Research & Development
TEVA Pharma
ark:/67375/WNG-81VH9D10-S
istex:B5DA68E3ADF465F9353610252FEF7EA574C095F4
Paracelsus-Klinike Germany
ArticleID:MDS26498
German Research Foundation - No. KA3179/2-1
Full financial disclosures and author roles may be found in the online version of this article.
Nothing to report.
Relevant conflicts of interest/financial disclosures
Funding agencies
Meike Kasten has received funding for the EPIPARK study from the German Research Foundation (KA3179/2‐1). DeNoPa was supported by unrestricted grants by the Paracelsus‐Klinike Germany and from TEVA Pharma as well as funding from GE Healthcare and the Deutsche Parkinsonvereinigung. The Oxford Discovery study was funded by the Monument Trust Discovery Award from Parkinson's UK; and supported by the National Institute for Health Research (NIHR) Oxford Biomedical Research Center based at Oxford University Hospitals NHS Trust and University of Oxford, and the Dementias and Neurodegenerative Diseases Research Network (DeNDRoN). The ABC‐PD study is supported by Janssen Research & Development, a division of Janssen Pharmaceutica NV. Baseline assessment of the MODEP study has been funded by Abbott. Further funding for the MODEP study has been provided by TEVA Pharma GmbH and UCB Deutschland.
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Funding agencies: Meike Kasten has received funding for the EPIPARK study from the German Research Foundation (KA3179/2‐1). DeNoPa was supported by unrestricted grants by the Paracelsus‐Klinike Germany and from TEVA Pharma as well as funding from GE Healthcare and the Deutsche Parkinsonvereinigung. The Oxford Discovery study was funded by the Monument Trust Discovery Award from Parkinson's UK; and supported by the National Institute for Health Research (NIHR) Oxford Biomedical Research Center based at Oxford University Hospitals NHS Trust and University of Oxford, and the Dementias and Neurodegenerative Diseases Research Network (DeNDRoN). The ABC‐PD study is supported by Janssen Research & Development, a division of Janssen Pharmaceutica NV. Baseline assessment of the MODEP study has been funded by Abbott. Further funding for the MODEP study has been provided by TEVA Pharma GmbH and UCB Deutschland.
Relevant conflicts of interest/financial disclosures: Nothing to report.
ISSN:0885-3185
1531-8257
1531-8257
DOI:10.1002/mds.26498