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The first series of cases of ketosis-prone type 2 diabetes (flatbush diabetes) in Brazilian adults

Ketosis-prone type 2 diabetes (KPD) is an emerging form of diabetes mellitus characterized by unprovoked ketoacidosis, absence of autoimmunity and beta-cell dysfunction. The KPD may improve after initial glycemic compensation and evolve to exogenous insulin independence, most cases were observed in...

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Autores principales: Ramaldes, Luana Aparecida de Lima, dos Santos, Sarah Simaan, de Sa, João Roberto, Dualib, Patrícia Médici, Dib, Sérgio Atala
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Endocrinologia e Metabologia 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065323/
https://www.ncbi.nlm.nih.gov/pubmed/33905625
http://dx.doi.org/10.20945/2359-3997000000329
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author Ramaldes, Luana Aparecida de Lima
dos Santos, Sarah Simaan
de Sa, João Roberto
Dualib, Patrícia Médici
Dib, Sérgio Atala
author_facet Ramaldes, Luana Aparecida de Lima
dos Santos, Sarah Simaan
de Sa, João Roberto
Dualib, Patrícia Médici
Dib, Sérgio Atala
author_sort Ramaldes, Luana Aparecida de Lima
collection PubMed
description Ketosis-prone type 2 diabetes (KPD) is an emerging form of diabetes mellitus characterized by unprovoked ketoacidosis, absence of autoimmunity and beta-cell dysfunction. The KPD may improve after initial glycemic compensation and evolve to exogenous insulin independence, most cases were observed in populations with African or Hispanic backgrounds. We reviewed the literature on KPD and, to date, only one case of KPD has been described in Brazil's multi-ethnic population. A group of adult Brazilian KPD patients without autoimmunity and insulinopenia was identified for this study. We report a retrospective study of four KPD cases (3 males) evaluated in southeast Brazil, the patients were overweight or obese, age between the third and fifth decades of life, had a family history of type 2 diabetes, hyperglycemia (809.5 ± 344.2 mg/dL), acidosis (pH 7.21 ± 0.07; normal range (nr): 7.35-7.45 and bicarbonate 9.1 ± 6.2; nr: 22-26 mEq/mL), ketonuria (142.5 ± 114.4 mg/dL; nr: absence), absence of glutamic acid decarboxylase antibodies (GAD-65), and beta-cell function reserve (C-peptide 1.19 ± 0.53 ng/mL - nr: 1.1-4.4 ng/mL) on diagnosis. After glycemic compensation, there was increase of C-peptide (2.21 ± 0.41) indicating the recovery of beta-cell function and the time to insulin independence was 7.7 ± 3.5 months. They evolved after the period of glucotoxicity with insulin withdrawal and could be treated with oral antidiabetic therapy. This is the first case series of KPD described in Brazil being characterized by ketoacidosis at diagnosis, absence of autoimmunity, recovery of beta-cell function and insulin independence.
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spelling pubmed-100653232023-04-01 The first series of cases of ketosis-prone type 2 diabetes (flatbush diabetes) in Brazilian adults Ramaldes, Luana Aparecida de Lima dos Santos, Sarah Simaan de Sa, João Roberto Dualib, Patrícia Médici Dib, Sérgio Atala Arch Endocrinol Metab Case Report Ketosis-prone type 2 diabetes (KPD) is an emerging form of diabetes mellitus characterized by unprovoked ketoacidosis, absence of autoimmunity and beta-cell dysfunction. The KPD may improve after initial glycemic compensation and evolve to exogenous insulin independence, most cases were observed in populations with African or Hispanic backgrounds. We reviewed the literature on KPD and, to date, only one case of KPD has been described in Brazil's multi-ethnic population. A group of adult Brazilian KPD patients without autoimmunity and insulinopenia was identified for this study. We report a retrospective study of four KPD cases (3 males) evaluated in southeast Brazil, the patients were overweight or obese, age between the third and fifth decades of life, had a family history of type 2 diabetes, hyperglycemia (809.5 ± 344.2 mg/dL), acidosis (pH 7.21 ± 0.07; normal range (nr): 7.35-7.45 and bicarbonate 9.1 ± 6.2; nr: 22-26 mEq/mL), ketonuria (142.5 ± 114.4 mg/dL; nr: absence), absence of glutamic acid decarboxylase antibodies (GAD-65), and beta-cell function reserve (C-peptide 1.19 ± 0.53 ng/mL - nr: 1.1-4.4 ng/mL) on diagnosis. After glycemic compensation, there was increase of C-peptide (2.21 ± 0.41) indicating the recovery of beta-cell function and the time to insulin independence was 7.7 ± 3.5 months. They evolved after the period of glucotoxicity with insulin withdrawal and could be treated with oral antidiabetic therapy. This is the first case series of KPD described in Brazil being characterized by ketoacidosis at diagnosis, absence of autoimmunity, recovery of beta-cell function and insulin independence. Sociedade Brasileira de Endocrinologia e Metabologia 2021-02-25 /pmc/articles/PMC10065323/ /pubmed/33905625 http://dx.doi.org/10.20945/2359-3997000000329 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ramaldes, Luana Aparecida de Lima
dos Santos, Sarah Simaan
de Sa, João Roberto
Dualib, Patrícia Médici
Dib, Sérgio Atala
The first series of cases of ketosis-prone type 2 diabetes (flatbush diabetes) in Brazilian adults
title The first series of cases of ketosis-prone type 2 diabetes (flatbush diabetes) in Brazilian adults
title_full The first series of cases of ketosis-prone type 2 diabetes (flatbush diabetes) in Brazilian adults
title_fullStr The first series of cases of ketosis-prone type 2 diabetes (flatbush diabetes) in Brazilian adults
title_full_unstemmed The first series of cases of ketosis-prone type 2 diabetes (flatbush diabetes) in Brazilian adults
title_short The first series of cases of ketosis-prone type 2 diabetes (flatbush diabetes) in Brazilian adults
title_sort first series of cases of ketosis-prone type 2 diabetes (flatbush diabetes) in brazilian adults
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065323/
https://www.ncbi.nlm.nih.gov/pubmed/33905625
http://dx.doi.org/10.20945/2359-3997000000329
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