Direct brain infusion of glial cell line-derived neurotrophic factor in Parkinson disease

被引:975
作者
Gill, SS [1 ]
Patel, NK
Hotton, GR
O'Sullivan, K
McCarter, R
Bunnage, M
Brooks, DJ
Svendsen, CN
Heywood, P
机构
[1] Frenchay Hosp, Inst Neurosci, Bristol BS16 1LE, Avon, England
[2] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Fac Med, MRC,Clin Sci Ctr, London, England
[3] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Fac Med, Div Neurosci, London, England
[4] Univ Wisconsin, Waisman Ctr, Stem Cell Res Program, Madison, WI 53705 USA
[5] Univ Wisconsin, Dept Neurol, Madison, WI 53706 USA
[6] Univ Wisconsin, Dept Anat, Madison, WI 53706 USA
关键词
D O I
10.1038/nm850
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glial cell line-derived neurotrophic factor (GDNF) is a potent neurotrophic factor with restorative effects in a wide variety of rodent and primate models of Parkinson disease, but penetration into brain tissue from either the blood or the cerebro-spinal fluid is limited. Here we delivered GDNF directly into the putamen of five Parkinson patients in a phase 1 safety trial. One catheter needed to be repositioned and there were changes in the magnetic resonance images that disappeared after lowering the concentration of GDNF. After one year, there were no serious clinical side effects, a 39% improvement in the off-medication motor sub-score of the Unified Parkinson's Disease Rating Scale (UPDRS) and a 61% improvement in the activities of daily living sub-score. Medication-induced dyskinesias were reduced by 64% and were not observed off medication during chronic GDNF delivery. Positron emission tomography (PET) scans of [F-18] dopamine uptake showed a significant 28% increase in putamen dopamine storage after 18 months, suggesting a direct effect of GDNF on dopamine function. This study warrants careful examination of GDNF as a treatment for Parkinson disease.
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收藏
页码:589 / 595
页数:7
相关论文
共 39 条
  • [31] THE DEVELOPMENT AND VALIDATION OF A SHORT MEASURE OF FUNCTIONING AND WELL-BEING FOR INDIVIDUALS WITH PARKINSONS-DISEASE
    PETO, V
    JENKINSON, C
    FITZPATRICK, R
    GREENHALL, R
    [J]. QUALITY OF LIFE RESEARCH, 1995, 4 (03) : 241 - 248
  • [32] OLFACTORY THRESHOLD IN PARKINSONS-DISEASE
    QUINN, NP
    ROSSOR, MN
    MARSDEN, CD
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1987, 50 (01) : 88 - 89
  • [33] Frontal, midbrain and striatal dopaminergic function in early and advanced Parkinson's disease -: A 3D [18F]dopa-PET study
    Rakshi, JS
    Uema, T
    Ito, K
    Bailey, DL
    Morrish, PK
    Ashburner, J
    Dagher, A
    Jenkins, IH
    Friston, KJ
    Brooks, DJ
    [J]. BRAIN, 1999, 122 : 1637 - 1650
  • [34] Treatment interventions for Parkinson's disease: an evidence based assessment
    Rascol, O
    Goetz, C
    Koller, W
    Poewe, W
    Sampaio, C
    [J]. LANCET, 2002, 359 (9317) : 1589 - 1598
  • [35] Nerve growth factor signaling, neuroprotection, and neural repair
    Sofroniew, MV
    Howe, CL
    Mobley, WC
    [J]. ANNUAL REVIEW OF NEUROSCIENCE, 2001, 24 : 1217 - 1281
  • [36] PROTECTION AND REPAIR OF THE NIGROSTRIATAL DOPAMINERGIC SYSTEM BY GDNF IN-VIVO
    TOMAC, A
    LINDQVIST, E
    LIN, LFH
    OGREN, SO
    YOUNG, D
    HOFFER, BJ
    OLSON, L
    [J]. NATURE, 1995, 373 (6512) : 335 - 339
  • [37] Short- and long-term survival and function of unilateral intrastriatal dopaminergic grafts in Parkinson's disease
    Wenning, GK
    Odin, P
    Morrish, P
    Rehncrona, S
    Widner, H
    Brundin, P
    Rothwell, JC
    Brown, R
    Gustavii, B
    Hagell, P
    Jahanshahi, M
    Sawle, G
    Bjorklund, A
    Brooks, DJ
    Marsden, CD
    Quinn, NP
    Lindvall, O
    [J]. ANNALS OF NEUROLOGY, 1997, 42 (01) : 95 - 107
  • [38] Whone AL, 2002, NEUROLOGY, V58, pA82
  • [39] Sustained delivery of GDNF: towards a treatment for Parkinson's disease
    Zurn, AD
    Widmer, HR
    Aebischer, P
    [J]. BRAIN RESEARCH REVIEWS, 2001, 36 (2-3) : 222 - 229