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Acanthosis Nigricans as a Clinical Predictor of Insulin Resistance in Obese Children
PURPOSE: This study aimed to evaluate the utility of acanthosis nigricans (AN) severity as an index for predicting insulin resistance in obese children. METHODS: The subjects comprised 74 obese pediatric patients who attended the Department of Pediatrics at Chosun University Hospital between January...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234421/ https://www.ncbi.nlm.nih.gov/pubmed/28090470 http://dx.doi.org/10.5223/pghn.2016.19.4.251 |
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author | Koh, Young Kwon Lee, Jae Hee Kim, Eun Young Moon, Kyung Rye |
author_facet | Koh, Young Kwon Lee, Jae Hee Kim, Eun Young Moon, Kyung Rye |
author_sort | Koh, Young Kwon |
collection | PubMed |
description | PURPOSE: This study aimed to evaluate the utility of acanthosis nigricans (AN) severity as an index for predicting insulin resistance in obese children. METHODS: The subjects comprised 74 obese pediatric patients who attended the Department of Pediatrics at Chosun University Hospital between January 2013 and March 2016. Waist circumference; body mass index; blood pressure; fasting glucose and fasting insulin levels; lipid profile; aspartate transaminase, alanine transaminase, glycated hemoglobin, C-peptide, and uric acid levels; and homeostatic model assessment insulin resistance (HOMA-IR) and quantitative insulin check sensitivity index (QUICKI) scores were compared between subjects with AN and those without AN. Receiver operating characteristic curves were used to investigate the utility of the AN score in predicting insulin resistance. HOMA-IR and QUICKI were compared according to AN severity. RESULTS: The With AN group had higher fasting insulin levels (24.1±21.0 mU/L vs. 9.8±3.6 mU/L, p<0.001) and HOMA-IR score (5.74±4.71 vs. 2.14±0.86, p<0.001) than the Without AN group. The AN score used to predict insulin resistance was 3 points or more (sensitivity 56.8%, specificity 83.9%). HOMA-IR scores increased with AN severity, from the Without AN group (mean, 2.15; 95% confidence interval [CI], 1.72-2.57) to the Mild AN (mean, 4.15; 95% CI, 3.04-5.25) and Severe AN groups (mean, 7.22; 95% CI, 5.08-9.35; p<0.001). CONCLUSION: Insulin resistance worsens with increasing AN severity, and patients with Severe AN (AN score ≥3) are at increased risk of insulin resistance. |
format | Online Article Text |
id | pubmed-5234421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition |
record_format | MEDLINE/PubMed |
spelling | pubmed-52344212017-01-13 Acanthosis Nigricans as a Clinical Predictor of Insulin Resistance in Obese Children Koh, Young Kwon Lee, Jae Hee Kim, Eun Young Moon, Kyung Rye Pediatr Gastroenterol Hepatol Nutr Original Article PURPOSE: This study aimed to evaluate the utility of acanthosis nigricans (AN) severity as an index for predicting insulin resistance in obese children. METHODS: The subjects comprised 74 obese pediatric patients who attended the Department of Pediatrics at Chosun University Hospital between January 2013 and March 2016. Waist circumference; body mass index; blood pressure; fasting glucose and fasting insulin levels; lipid profile; aspartate transaminase, alanine transaminase, glycated hemoglobin, C-peptide, and uric acid levels; and homeostatic model assessment insulin resistance (HOMA-IR) and quantitative insulin check sensitivity index (QUICKI) scores were compared between subjects with AN and those without AN. Receiver operating characteristic curves were used to investigate the utility of the AN score in predicting insulin resistance. HOMA-IR and QUICKI were compared according to AN severity. RESULTS: The With AN group had higher fasting insulin levels (24.1±21.0 mU/L vs. 9.8±3.6 mU/L, p<0.001) and HOMA-IR score (5.74±4.71 vs. 2.14±0.86, p<0.001) than the Without AN group. The AN score used to predict insulin resistance was 3 points or more (sensitivity 56.8%, specificity 83.9%). HOMA-IR scores increased with AN severity, from the Without AN group (mean, 2.15; 95% confidence interval [CI], 1.72-2.57) to the Mild AN (mean, 4.15; 95% CI, 3.04-5.25) and Severe AN groups (mean, 7.22; 95% CI, 5.08-9.35; p<0.001). CONCLUSION: Insulin resistance worsens with increasing AN severity, and patients with Severe AN (AN score ≥3) are at increased risk of insulin resistance. The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2016-12 2016-12-28 /pmc/articles/PMC5234421/ /pubmed/28090470 http://dx.doi.org/10.5223/pghn.2016.19.4.251 Text en Copyright © 2016 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Koh, Young Kwon Lee, Jae Hee Kim, Eun Young Moon, Kyung Rye Acanthosis Nigricans as a Clinical Predictor of Insulin Resistance in Obese Children |
title | Acanthosis Nigricans as a Clinical Predictor of Insulin Resistance in Obese Children |
title_full | Acanthosis Nigricans as a Clinical Predictor of Insulin Resistance in Obese Children |
title_fullStr | Acanthosis Nigricans as a Clinical Predictor of Insulin Resistance in Obese Children |
title_full_unstemmed | Acanthosis Nigricans as a Clinical Predictor of Insulin Resistance in Obese Children |
title_short | Acanthosis Nigricans as a Clinical Predictor of Insulin Resistance in Obese Children |
title_sort | acanthosis nigricans as a clinical predictor of insulin resistance in obese children |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234421/ https://www.ncbi.nlm.nih.gov/pubmed/28090470 http://dx.doi.org/10.5223/pghn.2016.19.4.251 |
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