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Population serum proteomics uncovers a prognostic protein classifier for metabolic syndrome
Metabolic syndrome (MetS) is a complex metabolic disorder with a global prevalence of 20%–25%. Early identification and intervention would help minimize the global burden on healthcare systems. Here, we measured over 400 proteins from ∼20,000 proteomes using data-independent acquisition mass spectro...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518601/ https://www.ncbi.nlm.nih.gov/pubmed/37652016 http://dx.doi.org/10.1016/j.xcrm.2023.101172 |
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author | Cai, Xue Xue, Zhangzhi Zeng, Fang-Fang Tang, Jun Yue, Liang Wang, Bo Ge, Weigang Xie, Yuting Miao, Zelei Gou, Wanglong Fu, Yuanqing Li, Sainan Gao, Jinlong Shuai, Menglei Zhang, Ke Xu, Fengzhe Tian, Yunyi Xiang, Nan Zhou, Yan Shan, Peng-Fei Zhu, Yi Chen, Yu-ming Zheng, Ju-Sheng Guo, Tiannan |
author_facet | Cai, Xue Xue, Zhangzhi Zeng, Fang-Fang Tang, Jun Yue, Liang Wang, Bo Ge, Weigang Xie, Yuting Miao, Zelei Gou, Wanglong Fu, Yuanqing Li, Sainan Gao, Jinlong Shuai, Menglei Zhang, Ke Xu, Fengzhe Tian, Yunyi Xiang, Nan Zhou, Yan Shan, Peng-Fei Zhu, Yi Chen, Yu-ming Zheng, Ju-Sheng Guo, Tiannan |
author_sort | Cai, Xue |
collection | PubMed |
description | Metabolic syndrome (MetS) is a complex metabolic disorder with a global prevalence of 20%–25%. Early identification and intervention would help minimize the global burden on healthcare systems. Here, we measured over 400 proteins from ∼20,000 proteomes using data-independent acquisition mass spectrometry for 7,890 serum samples from a longitudinal cohort of 3,840 participants with two follow-up time points over 10 years. We then built a machine-learning model for predicting the risk of developing MetS within 10 years. Our model, composed of 11 proteins and the age of the individuals, achieved an area under the curve of 0.774 in the validation cohort (n = 242). Using linear mixed models, we found that apolipoproteins, immune-related proteins, and coagulation-related proteins best correlated with MetS development. This population-scale proteomics study broadens our understanding of MetS and may guide the development of prevention and targeted therapies for MetS. |
format | Online Article Text |
id | pubmed-10518601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105186012023-09-26 Population serum proteomics uncovers a prognostic protein classifier for metabolic syndrome Cai, Xue Xue, Zhangzhi Zeng, Fang-Fang Tang, Jun Yue, Liang Wang, Bo Ge, Weigang Xie, Yuting Miao, Zelei Gou, Wanglong Fu, Yuanqing Li, Sainan Gao, Jinlong Shuai, Menglei Zhang, Ke Xu, Fengzhe Tian, Yunyi Xiang, Nan Zhou, Yan Shan, Peng-Fei Zhu, Yi Chen, Yu-ming Zheng, Ju-Sheng Guo, Tiannan Cell Rep Med Article Metabolic syndrome (MetS) is a complex metabolic disorder with a global prevalence of 20%–25%. Early identification and intervention would help minimize the global burden on healthcare systems. Here, we measured over 400 proteins from ∼20,000 proteomes using data-independent acquisition mass spectrometry for 7,890 serum samples from a longitudinal cohort of 3,840 participants with two follow-up time points over 10 years. We then built a machine-learning model for predicting the risk of developing MetS within 10 years. Our model, composed of 11 proteins and the age of the individuals, achieved an area under the curve of 0.774 in the validation cohort (n = 242). Using linear mixed models, we found that apolipoproteins, immune-related proteins, and coagulation-related proteins best correlated with MetS development. This population-scale proteomics study broadens our understanding of MetS and may guide the development of prevention and targeted therapies for MetS. Elsevier 2023-08-30 /pmc/articles/PMC10518601/ /pubmed/37652016 http://dx.doi.org/10.1016/j.xcrm.2023.101172 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Cai, Xue Xue, Zhangzhi Zeng, Fang-Fang Tang, Jun Yue, Liang Wang, Bo Ge, Weigang Xie, Yuting Miao, Zelei Gou, Wanglong Fu, Yuanqing Li, Sainan Gao, Jinlong Shuai, Menglei Zhang, Ke Xu, Fengzhe Tian, Yunyi Xiang, Nan Zhou, Yan Shan, Peng-Fei Zhu, Yi Chen, Yu-ming Zheng, Ju-Sheng Guo, Tiannan Population serum proteomics uncovers a prognostic protein classifier for metabolic syndrome |
title | Population serum proteomics uncovers a prognostic protein classifier for metabolic syndrome |
title_full | Population serum proteomics uncovers a prognostic protein classifier for metabolic syndrome |
title_fullStr | Population serum proteomics uncovers a prognostic protein classifier for metabolic syndrome |
title_full_unstemmed | Population serum proteomics uncovers a prognostic protein classifier for metabolic syndrome |
title_short | Population serum proteomics uncovers a prognostic protein classifier for metabolic syndrome |
title_sort | population serum proteomics uncovers a prognostic protein classifier for metabolic syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518601/ https://www.ncbi.nlm.nih.gov/pubmed/37652016 http://dx.doi.org/10.1016/j.xcrm.2023.101172 |
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