Reference : Prodromal Markers in Parkinson's Disease: Limitations in Longitudinal Studies and Les...
Scientific journals : Article
Human health sciences : Neurology
http://hdl.handle.net/10993/28237
Prodromal Markers in Parkinson's Disease: Limitations in Longitudinal Studies and Lessons Learned.
English
Heinzel, S. [> >]
Roeben, B. [> >]
Ben-Shlomo, Y. [> >]
Lerche, S. [> >]
Alves, G. [> >]
Barone, P. [> >]
Behnke, S. [> >]
Berendse, H. W. [> >]
Bloem, B. R. [> >]
Burn, D. [> >]
Dodel, R. [> >]
Grosset, D. G. [> >]
Hu, M. [> >]
Kasten, M. [> >]
Krüger, Rejko mailto [University of Luxembourg > Faculty of Science, Technology and Communication (FSTC) > Life Science Research Unit]
Moccia, M. [> >]
Mollenhauer, B. [> >]
Oertel, W. [> >]
Suenkel, U. [> >]
Walter, U. [> >]
Wirdefeldt, K. [> >]
Liepelt-Scarfone, I. [> >]
Maetzler, W. [> >]
Berg, D. [> >]
2016
Frontiers in aging neuroscience
8
147
Yes (verified by ORBilu)
1663-4365
1663-4365
Switzerland
[en] Parkinson's disease ; case-control ; clinical ; cohort ; longitudinal ; marker ; prodromal ; prospective
[en] A growing body of evidence supports a prodromal neurodegenerative process preceding the clinical onset of Parkinson's disease (PD). Studies have identified several different prodromal markers that may have the potential to predict the conversion from healthy to clinical PD but use considerably different approaches. We systematically reviewed 35 longitudinal studies reporting prodromal PD features and evaluated the methodological quality across 10 different predefined domains. We found limitations in the following domains: PD diagnosis (57% of studies), prodromal marker assessments (51%), temporal information on prodromal markers or PD diagnosis (34%), generalizability of results (17%), statistical methods (accounting for at least age as confounder; 17%), study design (14%), and sample size (9%). However, no limitations regarding drop-out (or bias investigation), or report of inclusion/exclusion criteria or
prodromal marker associations were revealed. Lessons learned from these limitations
and additional aspects of current prodromal marker studies in PD are discussed to
provide a basis for the evaluation of findings and the improvement of future research in
prodromal PD. The observed heterogeneity of studies, limitations and analyses might be
addressed in future longitudinal studies using a, yet to be established, modular minimal
set of assessments improving comparability of findings and enabling data sharing and
combined analyses across studies.
http://hdl.handle.net/10993/28237
10.3389/fnagi.2016.00147

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