Effect of donepezil for dementia prevention in Parkinson's disease with severe hyposmia (The DASH-PD study): A randomized long-term placebo-controlled trial

被引:10
作者
Baba, Toru [1 ,3 ]
Takeda, Atsushi [1 ,2 ,6 ]
Murakami, Aya [4 ]
Koga, Tadashi [4 ]
Isomura, Tatsuya
Mori, Etsuro [3 ,5 ]
机构
[1] Natl Hosp Org Sendai Nishitaga Hosp, Dept Neurol, Sendai, Miyagi, Japan
[2] Tohoku Univ Grad Sch Med, Dept Cognit Motor Aging, Sendai, Miyagi, Japan
[3] Tohoku Univ Grad Sch Med, Dept Behav Neurol & Cognit Neuroscience, Sendai, Miyagi, Japan
[4] Clin Study Support Inc, Nagoya, Aichi, Japan
[5] Osaka Univ, United Grad Sch Child Dev, EDepartment Behav Neurol & Neuropsychiatry, Suita, Osaka, Japan
[6] Natl Hosp Org Sendai Nishitaga Hosp, Dept Neurol, 2-11-11,Kagitorihoncho,Taihaku Ku, Sendai, Miyagi 9828555, Japan
关键词
Parkinson's disease; Hyposmia; Cholinesterase inhibitor; Dementia; Prevention; PREDICTS COGNITIVE DECLINE; OLFACTORY DYSFUNCTION; IMPAIRMENT; BIOMARKERS;
D O I
10.1016/j.eclinm.2022.101571
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Dementia greatly contributes to poor prognosis in patients with Parkinson's disease (PD). We previously reported that severe olfactory dysfunction may be a good predictor of Parkinson's disease dementia (PDD). In this trial, we investigated whether early administration of donepezil to patients with severe hyposmia can reduce the development of PDD. Methods This was a multi-centre, randomized, double-blind, parallel group, placebo-controlled trial in patients with non-demented PD with severe hyposmia (The Donepezil Application for Severe Hyposmic Parkinson's Disease [DASH-PD] study). A total of 201 patients were randomly allocated to receive donepezil or placebo in addition to standard therapy for PD. Patients were followed up every 6 months until the onset of PDD or for a maximum of 4 years. The primary endpoint was the onset of dementia. The secondary endpoint was cognitive impairment measured by Addenbrooke's Cognitive Examination-Revised (ACE-R) and the Clinical Dementia Rating (CDR). (UMIN000009958: February 2013 to May 2019). Findings A total of 201 hyposmic patients with PD were randomly assigned to a treatment: 103 to donepezil and 98 to placebo. Overall, 141 (70%) patients completed the 4-year intervention. During follow-up, 7 of 103 (6.8%) patients in the donepezil group and 12 of 98 (12.2%) patients in the placebo group developed PDD; however, the hazard ratio of PDD incidence was not statistically significant (hazard ratio (HR), 0.609; 95% confidence interval, 0.240 to 1.547; p = 0.2969). At week 208, the patients in the donepezil group had better scores on the ACE-R (p < 0.005) and the CDR (p < 0.005) than those taking placebo. Interpretation Administration of donepezil to PD patients with severe olfactory dysfunction for 4 years did not change the incidence of dementia but had a beneficial effect on neuropsychological function, with good tolerability. Copyright (C) 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
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页数:12
相关论文
共 34 条
[21]   The Addenbrooke's Cognitive Examination Revised (ACE-R): a brief cognitive test battery for dementia screening [J].
Mioshi, Eneida ;
Dawson, Kate ;
Mitchell, Joanna ;
Arnold, Robert ;
Hodges, John R. .
INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY, 2006, 21 (11) :1078-1085
[22]   THE CLINICAL DEMENTIA RATING (CDR) - CURRENT VERSION AND SCORING RULES [J].
MORRIS, JC .
NEUROLOGY, 1993, 43 (11) :2412-2414
[23]   SEQUENTIAL TREATMENT ASSIGNMENT WITH BALANCING FOR PROGNOSTIC FACTORS IN CONTROLLED CLINICAL TRIAL [J].
POCOCK, SJ ;
SIMON, R .
BIOMETRICS, 1975, 31 (01) :103-115
[24]   In vivo cholinergic basal forebrain atrophy predicts cognitive decline in de novo Parkinson's disease [J].
Ray, Nicola J. ;
Bradburn, Steven ;
Murgatroyd, Christopher ;
Toseeb, Umar ;
Mir, Pablo ;
Kountouriotis, George K. ;
Teipel, Stefan J. ;
Grothe, Michel J. .
BRAIN, 2018, 141 :165-176
[25]   Dementia in Parkinson's disease: a 20-year neuropsychological study (Sydney Multicentre Study) [J].
Reid, W. G. J. ;
Hely, M. A. ;
Morris, J. G. L. ;
Loy, C. ;
Halliday, G. M. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2011, 82 (09) :1033-1037
[26]   Development of a smell identification test using a novel stick-type odor presentation kit [J].
Saito, S ;
Ayabe-Kanamura, S ;
Takashima, Y ;
Gotow, N ;
Naito, N ;
Nozawa, T ;
Mise, M ;
Deguchi, Y ;
Kobayakawa, T .
CHEMICAL SENSES, 2006, 31 (04) :379-391
[27]   Clinical variables and biomarkers in prediction of cognitive CrossMark impairment in patients with newly diagnosed Parkinson's disease: a cohort study [J].
Schrag, Anette ;
Siddiqui, Uzma Faisal ;
Anastasiou, Zacharias ;
Weintraub, Daniel ;
Schott, Jonathan M. .
LANCET NEUROLOGY, 2017, 16 (01) :66-75
[28]   Nucleus basalis of Meynert degeneration precedes and predicts cognitive impairment in Parkinson's disease [J].
Schulz, Jonathan ;
Pagano, Gennaro ;
Bonfante, Juan Alberto Fernandez ;
Wilson, Heather ;
Politis, Marios .
BRAIN, 2018, 141 :1501-1516
[29]   Update on treatments for nonmotor symptoms of Parkinson's disease-an evidence-based medicine review [J].
Seppi, Klaus ;
Chaudhuri, K. Ray ;
Coelho, Miguel ;
Fox, Susan H. ;
Katzenschlager, Regina ;
Lloret, Santiago Perez ;
Weintraub, Daniel ;
Sampaio, Cristina ;
Chahine, Lana ;
Hametner, Eva-Maria ;
Heim, Beatrice ;
Lim, Shen-Yang ;
Poewe, Werner ;
Djamshidian-Tehrani, Atbin .
MOVEMENT DISORDERS, 2019, 34 (02) :180-198
[30]   Mapping of brain acetylcholinesterase alterations in Lewy body disease by PET [J].
Shimada, H. ;
Hirano, S. ;
Shinotoh, H. ;
Aotsuka, A. ;
Sato, K. ;
Tanaka, N. ;
Ota, T. ;
Asahina, M. ;
Fukushi, K. ;
Kuwabara, S. ;
Hattori, T. ;
Suhara, T. ;
Irie, T. .
NEUROLOGY, 2009, 73 (04) :273-278