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PMID: 21520231 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Plasma epidermal growth factor levels predict cognitive decline in Parkinson disease.

Annals of neurology ·Vol. 69 ·No. 4 ·2011-04-00 ·Pages 655-63

Chen-Plotkin AS, Hu WT, Siderowf A, Weintraub D, Goldmann Gross R, Hurtig HI, Xie SX, Arnold SE, Grossman M, Clark CM, Shaw LM, McCluskey L, Elman L, Van Deerlin VM, Lee VM, Soares H, Trojanowski JQ

Abstract

Most people with Parkinson disease (PD) eventually develop cognitive impairment (CI). However, neither the timing of onset nor the severity of cognitive symptoms can be accurately predicted. We sought plasma-based biomarkers for CI in PD. A discovery cohort of 70 PD patients was recruited. Cognitive status was evaluated with the Mattis Dementia Rating Scale-2 (DRS) at baseline and on annual follow-up visits, and baseline plasma levels of 102 proteins were determined with a bead-based immunoassay. Using linear regression, we identified biomarkers of CI in PD, that is, proteins whose levels correlated with cognitive performance at baseline and/or cognitive decline at follow-up. We then replicated the association between cognitive performance and levels of the top biomarker, using a different technical platform, with a separate cohort of 113 PD patients. Eleven proteins exhibited plasma levels correlating with baseline cognitive performance in the discovery cohort. The best candidate was epidermal growth factor (EGF, p < 0.001); many of the other 10 analytes covaried with EGF across samples. Low levels of EGF not only correlated with poor cognitive test scores at baseline, but also predicted an 8-fold greater risk of cognitive decline to dementia-range DRS scores at follow-up for those with intact baseline cognition. A weaker, but still significant, relationship between plasma EGF levels and cognitive performance was found in an independent replication cohort of 113 PD patients. Our data suggest that plasma EGF may be a biomarker for progression to CI in PD.

MeSH Terms
Aged Apolipoproteins E/genetics Biomarkers/blood Cognition Cognition Disorders/blood,etiology,prevention & control Epidermal Growth Factor/blood Female Genotype Humans Linear Models Male Middle Aged Parkinson Disease/blood,complications Predictive Value of Tests
Chemicals
Apolipoproteins E Biomarkers Epidermal Growth Factor
Authors & Affiliations
17 authors, click to expand affiliations / ORCID
Chen-Plotkin Alice S
Department of Neurology, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Hu William T
Siderowf Andrew
Weintraub Daniel
Goldmann Gross Rachel
Hurtig Howard I
Xie Sharon X
Arnold Steven E
Grossman Murray
Clark Christopher M
Shaw Leslie M
McCluskey Leo
Elman Lauren
Van Deerlin Vivianna M
Lee Virginia M-Y
Soares Holly
Trojanowski John Q
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Article Info
Journal
Annals of neurology
Abbr.
Ann Neurol
ISSN
1531-8249
Published
2011-04-00
Epub
2010-00-29
Pages
655-63
Language
English
Region
United States
NLM ID
7707449
PMCID
PMC3155276
Subset
IM
Grants
NIA NIH HHS · P30 AG010124-20 · United States
NIA NIH HHS · AG10124 · United States
NIA NIH HHS · P01 AG017586 · United States
NIA NIH HHS · AG024904 · United States
NIA NIH HHS · U01 AG024904 · United States
NIA NIH HHS · P01 AG017586-109002 · United States
NINDS NIH HHS · P50 NS053488 · United States
NIA NIH HHS · AG17586 · United States
NIA NIH HHS · K08 AG033101-03 · United States
NIA NIH HHS · AG033101 · United States
NINDS NIH HHS · P50 NS053488-05 · United States
NIA NIH HHS · P30 AG010124 · United States
NINDS NIH HHS · NS-053488 · United States
NIA NIH HHS · K08 AG033101 · United States
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