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Predictors of survival in a series of clinically diagnosed progressive supranuclear palsy patients
被引:67
|作者:
dell'Aquila, Claudia
[1
]
Zoccolella, Stefano
[1
]
Cardinali, Valentina
[1
]
de Mari, Michele
[1
]
Iliceto, Giovanni
[1
]
Tartaglione, Bruno
[1
]
Lamberti, Paolo
[1
]
Logroscino, Giancarlo
[1
]
机构:
[1] Univ Bari, Dept Basic Med Sci Neurosci & Organs Senses, I-70124 Bari, Italy
关键词:
Progressive supranuclear gaze palsy;
Steele-Richardson-Olszewski syndrome;
Parkinsonism;
Natural history;
Survival;
NATURAL-HISTORY;
FEATURES;
CRITERIA;
DISORDERS;
ACCURACY;
DISEASE;
GAIT;
D O I:
10.1016/j.parkreldis.2013.06.014
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Background: Investigations into prognostic factors in progressive supranuclear palsy have shown conflicting results. We performed a retrospective study in order to identify clinical predictors of survival in clinically diagnosed progressive supranuclear palsy patients referred to our centre. Methods: Data on medical history, survival and five clinical disability milestones (inability to walk unassisted, unintelligible speech, severe dysphagia, dementia and institutionalization) were collected from outpatients' medical records and by a telephone interview to caregivers. Patients were subdivided into Richardson's syndrome and PSP-Parkinsonism according to symptoms during the first 2 years of disease. Survival was analyzed by the Kaplan Meier method and Cox regression analysis. Results: Forty-three consecutive patients were enrolled (86% Richardson's syndrome). Motor disturbances were the most frequent symptoms of onset. During the follow-up, 60.5% of patients died after a median survival of 7.1 years (2.2-18). Older age at onset (> 63) (HR 2.8; 95% Cl: 1.3-5.7; p = 0.007), early dysphagia (HR 2.3;.95% Cl: 1-5.3; p = 0.05) and early cognitive deficits (HR 3.6; 95% Cl: 1.6-8.2; p = 0.002) were predictors of shorter survival. Compared to PSP-Parkinsonism patients, Richardson's syndrome patients had shorter survival and higher mortality risk although not statistically significant (HR 3 95% Cl: 0.9-9.9; p = 0.07). Seventy-seven percent of patients developed severe disability during follow-up: shorter time to the first clinical disability milestone predicted shorter survival (HR 7.8; 95% Cl: 2.3-26; p = 0.0008). Conclusions: early dysphagia, cognitive impairment, older age at onset, and time to disability were predictors of shorter survival; Richardson's syndrome had a less favorable course than PSP-Parkinsonism. Clinical milestones should be considered as possible endpoints in future clinical trials. (C) 2013 Elsevier Ltd. All rights reserved.
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页码:980 / 985
页数:6
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