An accumulating body of evidence suggests the involvement of an evolutionary conserved insulin/insulin-like growth factor-1 (IGF-1) signaling (IIS) pathway in the regulation of the life and health span in nematodes, flies, rodents, and humans. We studied the association between insulin/IGF-1 signaling and cognitive function among 1015 participants, 85 years old or older, of the population-based Leiden 85-Plus Study. A composite IIS6 score, based on expected effects (increased or decreased signaling) of selected variants in the IIS pathway, was calculated to estimate IIS pathway activity. Cognitive function was assessed at baseline and annually during a 5-year follow-up, using the Mini-Mental State Examination (MMSE). In women, but not in men, lower IIS6 scores (indicating decreased signaling) were associated with a lower risk of cognitive impairment (MMSE score ≤ 18) (p trend = .010). The IIS6 score was not associated with change in cognitive function. In addition to old age survival, genetically reduced IIS seems to be beneficial for cognitive function in women.

Cognitive function, Cohort study, Human, Insulin/IGF-1 signaling, aged, article, cognition, cognitive defect, female, follow up, genetic polymorphism, genetic variability, human, human experiment, insulin, lifespan, male, priority journal, risk assessment, scoring system, signal transduction, somatomedin C
Journals of Gerontology. Series A: Biological Sciences & Medical Sciences
Erasmus MC: University Medical Center Rotterdam

Euser, S.M, van Heemst, D, van Vliet, P, Breteler, M.M.B, & Westendorp, R.G.J. (2008). Insulin/insulin-like growth factor-1 signaling and cognitive function in humans. Journals of Gerontology. Series A: Biological Sciences & Medical Sciences, 907–910. Retrieved from