La maladie de Parkinson au Canada (serveur d'exploration)

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The role of radiotracer imaging in Parkinson disease

Identifieur interne : 000921 ( PascalFrancis/Corpus ); précédent : 000920; suivant : 000922

The role of radiotracer imaging in Parkinson disease

Auteurs : B. Ravina ; D. Eidelberg ; J. E. Ahlskog ; R. L. Albin ; D. J. Brooks ; M. Carbon ; V. Dhawan ; A. Feigin ; S. Fahn ; M. Guttman ; K. Gwinn-Hardy ; H. Mcfarland ; R. Innis ; R. G. Katz ; K. Kieburtz ; S. J. Kish ; N. Lange ; J. W. Langston ; K. Marek ; L. Morin ; C. Moy ; D. Murphy ; W. H. Oertel ; G. Oliver ; Y. Palesch ; W. Powers ; J. Seibyl ; K. D. Sethi ; C. W. Shults ; P. Sheehy ; A. J. Stoessl ; R. Holloway

Source :

RBID : Pascal:05-0185260

Descripteurs français

English descriptors

Abstract

Radiotracer imaging (RTI) of the nigrostriatal dopaminergic system is a widely used but controversial biomarker in Parkinson disease (PD). Here the authors review the concepts of biomarker development and the evidence to support the use of four radiotracers as biomarkers in PD: [18F]fluorodopa PET, (+)-[11C]dihydrotetrabenazine PET, [123I]β-CIT SPECT, and [18F]fluorodeoxyglucose PET. Biomarkers used to study disease biology and facilitate drug discovery and early human trials rely on evidence that they are measuring relevant biologic processes. The four tracers fulfill this criterion, although they do not measure the number or density of dopaminergic neurons. Biomarkers used as diagnostic tests, prognostic tools, or surrogate endpoints must not only have biologic relevance but also a strong linkage to the clinical outcome of interest. No radiotracers fulfill these criteria, and current evidence does not support the use of imaging as a diagnostic tool in clinical practice or as a surrogate endpoint in clinical trials. Mechanistic information added by RTI to clinical trials may be difficult to interpret because of uncertainty about the interaction between the interventions and the tracer.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A11 03  1    @1 AHLSKOG (J. E.)
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A11 10  1    @1 GUTTMAN (M.)
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A11 16  1    @1 KISH (S. J.)
A11 17  1    @1 LANGE (N.)
A11 18  1    @1 LANGSTON (J. W.)
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A11 24  1    @1 OLIVER (G.)
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A11 30  1    @1 SHEEHY (P.)
A11 31  1    @1 STOESSL (A. J.)
A11 32  1    @1 HOLLOWAY (R.)
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A14 18      @1 Department of Neurology, Medical College of Georgia @2 Augusta, GA @3 USA @Z 28 aut.
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C01 01    ENG  @0 Radiotracer imaging (RTI) of the nigrostriatal dopaminergic system is a widely used but controversial biomarker in Parkinson disease (PD). Here the authors review the concepts of biomarker development and the evidence to support the use of four radiotracers as biomarkers in PD: [18F]fluorodopa PET, (+)-[11C]dihydrotetrabenazine PET, [123I]β-CIT SPECT, and [18F]fluorodeoxyglucose PET. Biomarkers used to study disease biology and facilitate drug discovery and early human trials rely on evidence that they are measuring relevant biologic processes. The four tracers fulfill this criterion, although they do not measure the number or density of dopaminergic neurons. Biomarkers used as diagnostic tests, prognostic tools, or surrogate endpoints must not only have biologic relevance but also a strong linkage to the clinical outcome of interest. No radiotracers fulfill these criteria, and current evidence does not support the use of imaging as a diagnostic tool in clinical practice or as a surrogate endpoint in clinical trials. Mechanistic information added by RTI to clinical trials may be difficult to interpret because of uncertainty about the interaction between the interventions and the tracer.
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N44 01      @1 OTO
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Format Inist (serveur)

