Phosphorylation of Histone H2A.X in Peripheral Blood Mononuclear Cells May Be a Useful Marker for Monitoring Cardiometabolic Risk in Nondiabetic Individuals

Abstract EN

Phosphorylation of H2A.X (serine 139) in the histone H2A family located in the downstream of the DNA damage kinase signaling cascade is an important indicator of DNA damage.

Recently, phosphorylation of H2A.X was proposed as a sensitive biomarker of aging.

This study investigated if phosphorylation of H2A.X in peripheral blood mononuclear cells (PBMCs) is associated with cardiometabolic risk in nondiabetic individuals.

Basic parameters and oxidative stress/inflammatory markers were measured in nondiabetic healthy Koreans (n=119).

Phosphorylation of H2A.X was measured randomly among the study subjects using a flow cytometer.

According to the number of metabolic syndrome risk factor (MetS-RF), the study subjects were subdivided into “super healthy” (MetS−RF=0, n=71) and “MetS-risk” (MetS−RF≥1, n=48) groups.

Phosphorylation of H2A.X in PBMCs (percentages and mean fluorescence intensity) was significantly higher in the MetS-risk group than in the super healthy group after adjusting for age, sex, cigarette smoking, and alcohol consumption.

Phosphorylated H2A.X was positively correlated with the number of MetS-RF as well as waist circumference, blood pressures, triglyceride, HbA1C, oxidized LDL, high sensitivity C-reactive protein, tumor necrosis factor-alpha, and alanine aminotransferase after the adjustment.

The present study suggested that phosphorylated H2A.X in circulating PBMCs measured by flow cytometer may be a useful marker for monitoring cardiometabolic risk in nondiabetic individuals.