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Glycemia and Its Relationship to Outcomes in the Metformin in Gestational Diabetes Trial
OBJECTIVE: To determine how glucose control in women with GDM treated with metformin and/or insulin influenced pregnancy outcomes. RESEARCH DESIGN AND METHODS: Women randomly assigned to metformin or insulin treatment in the Metformin in Gestational Diabetes (MiG) trial had baseline glucose toleranc...
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Formato: | Texto |
Lenguaje: | English |
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American Diabetes Association
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797992/ https://www.ncbi.nlm.nih.gov/pubmed/19846793 http://dx.doi.org/10.2337/dc09-1407 |
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author | Rowan, Janet A. Gao, Wanzhen Hague, William M. McIntyre, Harold David |
author_facet | Rowan, Janet A. Gao, Wanzhen Hague, William M. McIntyre, Harold David |
author_sort | Rowan, Janet A. |
collection | PubMed |
description | OBJECTIVE: To determine how glucose control in women with GDM treated with metformin and/or insulin influenced pregnancy outcomes. RESEARCH DESIGN AND METHODS: Women randomly assigned to metformin or insulin treatment in the Metformin in Gestational Diabetes (MiG) trial had baseline glucose tolerance test (OGTT) results and A1C documented, together with all capillary glucose measurements during treatment. In the 724 women who had glucose data for analysis, tertiles of baseline glucose values and A1C and of mean capillary glucose values during treatment were calculated. The relationships between maternal factors, glucose values, and outcomes (including a composite of neonatal complications, preeclampsia, and large-for-gestational-age [LGA] and small-for-gestational-age infants) were examined with bivariable and multivariate models. RESULTS: Baseline OGTT did not predict outcomes, but A1C predicted LGA infants (P = 0.003). During treatment, fasting capillary glucose predicted neonatal complications (P < 0.001) and postprandial glucose predicted preeclampsia (P = 0.016) and LGA infants (P = 0.001). Obesity did not influence outcomes, and there was no interaction between glycemic control, randomized treatment, or maternal BMI in predicting outcomes. The lowest risk of complications was seen when fasting capillary glucose was <4.9 mmol/l (mean ± SD 4.6 ± 0.3 mmol/l) compared with 4.9–5.3 mmol/l or higher and when 2-h postprandial glucose was 5.9–6.4 mmol/l (6.2 ± 0.2 mmol/l) or lower. CONCLUSIONS: Glucose control in women with gestational diabetes mellitus treated with metformin and/or insulin is strongly related to outcomes. Obesity is not related to outcomes in this group. Targets for fasting and postprandial capillary glucose may need to be lower than currently recommended. |
format | Text |
id | pubmed-2797992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-27979922011-01-01 Glycemia and Its Relationship to Outcomes in the Metformin in Gestational Diabetes Trial Rowan, Janet A. Gao, Wanzhen Hague, William M. McIntyre, Harold David Diabetes Care Original Research OBJECTIVE: To determine how glucose control in women with GDM treated with metformin and/or insulin influenced pregnancy outcomes. RESEARCH DESIGN AND METHODS: Women randomly assigned to metformin or insulin treatment in the Metformin in Gestational Diabetes (MiG) trial had baseline glucose tolerance test (OGTT) results and A1C documented, together with all capillary glucose measurements during treatment. In the 724 women who had glucose data for analysis, tertiles of baseline glucose values and A1C and of mean capillary glucose values during treatment were calculated. The relationships between maternal factors, glucose values, and outcomes (including a composite of neonatal complications, preeclampsia, and large-for-gestational-age [LGA] and small-for-gestational-age infants) were examined with bivariable and multivariate models. RESULTS: Baseline OGTT did not predict outcomes, but A1C predicted LGA infants (P = 0.003). During treatment, fasting capillary glucose predicted neonatal complications (P < 0.001) and postprandial glucose predicted preeclampsia (P = 0.016) and LGA infants (P = 0.001). Obesity did not influence outcomes, and there was no interaction between glycemic control, randomized treatment, or maternal BMI in predicting outcomes. The lowest risk of complications was seen when fasting capillary glucose was <4.9 mmol/l (mean ± SD 4.6 ± 0.3 mmol/l) compared with 4.9–5.3 mmol/l or higher and when 2-h postprandial glucose was 5.9–6.4 mmol/l (6.2 ± 0.2 mmol/l) or lower. CONCLUSIONS: Glucose control in women with gestational diabetes mellitus treated with metformin and/or insulin is strongly related to outcomes. Obesity is not related to outcomes in this group. Targets for fasting and postprandial capillary glucose may need to be lower than currently recommended. American Diabetes Association 2010-01 2009-10-21 /pmc/articles/PMC2797992/ /pubmed/19846793 http://dx.doi.org/10.2337/dc09-1407 Text en © 2010 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 Rowan, Janet A. Gao, Wanzhen Hague, William M. McIntyre, Harold David Glycemia and Its Relationship to Outcomes in the Metformin in Gestational Diabetes Trial |
title | Glycemia and Its Relationship to Outcomes in the Metformin in Gestational Diabetes Trial |
title_full | Glycemia and Its Relationship to Outcomes in the Metformin in Gestational Diabetes Trial |
title_fullStr | Glycemia and Its Relationship to Outcomes in the Metformin in Gestational Diabetes Trial |
title_full_unstemmed | Glycemia and Its Relationship to Outcomes in the Metformin in Gestational Diabetes Trial |
title_short | Glycemia and Its Relationship to Outcomes in the Metformin in Gestational Diabetes Trial |
title_sort | glycemia and its relationship to outcomes in the metformin in gestational diabetes trial |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797992/ https://www.ncbi.nlm.nih.gov/pubmed/19846793 http://dx.doi.org/10.2337/dc09-1407 |
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