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1 型糖尿病的变化格局:最新进展和未来前沿。

The changing landscape of type 1 diabetes: recent developments and future frontiers.

机构信息

Pediatrics Epidemiology Center, Morsani College of Medicine, University of South Florida, 3650 Spectrum Blvd, Ste 100, Tampa, FL, 33612, USA,

出版信息

Curr Diab Rep. 2013 Oct;13(5):642-50. doi: 10.1007/s11892-013-0406-8.

DOI:10.1007/s11892-013-0406-8
PMID:23912764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3827778/
Abstract

Type 1 diabetes (T1D) research has made great strides over the past decade with advances in understanding the pathogenesis, natural history, candidate environmental exposures, exposure triggering time, disease prediction, and diagnosis. Major monitoring efforts have provided baseline historical measures, leading to better epidemiological studies incorporating longitudinal biosamples (ie, biobanks), which have allowed for new technologies ('omics') to further expose the etiological agents responsible for the initiation, progression, and eventual clinical onset of T1D. These new frontiers have brought forth high-dimensionality data, which have furthered the evidence of the heterogeneous nature of T1D pathogenesis and allowed for a more mechanistic approach in understanding the etiology of T1D. This review will expand on the most recent advances in the quest for T1D determinants, drawing upon novel research tools that epidemiology, genetics, microbiology, and immunology have provided, linking them to the major hypotheses associated with T1D etiology, and discussing the future frontiers.

摘要

在过去的十年中,随着对发病机制、自然史、候选环境暴露、暴露触发时间、疾病预测和诊断的深入理解,1 型糖尿病(T1D)的研究取得了重大进展。主要的监测工作提供了基线历史数据,从而使纳入纵向生物样本(即生物库)的流行病学研究更加完善,这也为新技术(组学)提供了条件,进一步揭示了导致 T1D 发生、进展和最终临床发作的病因。这些新的前沿领域带来了高维度的数据,进一步证明了 T1D 发病机制的异质性,并为理解 T1D 的病因提供了更具机制性的方法。本综述将扩展 T1D 决定因素的最新进展,借鉴流行病学、遗传学、微生物学和免疫学提供的新研究工具,将其与与 T1D 病因相关的主要假设联系起来,并讨论未来的前沿领域。

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本文引用的文献

1
Next generation sequencing reveals the association of DRB3*02:02 with type 1 diabetes.下一代测序揭示了 DRB3*02:02 与 1 型糖尿病的关联。
Diabetes. 2013 Jul;62(7):2618-22. doi: 10.2337/db12-1387. Epub 2013 Mar 5.
2
Revisiting the notion of type 1 diabetes being a T-cell-mediated autoimmune disease.重新审视 1 型糖尿病是 T 细胞介导的自身免疫性疾病这一概念。
Curr Opin Endocrinol Diabetes Obes. 2013 Apr;20(2):118-23. doi: 10.1097/MED.0b013e32835edb89.
3
Preclinical serum 25-hydroxyvitamin D levels and risk of type 1 diabetes in a cohort of US military personnel.美国军事人员队列研究中血清 25-羟维生素 D 水平与 1 型糖尿病风险
Am J Epidemiol. 2013 Mar 1;177(5):411-9. doi: 10.1093/aje/kws243. Epub 2013 Feb 3.
4
Pathogenesis of type 1 diabetes: lessons from natural history studies of high-risk individuals.1 型糖尿病的发病机制:高危个体自然史研究的启示。
Ann N Y Acad Sci. 2013 Apr;1281(1):1-15. doi: 10.1111/nyas.12021. Epub 2013 Jan 29.
5
Fecal microbiota composition differs between children with β-cell autoimmunity and those without.粪便微生物组成在β-细胞自身免疫的儿童和无β-细胞自身免疫的儿童之间存在差异。
Diabetes. 2013 Apr;62(4):1238-44. doi: 10.2337/db12-0526. Epub 2012 Dec 28.
6
The environment and the origins of islet autoimmunity and Type 1 diabetes.胰岛自身免疫和 1 型糖尿病的环境和起源。
Diabet Med. 2013 Feb;30(2):155-60. doi: 10.1111/dme.12099.
7
Projections of type 1 and type 2 diabetes burden in the U.S. population aged <20 years through 2050: dynamic modeling of incidence, mortality, and population growth.2050 年美国<20 岁人群 1 型和 2 型糖尿病负担预测:发病率、死亡率和人口增长的动态建模。
Diabetes Care. 2012 Dec;35(12):2515-20. doi: 10.2337/dc12-0669.
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Enterovirus RNA in peripheral blood may be associated with the variants of rs1990760, a common type 1 diabetes associated polymorphism in IFIH1.外周血中的肠道病毒 RNA 可能与 IFIH1 中常见的 1 型糖尿病相关多态性 rs1990760 的变体有关。
PLoS One. 2012;7(11):e48409. doi: 10.1371/journal.pone.0048409. Epub 2012 Nov 7.
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Investigation of the vitamin D receptor gene (VDR) and its interaction with protein tyrosine phosphatase, non-receptor type 2 gene (PTPN2) on risk of islet autoimmunity and type 1 diabetes: the Diabetes Autoimmunity Study in the Young (DAISY).维生素 D 受体基因(VDR)及其与蛋白酪氨酸磷酸酶非受体型 2 基因(PTPN2)在胰岛自身免疫和 1 型糖尿病发病风险中的相关性研究:青少年糖尿病自身免疫研究(DAISY)。
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Autologous regulatory T cells for the treatment of type 1 diabetes.自体调节性 T 细胞治疗 1 型糖尿病。
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