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. 2025 Dec 25;21(Suppl 4):e107372. doi: 10.1002/alz70858_107372

Baseline Results Investigate APOE‐Memory Connection in Latin‐American Population at Risk for Dementia ‐ LatAm‐FINGERS Initial Insights

Clarisse Vasconcelos Friedlaender 1,, Leonardo Cruz de Souza 2, Maira Tonidandel Barbosa 1, Karina Braga Gomes 2, Jessica Abdo Goncalves Tosatti 3, João Victor de Faria Rocha 1, Davi Melillo Cardoso 4, Marcelo Machado Prates 4, Andre Luis Lopes 5, Vitoria Silva Vieira 4, Vinicius Ribeiro Jeunon 6, Letícia Maria Ferreira de Souza 7, Lais Soares Figueiredo 3, Andreia de Andrades 1, Dias Teixeira 4, Ana Luisa Sosa 8, Ricardo Nitrini 9, Ricardo Allegri 10, Gustavo Sevlever 11, David Fernando Aguillón Niño 12, Daisy M Acosta 13, Luc¡a Crivelli 10, Ana Charamelo 14, Ivonne Z Jimenez‐Velazquez 15, Nilton Custodio 16, Lissette Duque 17, Jorge M Leon‐Salas 18,19, Carolina Delgado 20, María Isabel Cusicanqui 21, Belen Custodio 16, Rosa Maria Salinas‐Contreras 22, Gustavo Henrique Cançado 23, Ana Vigil‐Martinez 24, Maria Da Graça Morais Martin 25, Andrés Damian 26, Ezequiel Ignacio Surace 27, Natalia Acosta‐Baena 28, Ismael Luis Calandri 27, Monica Sanches Yassuda 29, Claudia Kimie Suemoto 30, Maria Eugenia Martin 31, Sonia Maria Dozzi Brucki 32, Heather M Snyder 33, Maria C Carrillo 33, Miia Kivipelto 34, Paulo Caramelli 3
PMCID: PMC12739714

Abstract

Background

Latin America (LA) faces heightened vulnerability to modifiable dementia risk factors. Early identification of at‐risk individuals is crucial for implementing effective preventive strategies. The Free and Cued Selective Reminding Test with Immediate Recall (FCSRT‐IR) is promising in early detection of mnemonic impairment, with high sensitivity and specificity for Alzheimer's Disease (AD) risk. While sociodemographic and genetic factors, including APOE ε4 genotype, are associated with elevated dementia risk, their influence on cognitive performance in LA populations remains unclear. We aim to investigate sociodemographic factors and APOE ε4 genotype influence on mnemonic performance in high‐risk LA individuals.

Method

Cross‐sectional analysis of LatAm‐FINGERS baseline data, a randomized, multicenter trial evaluating non‐pharmacological interventions for cognitive decline prevention in LA. Inclusion criteria: age 60‐77 years; CAIDE ≥ 6; ‐1.5 ≤ z score ≤ 0 on MMSE or CERAD word list. Exclusion criteria: MMSE < 20; dementia; illiteracy. Participants from Argentina, Brazil, Chile, and Uruguay were included. Memory assessment used FCSRT‐IR and SOMI (Stages of Objective Memory Impairment) classification. APOE genotyping was performed on blood samples using PCR‐RFLP analysis. Jamovi software (v2.3) analyzed correlations and associations (p < 0.05).

Result

Sample (N = 358 participants): age 67.75 ± 4.86 years; education 13.41 ± 3.14 years; 72.3% female; 61.2% white; 22.3% APOE ε4 carriers. FCSRT‐IR scores correlated significantly with sociodemographics (p < .001) and varied among countries (p < .001). SOMI distribution: 58% SOMI‐0 (preserved memory), 27.6% SOMI‐1/2 (mild impairment). Argentina showed 36% in SOMI‐3/4 (severe impairment); Uruguay 75% in SOMI‐0. No significant sociodemographic differences were found between APOE ε4 carriers/non‐carriers. Non‐carriers performed better on FCSRT‐IR, significant only for identification score (p = .017). No significant APOE ε4‐SOMI association.

Conclusion

Sociodemographic profile significantly influences memory performance, while APOE ε4 genotype shows limited association. This suggests environmental and social factors may play a more central role in cognitive performance than genetic predisposition in LA populations.


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