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Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations

BACKGROUND: Neonatal diabetes mellitus (NDM) is a rare (1:90,000 newborns) but potentially devastating metabolic disorder characterized by hyperglycemia combined with low levels of insulin. Dominantly-acting insulin (INS) gene mutations cause permanent NDM through single amino acid changes in the pr...

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Autores principales: Ngoc, Can Thi Bich, Dung, Vu Chi, De Franco, Elisa, Lan, Nguyen Ngoc, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Flanagan, Sarah E., Craig, Maria E., Hoang, Nguyen Huy, Dien, Tran Minh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063464/
https://www.ncbi.nlm.nih.gov/pubmed/35518939
http://dx.doi.org/10.3389/fendo.2022.866573
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author Ngoc, Can Thi Bich
Dung, Vu Chi
De Franco, Elisa
Lan, Nguyen Ngoc
Thao, Bui Phuong
Khanh, Nguyen Ngoc
Flanagan, Sarah E.
Craig, Maria E.
Hoang, Nguyen Huy
Dien, Tran Minh
author_facet Ngoc, Can Thi Bich
Dung, Vu Chi
De Franco, Elisa
Lan, Nguyen Ngoc
Thao, Bui Phuong
Khanh, Nguyen Ngoc
Flanagan, Sarah E.
Craig, Maria E.
Hoang, Nguyen Huy
Dien, Tran Minh
author_sort Ngoc, Can Thi Bich
collection PubMed
description BACKGROUND: Neonatal diabetes mellitus (NDM) is a rare (1:90,000 newborns) but potentially devastating metabolic disorder characterized by hyperglycemia combined with low levels of insulin. Dominantly-acting insulin (INS) gene mutations cause permanent NDM through single amino acid changes in the protein sequence leading to protein misfolding, which is retained within the endoplasmic reticulum (ER), causing ER stress and β-cell apoptosis. Over 90 dominantly-acting INS gene mutations have been identified in individuals with permanent NDM. PATIENTS AND METHODS: The study included 70 infants diagnosed with NDM in the first year of life between May 2008 and May 2021 at the Vietnam National Children’s Hospital. Sequencing analysis of all the genes known to cause NDM was performed at the Exeter Genomic Laboratory, UK. Clinical characteristics, molecular genetics, and annual data relating to glycemic control (HbA1c) and severe hypoglycemia of those with INS mutations were collected. The main outcomes of interest were HbA1c, daily insulin dose, growth, and cognitive/motor development. RESULTS: Fifty-five of 70 infants (78.5%) with NDM harbored a mutation in a known disease-causing gene and of these, 10 had six different de novo heterozygous INS mutations. Mean gestational age was 38.1 ± 2.5 weeks and mean birth weight was 2.8 ± 0.5 g. They presented with NDM at 20 ± 17 weeks of age; 6/10 had diabetic ketoacidosis with pH 7.13 ± 0.26; plasma glucose level 32.6 ± 14.3 mmol/l and HbA1C 81 ± 15% mmol/mol. After 5.5 ± 4.8 years of insulin treatment, 9/10 have normal development with a developmental quotient of 80-100% and HbA1C 64 ± 7.3 mmol/mol, 9/10 have normal height, weight, and BMI on follow-up. CONCLUSIONS: We report a series of Vietnamese NDM cases with dominant INS mutations. INS mutations are the third commonest cause of permanent NDM. We recommend screening of the INS gene in all children diagnosed with diabetes in the first year of life.
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spelling pubmed-90634642022-05-04 Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations Ngoc, Can Thi Bich Dung, Vu Chi De Franco, Elisa Lan, Nguyen Ngoc Thao, Bui Phuong Khanh, Nguyen Ngoc Flanagan, Sarah E. Craig, Maria E. Hoang, Nguyen Huy Dien, Tran Minh Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Neonatal diabetes mellitus (NDM) is a rare (1:90,000 newborns) but potentially devastating metabolic disorder characterized by hyperglycemia combined with low levels of insulin. Dominantly-acting insulin (INS) gene mutations cause permanent NDM through single amino acid changes in the protein sequence leading to protein misfolding, which is retained within the endoplasmic reticulum (ER), causing ER stress and β-cell apoptosis. Over 90 dominantly-acting INS gene mutations have been identified in individuals with permanent NDM. PATIENTS AND METHODS: The study included 70 infants diagnosed with NDM in the first year of life between May 2008 and May 2021 at the Vietnam National Children’s Hospital. Sequencing analysis of all the genes known to cause NDM was performed at the Exeter Genomic Laboratory, UK. Clinical characteristics, molecular genetics, and annual data relating to glycemic control (HbA1c) and severe hypoglycemia of those with INS mutations were collected. The main outcomes of interest were HbA1c, daily insulin dose, growth, and cognitive/motor development. RESULTS: Fifty-five of 70 infants (78.5%) with NDM harbored a mutation in a known disease-causing gene and of these, 10 had six different de novo heterozygous INS mutations. Mean gestational age was 38.1 ± 2.5 weeks and mean birth weight was 2.8 ± 0.5 g. They presented with NDM at 20 ± 17 weeks of age; 6/10 had diabetic ketoacidosis with pH 7.13 ± 0.26; plasma glucose level 32.6 ± 14.3 mmol/l and HbA1C 81 ± 15% mmol/mol. After 5.5 ± 4.8 years of insulin treatment, 9/10 have normal development with a developmental quotient of 80-100% and HbA1C 64 ± 7.3 mmol/mol, 9/10 have normal height, weight, and BMI on follow-up. CONCLUSIONS: We report a series of Vietnamese NDM cases with dominant INS mutations. INS mutations are the third commonest cause of permanent NDM. We recommend screening of the INS gene in all children diagnosed with diabetes in the first year of life. Frontiers Media S.A. 2022-04-19 /pmc/articles/PMC9063464/ /pubmed/35518939 http://dx.doi.org/10.3389/fendo.2022.866573 Text en Copyright © 2022 Ngoc, Dung, De Franco, Lan, Thao, Khanh, Flanagan, Craig, Hoang and Dien https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Ngoc, Can Thi Bich
Dung, Vu Chi
De Franco, Elisa
Lan, Nguyen Ngoc
Thao, Bui Phuong
Khanh, Nguyen Ngoc
Flanagan, Sarah E.
Craig, Maria E.
Hoang, Nguyen Huy
Dien, Tran Minh
Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations
title Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations
title_full Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations
title_fullStr Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations
title_full_unstemmed Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations
title_short Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations
title_sort genetic etiology of neonatal diabetes mellitus in vietnamese infants and characteristics of those with ins gene mutations
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063464/
https://www.ncbi.nlm.nih.gov/pubmed/35518939
http://dx.doi.org/10.3389/fendo.2022.866573
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