Abstract

ObjectiveType 2 diabetes (T2D) is a chronic low-grade inflammatory disease, which characterized by islet beta cell dysfunction. Serum adenosine deaminase (ADA) is an important enzyme that regulates the biological activity of insulin, and its levels are greatly increased in inflammatory diseases with insulin resistance. The present study was designed to explore the relationship between serum ADA levels and islet beta cell function in patients with T2D.MethodsThis cross-sectional study recruited 1573 patients with T2D from the Endocrinology Department of the Affiliated Hospital 2 of Nantong University between 2015 and 2018. All participants were received serum ADA test and oral glucose tolerance test (OGTT). Insulin sensitivity index (assessed by Matsuda index using C-peptide, ISIM-cp), insulin secretion index (assessed by ratio of area under the C-peptide curve to glucose curve, AUCcp/glu) and islet beta cell function (assessed by insulin secretion-sensitivity index 2 using C-peptide, ISSI2cp) were derived from OGTT. And other clinical parameters, such as HbA1c, were also collected.ResultsIt was showed that HbA1c was significantly increased, while ISIM-cp, AUCcp/glu and ISSI2cp significantly decreased, across ascending quartiles of serum ADA levels. Moreover, serum ADA levels were negatively correlated with ISSI2cp (r = − 0.267, p < 0.001). Furthermore, after adjusting for other clinical parameters by multiple linear regression analysis, serum ADA levels were still independently associated with ISSI2cp (β = − 0.125, t = − 5.397, p < 0.001, adjusted R2 = 0.459).ConclusionsSerum ADA levels are independently associated with islet beta cell function in patients with T2D.

Highlights

  • Adenosine deaminase (ADA) is a key enzyme in purine metabolism that catalyzes the irreversible conversion of adenosine and deoxyadenosine to inosine and deoxyinosine, respectively [1, 2]

  • Serum adenosine deaminase (ADA) levels were positively correlated with fasting plasma glucose (FPG), postprandial plasma glucose (PPG) and glycated hemoglobin (HbA1c) in patients with Type 2 diabetes (T2D) [1, 5, 16]

  • Clinical characteristics of study participants A total of 1573 participants diagnosed with T2D were recruited in this study and divided into four subgroups according to serum ADA levels

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Summary

Introduction

Adenosine deaminase (ADA) is a key enzyme in purine metabolism that catalyzes the irreversible conversion of adenosine and deoxyadenosine to inosine and deoxyinosine, respectively [1, 2]. ADA are directly related to the degree of inflammation [1, 5]. Recent studies showed that serum ADA levels and its isoenzymes are significantly higher in patients with T2D than in healthy controls [1, 5]. Serum ADA levels were positively correlated with fasting plasma glucose (FPG), postprandial plasma glucose (PPG) and glycated hemoglobin (HbA1c) in patients with T2D [1, 5, 16]. A previous study by Khemka et al [17] showed that there was no correlation between serum ADA levels and HbA1c in patients with T2D. The relationship between serum ADA levels and islet beta cell function in T2D has not been fully elucidated

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