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Early Gestational Diabetes Mellitus: Diagnostic Strategies and Clinical Implications
Preexisting diabetes mellitus (DM) should be ruled out early in pregnancy in those at risk. During screening, a significant proportion of women do not reach the threshold for overt DM but fulfill the criteria used for diagnosing conventional gestational DM (cGDM). There is no consensus on the manage...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8544345/ https://www.ncbi.nlm.nih.gov/pubmed/34698239 http://dx.doi.org/10.3390/medsci9040059 |
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author | Bhattacharya, Saptarshi Nagendra, Lakshmi Krishnamurthy, Aishwarya Lakhani, Om J. Kapoor, Nitin Kalra, Bharti Kalra, Sanjay |
author_facet | Bhattacharya, Saptarshi Nagendra, Lakshmi Krishnamurthy, Aishwarya Lakhani, Om J. Kapoor, Nitin Kalra, Bharti Kalra, Sanjay |
author_sort | Bhattacharya, Saptarshi |
collection | PubMed |
description | Preexisting diabetes mellitus (DM) should be ruled out early in pregnancy in those at risk. During screening, a significant proportion of women do not reach the threshold for overt DM but fulfill the criteria used for diagnosing conventional gestational DM (cGDM). There is no consensus on the management of pregnancies with intermediate levels of hyperglycemia thus diagnosed. We have used the term early gestational DM (eGDM) for this condition and reviewed the currently available literature. Fasting plasma glucose (FPG), oral glucose tolerance test, and glycated hemoglobin (HbA1c) are the commonly employed screening tools in early pregnancy. Observational studies suggest that early pregnancy FPG and Hba1c correlate with the risk of cGDM and adverse perinatal outcomes. However, specific cut-offs, including those proposed by the International Association of the Diabetes and Pregnancy Study Group, do not reliably predict the development of cGDM. Emerging data, though indicate that FPG ≥ 92 mg/dL (5.1 mmol/L), even in the absence of cGDM, signals the risk for perinatal complication. Elevated HbA1c, especially a level ≥ 5.9%, also correlates with the risk of cGDM and worsened outcome. HbA1c as a diagnostic test is however besieged with the usual caveats that occur in pregnancy. The studies that explored the effects of intervention present conflicting results, including a possibility of fetal malnutrition and small-for-date baby in the early treatment group. Diagnostic thresholds and glycemic targets in eGDM may differ, and large multicenter randomized controlled trials are necessary to define the appropriate strategy. |
format | Online Article Text |
id | pubmed-8544345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85443452021-10-26 Early Gestational Diabetes Mellitus: Diagnostic Strategies and Clinical Implications Bhattacharya, Saptarshi Nagendra, Lakshmi Krishnamurthy, Aishwarya Lakhani, Om J. Kapoor, Nitin Kalra, Bharti Kalra, Sanjay Med Sci (Basel) Review Preexisting diabetes mellitus (DM) should be ruled out early in pregnancy in those at risk. During screening, a significant proportion of women do not reach the threshold for overt DM but fulfill the criteria used for diagnosing conventional gestational DM (cGDM). There is no consensus on the management of pregnancies with intermediate levels of hyperglycemia thus diagnosed. We have used the term early gestational DM (eGDM) for this condition and reviewed the currently available literature. Fasting plasma glucose (FPG), oral glucose tolerance test, and glycated hemoglobin (HbA1c) are the commonly employed screening tools in early pregnancy. Observational studies suggest that early pregnancy FPG and Hba1c correlate with the risk of cGDM and adverse perinatal outcomes. However, specific cut-offs, including those proposed by the International Association of the Diabetes and Pregnancy Study Group, do not reliably predict the development of cGDM. Emerging data, though indicate that FPG ≥ 92 mg/dL (5.1 mmol/L), even in the absence of cGDM, signals the risk for perinatal complication. Elevated HbA1c, especially a level ≥ 5.9%, also correlates with the risk of cGDM and worsened outcome. HbA1c as a diagnostic test is however besieged with the usual caveats that occur in pregnancy. The studies that explored the effects of intervention present conflicting results, including a possibility of fetal malnutrition and small-for-date baby in the early treatment group. Diagnostic thresholds and glycemic targets in eGDM may differ, and large multicenter randomized controlled trials are necessary to define the appropriate strategy. MDPI 2021-09-23 /pmc/articles/PMC8544345/ /pubmed/34698239 http://dx.doi.org/10.3390/medsci9040059 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Bhattacharya, Saptarshi Nagendra, Lakshmi Krishnamurthy, Aishwarya Lakhani, Om J. Kapoor, Nitin Kalra, Bharti Kalra, Sanjay Early Gestational Diabetes Mellitus: Diagnostic Strategies and Clinical Implications |
title | Early Gestational Diabetes Mellitus: Diagnostic Strategies and Clinical Implications |
title_full | Early Gestational Diabetes Mellitus: Diagnostic Strategies and Clinical Implications |
title_fullStr | Early Gestational Diabetes Mellitus: Diagnostic Strategies and Clinical Implications |
title_full_unstemmed | Early Gestational Diabetes Mellitus: Diagnostic Strategies and Clinical Implications |
title_short | Early Gestational Diabetes Mellitus: Diagnostic Strategies and Clinical Implications |
title_sort | early gestational diabetes mellitus: diagnostic strategies and clinical implications |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8544345/ https://www.ncbi.nlm.nih.gov/pubmed/34698239 http://dx.doi.org/10.3390/medsci9040059 |
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