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. 2024 Oct 1;15(5):2205–2215. doi: 10.14336/AD.2023.1117

Table 4.

Associations between brain insulin signaling measures and the decline of late-life cognitive function after adjusting for APOEε4 allele (N=116).

Predictors Estimate (SE, p-value)
Global Cognition Episodic Memory Working Memory Semantic Memory Perceptual Speed Visuospatial Abilities
ELISA
pS307IRS1/total IRS1
Main Effect -0.071 (0.121,0.560) -0.149 (0.150,0.322) -0.110 (0.093,0.238) 0.060 (0.142,0.671) 0.069 (0.122,0.573) 0.021 (0.096,0.827)
Interaction with Time -0.002 (0.013,0.875) -0.002 (0.015,0.916) -0.001 (0.009,0.891) 0.005 (0.015,0.772) 0.001 (0.013,0.917) -0.002 (0.008,0.800)
pT308AKT1/total AKT1
Main Effect -0.228 (0.092,0.015) -0.320 (0.113,0.006) -0.204 (0.070,0.004) -0.102 (0.111,0.357) -0.133 (0.094,0.158) -0.122 (0.073,0.099)
Interaction with Time -0.017 (0.010,0.092) -0.020 (0.012,0.093) -0.017 (0.007,0.022) -0.003 (0.012,0.802) -0.011 (0.010,0.274) -0.014 (0.006,0.024)
Immunohistochemistry
pS616IRS1 cells/mm2
Main Effect -0.105 (0.080,0.242) -0.108 (0.111,0.335) -0.055 (0.070,0.429) -0.157 (0.105,0.137) -0.073 (0.090,0.419) -0.115 (0.071,0.106)
Interaction with Time 0.001 (0.010,0.908) -0.003 (0.012,0.810) 0.004 (0.008,0.599) -0.003 (0.012,0.796) 0.007 (0.010,0.481) -0.001 (0.007,0.914)

Note: All linear mixed-effects regression models were adjusted for age at death, sex, education, APOEε4, and their interaction with time. Data were from 116 participants with at least two longitudinal observations of cognitive function and available information on APOEε4 status. Bold values denote statistical significance (p<0.05).