The CamPaIGN study of Parkinson's disease: 10-year outlook in an incident population-based cohort

被引:451
作者
Williams-Gray, Caroline H. [1 ]
Mason, Sarah L. [1 ]
Evans, Jonathan R. [1 ]
Foltynie, Thomas [2 ]
Brayne, Carol [3 ]
Robbins, Trevor W. [4 ,5 ]
Barker, Roger A. [1 ]
机构
[1] Univ Cambridge, John Van Geest Ctr Brain Repair, Dept Clin Neurosci, Cambridge CB2 0PY, England
[2] UCL, Inst Neurol, Sobell Dept Motor Neurosci, London, England
[3] Univ Cambridge, Dept Publ Hlth & Primary Care, Cambridge, England
[4] Univ Cambridge, Dept Psychol, Cambridge, England
[5] Univ Cambridge, Behav & Clin Neurosci Inst, Cambridge, England
基金
美国国家卫生研究院; 英国医学研究理事会; 英国惠康基金;
关键词
SYDNEY MULTICENTER; COGNITIVE DECLINE; NATURAL-HISTORY; MOTOR SUBTYPE; DEMENTIA; MORTALITY; RISK; SURVIVAL; PROGRESSION; SUSCEPTIBILITY;
D O I
10.1136/jnnp-2013-305277
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Prognosis in Parkinson's disease (PD) remains poorly understood due to a lack of unbiased data on the natural history of treated PD. The CamPaIGN study has been the first to prospectively track disease evolution from diagnosis in an unselected population-representative incident cohort. We now report the 10-year follow-up data, focusing on three key irreversible milestones: postural instability (Hoehn and Yahr 3), dementia and death. Methods The cohort was collected between December 2000 and 2002. Those meeting diagnostic criteria (n=142) were followed-up until 1 January 2012. Clinical, neuropsychological and genetic testing were performed. Progression to key milestones was evaluated using Kaplan-Meier and Cox regression survival analyses. Results At 10 years, 55% had died, 68% had postural instability and 46% dementia. 23% had a good outcome at 10 years (surviving free of dementia/postural instability). Death rate was comparable with the UK population (standardised mortality ratio 1.29 (0.97-1.61)). Death certificates indicated PD was a substantial contributor in only 20%, with pneumonia being the commonest cause of death. Age, non-tremor-dominant motor phenotype and comorbidity predicted earlier postural instability. Baseline predictors of dementia were age, motor impairment, 'posterior-cortical' cognitive deficits and MAPT genotype. Conclusions (1) outlook in PD is heterogeneous, with most dying or developing dementia or postural instability by 10 years from diagnosis, but a quarter still doing well, with preserved mobility and intact cognition; (2) death is not directly related to PD in the majority; (3) baseline clinical and genetic variables are predictive of outcome and may be helpful in selecting patients for clinical trials.
引用
收藏
页码:1258 / 1264
页数:7
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