NO : PASCAL 05-0185260 INIST
ET : The role of radiotracer imaging in Parkinson disease
AU : RAVINA (B.); EIDELBERG (D.); AHLSKOG (J. E.); ALBIN (R. L.); BROOKS (D. J.); CARBON (M.); DHAWAN (V.); FEIGIN (A.); FAHN (S.); GUTTMAN (M.); GWINN-HARDY (K.); MCFARLAND (H.); INNIS (R.); KATZ (R. G.); KIEBURTZ (K.); KISH (S. J.); LANGE (N.); LANGSTON (J. W.); MAREK (K.); MORIN (L.); MOY (C.); MURPHY (D.); OERTEL (W. H.); OLIVER (G.); PALESCH (Y.); POWERS (W.); SEIBYL (J.); SETHI (K. D.); SHULTS (C. W.); SHEEHY (P.); STOESSL (A. J.); HOLLOWAY (R.)
AF : National Institute of Neurological Disorders and Stroke/Bethesda, MD/Etats-Unis (1 aut., 11 aut., 12 aut., 20 aut., 21 aut., 22 aut., 24 aut., 30 aut.); National Institutes of Health/Bethesda, MD/Etats-Unis (2 aut., 6 aut., 7 aut., 8 aut.); Center for Neurosciences, Institute for Medical Research, North Shore-Long Island Jewish Health System/Manhasset, NY/Etats-Unis (2 aut., 6 aut., 7 aut., 8 aut.); Department of Neurology, Mayo Clinic/Rochester, MN/Etats-Unis (3 aut.); Department of Neurology, University of Michigan and Ann Arbor VAMC GRECC/Ann Arbor, MI/Etats-Unis (4 aut.); Faculty of Medicine, Imperial College/London/Royaume-Uni (5 aut.); Department of Neurology, Columbia University/College of Physicians and Surgeons/New York, NY/Etats-Unis (9 aut.); Human Neurochemical Pathology Laboratory, Center for Addiction and Mental Health/Ontario/Canada (10 aut., 16 aut.); National Institute of Mental Health, National Institutes of Health/Bethesda, MD/Etats-Unis (13 aut.); US Food and Drug Administration/Rockville, MD/Etats-Unis (14 aut.); Department of Neurology, University of Rochester/NY/Etats-Unis (15 aut., 32 aut.); Departments of Psychiatry and Biostatistics, Harvard University Schools of Medicine and Public Health/Boston, MA/Etats-Unis (17 aut.); The Parkinson's Institute/Sunnyvale, CA/Etats-Unis (18 aut.); Institute for Neurodegenerative Disorders/New Haven, CT/Etats-Unis (19 aut., 27 aut.); Department of Neurology, Philipps University of Marburg/Marburg/Allemagne (23 aut.); Departments of Biometry and Epidemiology, Medical University of South Carolina/Charleston, SC/Etats-Unis (25 aut.); Department of Neurology, Washington University School of Medicine/St. Louis, MO/Etats-Unis (26 aut.); Department of Neurology, Medical College of Georgia/Augusta, GA/Etats-Unis (28 aut.); Department of Neuroscience, University of California, San Diego/CA/Etats-Unis (29 aut.); Pacific Parkinson's Research Center, University of British Columbia/Vancouver, British Columbia/Canada (31 aut.)
DT : Publication en série; Niveau analytique
SO : Neurology; ISSN 0028-3878; Coden NEURAI; Etats-Unis; Da. 2005; Vol. 64; No. 2; Pp. 208-215; Bibl. 60 ref.
LA : Anglais
EA : Radiotracer imaging (RTI) of the nigrostriatal dopaminergic system is a widely used but controversial biomarker in Parkinson disease (PD). Here the authors review the concepts of biomarker development and the evidence to support the use of four radiotracers as biomarkers in PD: [18F]fluorodopa PET, (+)-[11C]dihydrotetrabenazine PET, [123I]β-CIT SPECT, and [18F]fluorodeoxyglucose PET. Biomarkers used to study disease biology and facilitate drug discovery and early human trials rely on evidence that they are measuring relevant biologic processes. The four tracers fulfill this criterion, although they do not measure the number or density of dopaminergic neurons. Biomarkers used as diagnostic tests, prognostic tools, or surrogate endpoints must not only have biologic relevance but also a strong linkage to the clinical outcome of interest. No radiotracers fulfill these criteria, and current evidence does not support the use of imaging as a diagnostic tool in clinical practice or as a surrogate endpoint in clinical trials. Mechanistic information added by RTI to clinical trials may be difficult to interpret because of uncertainty about the interaction between the interventions and the tracer.
CC : 002B17; 002B17G; 002B24A06
FD : Système nerveux pathologie; Parkinson maladie
FG : Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Système nerveux central pathologie
ED : Nervous system diseases; Parkinson disease
EG : Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease
SD : Sistema nervioso patología; Parkinson enfermedad
LO : INIST-6345.354000125640020070
ID : 05-0185260

