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C1q/TNF-Related Protein5 (CTRP5) as a Biomarker to Predict Metabolic Syndrome and Each of Its Components

OBJECTIVE: C1q/TNF-related protein5 (CTRP5) is a member of the C1q/tumor necrosis factor α- (TNF-α-) related protein family and has been reported to be associated with the regulation of glucose and lipid metabolism. However, the clinical association between CTRP5 and metabolic syndrome (MetS) has no...

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Autores principales: Jiang, Feiyu, Yang, Min, Zhao, Xili, Liu, Rui, Yang, Gangyi, Liu, Dongfang, Liu, Hua, Zheng, Hongting, Zhu, Zhiming, Li, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282127/
https://www.ncbi.nlm.nih.gov/pubmed/30595692
http://dx.doi.org/10.1155/2018/7201473
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author Jiang, Feiyu
Yang, Min
Zhao, Xili
Liu, Rui
Yang, Gangyi
Liu, Dongfang
Liu, Hua
Zheng, Hongting
Zhu, Zhiming
Li, Ling
author_facet Jiang, Feiyu
Yang, Min
Zhao, Xili
Liu, Rui
Yang, Gangyi
Liu, Dongfang
Liu, Hua
Zheng, Hongting
Zhu, Zhiming
Li, Ling
author_sort Jiang, Feiyu
collection PubMed
description OBJECTIVE: C1q/TNF-related protein5 (CTRP5) is a member of the C1q/tumor necrosis factor α- (TNF-α-) related protein family and has been reported to be associated with the regulation of glucose and lipid metabolism. However, the clinical association between CTRP5 and metabolic syndrome (MetS) has not been reported. The aim of the current study is to investigate the association between CTRP5 and MetS by a cross-sectional study. METHODS: We performed a cross-sectional study in a Chinese population including 89 controls and 88 MetS individuals. Serum CTRP5 concentrations were determined by ELISA. The relationship between circulating CTRP5 and MetS and insulin resistance (IR) was assessed by Spearman's correlation and multiple stepwise regression analysis. RESULTS: Circulating CTRP5 concentrations were markedly decreased in MetS individuals relative to normal adults. Overweight/obese individuals (BMI ≥ 25 kg/m(2)) showed a lower serum CTRP5 level than lean subjects (BMI < 25 kg/m(2)) in the study population (124.1 (99.12–147.37) vs. 103.9 (79.15–124.25) μg/L; P < 0.01). Circulating CTRP5 was found to be correlated negatively with BMI, FAT%, FBG, WHR, SBP, HbA1c, TG, 2-hour blood glucose after glucose overload (2-hOGTT), FIns, and HOMA-IR and positively with HDL-C (P < 0.05 or P < 0.01). Binary logistic regression revealed that serum CTRP5 levels were associated with MetS. In addition, serum CTRP5 levels gradually decreased with the increase in MetS components. CONCLUSIONS: Circulating CTRP5 is relative to the elevated risk of MetS in humans and may be in part through the effect of insulin resistance. This trial is registered with ChiCTR-OCS-13003185.
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spelling pubmed-62821272018-12-30 C1q/TNF-Related Protein5 (CTRP5) as a Biomarker to Predict Metabolic Syndrome and Each of Its Components Jiang, Feiyu Yang, Min Zhao, Xili Liu, Rui Yang, Gangyi Liu, Dongfang Liu, Hua Zheng, Hongting Zhu, Zhiming Li, Ling Int J Endocrinol Research Article OBJECTIVE: C1q/TNF-related protein5 (CTRP5) is a member of the C1q/tumor necrosis factor α- (TNF-α-) related protein family and has been reported to be associated with the regulation of glucose and lipid metabolism. However, the clinical association between CTRP5 and metabolic syndrome (MetS) has not been reported. The aim of the current study is to investigate the association between CTRP5 and MetS by a cross-sectional study. METHODS: We performed a cross-sectional study in a Chinese population including 89 controls and 88 MetS individuals. Serum CTRP5 concentrations were determined by ELISA. The relationship between circulating CTRP5 and MetS and insulin resistance (IR) was assessed by Spearman's correlation and multiple stepwise regression analysis. RESULTS: Circulating CTRP5 concentrations were markedly decreased in MetS individuals relative to normal adults. Overweight/obese individuals (BMI ≥ 25 kg/m(2)) showed a lower serum CTRP5 level than lean subjects (BMI < 25 kg/m(2)) in the study population (124.1 (99.12–147.37) vs. 103.9 (79.15–124.25) μg/L; P < 0.01). Circulating CTRP5 was found to be correlated negatively with BMI, FAT%, FBG, WHR, SBP, HbA1c, TG, 2-hour blood glucose after glucose overload (2-hOGTT), FIns, and HOMA-IR and positively with HDL-C (P < 0.05 or P < 0.01). Binary logistic regression revealed that serum CTRP5 levels were associated with MetS. In addition, serum CTRP5 levels gradually decreased with the increase in MetS components. CONCLUSIONS: Circulating CTRP5 is relative to the elevated risk of MetS in humans and may be in part through the effect of insulin resistance. This trial is registered with ChiCTR-OCS-13003185. Hindawi 2018-11-22 /pmc/articles/PMC6282127/ /pubmed/30595692 http://dx.doi.org/10.1155/2018/7201473 Text en Copyright © 2018 Feiyu Jiang et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jiang, Feiyu
Yang, Min
Zhao, Xili
Liu, Rui
Yang, Gangyi
Liu, Dongfang
Liu, Hua
Zheng, Hongting
Zhu, Zhiming
Li, Ling
C1q/TNF-Related Protein5 (CTRP5) as a Biomarker to Predict Metabolic Syndrome and Each of Its Components
title C1q/TNF-Related Protein5 (CTRP5) as a Biomarker to Predict Metabolic Syndrome and Each of Its Components
title_full C1q/TNF-Related Protein5 (CTRP5) as a Biomarker to Predict Metabolic Syndrome and Each of Its Components
title_fullStr C1q/TNF-Related Protein5 (CTRP5) as a Biomarker to Predict Metabolic Syndrome and Each of Its Components
title_full_unstemmed C1q/TNF-Related Protein5 (CTRP5) as a Biomarker to Predict Metabolic Syndrome and Each of Its Components
title_short C1q/TNF-Related Protein5 (CTRP5) as a Biomarker to Predict Metabolic Syndrome and Each of Its Components
title_sort c1q/tnf-related protein5 (ctrp5) as a biomarker to predict metabolic syndrome and each of its components
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282127/
https://www.ncbi.nlm.nih.gov/pubmed/30595692
http://dx.doi.org/10.1155/2018/7201473
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