Gaps Between Aims and Achievements in Therapeutic Modification of Neuronal Damage ("Neuroprotection")

被引:26
作者
Wiendl, Heinz [1 ]
Elger, Christian [2 ]
Foerstl, Hans [3 ]
Hartung, Hans-Peter [4 ]
Oertel, Wolfgang [5 ]
Reichmann, Heinz [6 ]
Schwab, Stefan [7 ]
机构
[1] Univ Munster, Dept Neurol, D-48149 Munster, Germany
[2] Univ Bonn, Med Ctr, Dept Epileptol, Bonn, Germany
[3] Tech Univ Munich, Klin Psychiat & Psychotherapie, Munich, Germany
[4] Univ Dusseldorf, Dept Neurol, Dusseldorf, Germany
[5] Univ Marburg, Neurol Klin, Marburg, Germany
[6] Tech Univ Dresden, Univ Klinikum Carl Gustav Carus Dresden, Neurol Klin & Poliklin, D-01062 Dresden, Germany
[7] Univ Klinikum Erlangen, Neurol Klin, Erlangen, Germany
关键词
Neuroprotection; neurodegeneration; Alzheimer's disease; Parkinson's disease; multiple sclerosis; stroke; PROGRESSIVE MULTIPLE-SCLEROSIS; DISEASE; TRIALS; FINGOLIMOD; LESSONS;
D O I
10.1007/s13311-015-0348-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The term "neuroprotection" is often misused, overused, or misunderstood. A reasonable definition of neuroprotection refers to the preservation of "neuronal structure and/or function." Although our knowledge about the cellular and molecular mechanisms of neurodegeneration has expanded, experimental systems and animal models that mimic the process or allow translation into clinical success remain limited. This editorial discusses reasons for this gap and strategies to close it. Experimental models can only mirror certain aspects of disease mechanisms in humans. Therefore, findings in these models need to be linked with patient data to improve real-life relevance. Successful neuroprotection depends on finding the right "window of opportunity" which varies from very short (stroke) to very long (Alzheimer's disease), necessitating the need to focus on strategies for very early disease recognition. This need challenges the strategies to be chosen, trial approaches and methodologies, and the allocation of resources. Additionally, outcome measures are often not well suited to assess neuroprotection. To this end, surrogate measures, including biomarkers, are useful endpoints to demonstrate evidence of target directed therapeutic utility. Finally, studies have shown that neuroprotection is not likely to succeed when targeting only one pathway. These obstacles have reduced the level of enthusiasm for neuroprotection in certain disease areas (e.g., stroke). Academia, industry, regulatory authorities, funding agencies and patient organizations have to cooperate to a greater extent in order to overcome these impediments and to encourage nonclassical concepts. These concepts will be interdisciplinary in order to achieve meaningful disease modification.
引用
收藏
页码:449 / 454
页数:6
相关论文
共 21 条
[1]   Fingolimod is a potential novel therapy for multiple sclerosis [J].
Aktas, Orhan ;
Kuery, Patrick ;
Kieseier, Bernd ;
Hartung, Hans-Peter .
NATURE REVIEWS NEUROLOGY, 2010, 6 (07) :373-382
[2]   Neuroprotection, regeneration and immunomodulation: broadening the therapeutic repertoire in multiple sclerosis [J].
Aktas, Orhan ;
Kieseier, Bernd ;
Hartung, Hans-Peter .
TRENDS IN NEUROSCIENCES, 2010, 33 (03) :140-152
[3]   Staging of brain pathology related to sporadic Parkinson's disease [J].
Braak, H ;
Del Tredici, K ;
Rüb, U ;
de Vos, RAI ;
Steur, ENHJ ;
Braak, E .
NEUROBIOLOGY OF AGING, 2003, 24 (02) :197-211
[4]   Translational neuroprotection research in glaucoma: a review of definitions and principles [J].
Casson, Robert J. ;
Chidlow, Glyn ;
Ebneter, Andreas ;
Wood, John P. M. ;
Crowston, Jonathan ;
Goldberg, Ivan .
CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2012, 40 (04) :350-357
[5]  
Cedarbaum JM, 2015, NEUROTHERAPEUTICS, V12, P151, DOI 10.1007/s13311-014-0310-1
[6]   Adaptive Clinical Trial Design [J].
Chow, Shein-Chung .
ANNUAL REVIEW OF MEDICINE, VOL 65, 2014, 65 :405-415
[7]   Modeling Immunity and Inflammation in Stroke Can Mice Be Trusted? [J].
Dirnagl, Ulrich .
STROKE, 2014, 45 (09) :E177-E178
[8]   Progressive multiple sclerosis 2 Treatment of progressive multiple sclerosis: what works, what does not, and what is needed [J].
Feinstein, Anthony ;
Freeman, Jenny ;
Lo, Albert C. .
LANCET NEUROLOGY, 2015, 14 (02) :194-207
[9]   Tracking pathophysiological processes in Alzheimer's disease: an updated hypothetical model of dynamic biomarkers [J].
Jack, Clifford R., Jr. ;
Knopman, David S. ;
Jagust, William J. ;
Petersen, Ronald C. ;
Weiner, Michael W. ;
Aisen, Paul S. ;
Shaw, Leslie M. ;
Vemuri, Prashanthi ;
Wiste, Heather J. ;
Weigand, Stephen D. ;
Lesnick, Timothy G. ;
Pankratz, Vernon S. ;
Donohue, Michael C. ;
Trojanowski, John Q. .
LANCET NEUROLOGY, 2013, 12 (02) :207-216
[10]   Defining the clinical course of multiple sclerosis The 2013 revisions [J].
Lublin, Fred D. ;
Reingold, Stephen C. ;
Cohen, Jeffrey A. ;
Cutter, Gary R. ;
Sorensen, Per Soelberg ;
Thompson, Alan J. ;
Wolinsky, Jerry S. ;
Balcer, Laura J. ;
Banwell, Brenda ;
Barkhof, Frederik ;
Bebo, Bruce, Jr. ;
Calabresi, Peter A. ;
Clanet, Michel ;
Comi, Giancarlo ;
Fox, Robert J. ;
Freedman, Mark S. ;
Goodman, Andrew D. ;
Inglese, Matilde ;
Kappos, Ludwig ;
Kieseier, Bernd C. ;
Lincoln, John A. ;
Lubetzki, Catherine ;
Miller, Aaron E. ;
Montalban, Xavier ;
O'Connor, Paul W. ;
Petkau, John ;
Pozzilli, Carlo ;
Rudick, Richard A. ;
Sormani, Maria Pia ;
Stueve, Olaf ;
Waubant, Emmanuelle ;
Polman, Chris H. .
NEUROLOGY, 2014, 83 (03) :278-286