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Adiposity Mediates the Association between the Dietary Inflammatory Index and Markers of Type 2 Diabetes Risk in Middle-Aged Black South African Women

The dietary inflammatory index (DII(®)), a validated tool used to measure the inflammatory potential of the diet, has been associated with metabolic disorders in various settings, but not in African populations. The aim of this study was to investigate whether the DII is associated with markers of t...

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Autores principales: Mtintsilana, Asanda, Micklesfield, Lisa K., Chorell, Elin, Olsson, Tommy, Shivappa, Nitin, Hebert, James R, Kengne, Andre P., Goedecke, Julia H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628082/
https://www.ncbi.nlm.nih.gov/pubmed/31159253
http://dx.doi.org/10.3390/nu11061246
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author Mtintsilana, Asanda
Micklesfield, Lisa K.
Chorell, Elin
Olsson, Tommy
Shivappa, Nitin
Hebert, James R
Kengne, Andre P.
Goedecke, Julia H.
author_facet Mtintsilana, Asanda
Micklesfield, Lisa K.
Chorell, Elin
Olsson, Tommy
Shivappa, Nitin
Hebert, James R
Kengne, Andre P.
Goedecke, Julia H.
author_sort Mtintsilana, Asanda
collection PubMed
description The dietary inflammatory index (DII(®)), a validated tool used to measure the inflammatory potential of the diet, has been associated with metabolic disorders in various settings, but not in African populations. The aim of this study was to investigate whether the DII is associated with markers of type 2 diabetes (T2D) risk, and if this association is mediated by adiposity and/or low-grade inflammation, in black South Africa women. Energy-adjusted-DII (E-DII) scores were calculated in 190 women (median age, 53 years) from the Birth-to-Twenty plus cohort using a validated food frequency questionnaire. Fasting glucose, insulin, HbA1c, and inflammatory cytokines were measured, and an oral glucose tolerance test performed. Basic anthropometry and dual-energy x-ray absorptiometry-derived body fat, including estimate of visceral adipose tissue (VAT) area, were measured. E-DII scores were associated with all markers of T2D risk, namely, fasting glucose and insulin, HbA1c, HOMA2-IR, two-hour glucose and Matsuda index (all p < 0.05). After adjusting for age, measures of adiposity, but not inflammatory cytokines, mediated the association between E-DII and markers of T2D risk (p < 0.05). Measures of central obesity had proportionally higher (range: 23.5–100%) mediation effects than total obesity (range: 10–60%). The E-DII is associated with T2D risk through obesity, in particular central obesity, among black middle-aged South African women.
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spelling pubmed-66280822019-07-23 Adiposity Mediates the Association between the Dietary Inflammatory Index and Markers of Type 2 Diabetes Risk in Middle-Aged Black South African Women Mtintsilana, Asanda Micklesfield, Lisa K. Chorell, Elin Olsson, Tommy Shivappa, Nitin Hebert, James R Kengne, Andre P. Goedecke, Julia H. Nutrients Article The dietary inflammatory index (DII(®)), a validated tool used to measure the inflammatory potential of the diet, has been associated with metabolic disorders in various settings, but not in African populations. The aim of this study was to investigate whether the DII is associated with markers of type 2 diabetes (T2D) risk, and if this association is mediated by adiposity and/or low-grade inflammation, in black South Africa women. Energy-adjusted-DII (E-DII) scores were calculated in 190 women (median age, 53 years) from the Birth-to-Twenty plus cohort using a validated food frequency questionnaire. Fasting glucose, insulin, HbA1c, and inflammatory cytokines were measured, and an oral glucose tolerance test performed. Basic anthropometry and dual-energy x-ray absorptiometry-derived body fat, including estimate of visceral adipose tissue (VAT) area, were measured. E-DII scores were associated with all markers of T2D risk, namely, fasting glucose and insulin, HbA1c, HOMA2-IR, two-hour glucose and Matsuda index (all p < 0.05). After adjusting for age, measures of adiposity, but not inflammatory cytokines, mediated the association between E-DII and markers of T2D risk (p < 0.05). Measures of central obesity had proportionally higher (range: 23.5–100%) mediation effects than total obesity (range: 10–60%). The E-DII is associated with T2D risk through obesity, in particular central obesity, among black middle-aged South African women. MDPI 2019-05-31 /pmc/articles/PMC6628082/ /pubmed/31159253 http://dx.doi.org/10.3390/nu11061246 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mtintsilana, Asanda
Micklesfield, Lisa K.
Chorell, Elin
Olsson, Tommy
Shivappa, Nitin
Hebert, James R
Kengne, Andre P.
Goedecke, Julia H.
Adiposity Mediates the Association between the Dietary Inflammatory Index and Markers of Type 2 Diabetes Risk in Middle-Aged Black South African Women
title Adiposity Mediates the Association between the Dietary Inflammatory Index and Markers of Type 2 Diabetes Risk in Middle-Aged Black South African Women
title_full Adiposity Mediates the Association between the Dietary Inflammatory Index and Markers of Type 2 Diabetes Risk in Middle-Aged Black South African Women
title_fullStr Adiposity Mediates the Association between the Dietary Inflammatory Index and Markers of Type 2 Diabetes Risk in Middle-Aged Black South African Women
title_full_unstemmed Adiposity Mediates the Association between the Dietary Inflammatory Index and Markers of Type 2 Diabetes Risk in Middle-Aged Black South African Women
title_short Adiposity Mediates the Association between the Dietary Inflammatory Index and Markers of Type 2 Diabetes Risk in Middle-Aged Black South African Women
title_sort adiposity mediates the association between the dietary inflammatory index and markers of type 2 diabetes risk in middle-aged black south african women
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628082/
https://www.ncbi.nlm.nih.gov/pubmed/31159253
http://dx.doi.org/10.3390/nu11061246
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