Prodromal Dementia with Lewy Bodies: Clinical Characterization and Predictors of Progression

被引:54
作者
van de Beek, Marleen [1 ]
van Steenoven, Inger [1 ]
van der Zande, Jessica J. [1 ]
Barkhof, Frederik [2 ,3 ,4 ]
Teunissen, Charlotte E. [5 ,6 ,7 ]
van der Flier, Wiesje M. [1 ]
Lemstra, Afina W. [1 ]
机构
[1] Vrije Univ Amsterdam, Amsterdam Univ, Med Ctr, Alzheimer Ctr Amsterdam,Dept Neurol,Amsterdam Neu, Amsterdam, Netherlands
[2] Univ Amsterdam, Med Ctr, Amsterdam Neurosci, Dept Radiol & Nucl Med, Amsterdam, Netherlands
[3] UCL, Inst Neurol Engn, London, England
[4] UCL, Inst Healthcare Engn, London, England
[5] Vrije Univ Amsterdam, Amsterdam Neurosci, Dept Clin Chem, Neurochem Lab, Amsterdam, Netherlands
[6] Vrije Univ Amsterdam, Amsterdam Neurosci, Dept Clin Chem, Biobank, Amsterdam, Netherlands
[7] Univ Amsterdam, Med Ctr, Vrije Univ Amsterdam, Dept Epidemiol & Biostat, Amsterdam, Netherlands
关键词
Alzheimer's disease; dementia with Lewy bodies (DLB); Mild cognitive impairment (MCI); MILD COGNITIVE IMPAIRMENT; ALZHEIMERS ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; DISEASE; SYNUCLEINOPATHIES; RECOMMENDATIONS; PREVALENCE; SURVIVAL; ATROPHY;
D O I
10.1002/mds.27997
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective The objective of this study was to examine clinical characteristics, cognitive decline, and predictors for time to dementia in prodromal dementia with Lewy bodies with mild cognitive impairment (MCI-LB) compared with prodromal Alzheimer's disease (MCI-AD). Methods We included 73 MCI-LB patients (12% female; 68 +/- 6 years; Mini Mental State Examination, 27 +/- 2) and 124 MCI-AD patients (48% female; 68 +/- 7 years; Mini Mental State Examination, 27 +/- 2) from the Amsterdam Dementia Cohort. Follow-up was available for 61 MCI-LB patients and all MCI-AD patients (3 +/- 2 years). We evaluated dementia with Lewy bodies core features, neuropsychiatric symptoms, caregiver burden (Zarit caregiver burden interview), MRI, apolipoprotein genotype, and cerebrospinal fluid biomarkers (tau/A beta(1-42) ratio). Longitudinal outcome measures included cognitive slopes (memory, attention, executive functions, and language and visuospatial functions) and time to dementia. Results Parkinsonism was the most frequently present core feature in MCI-LB (69%). MCI-LB patients more often had neuropsychiatric symptoms and scored higher on ZARIT when compared with the MCI-AD patients. Linear mixed models showed that at baseline, MCI-LB patients performed worse on nonmemory cognitive domains, whereas memory performance was worse in MCI-AD patients. Over time, MCI-LB patients declined faster on attention, whereas MCI-AD patients declined faster on the Mini Mental State Examination and memory. Cox proportional hazards regressions showed that in the MCI-LB patients, lower attention (hazard ratio [HR] = 1.6; 95% confidence interval [CI], 1.1-2.3) and more posterior cortical atrophy (HR = 3.0; 95% CI, 1.5-5.8) predicted shorter time to dementia. In the MCI-AD patients, worse performance on memory (HR = 1.1; 95% CI, 1.0-1.2) and executive functions (HR = 1.3; 95% CI, 1.0-1.6) were independently associated with time to Alzheimer's dementia. Conclusion MCI-LB patients have distinct neuropsychiatric and cognitive profiles with prominent decline in attention when compared with MCI-AD patients. Our results highlight the importance of early diagnosis because symptoms already have an impact in the prodromal stages. (c) 2020 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
引用
收藏
页码:859 / 867
页数:9
相关论文
共 50 条
[1]   The diagnosis of mild cognitive impairment due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease [J].
Albert, Marilyn S. ;
DeKosky, Steven T. ;
Dickson, Dennis ;
Dubois, Bruno ;
Feldman, Howard H. ;
Fox, Nick C. ;
Gamst, Anthony ;
Holtzman, David M. ;
Jagust, William J. ;
Petersen, Ronald C. ;
Snyder, Peter J. ;
Carrillo, Maria C. ;
Thies, Bill ;
Phelps, Creighton H. .
ALZHEIMERS & DEMENTIA, 2011, 7 (03) :270-279
[2]  
[Anonymous], 1986, De 15-woordentest A en B (een voorlopige handleiding)
[3]   Neuropsychiatric Symptoms in Mild Dementia with Lewy Bodies and Alzheimer's Disease [J].
Bjoerke-Bertheussen, J. ;
Ehrt, U. ;
Rongve, A. ;
Ballard, C. ;
Aarsland, D. .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2012, 34 (01) :1-6
[4]   Quantitative electroencephalogram utility in predicting conversion of mild cognitive impairment to dementia with Lewy bodies [J].
Bonanni, Laura ;
Perfetti, Bernardo ;
Bifolchetti, Stefania ;
Taylor, John-Paul ;
Franciotti, Raffaella ;
Parnetti, Lucilla ;
Thomas, Astrid ;
Onofrj, Marco .
NEUROBIOLOGY OF AGING, 2015, 36 (01) :434-445
[5]   A Longitudinal Study of Neurocognition in Dementia with Lewy Bodies Compared to Alzheimer's Disease [J].
Breitve, Monica H. ;
Chwiszczuk, Luiza J. ;
Bronnick, Kolbjorn ;
Hynninen, Minna J. ;
Auestad, Bjorn H. ;
Aarsland, Dag ;
Rongve, Arvid .
FRONTIERS IN NEUROLOGY, 2018, 9
[6]   Clinical and Cognitive Phenotype of Mild Cognitive Impairment Evolving to Dementia with Lewy Bodies [J].
Cagnin, Annachiara ;
Bussse, Cinzia ;
Gardini, Simona ;
Jelcic, Nela ;
Guzzo, Caterina ;
Gnoato, Francesca ;
Mitolo, Micaela ;
Ermani, Mario ;
Caffarra, Paolo .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS EXTRA, 2015, 5 (03) :442-449
[7]   Prevalence and severity of microbleeds in a memory clinic setting [J].
Cordonnier, C ;
van der Flier, WM ;
Sluimer, JD ;
Leys, D ;
Barkhof, F ;
Scheltens, P .
NEUROLOGY, 2006, 66 (09) :1356-1360
[8]   The neuropsychiatric inventory: Assessing psychopathology in dementia patients [J].
Cummings, JL .
NEUROLOGY, 1997, 48 (05) :S10-S16
[9]   Memory impairment, but not cerebrovascular disease, predicts progression of MCI to dementia [J].
DeCarli, C ;
Mungas, D ;
Harvey, D ;
Reed, B ;
Weiner, M ;
Chui, H ;
Jagust, W .
NEUROLOGY, 2004, 63 (02) :220-227
[10]   Prodromal dementia with Lewy bodies [J].
Donaghy, P. C. ;
O'Brien, J. T. ;
Thomas, A. J. .
PSYCHOLOGICAL MEDICINE, 2015, 45 (02) :259-268