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Endocrine Disruptors and Polycystic Ovary Syndrome: Phthalates
OBJECTIVE: We aimed to investigate a possible role of the endocrine disruptors phthalates, di-2-ethylhexyl phthalate (DEHP) and mono (2-ethylhexyl) phthalate (MEHP), in polycystic ovary syndrome (PCOS) aetiopathogenesis. We also wished to evaluate the relationship between phthalates and metabolic di...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711640/ https://www.ncbi.nlm.nih.gov/pubmed/32431137 http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0037 |
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author | Akın, Leyla Kendirci, Mustafa Narin, Figen Kurtoglu, Selim Hatipoglu, Nihal Elmalı, Ferhan |
author_facet | Akın, Leyla Kendirci, Mustafa Narin, Figen Kurtoglu, Selim Hatipoglu, Nihal Elmalı, Ferhan |
author_sort | Akın, Leyla |
collection | PubMed |
description | OBJECTIVE: We aimed to investigate a possible role of the endocrine disruptors phthalates, di-2-ethylhexyl phthalate (DEHP) and mono (2-ethylhexyl) phthalate (MEHP), in polycystic ovary syndrome (PCOS) aetiopathogenesis. We also wished to evaluate the relationship between phthalates and metabolic disturbances in adolescents with PCOS. METHODS: A total of 124 adolescents were included. Serum MEHP and DEHP levels were determined by high-performance liquid chromatography. Insulin resistance was evaluated using homeostasis model assessment-insulin resistance, quantitative Insulin Sensitivity Check Index, fasting glucose/insulin ratio, Matsuda index, and total insulin levels during oral glucose tolerance test. Participants were further subdivided into lean and obese subgroups according to body mass index (BMI). RESULTS: Sixty-three PCOS and 61 controls, (mean age 15.2±1.5; range: 13-19 years) were enrolled. Serum DEHP and MEHP concentrations were not significantly different between PCOS and control groups. The mean (95% confidence interval) values of DEHP and MEHP were 2.62 (2.50-2.75) μg/mL vs 2.71 (2.52-2.90) μg/mL and 0.23 (0.19-0.29) μg/mL vs 0.36 (0.18-0.54) μg/mL in PCOS and the control groups respectively, p>0.05. Correlation analysis, adjusted for BMI, showed that both phthalates significantly correlated with insulin resistance indices and serum triglycerides in adolescents with PCOS. CONCLUSION: Serum DEHP and MEHP concentrations were not different between adolescents with or without PCOS. However, these phthalates are associated with metabolic disturbances such as dyslipidemia and insulin resistance, independently of obesity, in girls with PCOS. |
format | Online Article Text |
id | pubmed-7711640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Galenos Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-77116402020-12-08 Endocrine Disruptors and Polycystic Ovary Syndrome: Phthalates Akın, Leyla Kendirci, Mustafa Narin, Figen Kurtoglu, Selim Hatipoglu, Nihal Elmalı, Ferhan J Clin Res Pediatr Endocrinol Original Article OBJECTIVE: We aimed to investigate a possible role of the endocrine disruptors phthalates, di-2-ethylhexyl phthalate (DEHP) and mono (2-ethylhexyl) phthalate (MEHP), in polycystic ovary syndrome (PCOS) aetiopathogenesis. We also wished to evaluate the relationship between phthalates and metabolic disturbances in adolescents with PCOS. METHODS: A total of 124 adolescents were included. Serum MEHP and DEHP levels were determined by high-performance liquid chromatography. Insulin resistance was evaluated using homeostasis model assessment-insulin resistance, quantitative Insulin Sensitivity Check Index, fasting glucose/insulin ratio, Matsuda index, and total insulin levels during oral glucose tolerance test. Participants were further subdivided into lean and obese subgroups according to body mass index (BMI). RESULTS: Sixty-three PCOS and 61 controls, (mean age 15.2±1.5; range: 13-19 years) were enrolled. Serum DEHP and MEHP concentrations were not significantly different between PCOS and control groups. The mean (95% confidence interval) values of DEHP and MEHP were 2.62 (2.50-2.75) μg/mL vs 2.71 (2.52-2.90) μg/mL and 0.23 (0.19-0.29) μg/mL vs 0.36 (0.18-0.54) μg/mL in PCOS and the control groups respectively, p>0.05. Correlation analysis, adjusted for BMI, showed that both phthalates significantly correlated with insulin resistance indices and serum triglycerides in adolescents with PCOS. CONCLUSION: Serum DEHP and MEHP concentrations were not different between adolescents with or without PCOS. However, these phthalates are associated with metabolic disturbances such as dyslipidemia and insulin resistance, independently of obesity, in girls with PCOS. Galenos Publishing 2020-12 2020-11-25 /pmc/articles/PMC7711640/ /pubmed/32431137 http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0037 Text en ©Copyright 2020 by Turkish Pediatric Endocrinology and Diabetes Society | The Journal of Clinical Research in Pediatric Endocrinology published by Galenos Publishing House. http://creativecommons.org/licenses/by/2.5/ 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 | Original Article Akın, Leyla Kendirci, Mustafa Narin, Figen Kurtoglu, Selim Hatipoglu, Nihal Elmalı, Ferhan Endocrine Disruptors and Polycystic Ovary Syndrome: Phthalates |
title | Endocrine Disruptors and Polycystic Ovary Syndrome: Phthalates |
title_full | Endocrine Disruptors and Polycystic Ovary Syndrome: Phthalates |
title_fullStr | Endocrine Disruptors and Polycystic Ovary Syndrome: Phthalates |
title_full_unstemmed | Endocrine Disruptors and Polycystic Ovary Syndrome: Phthalates |
title_short | Endocrine Disruptors and Polycystic Ovary Syndrome: Phthalates |
title_sort | endocrine disruptors and polycystic ovary syndrome: phthalates |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711640/ https://www.ncbi.nlm.nih.gov/pubmed/32431137 http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0037 |
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