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      Long-term cognitive outcome of Alzheimer’s disease and dementia with Lewy bodies: dual disease is worse

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          Abstract

          Background

          Longitudinal studies of dementia with Lewy bodies (DLB) are rare. Clinically, DLB is usually considered to worsen into Alzheimer’s disease (AD). The aim of our study was to compare the rate of the cognitive decline in DLB, AD, and the association of the two diseases (AD + DLB).

          Methods

          Using the Regional Network for Diagnostic Aid and Management of Patients with Cognitive Impairment database, which includes all the patients seen at all memory clinics (medical consultation and day hospitals) in four French regions, and beta regression, we compared the longitudinal the Mini-Mental State Examination scores of 1159 patients with AD ( n = 1000), DLB ( n = 131) and AD + DLB (association of the two) ( n = 28) during follow-up of at least 4 years.

          Results

          The mean follow-up of the patients was 5.88 years. Using beta regression without propensity scores, the comparison of the decline of patients with AD and patients with DLB did not show a significant difference, but the decline of patients with AD + DLB was worse than that of either patients with DLB ( P = 0.006) or patients with AD ( P < 0.001). Using beta regression weighted by a propensity score, comparison of patients with AD and patients with DLB showed a faster decline for patients with DLB ( P < 0.001). The comparison of the decline of patients with AD + DLB with that of patients with DLB ( P < 0.001) and patients with AD ( P < 0.001) showed that the decline was clearly worse in the patients with dual disease.

          Conclusions

          Whatever the analysis, the rate of decline is faster in patients with AD + DLB dual disease. The identification of such patients is important to enable clinicians to optimise treatment and care and to better inform and help patients and caregivers.

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          Most cited references17

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          A systematic review of prevalence and incidence studies of dementia with Lewy bodies.

          Substantial variation in the prevalence of Dementia with Lewy Bodies (DLB) has been reported with estimates ranging from 0 to 26.3% of all dementia cases, potentially making it the second most common dementia subtype. The aim of this study was to review systematically and critically for the first time previous studies of the clinical prevalence and incidence of DLB in the population. A systematic literature search was performed using PubMed. Selected articles had to describe an original study that provided a prevalence and/or incidence number for the whole population for DLB as defined by pre-set clinical criteria and findings. Six studies reporting the prevalence of DLB and one study reporting the incidence of DLB met the inclusion criteria. Prevalence estimates, depending on case criteria, range from 0 to 5% with regard to the general population, and from 0 to 30.5% of all dementia cases. The only estimate for DLB incidence is 0.1% a year for the general population and 3.2% a year for all new dementia cases. The number of available studies was too small to hypothesise on the potential effect of age, sex and genetic background on the results. Although the literature on the prevalence and incidence of DLB is limited, there is a general consensus that DLB must be considered in the range of neurodegenerative conditions in the elderly. The move towards use of consensus criteria facilitates comparison and is welcome. Their application in a more routine way towards rigorously defined and selected study populations will lead to more comparable and generalisable studies in the future.
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            Incidence of dementia with Lewy bodies and Parkinson disease dementia.

            Epidemiologic data on dementia with Lewy bodies (DLB) and Parkinson disease dementia (PDD) remain limited in the United States and worldwide. These data are essential to guide research and clinical or public health interventions.
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              Are sex and educational level independent predictors of dementia and Alzheimer's disease? Incidence data from the PAQUID project.

              To examine the age specific risk of Alzheimer's disease according to sex, and to explore the role of education in a cohort of elderly community residents aged 65 years and older. A community based cohort of elderly people was studied longitudinally for 5 years for the development of dementia. Dementia diagnoses were made according to the DSM III R criteria and Alzheimer's disease was assessed using the NINCDS-ADRDA criteria. Among the 3675 non-demented subjects initially included in the cohort, 2881 participated in the follow up. Hazard ratios of dementia were estimated using a Cox model with delayed entry in which the time scale is the age of the subjects. During the 5 year follow up, 190 incident cases of dementia, including 140 cases of Alzheimer's disease were identified. The incidence rates of Alzheimer's disease were 0.8/100 person-years in men and 1.4/100 person-years in women. However, the incidence was higher in men than in women before the age of 80 and higher in women than in men after this age. A significant interaction between sex and age was found. The hazard ratio of Alzheimer's disease in women compared with men was estimated to be 0.8 at 75 years and 1.7 at 85 years. The risks of dementia and Alzheimer's disease were associated with a lower educational attainment (hazard ratio=1.8, p<0.001). The increased risk of Alzheimer's disease in women was not changed after adjustment for education. Women have a higher risk of developing dementia after the age of 80 than men. Low educational attainment is associated with a higher risk of Alzheimer's disease. However, the increased risk in women is not explained by a lower educational level.
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                Author and article information

