The Association of Alzheimer’s Disease-Related Blood-Based Biomarkers with Cognitive Screening Test Performance in the Congolese Population in Kinshasa

Author:

Schwinne Megan12,Alonso Alvaro2,Roberts Blaine R.3,Hickle Sabrina4,Verberk Inge M.W.5,Epenge Emmanuel67,Gikelekele Guy8,Tsengele Nathan89,Kavugho Immaculee10,Mampunza Samuel8,Yarasheski Kevin E.11,Teunissen Charlotte E.5,Stringer Anthony4,Levey Allan12,Ikanga Jean47

Affiliation:

1. Department of Biomedical Informatics, Emory University School of Medicine, Atlanta, GA, USA

2. Department of Epidemiology, Emory University Rollins School of Public Health, Atlanta, GA, USA

3. Department of Biochemistry, Department of Neurology, School of Medicine, Emory University, Atlanta, GA, USA

4. Department of Rehabilitation Medicine, Emory University School of Medicine, Atlanta, GA, USA

5. Department of Clinical Chemistry, Amsterdam Neuroscience, Neurodegeneration, Neurochemistry Laboratory, Amsterdam University Medical Centers, Vrije Universiteit, Amsterdam, The Netherlands

6. Department of Psychiatry, School of Medicine, University of Kinshasa and Catholic University of Congo, Kinshasa, Kinshasa I, Democratic Republic of Congo

7. Protestant University of Congo, Kinshasa, Kinshasa II, Democratic Republic of Congo

8. Department of Psychiatry, University of Kinshasa, Kinshasa, Kinshasa I, Democratic Republic of Congo

9. Faculty of Medicine, University of Kikwit, Democratic Republic of Congo

10. Memory Clinic of Kinshasa, Kinshasa, Kinshasa I, Democratic Republic of Congo

11. C N Diagnostics, Saint Louis, MO, USA

12. Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA

Abstract

Background: Alzheimer’s disease (AD), the most common cause of dementia, poses a significant global burden. Diagnosis typically involves invasive and costly methods like neuroimaging or cerebrospinal fluid (CSF) biomarker testing of phosphorylated tau (p-tau) and amyloid-β42/40 (Aβ42/40). Such procedures are especially impractical in resource-constrained regions, such as the Democratic Republic of Congo (DRC). Blood-based biomarker testing may provide a more accessible screening opportunity. Objective: This study aims to examine if AD-related blood-based biomarkers are associated with cognitive test performance in the Congolese population, where limited research has been conducted. Methods: In this cross-sectional study of 81 Congolese individuals, cognitive assessments (Alzheimer’s Questionnaire (AQ) and Community Screening Interview for Dementia (CSID)) distinguished dementia cases from controls. Blood draws were taken to assess p-tau 181 and Aβ42/40 biomarkers. Relationships between the biomarkers and cognitive performance were analyzed using multiple linear regression models. Results: Lower plasma Aβ42/40 was significantly associated with lower CSID scores and higher AQ scores, indicative of AD (p < 0.001). These relationships were observed in healthy controls (CSID p = 0.01, AQ p = 0.03), but not in dementia cases. However, p-tau 181 did not exhibit significant associations with either measure. Factors such as age, sex, education, presence of APOE ɛ4 allele, did not alter these relationships. Conclusions: Understanding relationships between AD-related screening tests and blood biomarkers is a step towards utilization of blood-based biomarker tests as a screening tool for AD, especially in resource-limited regions. Further research should be conducted to evaluate blood biomarker test efficacy in larger samples and other populations.

Publisher

IOS Press

Subject

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

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