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Glycans are a novel biomarker of chronological and biological ages. | LitMetric

AI Article Synopsis

  • The study investigates how changes in glycosylation of immunoglobulin G (IgG) molecules affect their function and inflammation as people age, analyzing data from over 5,000 individuals across four European populations.
  • It finds that specific IgG glycans change significantly with age, and a combination of three particular glycans can account for up to 58% of the differences in chronological age, outperforming other biological age markers like telomere lengths.
  • The research highlights the link between IgG glycosylation and both chronological and biological aging, suggesting that these changes could contribute to inflammation and have implications for disease prevention and treatment.

Article Abstract

Unlabelled: Fine structural details of glycans attached to the conserved N-glycosylation site significantly not only affect function of individual immunoglobulin G (IgG) molecules but also mediate inflammation at the systemic level. By analyzing IgG glycosylation in 5,117 individuals from four European populations, we have revealed very complex patterns of changes in IgG glycosylation with age. Several IgG glycans (including FA2B, FA2G2, and FA2BG2) changed considerably with age and the combination of these three glycans can explain up to 58% of variance in chronological age, significantly more than other markers of biological age like telomere lengths. The remaining variance in these glycans strongly correlated with physiological parameters associated with biological age. Thus, IgG glycosylation appears to be closely linked with both chronological and biological ages. Considering the important role of IgG glycans in inflammation, and because the observed changes with age promote inflammation, changes in IgG glycosylation also seem to represent a factor contributing to aging.

Significance Statement: Glycosylation is the key posttranslational mechanism that regulates function of immunoglobulins, with multiple systemic repercussions to the immune system. Our study of IgG glycosylation in 5,117 individuals from four European populations has revealed very extensive and complex changes in IgG glycosylation with age. The combined index composed of only three glycans explained up to 58% of variance in age, considerably more than other biomarkers of age like telomere lengths. The remaining variance in these glycans strongly correlated with physiological parameters associated with biological age; thus, IgG glycosylation appears to be closely linked with both chronological and biological ages. The ability to measure human biological aging using molecular profiling has practical applications for diverse fields such as disease prevention and treatment, or forensics.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049143PMC
http://dx.doi.org/10.1093/gerona/glt190DOI Listing

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