                Contributors
                + 33 3 88128638 , f.blanc@unistra.fr
                rmahmoudi@chu-reims.fr
                t.jonveaux@chu-nancy.fr
                jean-galmiche@orange.fr
                gilles.chopard@gmail.com
                benjamin.cretin@chru-strasbourg.fr
                catherine.demuynck@chru-strasbourg.fr
                catherine.martin-hunyadi@chru-strasbourg.fr
                nathalie.philippi@chru-strasbourg.fr
                francois.sellal@ch-colmar.fr
                jm.michel@ch-colmar.fr
                gtio@chu-besancon.fr
                melanie.stackfleth@chru-strasbourg.fr
                pierre.vandel@univ-fcomte.fr
                eloi.magnin@laposte.net
                jlnovella@chu-reims.fr
                georges.kaltenbach@chru-strasbourg.fr
                a.benetos@chu-nancy.fr
                ea.sauleau@chru-strasbourg.fr
                Journal
                Alzheimers Res Ther
                Alzheimers Res Ther
                Alzheimer's Research & Therapy
                BioMed Central (London )
                1758-9193
                27 June 2017
                27 June 2017
                2017
                : 9
                : 47
                Affiliations
                [1 ]ISNI 0000 0001 2177 138X, GRID grid.412220.7, Memory Resource and Research Centre (CM2R), Geriatrics Day Hospital, Geriatrics Department, , University Hospital of Strasbourg, ; 21 rue David Richard, 67091 Strasbourg Cedex, France
                [2 ]ISNI 0000 0001 2157 9291, GRID grid.11843.3f, , University of Strasbourg and French National Centre for Scientific Research (CNRS), ICube Laboratory and Fédération de Médecine Translationnelle de Strasbourg (FMTS), Team Imagerie Multimodale Intégrative en Santé (IMIS)/Neurocrypto, ; Strasbourg, France
                [3 ]ISNI 0000 0001 2157 9291, GRID grid.11843.3f, , University of Strasbourg, Laboratory of Biostatistics and French National Centre for Scientific Research (CNRS), ICube Laboratory, Team Modèles, Images et Vision (MIV), ; Strasbourg, France
                [4 ]ISNI 0000 0004 0472 3476, GRID grid.139510.f, Geriatrics Department, , Centre Hospitalier Universitaire Reims, Memory Resource and Research Centre (CM2R) Champagne-Ardenne, ; Reims, France
                [5 ]Geriatrics Department, Centre Hospitalier Universitaire Nancy, Université de Lorraine, Memory Resource and Research Centre (CM2R) Lorraine, Nancy, France
                [6 ]ISNI 0000 0004 0638 9213, GRID grid.411158.8, Psychiatry Department, , Centre Hospitalier Universitaire Besançon, Memory Resource and Research Centre (CM2R) Franche Comté, ; Besançon, France
                [7 ]ISNI 0000 0004 0638 9213, GRID grid.411158.8, Neurology Department, , Centre Hospitalier Universitaire Besançon, Memory Resource and Research Centre (CM2R) Franche Comté, ; Besançon, France
                [8 ]Association pour le Développement de la Neuropsychologie Appliquée (ADNA), Besançon, France
                [9 ]ISNI 0000 0001 0664 9183, GRID grid.418044.d, Geriatrics Department and Neurology Department, , Centre Hospitalier Général (CHG) de Colmar, Memory Resource and Research Centre (CM2R) Alsace, ; Colmar, France
                [10 ]Neurology Department, |Centre Hospitalier Général (CHG) de Colmar, Memory Resource and Research Centre (CM2R) Alsace, Colmar, France
                Author information
                http://orcid.org/0000-0002-6714-3247
                Article
                272
                10.1186/s13195-017-0272-8
                5488368
                28655337
                a68cedd4-762b-4595-833f-d978107b5ae6
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 6 January 2017
                : 2 June 2017
                Funding
                Funded by: Agence Régionale de Santé (ARS) Grand Est
                Funded by: ARS de Franche Comté
                Funded by: Projet Hospitalier de Recherche Clinique (PHRC)
                Award ID: 2012-A00992-41
                Categories
                Research
                Custom metadata
                © The Author(s) 2017

                Neurology
                dementia with lewy bodies,alzheimer’s disease,alzheimer’s dementia,lewy body disease,mmse,outcome

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