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Ceramide d18:1/24:1 as a potential biomarker to differentiate obesity subtypes with unfavorable health outcomes
BACKGROUND: The criteria for metabolically healthy obesity (MHO) and metabolically unhealthy obesity (MUO) remain controversial. This research aimed to identify a potential biomarker to differentiate the subtypes of obesity. METHODS: The study conducted a lipidomic evaluation of ceramide in the seru...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548646/ https://www.ncbi.nlm.nih.gov/pubmed/37794463 http://dx.doi.org/10.1186/s12944-023-01921-0 |
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author | Yu, Baowen Hu, Moran Jiang, Wanzi Ma, Yizhe Ye, Jingya Wu, Qinyi Guo, Wen Sun, Yan Zhou, Min Xu, Yiwen Wu, Zhoulu Wang, Yiwen Lam, Sin Man Shui, Guanghou Gu, Jingyu Li, John Zhong Fu, Zhenzhen Gong, Yingyun Zhou, Hongwen |
author_facet | Yu, Baowen Hu, Moran Jiang, Wanzi Ma, Yizhe Ye, Jingya Wu, Qinyi Guo, Wen Sun, Yan Zhou, Min Xu, Yiwen Wu, Zhoulu Wang, Yiwen Lam, Sin Man Shui, Guanghou Gu, Jingyu Li, John Zhong Fu, Zhenzhen Gong, Yingyun Zhou, Hongwen |
author_sort | Yu, Baowen |
collection | PubMed |
description | BACKGROUND: The criteria for metabolically healthy obesity (MHO) and metabolically unhealthy obesity (MUO) remain controversial. This research aimed to identify a potential biomarker to differentiate the subtypes of obesity. METHODS: The study conducted a lipidomic evaluation of ceramide in the serum of 77 Chinese adults who had undergone hyperinsulinemic-euglycemic clamps. These adults were divided into three groups according to the clinical data: normal weight control group (N = 21), MHO (N = 20), and MUO (N = 36). RESULTS: The serum Cer d18:1/24:1 level in the MHO group was lower than that in the MUO group. As the Cer d18:1/24:1 level increased, insulin sensitivity decreased, and the unfavorable parameters increased in parallel. Multivariate logistic regression analysis revealed that serum Cer d18:1/24:1 levels were independently correlated with MUO in obesity. Individuals with higher levels of Cer d18:1/24:1 also had an elevated risk of cardiovascular disease. Most ceramide subtype levels increased in obesity compared to normal-weight individuals, but the levels of serum Cer d18:0/18:0 and Cer d18:1/16:0 decreased in obesity. CONCLUSIONS: The relationships between ceramide subtypes and metabolic profiles might be heterogeneous in populations with different body weights. Cer d18:1/24:1 could be a biomarker that can be used to differentiate MUO from MHO, and to better predict who will develop unfavorable health outcomes among obese individuals. TRIAL REGISTRATION: The First Affiliated Hospital of Nanjing Medical University’s Institutional Review Board authorized this study protocol, and all participants provided written informed consent (2014-SR-003) prior to study entry. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-023-01921-0. |
format | Online Article Text |
id | pubmed-10548646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105486462023-10-05 Ceramide d18:1/24:1 as a potential biomarker to differentiate obesity subtypes with unfavorable health outcomes Yu, Baowen Hu, Moran Jiang, Wanzi Ma, Yizhe Ye, Jingya Wu, Qinyi Guo, Wen Sun, Yan Zhou, Min Xu, Yiwen Wu, Zhoulu Wang, Yiwen Lam, Sin Man Shui, Guanghou Gu, Jingyu Li, John Zhong Fu, Zhenzhen Gong, Yingyun Zhou, Hongwen Lipids Health Dis Research BACKGROUND: The criteria for metabolically healthy obesity (MHO) and metabolically unhealthy obesity (MUO) remain controversial. This research aimed to identify a potential biomarker to differentiate the subtypes of obesity. METHODS: The study conducted a lipidomic evaluation of ceramide in the serum of 77 Chinese adults who had undergone hyperinsulinemic-euglycemic clamps. These adults were divided into three groups according to the clinical data: normal weight control group (N = 21), MHO (N = 20), and MUO (N = 36). RESULTS: The serum Cer d18:1/24:1 level in the MHO group was lower than that in the MUO group. As the Cer d18:1/24:1 level increased, insulin sensitivity decreased, and the unfavorable parameters increased in parallel. Multivariate logistic regression analysis revealed that serum Cer d18:1/24:1 levels were independently correlated with MUO in obesity. Individuals with higher levels of Cer d18:1/24:1 also had an elevated risk of cardiovascular disease. Most ceramide subtype levels increased in obesity compared to normal-weight individuals, but the levels of serum Cer d18:0/18:0 and Cer d18:1/16:0 decreased in obesity. CONCLUSIONS: The relationships between ceramide subtypes and metabolic profiles might be heterogeneous in populations with different body weights. Cer d18:1/24:1 could be a biomarker that can be used to differentiate MUO from MHO, and to better predict who will develop unfavorable health outcomes among obese individuals. TRIAL REGISTRATION: The First Affiliated Hospital of Nanjing Medical University’s Institutional Review Board authorized this study protocol, and all participants provided written informed consent (2014-SR-003) prior to study entry. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-023-01921-0. BioMed Central 2023-10-04 /pmc/articles/PMC10548646/ /pubmed/37794463 http://dx.doi.org/10.1186/s12944-023-01921-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yu, Baowen Hu, Moran Jiang, Wanzi Ma, Yizhe Ye, Jingya Wu, Qinyi Guo, Wen Sun, Yan Zhou, Min Xu, Yiwen Wu, Zhoulu Wang, Yiwen Lam, Sin Man Shui, Guanghou Gu, Jingyu Li, John Zhong Fu, Zhenzhen Gong, Yingyun Zhou, Hongwen Ceramide d18:1/24:1 as a potential biomarker to differentiate obesity subtypes with unfavorable health outcomes |
title | Ceramide d18:1/24:1 as a potential biomarker to differentiate obesity subtypes with unfavorable health outcomes |
title_full | Ceramide d18:1/24:1 as a potential biomarker to differentiate obesity subtypes with unfavorable health outcomes |
title_fullStr | Ceramide d18:1/24:1 as a potential biomarker to differentiate obesity subtypes with unfavorable health outcomes |
title_full_unstemmed | Ceramide d18:1/24:1 as a potential biomarker to differentiate obesity subtypes with unfavorable health outcomes |
title_short | Ceramide d18:1/24:1 as a potential biomarker to differentiate obesity subtypes with unfavorable health outcomes |
title_sort | ceramide d18:1/24:1 as a potential biomarker to differentiate obesity subtypes with unfavorable health outcomes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548646/ https://www.ncbi.nlm.nih.gov/pubmed/37794463 http://dx.doi.org/10.1186/s12944-023-01921-0 |
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