Abstract

Dyshomeostasis of copper and zinc is linked to neurodegeneration. This study investigated the relationship between circulating copper and zinc and copper/zinc ratios and cognitive function, symptoms of depression and anxiety, and neurotrophic factors in older Australian adults. In this cross-sectional study (n = 139), plasma copper, serum zinc, and neurotrophic factors (brain-derived neurotrophic factor (BDNF), vascular endothelial growth factor, and insulin-like growth factor-1) were assessed. Cognition was assessed using the Cogstate battery and the Behavior Rating Inventory (BRI) of Executive Function (Adult version). Symptoms of anxiety and depression were assessed with the Hospital Anxiety and Depression Scale. Copper (β = −0.024; 95% CI = −0.044, −0.004; p = 0.019) and copper/zinc ratio (β = −1.99; 95% CI = −3.41, −0.57; p = 0.006) were associated with lower depressive symptoms, but not cognition. Plasma copper had a modest positive association with BDNF (β = −0.004; 95% CI = 0.000, 0.007; p = 0.021). Zinc was not associated with any of the outcomes. In conclusion, greater circulating copper concentrations and higher copper/zinc ratios were associated with lower depressive symptoms (but not cognition), with copper also positively associated with BDNF concentration, in a sample of community-dwelling older adults.

Highlights

  • Ageing is a naturally occurring physiological process which is characterized by both physical and cognitive decline

  • Decreased concentrations of such neurotrophic factors render brain cells more prone to damage caused by inflammatory processes and oxidative stress [4,5], which are key events in age-associated cognitive decline and neurodegenerative disease pathogenesis [6] experienced by many older adults

  • This is the first study to investigate the association between copper status and psychological distress in community-dwelling older adults, and comparisons with other studies conducted with a similar population are precluded

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Summary

Introduction

Ageing is a naturally occurring physiological process which is characterized by both physical and cognitive decline. Decreased concentrations of such neurotrophic factors render brain cells more prone to damage caused by inflammatory processes and oxidative stress [4,5], which are key events in age-associated cognitive decline and neurodegenerative disease pathogenesis [6] experienced by many older adults. It is estimated that dementia, a far-end result of cognitive decline, affects approximately 50 million people worldwide [7]. This number is expected to increase to 75 million by 2030 and 132 million by

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