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Published on: August 22, 2012
Public Health
Pablo Aguilar1,2,3, Carmen M Colceriu2, Alex López2
1Sant Pau Memory Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Background:
In aging and dementia research, the relationships between modifiable risk factors and biomarkers often vary across cohorts. We aim to evaluate the consistency and generalizability of the association between the area deprivation index (ADI) - an indicator of socioeconomic/resource disadvantage within a specific area - and cognition and Alzheimer's disease (AD) biomarkers across three distinct research cohorts, two from the U.S. (U.S. POINTER Imaging, ADNI) and one from Spain (UBRAIN).
Method:
We included a total of 3091 participants without dementia, 1879 from U.S. POINTER Imaging, 282 from ADNI and 930 from UBRAIN (Table 1). The ADI was calculated using validated indices from the US and Spain, with neighborhood deprivation ranked as Low, Moderate, and High in the US, and Low and High in Spain. Outcomes of interest included (1) the preclinical Alzheimer's cognitive composite (PACC-5), (2) MRI-derived gray matter volumes in AD-vulnerable regions and (3) PET or CSF-derived amyloid status (+/-). We ran logistic regression models with ADI level as predictor adjusted by sex, age, and APOE4 and considered education and race or ethnicity (only US cohorts) in our analyses.
Result:
Participants in more deprived areas had lower education across cohorts and were more likely to be female (U.S. POINTER) and African American (U.S. POINTER and ADNI, Table 1). Independent of age, sex and APOE4 status, higher ADI was associated with lower PACC in U.S. POINTER (Moderate: β=-0.165, p <0.001; High β=-0.412, p <0.001) and UBRAIN (ADI: High β=-0.096, p = 0.022) but not in ADNI (Figure 1). After controlling for education, this association remained significant in U.S. POINTER (Moderate: β=-0.166, p = 0.002; High: β=-0.248, p = 0.007) but not in UBRAIN (β=-0.021, p = 0.66). In U.S. POINTER, there was a trend towards an association of higher ADI with lower GM volume in AD-vulnerable regions (β=-0.126, p = 0.089) that was not observed in ADNI or UBRAIN (Figure 2). No associations between ADI and amyloid status were found across cohorts.
Conclusion:
We observed differing associations in neighborhood deprivation and cognition across US cohorts, as well as between the US and Spain cohorts. Country-specific factors and sample representativeness must be considered when investigating the pathophysiologic mechanisms underlying social determinants and disparities in AD.
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