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Screening for Gestational Diabetes Mellitus by Measuring Glycated Hemoglobin Can Reduce the Use of the Glucose Challenge Test
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 ) as a biomarker for gestational diabetes mellitus (GDM). Nevertheless, increasing evidence supports the use of HbA in GDM diagnostic strategies.We...
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Published in: | Annals of laboratory medicine 2019, 39(6), , pp.524-529 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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
) as a biomarker for gestational diabetes mellitus (GDM). Nevertheless, increasing evidence supports the use of HbA
in GDM diagnostic strategies.We studied HbA
as a biomarker of GDM and its possible use as a screening test to avoid the use of the glucose challenge test (GCT).
This case-control study involved 607 pregnant women between the 24th and 28th week of gestation. HbA
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.
The AUC for HbA
diagnostic performance was 0.68 (95% confidence interval 0.57-0.79). Using 4.6% HbA
(27 mmol/mol) as the lower cut-off (S=100%), 14% of participants could avoid the GCT. Using 5.5% HbA
(36 mmol/mol) as the upper cut-off (SP =94.5%), 6% of participants would be considered at high risk.
HbA
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. |
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ISSN: | 2234-3806 2234-3814 |
DOI: | 10.3343/alm.2019.39.6.524 |