Performance of plasma biomarkers for diagnosis and prediction of dementia in a Brazilian cohort

Abstract Background Dementia is a growing concern throughout the developing world and is severely underdiagnosed among the Brazilian population. Despite remarkable progress in the biomarker field in recent years, local testing and validation of plasma biomarkers of AD and dementia is still lacking in Brazil and Latin America. Method In this longitudinal cohort study of 145 participants, the diagnostic performance of plasma biomarkers was assessed based on clinical diagnosis and CSF biomarker positivity. Follow‐up data of up to 4.7 years were used to determine biomarker performance in predicting diagnostic conversions. The study was conducted at the Memory Clinic at the D’Or Institute for Research and Education (IDOR) in Rio de Janeiro. Participants were volunteers referred to the service. All were native Brazilians, had Portuguese as their first language and 60+ years of age. They were diagnosed (DSM‐5 criteria) and underwent extensive psychiatric and laboratory assessments. Diagnoses outside the scope of the study were excluded. CSF biomarker data was available for 34% of the sample. Participants were categorized as cognitively normal controls (n = 49), amnestic mild cognitive impairment (aMCI; n = 29), Alzheimer’s disease (AD; n = 37), Lewy body dementia (n = 23), or vascular dementia (n = 7). Plasma samples collected at initial and follow‐up visits were tested for relevant biomarkers. Result Plasma Tau, Aβ 40 , Aβ 42 , NfL, GFAP, pTau231 and pTau181 were measured on the SIMOA HD‐X platform. Results were evaluated against clinical diagnosis and CSF biomarker status. Plasma NfL and GFAP could discriminate between all‐cause dementia and controls with ROC AUCs of 0.79 (95% CI: [0.70–0.87]) and 0.74 [0.65–0.83], respectively. Plasma pTau181 had good diagnostic performance discriminating clinical AD (AUC = 0.89 [0.82–0.96]), CSF‐biomarker+ aMCI/AD (AUC = 0.90 [0.82–0.98]), or CSF‐biomarker‐confirmed AD (AUC = 0.95 [0.89–1.00]) from controls. Conclusion In this first description of the plasma biomarker profile of a Brazilian dementia cohort, plasma pTau181 confirmed its potential as a clinically useful diagnostic tool. This study comprises an initial step towards local validation and adoption of dementia biomarkers in Brazil and Latin America.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.095754
Primary Topic
Artificial Intelligence in Healthcare
Type
article
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article

Performance of plasma biomarkers for diagnosis and prediction of dementia in a Brazilian cohort

Fernanda G. Q. Barros‐Aragão, TC Pinheiro, Fernanda G. De Felice, Bart Vanderborght et al.
Alzheimer s & Dementia
Artificial Intelligence in Healthcare
article

Performance of plasma biomarkers for diagnosis and prediction of dementia in a Brazilian cohort

Fernanda G. Q. Barros‐Aragão, TC Pinheiro, Fernanda G. De Felice, Bart Vanderborght, Luís E. Santos, Felipe Kenji Sudo, Cláudia Drummond, Ananssa Silva, Fernanda Tovar‐Moll, Sérgio T. Ferreira, Paulo Mattos, Carlos Otávio Brandão
article en

Abstract

Abstract Background Dementia is a growing concern throughout the developing world and is severely underdiagnosed among the Brazilian population. Despite remarkable progress in the biomarker field in recent years, local testing and validation of plasma biomarkers of AD and dementia is still lacking in Brazil and Latin America. Method In this longitudinal cohort study of 145 participants, the diagnostic performance of plasma biomarkers was assessed based on clinical diagnosis and CSF biomarker positivity. Follow‐up data of up to 4.7 years were used to determine biomarker performance in predicting diagnostic conversions. The study was conducted at the Memory Clinic at the D’Or Institute for Research and Education (IDOR) in Rio de Janeiro. Participants were volunteers referred to the service. All were native Brazilians, had Portuguese as their first language and 60+ years of age. They were diagnosed (DSM‐5 criteria) and underwent extensive psychiatric and laboratory assessments. Diagnoses outside the scope of the study were excluded. CSF biomarker data was available for 34% of the sample. Participants were categorized as cognitively normal controls (n = 49), amnestic mild cognitive impairment (aMCI; n = 29), Alzheimer’s disease (AD; n = 37), Lewy body dementia (n = 23), or vascular dementia (n = 7). Plasma samples collected at initial and follow‐up visits were tested for relevant biomarkers. Result Plasma Tau, Aβ 40 , Aβ 42 , NfL, GFAP, pTau231 and pTau181 were measured on the SIMOA HD‐X platform. Results were evaluated against clinical diagnosis and CSF biomarker status. Plasma NfL and GFAP could discriminate between all‐cause dementia and controls with ROC AUCs of 0.79 (95% CI: [0.70–0.87]) and 0.74 [0.65–0.83], respectively. Plasma pTau181 had good diagnostic performance discriminating clinical AD (AUC = 0.89 [0.82–0.96]), CSF‐biomarker+ aMCI/AD (AUC = 0.90 [0.82–0.98]), or CSF‐biomarker‐confirmed AD (AUC = 0.95 [0.89–1.00]) from controls. Conclusion In this first description of the plasma biomarker profile of a Brazilian dementia cohort, plasma pTau181 confirmed its potential as a clinically useful diagnostic tool. This study comprises an initial step towards local validation and adoption of dementia biomarkers in Brazil and Latin America.

Alzheimer s & DementiaVol. 20(S8)
Universidade Federal do Rio de Janeiro (BR), Queen's University (CA), D’Or Institute for Research and Education (BR)
Openalex Percentile: Top 65%
Artificial Intelligence in Healthcare
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