diagnosis of parkinsons disease based on disease-specific autoantibody profiles in human sera帕金森病的诊断基于特定疾病在人类血清自身抗体的概要文件.pdfVIP
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diagnosis of parkinsons disease based on disease-specific autoantibody profiles in human sera帕金森病的诊断基于特定疾病在人类血清自身抗体的概要文件
Diagnosis of Parkinson’s Disease Based on Disease-
Specific Autoantibody Profiles in Human Sera
Min Han1,2., Eric Nagele3., Cassandra DeMarshall1,2, Nimish Acharya1,2, Robert Nagele2,3*
1 University of Medicine and Dentistry of New Jersey-Graduate School of Biomedical Sciences at the School of Osteopathic Medicine, Stratford, New Jersey, United States
of America, 2 New Jersey Institute for Successful Aging, University of Medicine and Dentistry of New Jersey, Stratford, New Jersey, United States of America, 3 Durin
Technologies, Inc. New Brunswick, New Jersey, United States of America
Abstract
Parkinson’s disease (PD), hallmarked by a variety of motor disorders and neurological decline, is the second most common
neurodegenerative disease worldwide. Currently, no diagnostic test exists to identify sufferers, and physicians must rely on a
combination of subjective physical and neurological assessments to make a diagnosis. The discovery of definitive blood-
borne biomarkers would be a major step towards early and reliable diagnosis. Despite attention devoted to this search, such
biomarkers have remained elusive. In the present study, we used human protein microarrays to reveal serum autoantibodies
that are differentially expressed among PD and control subjects. The diagnostic significance of each of these autoantibodies
was evaluated, resulting in the selection of 10 autoantibody biomarkers that can effectively differentiate PD sera from
control sera with a sensitivity of 93.1% and specificity of 100%. PD sera were also distinguishable from sera obtained from
Alzheimer’s disease, breast cancer, and multiple sclerosis patients with accuracies of 86.0%, 96.6%, and 100%, respectively.
Results demonstrate that serum autoantibodies can be used as highly specific and accurate biomarkers for PD diagnosis
throughout the course of the disease.
Citation: Han M, Nagele
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