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The serum level of a novel lipogenic protein Spot 14 was reduced in metabolic syndrome
Spot 14 (S14) protein is primarily expressed in adipogenic tissues. Compared to wild type, S14 knockout mice had better resistance to diet-induced obesity and glucose tolerance. However, the association between serum S14 level and metabolic variables in humans has never been investigated. The object...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375670/ https://www.ncbi.nlm.nih.gov/pubmed/30763384 http://dx.doi.org/10.1371/journal.pone.0212341 |
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author | Chen, Yen-Ting Tseng, Ping-Huei Tseng, Fen-Yu Chi, Yu-Chiao Han, Der-Sheng Yang, Wei-Shiung |
author_facet | Chen, Yen-Ting Tseng, Ping-Huei Tseng, Fen-Yu Chi, Yu-Chiao Han, Der-Sheng Yang, Wei-Shiung |
author_sort | Chen, Yen-Ting |
collection | PubMed |
description | Spot 14 (S14) protein is primarily expressed in adipogenic tissues. Compared to wild type, S14 knockout mice had better resistance to diet-induced obesity and glucose tolerance. However, the association between serum S14 level and metabolic variables in humans has never been investigated. The objectives of this study were to evaluate the associations between serum S14 concentrations with components of metabolic syndrome (MetS). A total of 327 subjects were recruited in this cross-sectional study and categorized by presence of MetS. The mean serum levels of S14 were significantly lower in subjects with MetS than those without (87.1±26.3 μg/L vs. 107.3±40.2 μg/L, p<0.001). In addition, the subjects with central obesity, low high density lipoprotein-C (HDL-C) or hypertriglyceridemia also had significantly lower S14 levels in comparison to those without. Adjusted with age and sex, diagnosis of MetS (β = -0.227, p<0.001), central obesity (β = -0.176, p = 0.001), low HDL-C (β = -0.149, p = 0.005), and high triglyceride (TG) (β = -0.198, p<0.001) were negatively associated with log transformation of serum S14 levels (logS14). With 25% logS14 increased, the risk of MetS (OR 0.65, 95% CI, 0.51–0.82, p<0.001), central obesity (OR 0.72, 95% CI, 0.58–0.89, p = 0.002), low HDL-C (OR 0.76, 95% CI, 0.61–0.95, p = 0.015) or high TG (OR 0.65, 95% CI, 0.51–0.83, p = 0.001) was reduced with a dose response trend. Our analysis revealed that patients with MetS had lower serum S14 levels than those without. Negative associations existed between MetS, central obesity, high TG, low HDL-C and logS14. |
format | Online Article Text |
id | pubmed-6375670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-63756702019-03-01 The serum level of a novel lipogenic protein Spot 14 was reduced in metabolic syndrome Chen, Yen-Ting Tseng, Ping-Huei Tseng, Fen-Yu Chi, Yu-Chiao Han, Der-Sheng Yang, Wei-Shiung PLoS One Research Article Spot 14 (S14) protein is primarily expressed in adipogenic tissues. Compared to wild type, S14 knockout mice had better resistance to diet-induced obesity and glucose tolerance. However, the association between serum S14 level and metabolic variables in humans has never been investigated. The objectives of this study were to evaluate the associations between serum S14 concentrations with components of metabolic syndrome (MetS). A total of 327 subjects were recruited in this cross-sectional study and categorized by presence of MetS. The mean serum levels of S14 were significantly lower in subjects with MetS than those without (87.1±26.3 μg/L vs. 107.3±40.2 μg/L, p<0.001). In addition, the subjects with central obesity, low high density lipoprotein-C (HDL-C) or hypertriglyceridemia also had significantly lower S14 levels in comparison to those without. Adjusted with age and sex, diagnosis of MetS (β = -0.227, p<0.001), central obesity (β = -0.176, p = 0.001), low HDL-C (β = -0.149, p = 0.005), and high triglyceride (TG) (β = -0.198, p<0.001) were negatively associated with log transformation of serum S14 levels (logS14). With 25% logS14 increased, the risk of MetS (OR 0.65, 95% CI, 0.51–0.82, p<0.001), central obesity (OR 0.72, 95% CI, 0.58–0.89, p = 0.002), low HDL-C (OR 0.76, 95% CI, 0.61–0.95, p = 0.015) or high TG (OR 0.65, 95% CI, 0.51–0.83, p = 0.001) was reduced with a dose response trend. Our analysis revealed that patients with MetS had lower serum S14 levels than those without. Negative associations existed between MetS, central obesity, high TG, low HDL-C and logS14. Public Library of Science 2019-02-14 /pmc/articles/PMC6375670/ /pubmed/30763384 http://dx.doi.org/10.1371/journal.pone.0212341 Text en © 2019 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chen, Yen-Ting Tseng, Ping-Huei Tseng, Fen-Yu Chi, Yu-Chiao Han, Der-Sheng Yang, Wei-Shiung The serum level of a novel lipogenic protein Spot 14 was reduced in metabolic syndrome |
title | The serum level of a novel lipogenic protein Spot 14 was reduced in metabolic syndrome |
title_full | The serum level of a novel lipogenic protein Spot 14 was reduced in metabolic syndrome |
title_fullStr | The serum level of a novel lipogenic protein Spot 14 was reduced in metabolic syndrome |
title_full_unstemmed | The serum level of a novel lipogenic protein Spot 14 was reduced in metabolic syndrome |
title_short | The serum level of a novel lipogenic protein Spot 14 was reduced in metabolic syndrome |
title_sort | serum level of a novel lipogenic protein spot 14 was reduced in metabolic syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375670/ https://www.ncbi.nlm.nih.gov/pubmed/30763384 http://dx.doi.org/10.1371/journal.pone.0212341 |
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