Predicting episodic memory performance using different biomarkers: results from argentinaalzheimer?s Disease Neuroimaging initiative

RUSSO MARÍA JULIETA; COHEN GABRIELA; CHREM MENDEZ PATRICIO; CAMPOS JORGE; NAHAS FEDERICO; SURACE EZEQUIEL; VAZQUEZ SILVIA; GUSTAFSON DEBORAH; GUINJOAN SALVADOR; ALLEGRI RICARDO FRANCISCO; SEVLEVER GUSTAVO

NEUROPSYCHIATRIC DISEASE AND TREATMENT

Dovepress

Año: 2016 vol. 12 p. 2199 - 2206

1178-2021

Purpose: Argentina-Alzheimer?s Disease Neuroimaging Initiative (Arg-ADNI) is the first ADNI study to be performed in Latin America at a medical center with the appropriate infrastructure. Our objective was to describe baseline characteristics and to examine whether biomarkers related to Alzheimer?s disease (AD) physiopathology were associated with worse memory performance. Patients and methods: Fifteen controls and 28 mild cognitive impairment and 13 AD dementia subjects were included. For Arg-ADNI, all biomarker parameters and neuropsychological tests of ADNI-II were adopted. Results of positron emission tomography (PET) with fluorodeoxyglucose and 11C-Pittsburgh compound-B (PIB-PET) were available from all participants. Cerebrospinal fluid biomarker results were available from 39 subjects. Results: A total of 56 participants were included and underwent baseline evaluation. The three groups were similar with respect to years of education and sex, and they differed in age (F=5.10, P=0.01). Mean scores for the baseline measurements of the neuropsychological evaluation differed significantly among the three groups at P,0.001, showing a continuum in their neuropsychological performance. No significant correlations were found between the principal measures (long-delay recall, C-Pittsburgh compound-B scan, left hippocampal volume, and APOEε4) and either age, sex, or education (P.0.1). Baseline amyloid deposition and left hippocampal volume separated the three diagnostic groups and correlated with the memory performance (P,0.001). Conclusion: Cross-sectional analysis of baseline data revealed links between cognition, structural changes, and biomarkers. Follow-up of a larger and more representative cohort, particularly analyzing cerebrospinal fluid and brain biomarkers, will allow better characterization of AD in our country.