Neuropsychiatric features in a multi‐ethnic population with Alzheimer disease and mild cognitive impairment

Author:

Celis Katrina1,Zaman Andrew1ORCID,Adams Larry Deon1,Gardner Olivia1,Farid Rajabli1,Starks Takiyah D.2,Lacroix Faina C.1,Hamilton‐Nelson Kara1,Mena Pedro1,Tejada Sergio1,Laux Renee3,Song Yeunjoo E.3,Caban‐Holt Allison2,Feliciano‐Astacio Briseida4,Vance Jeffery M.15,Haines Jonathan L.36,Byrd Goldie S.2,Beecham Gary W.15,Pericak‐Vance Margaret A.15,Cuccaro Michael L.15

Affiliation:

1. John P. Hussman Institute for Human Genomics University of Miami Miller School of Medicine Miami Florida USA

2. Maya Angelou Center for Health Equity Wake Forest University Winston‐Salem North Carolina USA

3. Department of Population & Quantitative Health Sciences Case Western Reserve University Cleveland Ohio USA

4. Universidad Central del Caribe Bayamon Puerto Rico USA

5. Dr. John T Macdonald Foundation Department of Human Genetics University of Miami Miller School of Medicine Miami Florida USA

6. Cleveland Institute for Computational Biology Cleveland Ohio USA

Abstract

AbstractBackgroundAlzheimer disease (AD) is more prevalent in African American (AA) and Hispanic White (HIW) compared to Non‐Hispanic White (NHW) individuals. Similarly, neuropsychiatric symptoms (NPS) vary by population in AD. This is likely the result of both sociocultural and genetic ancestral differences. However, the impact of these NPS on AD in different groups is not well understood.MethodsSelf‐declared AA, HIW, and NHW individuals were ascertained as part of ongoing AD genetics studies. Participants who scored higher than 0.5 on the Clinical Dementia Rating (CDR) Scale (CDR) were included. Group similarities and differences on Neuropsychiatric Inventory Questionnaire (NPI‐Q) outcomes (NPI‐Q total score, NPI‐Q items) were evaluated using univariate ANOVAs and post hoc comparisons after controlling for sex and CDR stage.ResultsOur sample consisted of 498 participants (26% AA; 30% HIW; 44% NHW). Overall, NPI‐Q total scores differed significantly between our groups, with HIW having the highest NPI‐Q total scores, and by AD stage as measured by CDR. We found no significant difference in NPI‐Q total score by sex. There were six NPI‐Q items with comparable prevalence in all groups and six items that significantly differed between the groups (Anxiety, Apathy, Depression, Disinhibition, Elation, and Irritability). Further, within the HIW group, differences were found between Puerto Rican and Cuban American Hispanics across several NPI‐Q items. Finally, Six NPI‐Q items were more prevalent in the later stages of AD including Agitation, Appetite, Hallucinations, Irritability, Motor Disturbance, and Nighttime Behavior.ConclusionsWe identified differences in NPS among HIW, AA, and NHW individuals. Most striking was the high burden of NPS in HIW, particularly for mood and anxiety symptoms. We suggest that NPS differences may represent the impact of sociocultural influences on symptom presentation as well as potential genetic factors rooted in ancestral background. Given the complex relationship between AD and NPS it is crucial to discern the presence of NPS to ensure appropriate interventions.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Psychiatry and Mental health,Geriatrics and Gerontology

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