Inflammatory Mediators and Type 2 Diabetes Risk Factors before and in Response to Lifestyle Intervention among Latino Adolescents with Obesity

Author:

Peña Armando123ORCID,Olson Micah L.34,Ayers Stephanie L.5,Sears Dorothy D.2ORCID,Vega-López Sonia25ORCID,Colburn Abigail T.67ORCID,Shaibi Gabriel Q.345

Affiliation:

1. Department of Health and Wellness Design, School of Public Health-Bloomington, Indiana University, Bloomington, IN 47405, USA

2. College of Health Solutions, Arizona State University, Phoenix, AZ 85004, USA

3. Center for Health Promotion and Disease Prevention, Arizona State University, Phoenix, AZ 85004, USA

4. Division of Pediatric Endocrinology and Diabetes, Phoenix Children’s Hospital, Phoenix, AZ 85016, USA

5. Southwestern Interdisciplinary Research Center, Arizona State University, Phoenix, AZ 85004, USA

6. Obstetrics, Gynecology and Reproductive Sciences, Yale School of Medicine, New Haven, CT 06510, USA

7. John B. Pierce Laboratory, Yale School of Medicine, New Haven, CT 06519, USA

Abstract

Obesity is associated with chronic inflammation that may contribute to T2D among youth. We examined the association between inflammatory biomarkers and insulin sensitivity and β-cell function and response to lifestyle intervention among Latino youth with obesity. Latino youth (n = 64) were randomized to six months of lifestyle intervention (INT, n = 40) or usual care (UC, n = 24). INT included nutrition education and physical activity. UC involved meeting with a pediatric endocrinologist and registered dietitian to discuss healthy lifestyles. At baseline, multiple linear regression assessed fasting serum interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), monocyte chemoattractant protein-1 (MCP-1), high-molecular weight adiponectin (HMW Adpn), IL-10, IL-1 receptor antagonist (IL-1ra) as predictors of insulin sensitivity (whole-body insulin sensitivity index, WBISI) and β-cell function (oral disposition index, oDI). Changes in outcomes between groups were assessed using covariance pattern models. At baseline, MCP-1 (β ± SE, −0.12 ± 0.05, p = 0.027) and IL-1ra (−0.03 ± 0.01, p = 0.005) were negatively associated with WBISI. Treatment effects were not observed for inflammatory markers. WBISI was significantly increased among both INT (from 1.8 ± 0.2 to 2.6 ± 0.4, p = 0.005) and UC (from 1.6 ± 0.2 to 2.8 ± 0.5, p = 0.002) with no significant differences between the groups. Obesity-related inflammatory mediators were associated with T2D risk factors but were unaffected by lifestyle intervention among Latino youth.

Funder

National Institutes of Health/National Institutes of Diabetes, Digestion, and Kidney Diseases

NIDDK Diversity Supplement

Diversity F31

Publisher

MDPI AG

Subject

Food Science,Nutrition and Dietetics

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