The Behavioral and Psychological Symptoms of Dementia in Down Syndrome Scale (BPSD-DS II): Optimization and Further Validation1

Author:

Dekker Alain D.12,Ulgiati Aurora M.12,Groen Henk3,Boxelaar Vincent A.4,Sacco Silvia5,Falquero Ségolène5,Carfi Angelo6,di Paola Antonella6,Benejam Bessy7,Valldeneu Silvia89,Fopma Roelie2,Oosterik Marjo10,Hermelink Marloes11,Beugelsdijk Gonny12,Schippers Mieke12,Henstra Hepie13,Scholten-Kuiper Martine14,Willink-Vos Judith15,de Ruiter Lisa16,Willems Liesbeth17,Loonstra-de Jong Anneke18,Coppus Antonia M.W.1920,Tollenaere Marleen2122,Fortea Juan789,Onder Graziano23,Rebillat Anne-Sophie5,Van Dam Debby121,De Deyn Peter P.12122

Affiliation:

1. Department of Neurology and Alzheimer Center, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands

2. Department of Practice-oriented Scientific Research (PWO), Alliade Care Group, Heerenveen, The Netherlands

3. Department of Epidemiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands

4. Center for Information Technology, University of Groningen, Groningen, The Netherlands

5. Institut Jérôme Lejeune, Paris, France

6. Department of Geriatrics, Fondazione Policlinico Universitario Gemelli IRCCS, Rome, Italy

7. Barcelona Down Medical Center, Fundació Catalana Síndrome de Down, Barcelona, Spain

8. Memory Unit and Biomedical Research Institute Sant Pau (IIB Sant Pau), Department of Neurology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

9. Centro de Investigación Biomédica en Red en Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain

10. Aveleijn, Borne, The Netherlands

11. De Twentse Zorgcentra, Enschede, The Netherlands

12. Ipse de Bruggen, Nieuwveen/Nootdorp, The Netherlands

13. Nieuw Woelwijck, Sappemeer, The Netherlands

14. Philadelphia Zorg, Amersfoort, The Netherlands

15. Severinus, Veldhoven, The Netherlands

16. Sherpa, Baarn, The Netherlands

17. Sprank, Zwolle, The Netherlands

18. Vanboeijen, Assen, The Netherlands

19. Department of Primary and Community Care, Radboud University Medical Center, Nijmegen, The Netherlands

20. Dichterbij, Gennep, The Netherlands

21. Laboratory of Neurochemistry and Behavior, Department of Biomedical Sciences and Institute Born-Bunge, University of Antwerp, Antwerp, Belgium

22. Department of Neurology and Memory Clinic, Hospital Network Antwerp (ZNA) Middelheim and Hoge Beuken, Antwerp, Belgium

23. Department of Cardiovascular, Endocrine-metabolic Diseases and Aging, Istituto Superiore di Sanitá, Rome, Italy

Abstract

Background: People with Down syndrome (DS) are at high risk to develop Alzheimer’s disease dementia (AD). Behavioral and psychological symptoms of dementia (BPSD) are common and may also serve as early signals for dementia. However, comprehensive evaluation scales for BPSD, adapted to DS, are lacking. Therefore, we previously developed the BPSD-DS scale to identify behavioral changes between the last six months and pre-existing life-long characteristic behavior. Objective: To optimize and further study the scale (discriminative ability and reliability) in a large representative DS study population. Methods: Optimization was based on item irrelevance and clinical experiences obtained in the initial study. Using the shortened and refined BPSD-DS II, informant interviews were conducted to evaluate 524 individuals with DS grouped according to dementia status: no dementia (DS, N = 292), questionable dementia (DS + Q, N = 119), and clinically diagnosed dementia (DS + AD, N = 113). Results: Comparing item change scores between groups revealed prominent changes in frequency and severity for anxious, sleep-related, irritable, restless/stereotypic, apathetic, depressive, and eating/drinking behavior. For most items, the proportion of individuals displaying an increased frequency was highest in DS + AD, intermediate in DS + Q, and lowest in DS. For various items within sections about anxious, sleep-related, irritable, apathetic, and depressive behaviors, the proportion of individuals showing an increased frequency was already substantial in DS + Q, suggesting that these changes may serve as early signals of AD in DS. Reliability data were promising. Conclusion: The optimized scale yields largely similar results as obtained with the initial version. Systematically evaluating BPSD in DS may increase understanding of changes among caregivers and (timely) adaptation of care/treatment.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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