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Histopathological placental lesions in mild gestational hyperglycemic and diabetic women

OBJECTIVE: To investigate and compare the incidence of histopathological placental lesions in mild gestational hyperglycemia, gestational diabetes and overt diabetes at term and preterm gestation. RESEARCH DESIGN AND METHODS: One-hundred-and-thirty-one placental samples were collected from Diabetes...

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Autores principales: Rudge, Marilza VC, Lima, César P, Damasceno, Débora C, Sinzato, Yuri K, Napoli, Gustavo, Rudge, Cibele VC, Gallego, Franciane Q, Calderon, Iracema MP
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3174871/
https://www.ncbi.nlm.nih.gov/pubmed/21831283
http://dx.doi.org/10.1186/1758-5996-3-19
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author Rudge, Marilza VC
Lima, César P
Damasceno, Débora C
Sinzato, Yuri K
Napoli, Gustavo
Rudge, Cibele VC
Gallego, Franciane Q
Calderon, Iracema MP
author_facet Rudge, Marilza VC
Lima, César P
Damasceno, Débora C
Sinzato, Yuri K
Napoli, Gustavo
Rudge, Cibele VC
Gallego, Franciane Q
Calderon, Iracema MP
author_sort Rudge, Marilza VC
collection PubMed
description OBJECTIVE: To investigate and compare the incidence of histopathological placental lesions in mild gestational hyperglycemia, gestational diabetes and overt diabetes at term and preterm gestation. RESEARCH DESIGN AND METHODS: One-hundred-and-thirty-one placental samples were collected from Diabetes mellitus (DM) positive screened patients. Two diagnostic tests, glycemic profile and 100 g oral glucose tolerance test (OGTT) in parallel identified 4 groups normoglycemic, mild gestational hyperglycemia (MGH), gestational DM (GDM) or overt DM (DM). Placental tissue specimens and sections from 4 groups were obtained by uniform random sampling and stained with hematoxylin-eosin. RESULTS: Placentas from MGH group presented 17 types of histopathological change and higher rates of syncytial nodes and endarteritis. GDM placentas presented only nine types of histopathological change, high rates of dysmaturity, low rates of calcification and no syncytial nodes. Overt DM placentas showed 22 types of histopathological change, 21 of which were present in the preterm period. There were histopathological similarities between MGH and DM placentas, but the former exhibited a higher incidence of endarteritis, which has been described as a "post-mortem" phenomenon. CONCLUSION: Our results confirmed that the distinct placental changes associated with DM and MGH depend on gestational period during which the diabetic insult occurs. It may reasonably be inferred that subclinical maternal hyperglycemia during pregnancy, as showed in MGH group, is responsible for increased placental endarteritis, a postmortem lesion in the live fetus.
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spelling pubmed-31748712011-09-17 Histopathological placental lesions in mild gestational hyperglycemic and diabetic women Rudge, Marilza VC Lima, César P Damasceno, Débora C Sinzato, Yuri K Napoli, Gustavo Rudge, Cibele VC Gallego, Franciane Q Calderon, Iracema MP Diabetol Metab Syndr Research OBJECTIVE: To investigate and compare the incidence of histopathological placental lesions in mild gestational hyperglycemia, gestational diabetes and overt diabetes at term and preterm gestation. RESEARCH DESIGN AND METHODS: One-hundred-and-thirty-one placental samples were collected from Diabetes mellitus (DM) positive screened patients. Two diagnostic tests, glycemic profile and 100 g oral glucose tolerance test (OGTT) in parallel identified 4 groups normoglycemic, mild gestational hyperglycemia (MGH), gestational DM (GDM) or overt DM (DM). Placental tissue specimens and sections from 4 groups were obtained by uniform random sampling and stained with hematoxylin-eosin. RESULTS: Placentas from MGH group presented 17 types of histopathological change and higher rates of syncytial nodes and endarteritis. GDM placentas presented only nine types of histopathological change, high rates of dysmaturity, low rates of calcification and no syncytial nodes. Overt DM placentas showed 22 types of histopathological change, 21 of which were present in the preterm period. There were histopathological similarities between MGH and DM placentas, but the former exhibited a higher incidence of endarteritis, which has been described as a "post-mortem" phenomenon. CONCLUSION: Our results confirmed that the distinct placental changes associated with DM and MGH depend on gestational period during which the diabetic insult occurs. It may reasonably be inferred that subclinical maternal hyperglycemia during pregnancy, as showed in MGH group, is responsible for increased placental endarteritis, a postmortem lesion in the live fetus. BioMed Central 2011-08-10 /pmc/articles/PMC3174871/ /pubmed/21831283 http://dx.doi.org/10.1186/1758-5996-3-19 Text en Copyright ©2011 Rudge et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Rudge, Marilza VC
Lima, César P
Damasceno, Débora C
Sinzato, Yuri K
Napoli, Gustavo
Rudge, Cibele VC
Gallego, Franciane Q
Calderon, Iracema MP
Histopathological placental lesions in mild gestational hyperglycemic and diabetic women
title Histopathological placental lesions in mild gestational hyperglycemic and diabetic women
title_full Histopathological placental lesions in mild gestational hyperglycemic and diabetic women
title_fullStr Histopathological placental lesions in mild gestational hyperglycemic and diabetic women
title_full_unstemmed Histopathological placental lesions in mild gestational hyperglycemic and diabetic women
title_short Histopathological placental lesions in mild gestational hyperglycemic and diabetic women
title_sort histopathological placental lesions in mild gestational hyperglycemic and diabetic women
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3174871/
https://www.ncbi.nlm.nih.gov/pubmed/21831283
http://dx.doi.org/10.1186/1758-5996-3-19
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