The Modulatory Effect of Gender and Cytomegalovirus-Seropositivity on Circulating Inflammatory Factors and Cognitive Performance in Elderly Individuals

Int J Mol Sci. 2019 Feb 25;20(4):990. doi: 10.3390/ijms20040990.

Abstract

Aging is characterized by a chronic increase in the systemic levels of inflammatory cytokines even in ostensibly healthy individuals. The drivers of age-related increase in systemic inflammation are unclear but one potential contributor may be a persistent infection with Cytomegalovirus (CMV). In this study, we characterized the inflammatory status of 161 older participants recruited to undergo a six-month training intervention. We investigated the influence of gender and CMV-seropositivity on the main inflammatory and anti-inflammatory circulating biomarkers, such as cytokines, receptor antagonist, soluble receptor, immune cells, and relevant metabolic markers. We found that both gender and CMV-seropositivity modulate circulating peripheral biomarkers, and that CMV-infection modifies associations among the latter. Moreover, we observed an interaction between CMV-serostatus and gender associations with cognitive abilities: gender differences in fluid intelligence (Gf) and working memory (WM) were noted only in CMV-negative individuals. Finally, we found that in the CMV-seronegative participants Gf, episodic memory (EM), and WM correlated negatively with pro-inflammatory tumor necrosis factor (TNF); and EM correlated positively with anti-inflammatory interleukin (IL)-10. In CMV-seropositive individuals EM and Gf correlated negatively with pro-inflammatory IL-6, while EM, Gf, and WM correlated negatively with anti-inflammatory IL-1RA. We conclude that both CMV-serostatus and gender may modulate neuroimmune factors, cognitive performance and the relationship between the two domains and should therefore be considered in comparative and interventional studies with elderly people.

Keywords: aging; anti-inflammatory cytokines; cognition; cytomegalovirus; gender; immunosenescence; inflammaging; pro-inflammatory cytokines.

MeSH terms

  • Aged
  • Aging / immunology*
  • Biomarkers / blood
  • Cognitive Aging*
  • Cytokines / blood*
  • Cytomegalovirus / immunology*
  • Cytomegalovirus Infections / immunology
  • Female
  • Healthy Volunteers
  • Humans
  • Inflammation / virology
  • Male
  • Middle Aged
  • Sex Factors

Substances

  • Biomarkers
  • Cytokines