Detrimental links between physical inactivity, metabolic risk and N-glycomic biomarkers of aging

Exp Gerontol. 2019 Sep:124:110626. doi: 10.1016/j.exger.2019.05.015. Epub 2019 May 31.

Abstract

Background: N-linked enzymatic glycosylation modulates the function of proteins and contributes to development of age-related metabolic abnormalities. Whether physical activity (PA) is linked to a specific N-glycan profile and can offset detrimental links between N-glycans and metabolic risk profile has never been explored. The aim of the present study is to assess serum N-glycan profile in older women with different PA levels and metabolic risk status.

Materials and methods: Components of the metabolic syndrome (MetS) and serum N-glycans analyzed using DSA-FACE technology were assessed in 109 older community-dwelling women (65-70 yrs). Ten peaks, each representing a unique N-glycan structure were detected. Moderate-to-vigorous PA (MVPA) was assessed objectively using accelerometry. All analyses were adjusted by covariates.

Results: Significantly elevated levels of NGA2FB (peak 2) and NA3F (peak 9) and lower level of the α(1,6)-arm monogalactosylated (NG1(6)A2F) (peak 3) were demonstrated in women with MetS compared to their healthier peers (p < 0.05). Importantly, women adhering to the PA guideline of time in MVPA had a 10% and a 12% lower level of NA3 (peak 8) and NA4 (peak 10), respectively, compared to those less active even after adjustment by MetS and covariates (p < 0.05). Interestingly, time spent in PA below the MVPA threshold was not linked to N-glycans.

Conclusion: Novel links between PA behaviors and N-glycan profile are demonstrated in older adults, regardless of metabolic risk status. This proposed effect on N-glycans requires engagement in MVPA. This supports public health efforts to promote adherence to PA guidelines in older adults across different stages of disease prevention.

MeSH terms

  • Accelerometry*
  • Aged
  • Aging*
  • Biomarkers / blood
  • Blood Proteins / analysis*
  • Exercise*
  • Female
  • Glycoproteins / analysis
  • Humans
  • Metabolic Syndrome / diagnosis*
  • Metabolic Syndrome / metabolism
  • Sedentary Behavior
  • Sweden

Substances

  • Biomarkers
  • Blood Proteins
  • Glycoproteins