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Is fibroblast growth factor 23 a new cardiovascular risk marker in gestational diabetes?
OBJECTIVE: This study was designed to compare the serum levels of fibroblast growth factor 23 (FGF23) among patients with gestational diabetes mellitus (GDM) and healthy pregnant women, and to evaluate the association between hormonal and metabolic parameters. SUBJECTS AND METHODS: A total of 82 pre...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Endocrinologia e Metabologia
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522065/ https://www.ncbi.nlm.nih.gov/pubmed/28977159 http://dx.doi.org/10.1590/2359-3997000000287 |
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author | Kizilgul, Muhammed Kan, Seyfullah Beysel, Selvihan Apaydin, Mahmut Ozcelik, Ozgur Caliskan, Mustafa Ozbek, Mustafa Ozdemir, Seyda Cakal, Erman |
author_facet | Kizilgul, Muhammed Kan, Seyfullah Beysel, Selvihan Apaydin, Mahmut Ozcelik, Ozgur Caliskan, Mustafa Ozbek, Mustafa Ozdemir, Seyda Cakal, Erman |
author_sort | Kizilgul, Muhammed |
collection | PubMed |
description | OBJECTIVE: This study was designed to compare the serum levels of fibroblast growth factor 23 (FGF23) among patients with gestational diabetes mellitus (GDM) and healthy pregnant women, and to evaluate the association between hormonal and metabolic parameters. SUBJECTS AND METHODS: A total of 82 pregnant women were consecutively enrolled in the study. Of these, 46 were diagnosed as having GDM; the remaining 36 healthy pregnant women served as controls in a cross-sectional study design. The womens’ ages ranged from 22 to 38 years and gestational ages, from 24 to 28 weeks. Serum samples were analyzed for FGF23 levels using an enzyme-linked immunosorbent assay. RESULTS: Serum FGF23 levels were increased in patients with GDM compared with controls (median, 65.3 for patients with GDM vs. 36.6 ng/mL for healthy controls; p = 0.019). Mean fasting glucose (105.6 ± 7.4 vs. 70.2 ± 7.2 mg/dL, p < 0.001), HbA1c (5.6 ± 0.5 vs. 4.9 ± 0.5%, p < 0.001), insulin (median, 11.1 vs. 8.7 µIU/mL, p = 0.006) and HOMA-IR (3.0 (1.8) vs 1.4 (0.6), p < 0.001) levels were significantly higher in patients with GDM than in controls. Serum FGF23 level was positively correlated with body mass index (r(2) = 0.346, p < 0.05), FPG (r(2) = 0.264, p < 0.05), insulin (r(2) = 0.388, p < 0.05), HOMA-IR (r(2) = 0.384, p < 0.05). CONCLUSION: Serum FGF23 levels were higher in women with GDM compared with controls. The present findings suggest that FGF23 could be a useful marker of cardiovascular disease in GDM. |
format | Online Article Text |
id | pubmed-10522065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Sociedade Brasileira de Endocrinologia e Metabologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-105220652023-09-27 Is fibroblast growth factor 23 a new cardiovascular risk marker in gestational diabetes? Kizilgul, Muhammed Kan, Seyfullah Beysel, Selvihan Apaydin, Mahmut Ozcelik, Ozgur Caliskan, Mustafa Ozbek, Mustafa Ozdemir, Seyda Cakal, Erman Arch Endocrinol Metab Articles OBJECTIVE: This study was designed to compare the serum levels of fibroblast growth factor 23 (FGF23) among patients with gestational diabetes mellitus (GDM) and healthy pregnant women, and to evaluate the association between hormonal and metabolic parameters. SUBJECTS AND METHODS: A total of 82 pregnant women were consecutively enrolled in the study. Of these, 46 were diagnosed as having GDM; the remaining 36 healthy pregnant women served as controls in a cross-sectional study design. The womens’ ages ranged from 22 to 38 years and gestational ages, from 24 to 28 weeks. Serum samples were analyzed for FGF23 levels using an enzyme-linked immunosorbent assay. RESULTS: Serum FGF23 levels were increased in patients with GDM compared with controls (median, 65.3 for patients with GDM vs. 36.6 ng/mL for healthy controls; p = 0.019). Mean fasting glucose (105.6 ± 7.4 vs. 70.2 ± 7.2 mg/dL, p < 0.001), HbA1c (5.6 ± 0.5 vs. 4.9 ± 0.5%, p < 0.001), insulin (median, 11.1 vs. 8.7 µIU/mL, p = 0.006) and HOMA-IR (3.0 (1.8) vs 1.4 (0.6), p < 0.001) levels were significantly higher in patients with GDM than in controls. Serum FGF23 level was positively correlated with body mass index (r(2) = 0.346, p < 0.05), FPG (r(2) = 0.264, p < 0.05), insulin (r(2) = 0.388, p < 0.05), HOMA-IR (r(2) = 0.384, p < 0.05). CONCLUSION: Serum FGF23 levels were higher in women with GDM compared with controls. The present findings suggest that FGF23 could be a useful marker of cardiovascular disease in GDM. Sociedade Brasileira de Endocrinologia e Metabologia 2017-09-04 /pmc/articles/PMC10522065/ /pubmed/28977159 http://dx.doi.org/10.1590/2359-3997000000287 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Kizilgul, Muhammed Kan, Seyfullah Beysel, Selvihan Apaydin, Mahmut Ozcelik, Ozgur Caliskan, Mustafa Ozbek, Mustafa Ozdemir, Seyda Cakal, Erman Is fibroblast growth factor 23 a new cardiovascular risk marker in gestational diabetes? |
title | Is fibroblast growth factor 23 a new cardiovascular risk marker in gestational diabetes? |
title_full | Is fibroblast growth factor 23 a new cardiovascular risk marker in gestational diabetes? |
title_fullStr | Is fibroblast growth factor 23 a new cardiovascular risk marker in gestational diabetes? |
title_full_unstemmed | Is fibroblast growth factor 23 a new cardiovascular risk marker in gestational diabetes? |
title_short | Is fibroblast growth factor 23 a new cardiovascular risk marker in gestational diabetes? |
title_sort | is fibroblast growth factor 23 a new cardiovascular risk marker in gestational diabetes? |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522065/ https://www.ncbi.nlm.nih.gov/pubmed/28977159 http://dx.doi.org/10.1590/2359-3997000000287 |
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