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Peripheral invariant natural killer T cell deficiency in metabolically unhealthy but normal weight versus metabolically healthy but obese individuals
OBJECTIVE: To investigate the proportion of circulating invariant natural killer T (iNKT) cells in four body health types. METHODS: In this cross-sectional study, participants were classified into four body health types according to the body mass index and metabolic status: metabolically healthy and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536764/ https://www.ncbi.nlm.nih.gov/pubmed/28322093 http://dx.doi.org/10.1177/0300060516663778 |
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author | Wang, Xiao-Li Chang, Xiang-Yun Tang, Xiao-Xiao Chen, Zhi-Gang Zhou, Ting Sun, Kan |
author_facet | Wang, Xiao-Li Chang, Xiang-Yun Tang, Xiao-Xiao Chen, Zhi-Gang Zhou, Ting Sun, Kan |
author_sort | Wang, Xiao-Li |
collection | PubMed |
description | OBJECTIVE: To investigate the proportion of circulating invariant natural killer T (iNKT) cells in four body health types. METHODS: In this cross-sectional study, participants were classified into four body health types according to the body mass index and metabolic status: metabolically healthy and normal weight (MHNW), metabolically unhealthy but normal weight (MUNW), metabolically healthy but obese (MHO), or metabolically unhealthy and obese (MUO). Demographic and clinical characteristics were measured, and the homeostasis model assessment of insulin resistance (HOMA-IR) and visceral adiposity index (VAI) were calculated. The proportion of circulating iNKT cells was also evaluated by flow cytometry. RESULTS: The study enrolled 41 MHNW, 37 MUNW, 30 MHO, and 43 MUO participants. Compared with the MHNW group, the MUNW, MHO, and MUO groups had significantly lower iNKT cell proportions. The iNKT cell proportion was significantly higher in the MHO group than the MUNW and MUO groups. The iNKT cell proportion was inversely correlated with high-sensitivity C-reactive protein, HOMA-IR, and VAI values. CONCLUSION: The proportion of iNKT cells was lower in people (lean or obese) with excessive visceral fat accumulation, suggesting that iNKT cell deficiency may be involved in the pathophysiology of obesity-related metabolic disorders. |
format | Online Article Text |
id | pubmed-5536764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-55367642017-10-03 Peripheral invariant natural killer T cell deficiency in metabolically unhealthy but normal weight versus metabolically healthy but obese individuals Wang, Xiao-Li Chang, Xiang-Yun Tang, Xiao-Xiao Chen, Zhi-Gang Zhou, Ting Sun, Kan J Int Med Res Research Reports OBJECTIVE: To investigate the proportion of circulating invariant natural killer T (iNKT) cells in four body health types. METHODS: In this cross-sectional study, participants were classified into four body health types according to the body mass index and metabolic status: metabolically healthy and normal weight (MHNW), metabolically unhealthy but normal weight (MUNW), metabolically healthy but obese (MHO), or metabolically unhealthy and obese (MUO). Demographic and clinical characteristics were measured, and the homeostasis model assessment of insulin resistance (HOMA-IR) and visceral adiposity index (VAI) were calculated. The proportion of circulating iNKT cells was also evaluated by flow cytometry. RESULTS: The study enrolled 41 MHNW, 37 MUNW, 30 MHO, and 43 MUO participants. Compared with the MHNW group, the MUNW, MHO, and MUO groups had significantly lower iNKT cell proportions. The iNKT cell proportion was significantly higher in the MHO group than the MUNW and MUO groups. The iNKT cell proportion was inversely correlated with high-sensitivity C-reactive protein, HOMA-IR, and VAI values. CONCLUSION: The proportion of iNKT cells was lower in people (lean or obese) with excessive visceral fat accumulation, suggesting that iNKT cell deficiency may be involved in the pathophysiology of obesity-related metabolic disorders. SAGE Publications 2016-11-07 2016-12 /pmc/articles/PMC5536764/ /pubmed/28322093 http://dx.doi.org/10.1177/0300060516663778 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Reports Wang, Xiao-Li Chang, Xiang-Yun Tang, Xiao-Xiao Chen, Zhi-Gang Zhou, Ting Sun, Kan Peripheral invariant natural killer T cell deficiency in metabolically unhealthy but normal weight versus metabolically healthy but obese individuals |
title | Peripheral invariant natural killer T cell deficiency in metabolically unhealthy but normal weight versus metabolically healthy but obese individuals |
title_full | Peripheral invariant natural killer T cell deficiency in metabolically unhealthy but normal weight versus metabolically healthy but obese individuals |
title_fullStr | Peripheral invariant natural killer T cell deficiency in metabolically unhealthy but normal weight versus metabolically healthy but obese individuals |
title_full_unstemmed | Peripheral invariant natural killer T cell deficiency in metabolically unhealthy but normal weight versus metabolically healthy but obese individuals |
title_short | Peripheral invariant natural killer T cell deficiency in metabolically unhealthy but normal weight versus metabolically healthy but obese individuals |
title_sort | peripheral invariant natural killer t cell deficiency in metabolically unhealthy but normal weight versus metabolically healthy but obese individuals |
topic | Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536764/ https://www.ncbi.nlm.nih.gov/pubmed/28322093 http://dx.doi.org/10.1177/0300060516663778 |
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