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Abstract 61: Prevalence and clinical profile of maturity onset diabetes of the young among people with diabetes attending a tertiary care institute in North India

Background: Maturity onset diabetes of young (MODY) is considered to be the most underdiagnosed condition and correct diagnosis has a definite bearing on the outcome and clinical course of the disease. Aims and Objectives: To determine the prevalence and clinical profile of MODY among young diabetic...

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Autores principales: Bhat, Javaid Ahmad, Masoodi1, Shariq Rashid, Bhat, Mohammad Hayat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067748/
http://dx.doi.org/10.4103/2230-8210.342178
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author Bhat, Javaid Ahmad
Masoodi1, Shariq Rashid
Bhat, Mohammad Hayat
author_facet Bhat, Javaid Ahmad
Masoodi1, Shariq Rashid
Bhat, Mohammad Hayat
author_sort Bhat, Javaid Ahmad
collection PubMed
description Background: Maturity onset diabetes of young (MODY) is considered to be the most underdiagnosed condition and correct diagnosis has a definite bearing on the outcome and clinical course of the disease. Aims and Objectives: To determine the prevalence and clinical profile of MODY among young diabetic patients attending Endocrinology department at SKIMS, India. Methods: This was a cross-sectional study involving 1094 consenting patients with diabetes and age of onset of diabetes (DM) ≤30 years (<25 years in 858 patients). All patients were screened for MODY using clinical criteria and MODY probability calculator (available on diabetesgenes.org). Patients with high clinical probability of MODY and negative anti-GAD65 antibody but fasting serum C-peptide levels >0.6 ng/ml were subjected to the Ala98Val polymorphism (SNP) in HNF1α gene. Results: The prevalence of MODY as per clinical criteria was 7.7%. The patients with MODY were younger (p<0.001), leaner (p<0.001), had younger age at onset of DM (p<0.001) and lower frequency of features of insulin resistance. Among 40patients who were subjected to SNP analysis in HNF1α gene (MODY3), the mutant genotype was seen in 20 (50%) patients. Conclusion: We report a higher prevalence of MODY3 in our young diabetic patients. A high index of suspicion is required to diagnose MODY as misdiagnosis and inappropriate treatment may have a significant impact on quality of life.
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spelling pubmed-90677482022-05-05 Abstract 61: Prevalence and clinical profile of maturity onset diabetes of the young among people with diabetes attending a tertiary care institute in North India Bhat, Javaid Ahmad Masoodi1, Shariq Rashid Bhat, Mohammad Hayat Indian J Endocrinol Metab Abstracts … Esicon 2021 Background: Maturity onset diabetes of young (MODY) is considered to be the most underdiagnosed condition and correct diagnosis has a definite bearing on the outcome and clinical course of the disease. Aims and Objectives: To determine the prevalence and clinical profile of MODY among young diabetic patients attending Endocrinology department at SKIMS, India. Methods: This was a cross-sectional study involving 1094 consenting patients with diabetes and age of onset of diabetes (DM) ≤30 years (<25 years in 858 patients). All patients were screened for MODY using clinical criteria and MODY probability calculator (available on diabetesgenes.org). Patients with high clinical probability of MODY and negative anti-GAD65 antibody but fasting serum C-peptide levels >0.6 ng/ml were subjected to the Ala98Val polymorphism (SNP) in HNF1α gene. Results: The prevalence of MODY as per clinical criteria was 7.7%. The patients with MODY were younger (p<0.001), leaner (p<0.001), had younger age at onset of DM (p<0.001) and lower frequency of features of insulin resistance. Among 40patients who were subjected to SNP analysis in HNF1α gene (MODY3), the mutant genotype was seen in 20 (50%) patients. Conclusion: We report a higher prevalence of MODY3 in our young diabetic patients. A high index of suspicion is required to diagnose MODY as misdiagnosis and inappropriate treatment may have a significant impact on quality of life. Wolters Kluwer - Medknow 2022-03 /pmc/articles/PMC9067748/ http://dx.doi.org/10.4103/2230-8210.342178 Text en Copyright: © 2022 Indian Journal of Endocrinology and Metabolism https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Abstracts … Esicon 2021
Bhat, Javaid Ahmad
Masoodi1, Shariq Rashid
Bhat, Mohammad Hayat
Abstract 61: Prevalence and clinical profile of maturity onset diabetes of the young among people with diabetes attending a tertiary care institute in North India
title Abstract 61: Prevalence and clinical profile of maturity onset diabetes of the young among people with diabetes attending a tertiary care institute in North India
title_full Abstract 61: Prevalence and clinical profile of maturity onset diabetes of the young among people with diabetes attending a tertiary care institute in North India
title_fullStr Abstract 61: Prevalence and clinical profile of maturity onset diabetes of the young among people with diabetes attending a tertiary care institute in North India
title_full_unstemmed Abstract 61: Prevalence and clinical profile of maturity onset diabetes of the young among people with diabetes attending a tertiary care institute in North India
title_short Abstract 61: Prevalence and clinical profile of maturity onset diabetes of the young among people with diabetes attending a tertiary care institute in North India
title_sort abstract 61: prevalence and clinical profile of maturity onset diabetes of the young among people with diabetes attending a tertiary care institute in north india
topic Abstracts … Esicon 2021
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067748/
http://dx.doi.org/10.4103/2230-8210.342178
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