Exploring the severity and early onset of familial type 1 diabetes in Romania: genetic and microbiota insights.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Archive of clinical cases Pub Date : 2024-04-30 eCollection Date: 2024-01-01 DOI:10.22551/2024.42.1101.10283
Amalia Ioana Arhire, Dorian Sorin Ioacara, Teodora Papuc, Gratiela Gradisteanu Parcalibioru, Simona Fica
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Abstract

Type 1 diabetes mellitus (T1DM) is a chronic condition characterized by pancreatic autoimmunity and destruction of the insulin producing beta-cells. The risk of familial type 1 diabetes (FT1DM) is greater in families with paternal T1DM. The children with paternal FT1DM have a more severe form of the disease with diabetic ketoacidosis. Three families with FT1DM, out of which two with paternal diabetes and daughters diagnosed with this disease, and one family with sibling FT1DM were evaluated between 2019-2021 in the Pediatric Diabetes and the Diabetes, Nutrition and Metabolic Departments of a tertiary hospital. Clinical, biological, and genetic evaluations were performed, together with an assessment of the gastrointestinal microbiota. The Romanian children with FT1DM had a more severe onset, a median of age at onset of 9 years old and a genetic predisposition with positive HLA DR3/R4, DQB1*02:01. The protecting allele, DPB1*04:01, was found only in the siblings with FT1DM. A gastrointestinal dysbiosis, characterized by pro-inflammatory bacteria, with high levels of Enterobacteriaceae and Candida, was observed in the gut microbiota. This is the first case series of FT1DM in Romanian patients that shows the presence of genetic determinants but also a pathological microbiota which may determine a more severe and an early-age onset of disease.

探索罗马尼亚家族性 1 型糖尿病的严重性和早期发病情况:遗传和微生物群的启示。
1 型糖尿病(T1DM)是一种慢性疾病,其特点是胰腺自身免疫和产生胰岛素的 beta 细胞遭到破坏。在父系患有 T1DM 的家族中,患家族性 1 型糖尿病(FT1DM)的风险更大。父系 FT1DM 患儿的病情更为严重,会出现糖尿病酮症酸中毒。一家三甲医院的儿童糖尿病科和糖尿病、营养与代谢科在2019-2021年间对三个FT1DM家庭进行了评估,其中两个家庭的父亲患有糖尿病,女儿也被诊断患有此病,还有一个家庭的兄弟姐妹都患有FT1DM。他们进行了临床、生物学和遗传学评估,并对胃肠道微生物群进行了评估。患有 FT1DM 的罗马尼亚儿童发病较严重,发病年龄中位数为 9 岁,遗传倾向为 HLA DR3/R4、DQB1*02:01 阳性。保护性等位基因 DPB1*04:01 仅在患有 FT1DM 的兄弟姐妹中发现。在肠道微生物群中观察到胃肠道菌群失调,其特征是肠道微生物群中含有大量肠杆菌科和白色念珠菌的促炎细菌。这是罗马尼亚 FT1DM 患者的首例系列病例,显示了遗传决定因素和病理微生物群的存在,而病理微生物群可能决定疾病的严重程度和发病年龄。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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