Abstract

BackgroundInterleukin-33 (IL-33) plays a pivotal role in regulating innate immune response and metabolic homeostasis. However, whether its circulating level is correlated with obesity and metabolic disorders in humans remains largely unknown. We aimed to address this gap by determining IL-33 serum level and its downstream type 2 inflammatory cytokines interleukin-5 (IL-5) and interleukin-13 (IL-13) in overweight/obese population, and analyzing the specific associations between IL-33 and obesity metabolic phenotypes.Methods217 subjects were enrolled and divided into three groups: healthy control (HC) subjects, metabolically healthy overweight/obese (MHOO) subjects and metabolically unhealthy overweight/obese (MUOO) subjects. Circulating levels of IL-33, IL-5 and IL-13 were measured using ELISA analyses. Multivariate regression analyses were further performed to determine the independent association between IL-33 and obesity metabolic phenotypes.ResultsCirculating levels of IL-33 were significantly elevated in subjects of MUOO group compared with HC group and MHOO group, while no significant difference was observed between the latter two groups in IL-33 levels. Consistent with this, serum levels of IL-5/13 were higher in the MUOO group compared with HC and MHOO groups. After adjusted for all confounders, MUOO phenotype was significantly associated with increased IL-33 serum levels (OR = 1.70; 95% CI 1.09–2.64; p = 0.019). With the MHOO group as the reference population, higher circulating level of IL-33 was also positively associated with MUOO phenotype after adjusting for confounders (OR = 1.50; 95% CI 1.20–1.88; p = 2.91E−4). However, there was no significant association between MHOO phenotype and IL-33 levels (p = 0.942). Trend analysis further confirmed the positive correlation between MUOO phenotype and IL-33 level (p for trend = 0.019). Additionally, IL-33 was significantly and positively correlated with diastolic blood pressure (DBP), total cholesterol (TC), alanine aminotransferase (ALT), aspartate aminotransferase (AST), white blood cell (WBC), neutrophil and IL-5 only in MUOO group, while inversely correlated with high density lipoprotein cholesterol (HDL-C) in MHOO subjects.ConclusionCirculating levels of IL-33 were significantly elevated in overweight/obese Chinese adults with metabolic disorders. Increased levels of IL-33 were positively associated with metabolically unhealthy overweight/obese phenotype and several metabolic syndrome risk factors.

Highlights

  • Obesity and its related metabolic complications have become important public health issues globally, contributing to disease burden worldwide [1,2,3,4]

  • Our results showed that circulating levels of IL-33 in overweight/obese subjects were significantly higher than those in healthy control (HC) subjects, which was partly in agreement with the findings of IL-33 expression in human adipose tissue was upregulated by severe obesity [13]

  • We analyzed the correlation between IL-33 and metabolic phenotypes of obesity and the results showed that IL-33 was significantly and positively associated with metabolically unhealthy overweight/obese (MUOO) phenotype, but not associated with metabolically healthy overweight/obese (MHOO) phenotype

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Summary

Introduction

Obesity and its related metabolic complications have become important public health issues globally, contributing to disease burden worldwide [1,2,3,4]. With the occurrence and development of obesity, inflammatory immune cells infiltrated into adipose tissue and other metabolically active organs, causing inflammation and insulin resistance [5, 6]. Obesity has been well documented as a low-grade but chronic inflammatory disease [6,7,8], which contributes to the development and progression of its related metabolic complications such as cardiovascular diseases and type 2 diabetes mellitus (T2DM) [2]. Several reports have shown that IL-33 is important for maintaining immune cell homeostasis in adipose tissue [6] as well as the involvement of adipose tissue microenvironment in the obesity-related inflammation and complications [13].

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