Links to Exploration step

Pascal:05-0185260

Le document en format XML

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<s1>Pacific Parkinson's Research Center, University of British Columbia</s1>
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<name sortKey="Holloway, R" sort="Holloway, R" uniqKey="Holloway R" first="R." last="Holloway">R. Holloway</name>
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<title xml:lang="en" level="a">The role of radiotracer imaging in Parkinson disease</title>
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<s1>National Institute of Neurological Disorders and Stroke</s1>
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<name sortKey="Katz, R G" sort="Katz, R G" uniqKey="Katz R" first="R. G." last="Katz">R. G. Katz</name>
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<name sortKey="Oliver, G" sort="Oliver, G" uniqKey="Oliver G" first="G." last="Oliver">G. Oliver</name>
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<name sortKey="Seibyl, J" sort="Seibyl, J" uniqKey="Seibyl J" first="J." last="Seibyl">J. Seibyl</name>
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<AU>RAVINA (B.); EIDELBERG (D.); AHLSKOG (J. E.); ALBIN (R. L.); BROOKS (D. J.); CARBON (M.); DHAWAN (V.); FEIGIN (A.); FAHN (S.); GUTTMAN (M.); GWINN-HARDY (K.); MCFARLAND (H.); INNIS (R.); KATZ (R. G.); KIEBURTZ (K.); KISH (S. J.); LANGE (N.); LANGSTON (J. W.); MAREK (K.); MORIN (L.); MOY (C.); MURPHY (D.); OERTEL (W. H.); OLIVER (G.); PALESCH (Y.); POWERS (W.); SEIBYL (J.); SETHI (K. D.); SHULTS (C. W.); SHEEHY (P.); STOESSL (A. J.); HOLLOWAY (R.)</AU>
<AF>National Institute of Neurological Disorders and Stroke/Bethesda, MD/Etats-Unis (1 aut., 11 aut., 12 aut., 20 aut., 21 aut., 22 aut., 24 aut., 30 aut.); National Institutes of Health/Bethesda, MD/Etats-Unis (2 aut., 6 aut., 7 aut., 8 aut.); Center for Neurosciences, Institute for Medical Research, North Shore-Long Island Jewish Health System/Manhasset, NY/Etats-Unis (2 aut., 6 aut., 7 aut., 8 aut.); Department of Neurology, Mayo Clinic/Rochester, MN/Etats-Unis (3 aut.); Department of Neurology, University of Michigan and Ann Arbor VAMC GRECC/Ann Arbor, MI/Etats-Unis (4 aut.); Faculty of Medicine, Imperial College/London/Royaume-Uni (5 aut.); Department of Neurology, Columbia University/College of Physicians and Surgeons/New York, NY/Etats-Unis (9 aut.); Human Neurochemical Pathology Laboratory, Center for Addiction and Mental Health/Ontario/Canada (10 aut., 16 aut.); National Institute of Mental Health, National Institutes of Health/Bethesda, MD/Etats-Unis (13 aut.); US Food and Drug Administration/Rockville, MD/Etats-Unis (14 aut.); Department of Neurology, University of Rochester/NY/Etats-Unis (15 aut., 32 aut.); Departments of Psychiatry and Biostatistics, Harvard University Schools of Medicine and Public Health/Boston, MA/Etats-Unis (17 aut.); The Parkinson's Institute/Sunnyvale, CA/Etats-Unis (18 aut.); Institute for Neurodegenerative Disorders/New Haven, CT/Etats-Unis (19 aut., 27 aut.); Department of Neurology, Philipps University of Marburg/Marburg/Allemagne (23 aut.); Departments of Biometry and Epidemiology, Medical University of South Carolina/Charleston, SC/Etats-Unis (25 aut.); Department of Neurology, Washington University School of Medicine/St. Louis, MO/Etats-Unis (26 aut.); Department of Neurology, Medical College of Georgia/Augusta, GA/Etats-Unis (28 aut.); Department of Neuroscience, University of California, San Diego/CA/Etats-Unis (29 aut.); Pacific Parkinson's Research Center, University of British Columbia/Vancouver, British Columbia/Canada (31 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
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<EA>Radiotracer imaging (RTI) of the nigrostriatal dopaminergic system is a widely used but controversial biomarker in Parkinson disease (PD). Here the authors review the concepts of biomarker development and the evidence to support the use of four radiotracers as biomarkers in PD: [
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   |texte=   The role of radiotracer imaging in Parkinson disease
}}

Wicri

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