Abstract

To investigate the role of NAMPT/visfatin in euthyroid patients with Graves’ disease without (GD) and with Graves’ ophthalmopathy (GO), we analyzed NAMPT leukocyte expression and its serum concentration. This was a single-center, cross-sectional study with consecutive enrollment. In total, 149 patients diagnosed with Graves’ disease were enrolled in the study. We excluded subjects with hyper- or hypothyroidism, diabetes mellitus, other autoimmune disorders, active neoplastic disease, and infection. The control group was recruited among healthy volunteers adjusted for age, sex, and BMI with normal thyroid function and negative thyroid antibodies. Serum levels of visfatin, TSH, FT4, FT3, antibodies against TSH receptor (TRAb), antithyroperoxidase antibodies, antithyroglobulin antibodies, fasting glucose, and insulin were measured. NAMPT mRNA leukocyte expression was assessed using RT-qPCR. NAMPT/visfatin serum concentration was higher in GD (n = 44) and GO (n = 49) patients than in the control group (n = 40) (p = 0.0275). NAMPT leukocyte expression was higher in patients with GO (n = 30) than in GD patients (n = 27) and the control group (n = 29) (p < 0.0001). Simple linear regression analysis revealed that NAMPT/visfatin serum concentration was significantly associated with GD (β = 1.5723; p = 0.021). When NAMPT leukocyte expression was used as a dependent variable, simple regression analysis found association with TRAb, fasting insulin level, HOMA-IR, GD, and GO. In the stepwise multiple regression analysis, we confirmed the association between higher serum NAMPT/visfatin level and GD (coefficient = 1.5723; p = 0.0212), and between NAMPT leukocyte expression and GO (coefficient = 2.4619; p = 0.0001) and TRAb (coefficient = 0.08742; p = 0.006). Increased NAMPT leukocyte expression in patients with GO might suggest a presently undefined role in the pathogenesis of GO.

Highlights

  • Visfatin, primarily identified as a cytokine pre-B cell colony-enhancing factor (PBEF), known as nicotinamide phosphoribosyltransferase (NAMPT), has nomenclature that reflects its complex functional aspects [1]

  • NAMPT leukocyte expression was higher in patients with Graves’ ophthalmopathy (GO) (n = 30) than in Graves’ disease without (GD) patients (n = 27) and the control group (n = 29) (p \ 0.0001)

  • Simple linear regression analysis revealed that NAMPT/visfatin serum concentration was significantly associated with GD (b = 1.5723; p = 0.021)

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Summary

Introduction

Primarily identified as a cytokine pre-B cell colony-enhancing factor (PBEF), known as nicotinamide phosphoribosyltransferase (NAMPT), has nomenclature that reflects its complex functional aspects [1]. NAMPT/visfatin is secreted by adipose tissue and leukocytes as an extracellular protein, but its main source is still elusive [2, 3]. The protein is involved in metabolic regulation and its elevated levels were observed in patients with diabetes mellitus type 2 and obesity [4, 5]. Both hypo- and hyperthyroidism influence NAMPT/visfatin level [6, 7].

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