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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  • Λέξεις κλειδιά

Identification of a prospective early motor progression cluster of Parkinson's disease: Data from the PPMI study

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Συγγραφέας
Vavougios G.D., Doskas T., Kormas C., Krogfelt K.A., Zarogiannis S.G., Stefanis L.
Ημερομηνία
2018
Γλώσσα
en
DOI
10.1016/j.jns.2018.01.025
Λέξη-κλειδί
alpha synuclein
biological marker
somatomedin C
biological marker
aged
Article
cerebrospinal fluid
clinical assessment
cluster analysis
decision making
disease course
female
Hopkins verbal learning test
human
major clinical study
male
motor progression
neuroimaging
neuropsychological test
Parkinson disease
phenotype
priority journal
semantics
serum
bibliographic database
blood
cerebrospinal fluid
diagnostic imaging
disease exacerbation
middle aged
nonparametric test
nuclear magnetic resonance imaging
Parkinson disease
pathophysiology
statistical model
statistics and numerical data
Aged
Biomarkers
Cluster Analysis
Databases, Bibliographic
Disease Progression
Female
Humans
Logistic Models
Magnetic Resonance Imaging
Male
Middle Aged
Parkinson Disease
Phenotype
Statistics, Nonparametric
Elsevier B.V.
Εμφάνιση Μεταδεδομένων
Επιτομή
Aim: The aim of our study is to phenotype PD motor progression, and to detect whether serum, cerebrospinal fluid (CSF), neuroimaging biomarkers and neuropsychological measures characterize PD motor progression phenotypes. Methods: We defined motor progression as a difference of at least one point in the Hoehn & Yahr (H&Y) scale between the baseline (Visit 0, V0), 12 months (Visit 04, V04) and 36 months (Visit 08, V08) milestones of the Progression Markers Initiative (PPMI) study. H&Y progression events were recorded at each milestone in order to be used as cluster analysis variables, in order to produce progression phenotypes. Subsequently, cross-cluster comparisons prior to and following (pairwise) propensity score matching were performed in order to assess phenotype – defining characteristics. Results: Four progression clusters where identified: SPPD: Secondarily Progressive PD, H&Y progression between V04 and V08; EPPD: Early Progressive PD. H&Y progression between V0 and V04; NPPD: Non Progressive PD, no H&Y progression; MIPD: Minimally Improving PD, i.e. Minimal H&Y improvement H&Y progression between V04 and V08;. Independent Samples Mann Whitney U tests determined CSF aSyn (p = 0.006, adj p-value = 0.036. I) and Semantic Animal fluency T-score (SFT, p = 0.003, adjusted p-value = 0.016.) as statistically significant cross-cluster characteristics. Following Propensity Score Matching, SFT, Hopkins Verbal Learning Test (Retention/Recall), Serum IGF1, CSF aSyn, DaT-SPECT binding ratios (SBRs) and the Benton Judgement of Line Orientation Test (BJLOT) were determined as statistically significant predictors of cluster differentiation (p < 0.05). Discussion: SFT, Serum IGF1, CSF aSyn and DaT-SPECT-derived, basal ganglia Striatal Binding Ratios warrant further investigation as possible motor progression biomarkers. © 2018 Elsevier B.V.
URI
http://hdl.handle.net/11615/80530
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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    SARS-CoV-2 pathophysiology and its clinical implications: An integrative overview of the pharmacotherapeutic management of COVID-19 

    Tsatsakis A., Calina D., Falzone L., Petrakis D., Mitrut R., Siokas V., Pennisi M., Lanza G., Libra M., Doukas S.G., Doukas P.G., Kavali L., Bukhari A., Gadiparthi C., Vageli D.P., Kofteridis D.P., Spandidos D.A., Paoliello M.M.B., Aschner M., Docea A.O. (2020)
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