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Fasting Indicators of Insulin Sensitivity: Effects of Ethnicity and Pubertal Status
OBJECTIVE: To examine the relationship of fasting indicators of insulin sensitivity with a more invasive measure of insulin sensitivity (frequently sampled intravenous glucose tolerance test [FSIVGTT]) and the effect of Tanner stage and ethnicity on that relationship. RESEARCH DESIGN AND METHODS: Da...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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American Diabetes Association
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3064063/ https://www.ncbi.nlm.nih.gov/pubmed/21357795 http://dx.doi.org/10.2337/dc10-1593 |
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author | Adam, Tanja C. Hasson, Rebecca E. Lane, Christianne J. Davis, Jaimie N. Weigensberg, Marc J. Spruijt-Metz, Donna Goran, Michael I. |
author_facet | Adam, Tanja C. Hasson, Rebecca E. Lane, Christianne J. Davis, Jaimie N. Weigensberg, Marc J. Spruijt-Metz, Donna Goran, Michael I. |
author_sort | Adam, Tanja C. |
collection | PubMed |
description | OBJECTIVE: To examine the relationship of fasting indicators of insulin sensitivity with a more invasive measure of insulin sensitivity (frequently sampled intravenous glucose tolerance test [FSIVGTT]) and the effect of Tanner stage and ethnicity on that relationship. RESEARCH DESIGN AND METHODS: Data were analyzed from 149 overweight girls (97 Hispanic and 52 African American) who were either in the early stages of maturation defined by Tanner stages 1 or 2 (52 Hispanic and 18 African American) or in the later stages of maturation defined by Tanner stages 4 and 5 (45 Hispanic and 34 African American). Fasting indicators of insulin sensitivity (IS) included fasting insulin and glucose and the homeostasis model assessment of insulin resistance (HOMA-IR). IS was derived from an FSIVGTT with minimal modeling. RESULTS: In Tanner stages 1 and 2, all fasting indicators were significantly associated with IS: (fasting insulin: r = −0.67, P < 0.01; HOMA: r = −0.66, P < 0.01) with no significant influence of ethnicity on these relationships. In Tanner stages 4 and 5, however, all fasting indicators were associated with IS in African American girls (fasting insulin: r = −0.55, P < 0.01; HOMA: r = −0.47, P < 0.01), but none of the indicators were significantly associated with IS in Hispanic girls. CONCLUSIONS: Fasting indicators were reflective of IS for girls in Tanner stages 1 and 2, regardless of ethnicity and may provide a clinical measure of future risk for type 2 diabetes. In the latter stages of maturation, however, more invasive measures are warranted to adequately determine IS in clinical practice. |
format | Text |
id | pubmed-3064063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-30640632012-04-01 Fasting Indicators of Insulin Sensitivity: Effects of Ethnicity and Pubertal Status Adam, Tanja C. Hasson, Rebecca E. Lane, Christianne J. Davis, Jaimie N. Weigensberg, Marc J. Spruijt-Metz, Donna Goran, Michael I. Diabetes Care Original Research OBJECTIVE: To examine the relationship of fasting indicators of insulin sensitivity with a more invasive measure of insulin sensitivity (frequently sampled intravenous glucose tolerance test [FSIVGTT]) and the effect of Tanner stage and ethnicity on that relationship. RESEARCH DESIGN AND METHODS: Data were analyzed from 149 overweight girls (97 Hispanic and 52 African American) who were either in the early stages of maturation defined by Tanner stages 1 or 2 (52 Hispanic and 18 African American) or in the later stages of maturation defined by Tanner stages 4 and 5 (45 Hispanic and 34 African American). Fasting indicators of insulin sensitivity (IS) included fasting insulin and glucose and the homeostasis model assessment of insulin resistance (HOMA-IR). IS was derived from an FSIVGTT with minimal modeling. RESULTS: In Tanner stages 1 and 2, all fasting indicators were significantly associated with IS: (fasting insulin: r = −0.67, P < 0.01; HOMA: r = −0.66, P < 0.01) with no significant influence of ethnicity on these relationships. In Tanner stages 4 and 5, however, all fasting indicators were associated with IS in African American girls (fasting insulin: r = −0.55, P < 0.01; HOMA: r = −0.47, P < 0.01), but none of the indicators were significantly associated with IS in Hispanic girls. CONCLUSIONS: Fasting indicators were reflective of IS for girls in Tanner stages 1 and 2, regardless of ethnicity and may provide a clinical measure of future risk for type 2 diabetes. In the latter stages of maturation, however, more invasive measures are warranted to adequately determine IS in clinical practice. American Diabetes Association 2011-04 2011-03-21 /pmc/articles/PMC3064063/ /pubmed/21357795 http://dx.doi.org/10.2337/dc10-1593 Text en © 2011 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. |
spellingShingle | Original Research Adam, Tanja C. Hasson, Rebecca E. Lane, Christianne J. Davis, Jaimie N. Weigensberg, Marc J. Spruijt-Metz, Donna Goran, Michael I. Fasting Indicators of Insulin Sensitivity: Effects of Ethnicity and Pubertal Status |
title | Fasting Indicators of Insulin Sensitivity: Effects of Ethnicity and Pubertal Status |
title_full | Fasting Indicators of Insulin Sensitivity: Effects of Ethnicity and Pubertal Status |
title_fullStr | Fasting Indicators of Insulin Sensitivity: Effects of Ethnicity and Pubertal Status |
title_full_unstemmed | Fasting Indicators of Insulin Sensitivity: Effects of Ethnicity and Pubertal Status |
title_short | Fasting Indicators of Insulin Sensitivity: Effects of Ethnicity and Pubertal Status |
title_sort | fasting indicators of insulin sensitivity: effects of ethnicity and pubertal status |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3064063/ https://www.ncbi.nlm.nih.gov/pubmed/21357795 http://dx.doi.org/10.2337/dc10-1593 |
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