Abstract

Background:Altered cerebral glucose metabolism, especially prominent in APOE ɛ4 carriers, occurs years prior to symptoms in Alzheimer’s disease (AD). We recently found an association between a higher ratio of plasma apolipoprotein E4 (apoE4) over apoE3, and cerebral glucose hypometabolism in cognitively healthy APOE ɛ3/ɛ4 subjects. Plasma apoE does not cross the blood-brain barrier, hence we speculate that apoE is linked to peripheral glucose metabolism which is known to affect glucose metabolism in the brain.Objective:Explore potential associations between levels of plasma insulin and glucose with previously acquired plasma apoE, cerebral metabolic rate of glucose (CMRgl), gray matter volume, and neuropsychological test scores.Methods:Plasma insulin and glucose levels were determined by ELISA and a glucose oxidase assay whereas apoE levels were earlier quantified by mass-spectrometry in 128 cognitively healthy APOE ɛ3/ɛ4 subjects. Twenty-five study subjects had previously undergone FDG-PET and structural MRI.Results:Lower plasma apoE3 associated with higher plasma glucose but not insulin in male subjects and subjects with a body mass index above 25. Negative correlations were found between plasma glucose and CMRgl in the left prefrontal and bilateral occipital regions. These associations may have functional implications since glucose levels in turn were negatively associated with neuropsychological test scores.Conclusion:Plasma apoE3 but not apoE4 may be involved in insulin-independent processes governing plasma glucose levels. Higher plasma glucose, which negatively affects brain glucose metabolism, was associated with lower plasma apoE levels in APOE ɛ3/ɛ4 subjects. High plasma glucose and low apoE levels may be a hazardous combination leading to an increased risk of AD.

Highlights

  • Apolipoprotein E is a 299 amino acid long glycoprotein, existing in three common isoforms due to polymorphism in the human APOE gene locatedA.K

  • We aimed to investigate whether plasma Apolipoprotein E (apoE) levels are directly associated with plasma glucose and/or insulin levels, which potentially could help explain our previous findings of an association between the plasma apolipoprotein E4 (apoE4)/ E3 ratio and alterations in brain glucose metabolism and gray matter volume (GMV)

  • Using the same cohort of subjects examined in the current study, we have reported that a higher relative plasma concentration ratio between the apoE4 and apoE3 isoforms was associated with reduced GMV and cerebral glucose metabolism in the hippocampus [21]

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Summary

Introduction

Apolipoprotein E (apoE) is a 299 amino acid long glycoprotein, existing in three common isoforms due to polymorphism in the human APOE gene locatedA.K. Greater peripheral insulin resistance, indexed with the Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), was reported to be negatively associated with FDG-uptake and AD-like reduction in cerebral metabolic rate of glucose (CMRgl) in frontal, parieto-temporal and cingulate regions in cognitively normal elderly with pre-diabetes and T2DM [16]. We recently found an association between a higher ratio of plasma apolipoprotein E4 (apoE4) over apoE3, and cerebral glucose hypometabolism in cognitively healthy APOE ␧3/␧4 subjects. Objective: Explore potential associations between levels of plasma insulin and glucose with previously acquired plasma apoE, cerebral metabolic rate of glucose (CMRgl), gray matter volume, and neuropsychological test scores. Higher plasma glucose, which negatively affects brain glucose metabolism, was associated with lower plasma apoE levels in APOE ␧3/␧4 subjects.

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