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Relation between abdominal subcutaneous fat tissue thickness and inflammatory markers during pregnancy
INTRODUCTION: Subcutaneous abdominal fat thickness (SCFT) is important for predisposition to metabolic and cardiovascular diseases. Our aim was to evaluate maternal SCFT and metabolic changes (such as insulin resistance and high inflammatory markers) during pregnancy. MATERIAL AND METHODS: A total o...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4175775/ https://www.ncbi.nlm.nih.gov/pubmed/25276159 http://dx.doi.org/10.5114/aoms.2014.44865 |
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author | Köşüş, Nermin Köşüş, Aydın Turhan, Nilgün |
author_facet | Köşüş, Nermin Köşüş, Aydın Turhan, Nilgün |
author_sort | Köşüş, Nermin |
collection | PubMed |
description | INTRODUCTION: Subcutaneous abdominal fat thickness (SCFT) is important for predisposition to metabolic and cardiovascular diseases. Our aim was to evaluate maternal SCFT and metabolic changes (such as insulin resistance and high inflammatory markers) during pregnancy. MATERIAL AND METHODS: A total of 92 pregnant women between 24–28 weeks of gestation were enrolled in the study. The SCFT was measured by ultrasonography and patients were divided into 2 groups according to thickness of maternal SCFT and body mass index (BMI). Groups were compared with each other for oral glucose loading test (OGL) results, and for haematological, biochemical and fetal biometric parameters. RESULTS: After analysis of frequency for SCFT, the most appropriate cut-off value for grouping patients was found to be 15 mm for SCFT. In 48 cases SCFT was over 15 mm. High C reactive protein (CRP) was found in 47.9% (23) of cases with SCFT over 15 mm. Serum haemoglobin A(1c) (HbA(1c)) level was significantly correlated with SCFT thickness. The most important factors for determination of OGL level were found to be serum HbA(1c) level, BMI and SCFT. In obese subjects (BMI ≥ 25 kg/m(2)), levels of inflammatory markers and SCFT thickness were higher. The CRP and γ-glutamyltransferase (GGT) levels were significantly correlated with BMI and SCFT. CONCLUSIONS: High SCFT during pregnancy is associated with elevated inflammatory marker levels and HbA(1c). Pregnant women with thicker SCFT may be susceptible to the development of metabolic complications of pregnancy, such as gestational diabetes mellitus (GDM) and hypertension, as well as risk of future metabolic and cardiovascular disease. |
format | Online Article Text |
id | pubmed-4175775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-41757752014-09-30 Relation between abdominal subcutaneous fat tissue thickness and inflammatory markers during pregnancy Köşüş, Nermin Köşüş, Aydın Turhan, Nilgün Arch Med Sci Clinical Research INTRODUCTION: Subcutaneous abdominal fat thickness (SCFT) is important for predisposition to metabolic and cardiovascular diseases. Our aim was to evaluate maternal SCFT and metabolic changes (such as insulin resistance and high inflammatory markers) during pregnancy. MATERIAL AND METHODS: A total of 92 pregnant women between 24–28 weeks of gestation were enrolled in the study. The SCFT was measured by ultrasonography and patients were divided into 2 groups according to thickness of maternal SCFT and body mass index (BMI). Groups were compared with each other for oral glucose loading test (OGL) results, and for haematological, biochemical and fetal biometric parameters. RESULTS: After analysis of frequency for SCFT, the most appropriate cut-off value for grouping patients was found to be 15 mm for SCFT. In 48 cases SCFT was over 15 mm. High C reactive protein (CRP) was found in 47.9% (23) of cases with SCFT over 15 mm. Serum haemoglobin A(1c) (HbA(1c)) level was significantly correlated with SCFT thickness. The most important factors for determination of OGL level were found to be serum HbA(1c) level, BMI and SCFT. In obese subjects (BMI ≥ 25 kg/m(2)), levels of inflammatory markers and SCFT thickness were higher. The CRP and γ-glutamyltransferase (GGT) levels were significantly correlated with BMI and SCFT. CONCLUSIONS: High SCFT during pregnancy is associated with elevated inflammatory marker levels and HbA(1c). Pregnant women with thicker SCFT may be susceptible to the development of metabolic complications of pregnancy, such as gestational diabetes mellitus (GDM) and hypertension, as well as risk of future metabolic and cardiovascular disease. Termedia Publishing House 2014-08-29 2014-08-29 /pmc/articles/PMC4175775/ /pubmed/25276159 http://dx.doi.org/10.5114/aoms.2014.44865 Text en Copyright © 2014 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Research Köşüş, Nermin Köşüş, Aydın Turhan, Nilgün Relation between abdominal subcutaneous fat tissue thickness and inflammatory markers during pregnancy |
title | Relation between abdominal subcutaneous fat tissue thickness and inflammatory markers during pregnancy |
title_full | Relation between abdominal subcutaneous fat tissue thickness and inflammatory markers during pregnancy |
title_fullStr | Relation between abdominal subcutaneous fat tissue thickness and inflammatory markers during pregnancy |
title_full_unstemmed | Relation between abdominal subcutaneous fat tissue thickness and inflammatory markers during pregnancy |
title_short | Relation between abdominal subcutaneous fat tissue thickness and inflammatory markers during pregnancy |
title_sort | relation between abdominal subcutaneous fat tissue thickness and inflammatory markers during pregnancy |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4175775/ https://www.ncbi.nlm.nih.gov/pubmed/25276159 http://dx.doi.org/10.5114/aoms.2014.44865 |
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