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Diabetes Obes Metab. 2020 Jul;22(7):1009-1013. doi: 10.1111/dom.14022. Epub 2020 Mar 24.
2
Gluten Intake and Risk of Islet Autoimmunity and Progression to Type 1 Diabetes in Children at Increased Risk of the Disease: The Diabetes Autoimmunity Study in the Young (DAISY).谷物摄入量与儿童胰岛自身免疫及向 1 型糖尿病进展的风险:儿童糖尿病自身免疫研究(DAISY)。
Diabetes Care. 2019 May;42(5):789-796. doi: 10.2337/dc18-2315. Epub 2019 Feb 22.
3
The human gut microbiome in early-onset type 1 diabetes from the TEDDY study.TEDDY 研究中的早发性 1 型糖尿病患者的人类肠道微生物组。
Nature. 2018 Oct;562(7728):589-594. doi: 10.1038/s41586-018-0620-2. Epub 2018 Oct 24.
4
The Environmental Determinants of Diabetes in the Young (TEDDY) Study: 2018 Update.《儿童期糖尿病的环境决定因素研究(TEDDY):2018 更新》。
Curr Diab Rep. 2018 Oct 23;18(12):136. doi: 10.1007/s11892-018-1113-2.
5
Incidence and risk of celiac disease after type 1 diabetes: A population-based cohort study using the health improvement network database.1 型糖尿病后乳糜泻的发病风险:一项基于人群的队列研究,使用健康改善网络数据库。
Pediatr Diabetes. 2018 Dec;19(8):1422-1428. doi: 10.1111/pedi.12770. Epub 2018 Oct 9.
6
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7
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8
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10
Coxsackievirus B1 infections are associated with the initiation of insulin-driven autoimmunity that progresses to type 1 diabetes.柯萨奇病毒 B1 感染与胰岛素驱动的自身免疫的启动有关,而后者会进展为 1 型糖尿病。
Diabetologia. 2018 May;61(5):1193-1202. doi: 10.1007/s00125-018-4561-y. Epub 2018 Feb 5.

识别1型糖尿病环境决定因素的挑战:寻找圣杯

The Challenges of Identifying Environmental Determinants of Type 1 Diabetes: In Search of the Holy Grail.

作者信息

Butalia Sonia, Kaplan Gilaad G, Khokhar Bushra, Haubrich Sydney, Rabi Doreen M

机构信息

Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

出版信息

Diabetes Metab Syndr Obes. 2020 Dec 9;13:4885-4895. doi: 10.2147/DMSO.S275080. eCollection 2020.

DOI:10.2147/DMSO.S275080
PMID:33328748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7734044/
Abstract

Type 1 diabetes is the result of autoimmune-mediated destruction and inflammation of the insulin-producing β-cells of the pancreas. The excess morbidity and mortality from its complications coupled with its increasing incidence emphasize the importance to better understand the etiology of this condition. It has a strong genetic component, but a genetic predisposition is not the sole contributor to disease development as only 30% to 50% of identical twins both develop the disease. In addition, there are multiple lines of evidence to support that environmental factors contribute to the pathogenesis of type 1 diabetes. Environmental risk factors that have been proposed include infections, dietary factors, air pollution, vaccines, location of residence, childhood obesity, family environment and stress. Researchers have conducted many observational studies to identify and characterize these potential environmental factors, but findings have been inconsistent or inconclusive. Many studies have had inherent methodological issues in recruitment, participation, defining cases and exposures, and/or data analysis which may limit the interpretability of findings. Identifying and addressing these limitations may allow for greatly needed advances in our understanding of type 1 diabetes. As such, the purpose of this article is to review and discuss the limitations of observational studies that aim to determine environmental risk factors for type 1 diabetes and propose recommendations to overcome them.

摘要

1型糖尿病是胰腺中产生胰岛素的β细胞受到自身免疫介导的破坏和炎症的结果。其并发症导致的过高发病率和死亡率,以及发病率的不断上升,凸显了更好地了解这种疾病病因的重要性。它有很强的遗传成分,但遗传易感性并非疾病发展的唯一因素,因为只有30%至50%的同卵双胞胎都会患这种疾病。此外,有多项证据支持环境因素在1型糖尿病发病机制中起作用。已提出的环境风险因素包括感染、饮食因素、空气污染、疫苗、居住地点、儿童肥胖、家庭环境和压力。研究人员进行了许多观察性研究来识别和描述这些潜在的环境因素,但结果并不一致或尚无定论。许多研究在招募、参与、定义病例和暴露因素以及/或者数据分析方面存在固有的方法学问题,这可能会限制研究结果的可解释性。识别并解决这些局限性可能会使我们在对1型糖尿病的理解上取得急需的进展。因此,本文的目的是回顾和讨论旨在确定1型糖尿病环境风险因素的观察性研究的局限性,并提出克服这些局限性的建议。