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Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship.

Authors :
Özsu, Elif
Çetinkaya, Semra
Bolu, Semih
Hatipoğlu, Nihal
Erdeve, Şenay Savaş
Evliyaoğlu, Olcay
Baş, Firdevs
Çayır, Atilla
Dündar, İsmail
Akbaş, Emine Demet
Uçaktürk, Seyid Ahmet
Berberoğlu, Merih
Şıklar, Zeynep
Özalkak, Şervan
Şahin, Nursel Muratoğlu
Keskin, Melikşah
Şiraz, Ülkü Gül
Turan, Hande
Öztürk, Ayşe Pınar
Mengen, Eda
Source :
Journal of Clinical Research in Pediatric Endocrinology; Sep2024, Vol. 16 Issue 3, p297-305, 9p
Publication Year :
2024

Abstract

Objective: Maturity onset diabetes of the young (MODY) occurs due to mutations in genes involved in pancreatic beta cell function and insulin secretion, has heterogeneous clinical and laboratory features, and account for 1-5% of all diabetes cases. The prevalence and distribution of MODY subtypes vary between countries. The aim of this study was to evaluate the clinical and laboratory characteristics, mutation distribution, and phenotype-genotype relationship in a large case series of pediatric Turkish patients genetically diagnosed with MODY. Methods: MODY cases from 14 different pediatric endocrinology departments were included. Diagnosis, treatment, follow-up data, and results of genetic analysis were evaluated. Results: A total of 224 patients were included, of whom 101 (45%) were female, and the mean age at diagnosis was 9.4±4.1 years. Gene variant distribution was: 146 (65%) GCK; 43 (19%) HNF1A; 8 (3.6%) HNF4A, 8 (3.6%) KLF11 and 7 (3.1%) HNF1B. The remaining 12 variants were: PDX (n=1), NEUROD1 (n=3), CEL (n=1), INS (n=3), ABCC8 (n= 3) and KJNC11 (n=1). Of the cases, 197 (87.9%) were diagnosed with incidental hyperglycemia, 16 with ketosis (7%) and 7 (3%) with diabetic ketoacidosis (DKA), while 30% presented with classical symptoms of diabetes. Two-hundred (89%) had a family history of diabetes. Anti-GAD antibody was detected in 13 cases, anti-islet antibody in eight and anti-insulin antibody in four. Obesity was present in 16. Distribution of therapy was: 158 (71%) diet only; 23 (11%) intensive insulin treatment; 17 (7.6%) sulfonylureas; 10 (4.5%) metformin; and 6 (2.7%) insulin and oral anti-diabetic treatment. Conclusion: This was the largest genetically diagnosed series from Turkey. The most common gene variants were GCK and HNF1A with much lower proportions for other MODY types. Hyperglycemia was the most common presenting symptom while 11% of patients had diabetes-associated autoantibodies and 7% were obese. The majority of patients received dietary management only. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13085727
Volume :
16
Issue :
3
Database :
Complementary Index
Journal :
Journal of Clinical Research in Pediatric Endocrinology
Publication Type :
Academic Journal
Accession number :
179504313
Full Text :
https://doi.org/10.4274/jcrpe.galenos.2024.2023-10-16