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GDF15 Is a Novel Biomarker for Impaired Fasting Glucose
BACKGROUND: Growth differentiation factor-15 (GDF15) is a protein that belongs to the transforming growth factor β superfamily. An elevated serum level of GDF15 was found to be associated with type 2 diabetes mellitus (T2DM). T2DM is an inflammatory disease that progresses from normal glucose tolera...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Diabetes Association
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273034/ https://www.ncbi.nlm.nih.gov/pubmed/25541611 http://dx.doi.org/10.4093/dmj.2014.38.6.472 |
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author | Hong, Jun Hwa Chung, Hyo Kyun Park, Hye Yoon Joung, Kyong-Hye Lee, Ju Hee Jung, Jin Gyu Kim, Koon Soon Kim, Hyun Jin Ku, Bon Jeong Shong, Minho |
author_facet | Hong, Jun Hwa Chung, Hyo Kyun Park, Hye Yoon Joung, Kyong-Hye Lee, Ju Hee Jung, Jin Gyu Kim, Koon Soon Kim, Hyun Jin Ku, Bon Jeong Shong, Minho |
author_sort | Hong, Jun Hwa |
collection | PubMed |
description | BACKGROUND: Growth differentiation factor-15 (GDF15) is a protein that belongs to the transforming growth factor β superfamily. An elevated serum level of GDF15 was found to be associated with type 2 diabetes mellitus (T2DM). T2DM is an inflammatory disease that progresses from normal glucose tolerance (NGT) to impaired fasting glucose (IFG). Hence, we aimed to validate the relationship between GDF15 and IFG. METHODS: The participants were divided into the following three groups: NGT (n=137), IFG (n=29), and T2DM (n=75). The controls and T2DM outpatients visited the hospital for routine health check-ups. We used fasting blood glucose to detect IFG in nondiabetic patients. We checked the body mass index (BMI), C-reactive protein level, metabolic parameters, and fasting serum GDF15 level. RESULTS: Age, BMI, triglyceride, insulin, glucose, homeostatic model assessment-insulin resistance (HOMA-IR), and GDF15 levels were elevated in the IFG and T2DM groups compared to the NGT group. In the correlation analysis between metabolic parameters and GDF15, age and HOMA-IR had a significant positive correlation with GDF15 levels. GDF15 significantly discriminated between IFG and NGT, independent of age, BMI, and HOMA-IR. The serum levels of GDF15 were more elevated in men than in women. As a biomarker for IFG based on the receiver operating characteristic curve analysis, the cutoff value of GDF15 was 510 pg/mL in males and 400 pg/mL in females. CONCLUSION: GDF15 had a positive correlation with IR independent of age and BMI, and the serum level of GDF15 was increased in the IFG and T2DM groups. GDF15 may be a novel biomarker for detecting IFG in nondiabetic patients. |
format | Online Article Text |
id | pubmed-4273034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Korean Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-42730342014-12-25 GDF15 Is a Novel Biomarker for Impaired Fasting Glucose Hong, Jun Hwa Chung, Hyo Kyun Park, Hye Yoon Joung, Kyong-Hye Lee, Ju Hee Jung, Jin Gyu Kim, Koon Soon Kim, Hyun Jin Ku, Bon Jeong Shong, Minho Diabetes Metab J Original Article BACKGROUND: Growth differentiation factor-15 (GDF15) is a protein that belongs to the transforming growth factor β superfamily. An elevated serum level of GDF15 was found to be associated with type 2 diabetes mellitus (T2DM). T2DM is an inflammatory disease that progresses from normal glucose tolerance (NGT) to impaired fasting glucose (IFG). Hence, we aimed to validate the relationship between GDF15 and IFG. METHODS: The participants were divided into the following three groups: NGT (n=137), IFG (n=29), and T2DM (n=75). The controls and T2DM outpatients visited the hospital for routine health check-ups. We used fasting blood glucose to detect IFG in nondiabetic patients. We checked the body mass index (BMI), C-reactive protein level, metabolic parameters, and fasting serum GDF15 level. RESULTS: Age, BMI, triglyceride, insulin, glucose, homeostatic model assessment-insulin resistance (HOMA-IR), and GDF15 levels were elevated in the IFG and T2DM groups compared to the NGT group. In the correlation analysis between metabolic parameters and GDF15, age and HOMA-IR had a significant positive correlation with GDF15 levels. GDF15 significantly discriminated between IFG and NGT, independent of age, BMI, and HOMA-IR. The serum levels of GDF15 were more elevated in men than in women. As a biomarker for IFG based on the receiver operating characteristic curve analysis, the cutoff value of GDF15 was 510 pg/mL in males and 400 pg/mL in females. CONCLUSION: GDF15 had a positive correlation with IR independent of age and BMI, and the serum level of GDF15 was increased in the IFG and T2DM groups. GDF15 may be a novel biomarker for detecting IFG in nondiabetic patients. Korean Diabetes Association 2014-12 2014-12-15 /pmc/articles/PMC4273034/ /pubmed/25541611 http://dx.doi.org/10.4093/dmj.2014.38.6.472 Text en Copyright © 2014 Korean Diabetes Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hong, Jun Hwa Chung, Hyo Kyun Park, Hye Yoon Joung, Kyong-Hye Lee, Ju Hee Jung, Jin Gyu Kim, Koon Soon Kim, Hyun Jin Ku, Bon Jeong Shong, Minho GDF15 Is a Novel Biomarker for Impaired Fasting Glucose |
title | GDF15 Is a Novel Biomarker for Impaired Fasting Glucose |
title_full | GDF15 Is a Novel Biomarker for Impaired Fasting Glucose |
title_fullStr | GDF15 Is a Novel Biomarker for Impaired Fasting Glucose |
title_full_unstemmed | GDF15 Is a Novel Biomarker for Impaired Fasting Glucose |
title_short | GDF15 Is a Novel Biomarker for Impaired Fasting Glucose |
title_sort | gdf15 is a novel biomarker for impaired fasting glucose |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273034/ https://www.ncbi.nlm.nih.gov/pubmed/25541611 http://dx.doi.org/10.4093/dmj.2014.38.6.472 |
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