Biomarker candidates of neurodegeneration in Parkinson’s disease for the evaluation of disease-modifying therapeutics

被引:0
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作者
Manfred Gerlach
Walter Maetzler
Karl Broich
Harald Hampel
Lucas Rems
Torsten Reum
Peter Riederer
Albrecht Stöffler
Johannes Streffer
Daniela Berg
机构
[1] University of Würzburg,Department for Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy
[2] University of Tübingen,Center of Neurology, Department of Neurodegeneration and Hertie Institute for Clinical Brain Research
[3] DZNE,Department of Psychiatry, Psychosomatic Medicine and Psychotherapy
[4] German Center for Neurodegenerative Diseases,Boehringer Ingelheim Pharma GmbH and Co KG
[5] Bundesinstitut für Arzneimittel und Medizinprodukte,Department for Psychiatry, Psychosomatics and Psychotherapy
[6] Johann Wolfgang Goethe-University,Janssen
[7] Therapeutic Area CNS/General Medicine,Cilag GmbH
[8] University of Würzburg,undefined
[9] Medizinischer Fachbereich ZNS,undefined
来源
关键词
Parkinson’s disease; Disease-modifying therapies; Neuroprotection; Biomarkers; Surrogate endpoints; Drug development; Disease progression;
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摘要
Reliable biomarkers that can be used for early diagnosis and tracking disease progression are the cornerstone of the development of disease-modifying treatments for Parkinson’s disease (PD). The German Society of Experimental and Clinical Neurotherapeutics (GESENT) has convened a Working Group to review the current status of proposed biomarkers of neurodegeneration according to the following criteria and to develop a consensus statement on biomarker candidates for evaluation of disease-modifying therapeutics in PD. The criteria proposed are that the biomarker should be linked to fundamental features of PD neuropathology and mechanisms underlying neurodegeneration in PD, should be correlated to disease progression assessed by clinical rating scales, should monitor the actual disease status, should be pre-clinically validated, and confirmed by at least two independent studies conducted by qualified investigators with the results published in peer-reviewed journals. To date, available data have not yet revealed one reliable biomarker to detect early neurodegeneration in PD and to detect and monitor effects of drug candidates on the disease process, but some promising biomarker candidates, such as antibodies against neuromelanin, pathological forms of α-synuclein, DJ-1, and patterns of gene expression, metabolomic and protein profiling exist. Almost all of the biomarker candidates were not investigated in relation to effects of treatment, validated in experimental models of PD and confirmed in independent studies.
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页码:39 / 52
页数:13
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