青少年成熟型糖尿病(MODY)的流行病学、分子发病机制、诊断和治疗。

Ken Munene Nkonge, Dennis Karani Nkonge, Teresa Njeri Nkonge
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引用次数: 66

摘要

背景:最常见的单基因糖尿病类型是青年成熟型糖尿病(MODY),这是一种临床和遗传异质性的内分泌紊乱组,影响1-5%的糖尿病患者。MODY的特点是常染色体显性遗传,但也有新发突变的报道。MODY的临床特征包括年轻时出现高血糖、胰腺功能残留、缺乏β细胞自身免疫或胰岛素抵抗。降糖药物是MODY的主要治疗选择。临床医生、研究人员和政府日益认识到MODY的临床和公共卫生意义,这可能会改善筛查和诊断实践。因此,本文结合1975年至2020年发表的相关文献,对MODY的流行病学、发病机制、诊断和治疗进行综述。主体:欧洲队列中MODY的估计患病率为成人1 / 10,000,儿童1 / 23,000。由于对MODY在非洲、亚洲、南美和中东人群中的患病率知之甚少,因此需要对非欧洲人群进行进一步研究,以帮助阐明MODY的确切患病率。目前,通过临床评估和基因分析可以诊断出14种不同的MODY亚型。多种基因突变和疾病机制参与了MODY的发病机制。MODY的治疗是亚型特异性的,包括饮食、口服降糖药或胰岛素。结论:MODY的发病率和患病率估计来自欧洲、澳大利亚和北美的年轻糖尿病患者的流行病学研究。MODY的发病机制包括转录调控缺陷、代谢酶异常、蛋白质错误折叠、离子通道功能障碍或信号转导受损。临床医生应该了解MODY的流行病学和发病机制,因为这些知识对于准确诊断,个性化患者管理和家庭成员筛查至关重要。
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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The epidemiology, molecular pathogenesis, diagnosis, and treatment of maturity-onset diabetes of the young (MODY).

Background: The most common type of monogenic diabetes is maturity-onset diabetes of the young (MODY), a clinically and genetically heterogeneous group of endocrine disorders that affect 1-5% of all patients with diabetes mellitus. MODY is characterized by autosomal dominant inheritance but de novo mutations have been reported. Clinical features of MODY include young-onset hyperglycemia, evidence of residual pancreatic function, and lack of beta cell autoimmunity or insulin resistance. Glucose-lowering medications are the main treatment options for MODY. The growing recognition of the clinical and public health significance of MODY by clinicians, researchers, and governments may lead to improved screening and diagnostic practices. Consequently, this review article aims to discuss the epidemiology, pathogenesis, diagnosis, and treatment of MODY based on relevant literature published from 1975 to 2020.

Main body: The estimated prevalence of MODY from European cohorts is 1 per 10,000 in adults and 1 per 23,000 in children. Since little is known about the prevalence of MODY in African, Asian, South American, and Middle Eastern populations, further research in non-European cohorts is needed to help elucidate MODY's exact prevalence. Currently, 14 distinct subtypes of MODY can be diagnosed through clinical assessment and genetic analysis. Various genetic mutations and disease mechanisms contribute to the pathogenesis of MODY. Management of MODY is subtype-specific and includes diet, oral antidiabetic drugs, or insulin.

Conclusions: Incidence and prevalence estimates for MODY are derived from epidemiologic studies of young people with diabetes who live in Europe, Australia, and North America. Mechanisms involved in the pathogenesis of MODY include defective transcriptional regulation, abnormal metabolic enzymes, protein misfolding, dysfunctional ion channels, or impaired signal transduction. Clinicians should understand the epidemiology and pathogenesis of MODY because such knowledge is crucial for accurate diagnosis, individualized patient management, and screening of family members.

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来源期刊
自引率
0.00%
发文量
7
审稿时长
8 weeks
期刊介绍: Clinical Diabetes and Endocrinology is an open access journal publishing within the field of diabetes and endocrine disease. The journal aims to provide a widely available resource for people working within the field of diabetes and endocrinology, in order to improve the care of people affected by these conditions. The audience includes, but is not limited to, physicians, researchers, nurses, nutritionists, pharmacists, podiatrists, psychologists, epidemiologists, exercise physiologists and health care researchers. Research articles include patient-based research (clinical trials, clinical studies, and others), translational research (translation of basic science to clinical practice, translation of clinical practice to policy and others), as well as epidemiology and health care research. Clinical articles include case reports, case seminars, consensus statements, clinical practice guidelines and evidence-based medicine. Only articles considered to contribute new knowledge to the field will be considered for publication.
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