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Hyperinsulinemia: an early biomarker of metabolic dysfunction
INTRODUCTION: Hyperinsulinemia in the absence of impaired glucose tolerance and normal HbA1c is considered indicative of pre-diabetes. Very few Indian studies have focused on hyperinsulinemia particularly in young adults. The present study aimed to determine whether hyperinsulinemia may be present d...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186728/ https://www.ncbi.nlm.nih.gov/pubmed/37200851 http://dx.doi.org/10.3389/fcdhc.2023.1159664 |
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author | Vaidya, Rama A. Desai, Sharvari Moitra, Panchali Salis, Sheryl Agashe, Shubhada Battalwar, Rekha Mehta, Anushree Madan, Jagmeet Kalita, Soumik Udipi, Shobha A. Vaidya, Ashok B. |
author_facet | Vaidya, Rama A. Desai, Sharvari Moitra, Panchali Salis, Sheryl Agashe, Shubhada Battalwar, Rekha Mehta, Anushree Madan, Jagmeet Kalita, Soumik Udipi, Shobha A. Vaidya, Ashok B. |
author_sort | Vaidya, Rama A. |
collection | PubMed |
description | INTRODUCTION: Hyperinsulinemia in the absence of impaired glucose tolerance and normal HbA1c is considered indicative of pre-diabetes. Very few Indian studies have focused on hyperinsulinemia particularly in young adults. The present study aimed to determine whether hyperinsulinemia may be present despite HbA1c being normal. METHODS: This was a cross–sectional study conducted on adolescents and young adults aged 16-25 years living in Mumbai, India. The participants attended various academic institutions and were those who underwent screening as the first step of a clinical trial for studying the efficacy of almond intake in prediabetes. RESULTS: Among this young population (n=1313), 4.2% (n=55) of the participants were found to be prediabetic (ADA criteria) and 19.7% of them had HbA1c levels between 5.7%-6.4%. However, almost, 30.5% had hyperinsulinemia inspite of normal blood glucose levels and normal HbA1c. Among those with HbA1c<5.7 (n=533), 10.5% (n=56) participants had fasting insulin>15 mIU/L and a higher percentage (39.4%, n=260) had stimulated insulin above 80 mIU/L. These participants had higher mean anthropometric markers than those with normal fasting and/or stimulated insulin. CONCLUSION: Hyperinsulinaemia in the absence of impaired glucose tolerance and normal HbA1c may provide a much earlier indicator of detection for risk of metabolic disease and progression to metabolic syndrome and diabetes mellitus. |
format | Online Article Text |
id | pubmed-10186728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101867282023-05-17 Hyperinsulinemia: an early biomarker of metabolic dysfunction Vaidya, Rama A. Desai, Sharvari Moitra, Panchali Salis, Sheryl Agashe, Shubhada Battalwar, Rekha Mehta, Anushree Madan, Jagmeet Kalita, Soumik Udipi, Shobha A. Vaidya, Ashok B. Front Clin Diabetes Healthc Clinical Diabetes and Healthcare INTRODUCTION: Hyperinsulinemia in the absence of impaired glucose tolerance and normal HbA1c is considered indicative of pre-diabetes. Very few Indian studies have focused on hyperinsulinemia particularly in young adults. The present study aimed to determine whether hyperinsulinemia may be present despite HbA1c being normal. METHODS: This was a cross–sectional study conducted on adolescents and young adults aged 16-25 years living in Mumbai, India. The participants attended various academic institutions and were those who underwent screening as the first step of a clinical trial for studying the efficacy of almond intake in prediabetes. RESULTS: Among this young population (n=1313), 4.2% (n=55) of the participants were found to be prediabetic (ADA criteria) and 19.7% of them had HbA1c levels between 5.7%-6.4%. However, almost, 30.5% had hyperinsulinemia inspite of normal blood glucose levels and normal HbA1c. Among those with HbA1c<5.7 (n=533), 10.5% (n=56) participants had fasting insulin>15 mIU/L and a higher percentage (39.4%, n=260) had stimulated insulin above 80 mIU/L. These participants had higher mean anthropometric markers than those with normal fasting and/or stimulated insulin. CONCLUSION: Hyperinsulinaemia in the absence of impaired glucose tolerance and normal HbA1c may provide a much earlier indicator of detection for risk of metabolic disease and progression to metabolic syndrome and diabetes mellitus. Frontiers Media S.A. 2023-05-02 /pmc/articles/PMC10186728/ /pubmed/37200851 http://dx.doi.org/10.3389/fcdhc.2023.1159664 Text en Copyright © 2023 Vaidya, Desai, Moitra, Salis, Agashe, Battalwar, Mehta, Madan, Kalita, Udipi and Vaidya https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Clinical Diabetes and Healthcare Vaidya, Rama A. Desai, Sharvari Moitra, Panchali Salis, Sheryl Agashe, Shubhada Battalwar, Rekha Mehta, Anushree Madan, Jagmeet Kalita, Soumik Udipi, Shobha A. Vaidya, Ashok B. Hyperinsulinemia: an early biomarker of metabolic dysfunction |
title | Hyperinsulinemia: an early biomarker of metabolic dysfunction |
title_full | Hyperinsulinemia: an early biomarker of metabolic dysfunction |
title_fullStr | Hyperinsulinemia: an early biomarker of metabolic dysfunction |
title_full_unstemmed | Hyperinsulinemia: an early biomarker of metabolic dysfunction |
title_short | Hyperinsulinemia: an early biomarker of metabolic dysfunction |
title_sort | hyperinsulinemia: an early biomarker of metabolic dysfunction |
topic | Clinical Diabetes and Healthcare |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186728/ https://www.ncbi.nlm.nih.gov/pubmed/37200851 http://dx.doi.org/10.3389/fcdhc.2023.1159664 |
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