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Cerebrospinal fluid biomarkers in Parkinson’s disease with freezing of gait: an exploratory analysis
被引:0
|作者:
J. M. Hatcher-Martin
J. L. McKay
A. F. Pybus
B. Sommerfeld
J. C. Howell
F. C. Goldstein
L. Wood
W. T. Hu
S. A. Factor
机构:
[1] Emory University,Jean & Paul Amos PD & Movement Disorders Program, Department of Neurology
[2] Emory University,Department of Biomedical Informatics
[3] Georgia Tech and Emory University,Wallace H. Coulter Department of Biomedical Engineering
[4] Georgia Tech,Department of Mechanical Engineering
[5] Neurology Consultants of Dallas,Neuropsychology Program, Department of Neurology
[6] Emory University,Alzheimer’s Disease Research Center, Emory University and Cognitive Neurology Division, Rutgers
[7] Health Care Policy,Robert Wood Johnson Medical School and Institute for Health
[8] and Aging Research,Department of Neurology
[9] SOC Telemed,undefined
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摘要:
We explore the association between three Alzheimer’s disease-related and ten inflammation-related CSF markers and freezing of gait (FOG) in patients with Parkinson’s disease (PD). The study population includes PD patients with FOG (PD-FOG, N = 12), without FOG (PD-NoFOG, N = 19), and healthy controls (HC, N = 12). Age and PD duration are not significantly different between groups. After adjusting for covariates and multiple comparisons, the anti-inflammatory marker, fractalkine, is significantly decreased in the PD groups compared to HC (P = 0.002), and further decreased in PD-FOG compared to PD-NoFOG (P = 0.007). The Alzheimer’s disease-related protein, Aβ42, is increased in PD-FOG compared to PD-NoFOG and HC (P = 0.001). Group differences obtained in individual biomarker analyses are confirmed with multivariate discriminant partial least squares regression (P < 0.001). High levels of Aβ42 in PD-FOG patients supports an increase over time from early to advanced state. Low levels of fractalkine might suggest anti-inflammatory effect. These findings warrant replication.
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