Clinical and Laboratory Characteristics of MODY (Maturity Onset Diabetes of Young) Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship.

Childhood Diagnosis MODY

Journal

Journal of clinical research in pediatric endocrinology
ISSN: 1308-5735
Titre abrégé: J Clin Res Pediatr Endocrinol
Pays: Turkey
ID NLM: 101519456

Informations de publication

Date de publication:
26 Apr 2024
Historique:
medline: 26 4 2024
pubmed: 26 4 2024
entrez: 26 4 2024
Statut: aheadofprint

Résumé

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. MODY cases from 14 different pediatric endocrinology departments were included. Diagnosis, treatment, follow-up data, and results of genetic analysis were evaluated. 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 antidiabetic treatment. 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.

Identifiants

pubmed: 38665000
doi: 10.4274/jcrpe.galenos.2024.2023-10-16
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Elif Özsu (E)

Department of Pediatric Endocrinology, Ankara University Faculty of Medicine, Ankara, Turkiye.

Semra Çetinkaya (S)

Department of Pediatric Endocrinology, Pediatric Health and Disease Training and Research Hospital, Dr. Sami Ulus Obstetrics and Gynecology, Ankara, Turkey.

Semih Bolu (S)

Department of Pediatric Endocrinology Adıyaman Training and Research Hospital, Adıyaman, Turkey.

Nihal Hatipoğlu (N)

Department of Pediatric Endocrinology, Erciyes University Faculty of Medicine, Kayseri, Turkey.

Şenay Savaş Erdeve (Ş)

Department of Pediatric Endocrinology, Pediatric Health and Disease Training and Research Hospital, Dr. Sami Ulus Obstetrics and Gynecology, Ankara, Turkey.

Olcay Evliyaoğlu (O)

Department of Pediatric Endocrinology, İstanbul University Cerrahpaşa Faculty of Medicine, Istanbul, Turkey.

Firdevs Baş (F)

Department of Pediatric Endocrinology,İstanbul University Istanbul Faculty of Medicine, Istanbul ,Turkey.

Atilla Çayır (A)

Department of Pediatric Endocrinology, Erzurum Regional Training and Research Hospital, Erzurum, Turkey.

İsmail Dündar (İ)

Department of Pediatric Endocrinology, Malatya Training and Research Hospital, Malatya, Turkey.

Emine Demet Akbaş (ED)

Department of Pediatric Endocrinology, Adana Tranining and Research Hospital, Adana, Turkey.

Seyid Ahmet Uçaktürk (SA)

Department of Pediatric Endocrinology, Adana Tranining and Research Hospital, Adana, Turkey.

Merih Berberoğlu (M)

Department of Pediatric Endocrinology, Ankara University Faculty of Medicine, Ankara, Turkiye.

Zeynep Şıklar (Z)

Department of Pediatric Endocrinology, Ankara University Faculty of Medicine, Ankara, Turkiye.

Şervan Özalkak (Ş)

Department of Pediatric Endocrinology, Pediatric Health and Disease Training and Research Hospital, Dr. Sami Ulus Obstetrics and Gynecology, Ankara, Turkey.

Nursel Muratoğlu Şahin (N)

Department of Pediatric Endocrinology, Pediatric Health and Disease Training and Research Hospital, Dr. Sami Ulus Obstetrics and Gynecology, Ankara, Turkey.

Melikşah Keskin (M)

Department of Pediatric Endocrinology, Pediatric Health and Disease Training and Research Hospital, Dr. Sami Ulus Obstetrics and Gynecology, Ankara, Turkey.

Ülkü Gül Şiraz (ÜG)

Department of Pediatric Endocrinology, Erciyes University Faculty of Medicine, Kayseri, Turkey.

Hande Turan (H)

Department of Pediatric Endocrinology, İstanbul University Cerrahpaşa Faculty of Medicine, Istanbul, Turkey.

Ayşe Pınar Öztürk (AP)

Department of Pediatric Endocrinology,İstanbul University Istanbul Faculty of Medicine, Istanbul ,Turkey.

Eda Mengen (E)

Department of Pediatric Endocrinology, Cukurova University School of Medicine, Adana, Turkey.

Elif Sağsak (E)

Department of Pediatric Endocrinology Yeditepe University School of Medicine, İstanbul, Turkey.

Fatma Dursun (F)

Department of Pediatric Endocrinology, Ümraniye Training and Research Hospital, Istanbul, Turkey.

Nesibe Akyürek (N)

Department of Pediatric Endocrinology, Başkent University Konya Training and Research Hospital, Konya, Turkey.

Sevinç Odabaşı Guneş (S)

Department of Pediatric Endocrinology, Gülhane Training and Research Hospital, Ankara, Turkey.

Zehra Aycan (Z)

Department of Pediatric Endocrinology, Ankara University Faculty of Medicine, Ankara, Turkiye.

Classifications MeSH