An alternatively spliced soluble TNF-α receptor is associated with metabolic disorders A replication study

Abstract In a previous study, we identified a biologically active form of tumor necrosis factor-alpha receptor 2 (sTNFR2) produced by differential splicing (DS-TNFR2) which antagonized TNF-α biological activity. Obesity, insulin resistance and type 2 diabetes are linked to increased TNF-α action. We hypothesized that subjects with detectable DS-TNFR2 would be protected from developing obesity and related metabolic disorders. Thus, we investigated if circulating DS-TNFR2 concentration was associated with components of the so-called metabolic syndrome among 269 consecutive subjects from the general population. DS-TNFR2 was measured using a monoclonal antibody against an epitope present in TNFR2 (first 14 residues of the juxtamembrane region) but predicted to be absent in soluble proteolytic cleavage-produced TNFR2. Plasma DS-TNFR2 concentration was significantly decreased among patients with glucose intolerance or type 2 diabetes mellitus ( p  = 0.026). DS-TNFR2 tended to be associated with fasting and post-load glucose (both r  = − 0.11, p  = 0.054), and with diastolic blood pressure in men ( r  = − 0.16, p  = 0.07). Serum DS-TNFR2 concentration was significantly associated with LDL cholesterol ( r  = − 0.28, p  = 0.002), uric acid ( r  = − 0.13, p  = 0.04) and with blood glycated hemoglobin ( r  = − 0.13, p  = 0.04). DS-TNFR2 declined with increased number of components of the metabolic syndrome ( p  = 0.03). Those subjects with 2 or more components had significantly decreased circulating DS-TNFR2 levels (0.96 ± 2.2 versus 1.7 ± 3.2, p  = 0.033). In summary, the circulating concentration of DS-TNFR2 seems to be inversely linked to metabolic disorders, hinting at a possible anti-inflammatory role.