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

IF 1.5 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Journal of Clinical Research in Pediatric Endocrinology Pub Date : 2024-09-05 Epub Date: 2024-04-26 DOI:10.4274/jcrpe.galenos.2024.2023-10-16
Elif Özsu, Semra Çetinkaya, Semih Bolu, Nihal Hatipoğlu, Şenay Savaş Erdeve, Olcay Evliyaoğlu, Firdevs Baş, Atilla Çayır, İsmail Dündar, Emine Demet Akbaş, Seyid Ahmet Uçaktürk, Merih Berberoğlu, Zeynep Şıklar, Şervan Özalkak, Nursel Muratoğlu Şahin, Melikşah Keskin, Ülkü Gül Şiraz, Hande Turan, Ayşe Pınar Öztürk, Eda Mengen, Elif Sağsak, Fatma Dursun, Nesibe Akyürek, Sevinç Odabaşı Güneş, Zehra Aycan
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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.

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MODY(青年成熟型糖尿病)病例的临床和实验室特征、基因突变谱和表型-基因型关系。
目的:成熟-发病型青年糖尿病(MODY)是由于参与胰岛β细胞功能和胰岛素分泌的基因发生突变而引起的,具有不同的临床和实验室特征,占所有糖尿病病例的 1-5%。不同国家 MODY 亚型的发病率和分布情况各不相同。本研究的目的是评估经基因诊断为 MODY 的土耳其儿科患者的临床和实验室特征、突变分布以及表型与基因型的关系:方法:纳入来自 14 个不同儿科内分泌科的 MODY 病例。方法:纳入来自 14 个不同儿科内分泌科的 MODY 病例,对诊断、治疗、随访数据和基因分析结果进行评估:结果:共纳入 224 例患者,其中 101 例(45%)为女性,诊断时的平均年龄为(9.4±4.1)岁。基因变异分布为:146个(65%)GCK、43个(19%)HNF1A、8个(3.6%)HNF4A、8个(3.6%)KLF11和7个(3.1%)HNF1B。其余 12 个变异体分别是PDX(n=1)、NEUROD1(n=3)、CEL(n=1)、INS(n=3)、ABCC8(n=3)和KJNC11(n=1)。在这些病例中,197 例(87.9%)被诊断为偶发性高血糖,16 例(7%)被诊断为酮症,7 例(3%)被诊断为糖尿病酮症酸中毒(DKA),30%的病例表现为典型的糖尿病症状。200人(89%)有糖尿病家族史。13 例患者检测出抗 GAD 抗体,8 例检测出抗胰岛素抗体,4 例检测出抗胰岛素抗体。肥胖症患者有 16 例。治疗分布情况为:158 例(71%)仅接受饮食治疗;23 例(11%)接受胰岛素强化治疗;17 例(7.6%)接受磺脲类药物治疗;10 例(4.5%)接受二甲双胍治疗;6 例(2.7%)接受胰岛素和口服抗糖尿病药物治疗:这是土耳其最大的基因诊断系列。最常见的基因变异是 GCK 和 HNF1A,其他 MODY 类型的比例要低得多。高血糖是最常见的症状,11%的患者有糖尿病相关自身抗体,7%的患者肥胖。大多数患者只接受饮食治疗。
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来源期刊
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology ENDOCRINOLOGY & METABOLISM-PEDIATRICS
CiteScore
3.60
自引率
5.30%
发文量
73
审稿时长
20 weeks
期刊介绍: The Journal of Clinical Research in Pediatric Endocrinology (JCRPE) publishes original research articles, reviews, short communications, letters, case reports and other special features related to the field of pediatric endocrinology. JCRPE is published in English by the Turkish Pediatric Endocrinology and Diabetes Society quarterly (March, June, September, December). The target audience is physicians, researchers and other healthcare professionals in all areas of pediatric endocrinology.
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