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The contribution of cerebrovascular risk factors, metabolic and inflammatory changes to cognitive decline in Parkinson's disease: preliminary observations
B. Veselý, E. Koriťáková, NI. Bohnen, D. Viszlayová, S. Királová, P. Valkovič, E. Kurča, I. Rektor,
Jazyk angličtina Země Rakousko
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
I01 RX001631
RRD VA - United States
P01 NS015655
NINDS NIH HHS - United States
P50 NS091856
NINDS NIH HHS - United States
NV16-33798A
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
NLK
Medline Complete (EBSCOhost)
od 2000-01-01 do Před 1 rokem
- MeSH
- cerebrovaskulární poruchy diagnóza epidemiologie metabolismus MeSH
- kognitivní dysfunkce diagnóza epidemiologie metabolismus MeSH
- kohortové studie MeSH
- lidé středního věku MeSH
- lidé MeSH
- longitudinální studie MeSH
- mediátory zánětu metabolismus MeSH
- metabolické nemoci diagnóza epidemiologie metabolismus MeSH
- následné studie MeSH
- Parkinsonova nemoc diagnóza epidemiologie metabolismus MeSH
- rizikové faktory MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
To determine whether systemic medical factors, such as vascular risk factors, metabolic and inflammatory markers contribute to cognitive decline in Parkinson's disease (PD); if confirmed to determine whether a clinically applicable risk factor model can predict the conversion from normal cognition (NC) to mild cognitive impairment (MCI). 58 patients who met the UK Brain Bank Criteria for PD underwent clinical and laboratory assessment at study entry; 47 patients were re-assessed after 2 years. Medical history, vascular risk (QRISK2), blood metabolic and inflammatory factors, brain vessel examinations, activity of daily living, and neuropsychological testing were performed. Forty patients had NC and 18 patients had MCI at baseline. Patients with MCI had higher level of interleukin 6, folic acid below normal range and higher L-dopa equivalent dose compared to cognitive normal patients at baseline. Patients with NC at baseline were classified into two groups: patients who remained cognitively normal (non-converters, n = 23) and patients who progressed to MCI (converters, n = 11). MCI converters were older at baseline and had higher QRISK2 than the non-converters. Patients with higher QRISK2, lower uric acid level and lower activity of daily living scale at baseline had a higher risk of converting from NC to MCI with a sensitivity of 72.2%, a specificity of 87%, and an overall accuracy of 82.4%. Systemic medical factors are associated with cognitive impairment in PD both cross-sectionally and longitudinally. A risk factor model predicting the decline from NC to MCI could be constructed.
2nd Department of Neurology Comenius University School of Medicine Bratislava Slovak Republic
Clinic of Neurology Comenius University Jessenius Faculty of Medicine Martin Slovak Republic
Department of Neurology Charles University Faculty of Medicine Hradec Králové Czech Republic
Citace poskytuje Crossref.org
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- $a Veselý, Branislav $u Department of Neurology, Faculty Hospital, Constantine the Philosopher University, Nitra, Slovak Republic. Central European Institute of Technology (CEITEC), Brain and Mind Research Program, Masaryk University, Pekařská 664/53, 656 91, Brno, Czech Republic.
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