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Screening for Gestational Diabetes Mellitus by Measuring Glycated Hemoglobin Can Reduce the Use of the Glucose Challenge Test
BACKGROUND: Physiological changes during pregnancy, such as dilutional anemia and a reduced half-life of red blood cells, have prevented the use of glycated Hb (HbA(1c)) as a biomarker for gestational diabetes mellitus (GDM). Nevertheless, increasing evidence supports the use of HbA(1c) in GDM diagn...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society for Laboratory Medicine
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6660334/ https://www.ncbi.nlm.nih.gov/pubmed/31240879 http://dx.doi.org/10.3343/alm.2019.39.6.524 |
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author | Maesa, Jose-Maria Fernandez-Riejos, Patricia Gonzalez-Rodriguez, Concepcion Sanchez-Margalet, Victor |
author_facet | Maesa, Jose-Maria Fernandez-Riejos, Patricia Gonzalez-Rodriguez, Concepcion Sanchez-Margalet, Victor |
author_sort | Maesa, Jose-Maria |
collection | PubMed |
description | BACKGROUND: Physiological changes during pregnancy, such as dilutional anemia and a reduced half-life of red blood cells, have prevented the use of glycated Hb (HbA(1c)) as a biomarker for gestational diabetes mellitus (GDM). Nevertheless, increasing evidence supports the use of HbA(1c) in GDM diagnostic strategies.We studied HbA(1c) as a biomarker of GDM and its possible use as a screening test to avoid the use of the glucose challenge test (GCT). METHODS: This case-control study involved 607 pregnant women between the 24th and 28th week of gestation. HbA(1c) level was determined, and GDM was diagnosed according to the National Diabetes Data Group criteria. The area under the ROC curve (AUC) was determined; two low and two high cut-off points were established to rule out GDM and classify high-risk pregnant women, respectively. For each cut-off, sensitivity (S), specificity (SP), and total number and percentage of GCTs avoided were determined. RESULTS: The AUC for HbA(1c) diagnostic performance was 0.68 (95% confidence interval 0.57–0.79). Using 4.6% HbA(1c) (27 mmol/mol) as the lower cut-off (S=100%), 14% of participants could avoid the GCT. Using 5.5% HbA(1c) (36 mmol/mol) as the upper cut-off (SP =94.5%), 6% of participants would be considered at high risk. CONCLUSIONS: HbA(1c) can be used as a screening test prior to the GCT, thereby reducing the need for the GCT among pregnant women at a low risk of GDM. |
format | Online Article Text |
id | pubmed-6660334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Korean Society for Laboratory Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-66603342019-11-01 Screening for Gestational Diabetes Mellitus by Measuring Glycated Hemoglobin Can Reduce the Use of the Glucose Challenge Test Maesa, Jose-Maria Fernandez-Riejos, Patricia Gonzalez-Rodriguez, Concepcion Sanchez-Margalet, Victor Ann Lab Med Original Article BACKGROUND: Physiological changes during pregnancy, such as dilutional anemia and a reduced half-life of red blood cells, have prevented the use of glycated Hb (HbA(1c)) as a biomarker for gestational diabetes mellitus (GDM). Nevertheless, increasing evidence supports the use of HbA(1c) in GDM diagnostic strategies.We studied HbA(1c) as a biomarker of GDM and its possible use as a screening test to avoid the use of the glucose challenge test (GCT). METHODS: This case-control study involved 607 pregnant women between the 24th and 28th week of gestation. HbA(1c) level was determined, and GDM was diagnosed according to the National Diabetes Data Group criteria. The area under the ROC curve (AUC) was determined; two low and two high cut-off points were established to rule out GDM and classify high-risk pregnant women, respectively. For each cut-off, sensitivity (S), specificity (SP), and total number and percentage of GCTs avoided were determined. RESULTS: The AUC for HbA(1c) diagnostic performance was 0.68 (95% confidence interval 0.57–0.79). Using 4.6% HbA(1c) (27 mmol/mol) as the lower cut-off (S=100%), 14% of participants could avoid the GCT. Using 5.5% HbA(1c) (36 mmol/mol) as the upper cut-off (SP =94.5%), 6% of participants would be considered at high risk. CONCLUSIONS: HbA(1c) can be used as a screening test prior to the GCT, thereby reducing the need for the GCT among pregnant women at a low risk of GDM. The Korean Society for Laboratory Medicine 2019-11 2019-06-25 /pmc/articles/PMC6660334/ /pubmed/31240879 http://dx.doi.org/10.3343/alm.2019.39.6.524 Text en © The Korean Society for Laboratory Medicine 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 Maesa, Jose-Maria Fernandez-Riejos, Patricia Gonzalez-Rodriguez, Concepcion Sanchez-Margalet, Victor Screening for Gestational Diabetes Mellitus by Measuring Glycated Hemoglobin Can Reduce the Use of the Glucose Challenge Test |
title | Screening for Gestational Diabetes Mellitus by Measuring Glycated Hemoglobin Can Reduce the Use of the Glucose Challenge Test |
title_full | Screening for Gestational Diabetes Mellitus by Measuring Glycated Hemoglobin Can Reduce the Use of the Glucose Challenge Test |
title_fullStr | Screening for Gestational Diabetes Mellitus by Measuring Glycated Hemoglobin Can Reduce the Use of the Glucose Challenge Test |
title_full_unstemmed | Screening for Gestational Diabetes Mellitus by Measuring Glycated Hemoglobin Can Reduce the Use of the Glucose Challenge Test |
title_short | Screening for Gestational Diabetes Mellitus by Measuring Glycated Hemoglobin Can Reduce the Use of the Glucose Challenge Test |
title_sort | screening for gestational diabetes mellitus by measuring glycated hemoglobin can reduce the use of the glucose challenge test |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6660334/ https://www.ncbi.nlm.nih.gov/pubmed/31240879 http://dx.doi.org/10.3343/alm.2019.39.6.524 |
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