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Racial and Ethnic Differences in Metabolic Disease in Adolescents With Obesity and Polycystic Ovary Syndrome

CONTEXT: Polycystic ovary syndrome (PCOS) is common and associated with metabolic syndrome. In the general population, metabolic disease varies by race and ethnicity. OBJECTIVE: This work aimed to examine in depth the interaction of race and ethnicity with PCOS-related metabolic disease in adolescen...

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Autores principales: Andrisse, Stanley, Garcia-Reyes, Yesenia, Pyle, Laura, Kelsey, Megan M, Nadeau, Kristen J, Cree-Green, Melanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896356/
https://www.ncbi.nlm.nih.gov/pubmed/33644620
http://dx.doi.org/10.1210/jendso/bvab008
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author Andrisse, Stanley
Garcia-Reyes, Yesenia
Pyle, Laura
Kelsey, Megan M
Nadeau, Kristen J
Cree-Green, Melanie
author_facet Andrisse, Stanley
Garcia-Reyes, Yesenia
Pyle, Laura
Kelsey, Megan M
Nadeau, Kristen J
Cree-Green, Melanie
author_sort Andrisse, Stanley
collection PubMed
description CONTEXT: Polycystic ovary syndrome (PCOS) is common and associated with metabolic syndrome. In the general population, metabolic disease varies by race and ethnicity. OBJECTIVE: This work aimed to examine in depth the interaction of race and ethnicity with PCOS-related metabolic disease in adolescent youth. METHODS: A secondary analysis was conducted of data from girls (age 12-21 years) with overweight or obesity (> 90 body mass index [BMI] percentile) and PCOS. Measurements included fasting hormone and metabolic measures, a 2-hour oral glucose tolerance test (OGTT), and magnetic resonance imaging for hepatic fat. Groups were categorized by race or ethnicity. RESULTS: Participants included 39 non-Hispanic White (NHW, age 15.7 ± 0.2 years; BMI 97.7 ± 0.2 percentile), 50 Hispanic (HW, 15.2 ± 0.3 years; 97.9 ± 0.3 percentile), and 12 non-Hispanic Black (NHB, 16.0 ± 0.6 years; 98.6 ± 0.4 percentile) adolescents. Hepatic markers of insulin resistance were worse in NHW, including lower sex hormone–binding globulin and higher triglycerides over high-density lipoprotein cholesterol (TGs/HDL-C) ratio (P = .002 overall, HW vs NHB [P = .009] vs NHW [P = 0.020]), although homeostasis model assessment of estimated insulin resistance was worst in NHB (P = .010 overall, NHW vs NHB P = .014). Fasting and 2-hour OGTT glucose were not different between groups, although glycated hemoglobin A(1c) (HbA(1c)) was lowest in NHW (overall P < .001, NHW 5.2 ± 0.3 vs HW 5.5 ± 0.3 P < .001 vs 5.7 ± 0.4%, P < .001). The frequency of hepatic steatosis (HW 62%, NHW 42%, NHB 25%, P = .032); low HDL-C < 40 mg/dL (HW 82%, NHW 61%, NHB 50%, P < .001) and prediabetes HbA(1c) 5.7% to 6.4% (NHB 50%, HW 36%, NHW 5%, P < .001) were different between the groups. CONCLUSION: Adolescents with PCOS appear to show similar racial and ethnic variation to the general population in terms of metabolic disease components.
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spelling pubmed-78963562021-02-25 Racial and Ethnic Differences in Metabolic Disease in Adolescents With Obesity and Polycystic Ovary Syndrome Andrisse, Stanley Garcia-Reyes, Yesenia Pyle, Laura Kelsey, Megan M Nadeau, Kristen J Cree-Green, Melanie J Endocr Soc Clinical Research Articles CONTEXT: Polycystic ovary syndrome (PCOS) is common and associated with metabolic syndrome. In the general population, metabolic disease varies by race and ethnicity. OBJECTIVE: This work aimed to examine in depth the interaction of race and ethnicity with PCOS-related metabolic disease in adolescent youth. METHODS: A secondary analysis was conducted of data from girls (age 12-21 years) with overweight or obesity (> 90 body mass index [BMI] percentile) and PCOS. Measurements included fasting hormone and metabolic measures, a 2-hour oral glucose tolerance test (OGTT), and magnetic resonance imaging for hepatic fat. Groups were categorized by race or ethnicity. RESULTS: Participants included 39 non-Hispanic White (NHW, age 15.7 ± 0.2 years; BMI 97.7 ± 0.2 percentile), 50 Hispanic (HW, 15.2 ± 0.3 years; 97.9 ± 0.3 percentile), and 12 non-Hispanic Black (NHB, 16.0 ± 0.6 years; 98.6 ± 0.4 percentile) adolescents. Hepatic markers of insulin resistance were worse in NHW, including lower sex hormone–binding globulin and higher triglycerides over high-density lipoprotein cholesterol (TGs/HDL-C) ratio (P = .002 overall, HW vs NHB [P = .009] vs NHW [P = 0.020]), although homeostasis model assessment of estimated insulin resistance was worst in NHB (P = .010 overall, NHW vs NHB P = .014). Fasting and 2-hour OGTT glucose were not different between groups, although glycated hemoglobin A(1c) (HbA(1c)) was lowest in NHW (overall P < .001, NHW 5.2 ± 0.3 vs HW 5.5 ± 0.3 P < .001 vs 5.7 ± 0.4%, P < .001). The frequency of hepatic steatosis (HW 62%, NHW 42%, NHB 25%, P = .032); low HDL-C < 40 mg/dL (HW 82%, NHW 61%, NHB 50%, P < .001) and prediabetes HbA(1c) 5.7% to 6.4% (NHB 50%, HW 36%, NHW 5%, P < .001) were different between the groups. CONCLUSION: Adolescents with PCOS appear to show similar racial and ethnic variation to the general population in terms of metabolic disease components. Oxford University Press 2021-02-02 /pmc/articles/PMC7896356/ /pubmed/33644620 http://dx.doi.org/10.1210/jendso/bvab008 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Research Articles
Andrisse, Stanley
Garcia-Reyes, Yesenia
Pyle, Laura
Kelsey, Megan M
Nadeau, Kristen J
Cree-Green, Melanie
Racial and Ethnic Differences in Metabolic Disease in Adolescents With Obesity and Polycystic Ovary Syndrome
title Racial and Ethnic Differences in Metabolic Disease in Adolescents With Obesity and Polycystic Ovary Syndrome
title_full Racial and Ethnic Differences in Metabolic Disease in Adolescents With Obesity and Polycystic Ovary Syndrome
title_fullStr Racial and Ethnic Differences in Metabolic Disease in Adolescents With Obesity and Polycystic Ovary Syndrome
title_full_unstemmed Racial and Ethnic Differences in Metabolic Disease in Adolescents With Obesity and Polycystic Ovary Syndrome
title_short Racial and Ethnic Differences in Metabolic Disease in Adolescents With Obesity and Polycystic Ovary Syndrome
title_sort racial and ethnic differences in metabolic disease in adolescents with obesity and polycystic ovary syndrome
topic Clinical Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896356/
https://www.ncbi.nlm.nih.gov/pubmed/33644620
http://dx.doi.org/10.1210/jendso/bvab008
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