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Makale Tam Makale Uluslararası 2024

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

ELİF ÖZSU, Semra Cetinkaya, Semih Bolu, NİHAL HATİPOĞLU, Senay Savas Erdeve, SAADET OLCAY EVLİYAOĞLU, Firdevs BAŞ, Atilla Çayır, İSMAİL DÜNDAR, Emine Demet Akbas, Seyid Ahmet Ucakturk, Merih Berberoglu, Zeynep Siklar, Servan Ozalkak, Nursel Muratoglu Sahin, Meliksah Keskin, Ulku Gul Siraz, Hande Turan, Ayse Pinar Ozturk, Eda Mengen, Elif Sagsak, Fatma Dursun, Nesibe Akyurek, Sevinc Odabasi Gunes, Zehra Aycan

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY Cilt 16 · Sayı 3 · ss. 297–305 · 01.09.2024
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Özet

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.

Sürdürülebilir Kalkınma Amaçları

  • SKA 3: Sağlıklı Bireyler

Atıf için künye

ÖZSU, E., Cetinkaya, S., Bolu, S., HATİPOĞLU, N., Erdeve, S. S., EVLİYAOĞLU, S. O., BAŞ, F., Çayır, A., DÜNDAR, İ., Akbas, E. D., Ucakturk, S. A., Berberoglu, M., Siklar, Z., Ozalkak, S., Sahin, N. M., Keskin, M., Siraz, U. G., Turan, H., Ozturk, A. P., … Aycan, Z. (2024). Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, 16(3), 297–305. https://doi.org/10.4274/jcrpe.galenos.2024.2023-10-16

BibTeX
@article{ozsu2024-246729,
  author = {ÖZSU, ELİF and Cetinkaya, Semra and Bolu, Semih and HATİPOĞLU, NİHAL and Erdeve, Senay Savas and EVLİYAOĞLU, SAADET OLCAY and BAŞ, Firdevs and Çayır, Atilla and DÜNDAR, İSMAİL and Akbas, Emine Demet and Ucakturk, Seyid Ahmet and Berberoglu, Merih and Siklar, Zeynep and Ozalkak, Servan and Sahin, Nursel Muratoglu and Keskin, Meliksah and Siraz, Ulku Gul and Turan, Hande and Ozturk, Ayse Pinar and Mengen, Eda and Sagsak, Elif and Dursun, Fatma and Akyurek, Nesibe and Gunes, Sevinc Odabasi and Aycan, Zehra},
  title = {Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship},
  journal = {JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY},
  year = {2024},
  volume = {16},
  number = {3},
  pages = {297--305},
  issn = {1308-5727},
  doi = {10.4274/jcrpe.galenos.2024.2023-10-16},
  url = {https://akademik.atauni.edu.tr/yayinlar/246729-clinical-and-laboratory-characteristics-of-mody-cases-genetic-mutation-spectrum}
}