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Metabolomics for predicting hyperglycemia in pregnancy: a protocol for a systematic review and potential meta-analysis

BACKGROUND: Hyperglycemia in pregnancy (HIP) has been recently differentiated between diabetes in pregnancy (DIP) and gestational diabetes mellitus (GDM). The proposed protocol is relevant, and clinical concern is due to the higher risk of adverse pregnancy outcomes (APO) and long-term effects on bo...

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Autores principales: Nicolosi, Bianca Fioravanti, Leite, Debora F., Mayrink, Jussara, Souza, Renato T., Cecatti, José Guilherme, Calderon, Iracema de Mattos Paranhos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708156/
https://www.ncbi.nlm.nih.gov/pubmed/31445518
http://dx.doi.org/10.1186/s13643-019-1129-y
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author Nicolosi, Bianca Fioravanti
Leite, Debora F.
Mayrink, Jussara
Souza, Renato T.
Cecatti, José Guilherme
Calderon, Iracema de Mattos Paranhos
author_facet Nicolosi, Bianca Fioravanti
Leite, Debora F.
Mayrink, Jussara
Souza, Renato T.
Cecatti, José Guilherme
Calderon, Iracema de Mattos Paranhos
author_sort Nicolosi, Bianca Fioravanti
collection PubMed
description BACKGROUND: Hyperglycemia in pregnancy (HIP) has been recently differentiated between diabetes in pregnancy (DIP) and gestational diabetes mellitus (GDM). The proposed protocol is relevant, and clinical concern is due to the higher risk of adverse pregnancy outcomes (APO) and long-term effects on both the mother and the fetus. Fasting plasma glucose level (FPG) and oral glucose tolerance test (OGTT) are current diagnostic tools. However, controversy persists concerning diagnostic criteria, cut-off points, and even selective or universal screening. The objective of this systematic review is to assess the performance of metabolomic markers in the prediction of HIP. METHODS: This is a protocol for a systematic review with potential meta-analysis. The primary outcome is GDM, defined as glucose intolerance identified in the second and third trimesters of pregnancy (any FPG ≥ 92 mg/dL and < 126 mg/dL OR when 75-g OGTT shows one altered value among these: FPG ≥ 92 mg/dL or 1-h post glucose load ≥ 180 mg/dL or 2-h post glucose load ≥ 153 mg/dL); the secondary outcome is HIP, defined as hyperglycemia detected in the first trimester of pregnancy (any FPG ≥ 126 mg/dL). A detailed systematic literature search will be carried out in electronic databases and conference abstracts, using the keywords “gestational diabetes mellitus,” “metabolomics,” “pregnancy,” and “screening” (and their variations). We will include original peer-reviewed articles published from Jan 1, 1999, to Dec 31, 2018. Original studies including diabetes diagnosed before pregnancy (T2DM and T1DM), multiple pregnancies, and congenital malformations will be excluded. All results regarding samples, participant characteristics, metabolomic techniques, and diagnostic accuracy measures will be retrieved and analyzed. Since this is a systematic review, no ethical approval is necessary. DISCUSSION: This systematic review may have the potential to provide significant evidence-based findings on the prediction performance of metabolomics. There are short and long-term repercussions for the mother and the newborn. Therefore, both may benefit from an accurate prediction technique for HIP. SYSTEMATIC REVIEW REGISTRATION: This protocol was registered in the PROSPERO platform under number CRD42018100175. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13643-019-1129-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-67081562019-08-28 Metabolomics for predicting hyperglycemia in pregnancy: a protocol for a systematic review and potential meta-analysis Nicolosi, Bianca Fioravanti Leite, Debora F. Mayrink, Jussara Souza, Renato T. Cecatti, José Guilherme Calderon, Iracema de Mattos Paranhos Syst Rev Protocol BACKGROUND: Hyperglycemia in pregnancy (HIP) has been recently differentiated between diabetes in pregnancy (DIP) and gestational diabetes mellitus (GDM). The proposed protocol is relevant, and clinical concern is due to the higher risk of adverse pregnancy outcomes (APO) and long-term effects on both the mother and the fetus. Fasting plasma glucose level (FPG) and oral glucose tolerance test (OGTT) are current diagnostic tools. However, controversy persists concerning diagnostic criteria, cut-off points, and even selective or universal screening. The objective of this systematic review is to assess the performance of metabolomic markers in the prediction of HIP. METHODS: This is a protocol for a systematic review with potential meta-analysis. The primary outcome is GDM, defined as glucose intolerance identified in the second and third trimesters of pregnancy (any FPG ≥ 92 mg/dL and < 126 mg/dL OR when 75-g OGTT shows one altered value among these: FPG ≥ 92 mg/dL or 1-h post glucose load ≥ 180 mg/dL or 2-h post glucose load ≥ 153 mg/dL); the secondary outcome is HIP, defined as hyperglycemia detected in the first trimester of pregnancy (any FPG ≥ 126 mg/dL). A detailed systematic literature search will be carried out in electronic databases and conference abstracts, using the keywords “gestational diabetes mellitus,” “metabolomics,” “pregnancy,” and “screening” (and their variations). We will include original peer-reviewed articles published from Jan 1, 1999, to Dec 31, 2018. Original studies including diabetes diagnosed before pregnancy (T2DM and T1DM), multiple pregnancies, and congenital malformations will be excluded. All results regarding samples, participant characteristics, metabolomic techniques, and diagnostic accuracy measures will be retrieved and analyzed. Since this is a systematic review, no ethical approval is necessary. DISCUSSION: This systematic review may have the potential to provide significant evidence-based findings on the prediction performance of metabolomics. There are short and long-term repercussions for the mother and the newborn. Therefore, both may benefit from an accurate prediction technique for HIP. SYSTEMATIC REVIEW REGISTRATION: This protocol was registered in the PROSPERO platform under number CRD42018100175. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13643-019-1129-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-24 /pmc/articles/PMC6708156/ /pubmed/31445518 http://dx.doi.org/10.1186/s13643-019-1129-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Protocol
Nicolosi, Bianca Fioravanti
Leite, Debora F.
Mayrink, Jussara
Souza, Renato T.
Cecatti, José Guilherme
Calderon, Iracema de Mattos Paranhos
Metabolomics for predicting hyperglycemia in pregnancy: a protocol for a systematic review and potential meta-analysis
title Metabolomics for predicting hyperglycemia in pregnancy: a protocol for a systematic review and potential meta-analysis
title_full Metabolomics for predicting hyperglycemia in pregnancy: a protocol for a systematic review and potential meta-analysis
title_fullStr Metabolomics for predicting hyperglycemia in pregnancy: a protocol for a systematic review and potential meta-analysis
title_full_unstemmed Metabolomics for predicting hyperglycemia in pregnancy: a protocol for a systematic review and potential meta-analysis
title_short Metabolomics for predicting hyperglycemia in pregnancy: a protocol for a systematic review and potential meta-analysis
title_sort metabolomics for predicting hyperglycemia in pregnancy: a protocol for a systematic review and potential meta-analysis
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708156/
https://www.ncbi.nlm.nih.gov/pubmed/31445518
http://dx.doi.org/10.1186/s13643-019-1129-y
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