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本文引用的文献

1
Growth and development of islet autoimmunity and type 1 diabetes in children genetically at risk.胰岛自身免疫和 1 型糖尿病在遗传风险儿童中的生长和发育。
Diabetologia. 2021 Apr;64(4):826-835. doi: 10.1007/s00125-020-05358-3. Epub 2021 Jan 21.
2
Association between family history, early growth and the risk of beta cell autoimmunity in children at risk for type 1 diabetes.家族史、早期生长与 1 型糖尿病高危儿童胰岛自身免疫风险的相关性。
Diabetologia. 2021 Jan;64(1):119-128. doi: 10.1007/s00125-020-05287-1. Epub 2020 Oct 7.
3
Thyroid peroxidase antibodies are common in children with HLA-conferred susceptibility to type 1 diabetes, but are weakly associated with thyroid function.甲状腺过氧化物酶抗体在具有HLA基因赋予1型糖尿病易感性的儿童中很常见,但与甲状腺功能的关联较弱。
J Pediatr Endocrinol Metab. 2020 Jul 7. doi: 10.1515/jpem-2019-0512.
4
Fluctuations in the incidence of type 1 diabetes in the United States from 2001 to 2015: a longitudinal study.2001年至2015年美国1型糖尿病发病率的波动:一项纵向研究。
BMC Med. 2017 Nov 8;15(1):199. doi: 10.1186/s12916-017-0958-6.
5
Growth and Risk for Islet Autoimmunity and Progression to Type 1 Diabetes in Early Childhood: The Environmental Determinants of Diabetes in the Young Study.幼儿期胰岛自身免疫的生长与风险及1型糖尿病进展:青少年糖尿病环境决定因素研究
Diabetes. 2016 Jul;65(7):1988-95. doi: 10.2337/db15-1180. Epub 2016 Mar 18.
6
Prediction and prevention of type 1 diabetes: update on success of prediction and struggles at prevention.1型糖尿病的预测与预防:预测成果及预防难题的最新进展
Pediatr Diabetes. 2015 Nov;16(7):465-84. doi: 10.1111/pedi.12299. Epub 2015 Jul 23.
7
Circulating IGF1 and IGFBP3 in relation to the development of β-cell autoimmunity in young children.循环 IGF1 和 IGFBP3 与幼儿胰岛自身免疫的发展有关。
Eur J Endocrinol. 2015 Aug;173(2):129-37. doi: 10.1530/EJE-14-1078. Epub 2015 May 6.
8
Prevalence of obesity was related to HLA-DQ in 2-4-year-old children at genetic risk for type 1 diabetes.在有1型糖尿病遗传风险的2至4岁儿童中,肥胖患病率与HLA - DQ相关。
Int J Obes (Lond). 2014 Dec;38(12):1491-6. doi: 10.1038/ijo.2014.55. Epub 2014 Apr 3.
9
Early postnatal growth in children with HLA-conferred susceptibility to type 1 diabetes.1 型糖尿病 HLA 易感患儿的早期产后生长。
Diabetes Metab Res Rev. 2014 Jan;30(1):60-8. doi: 10.1002/dmrr.2449.
10
Association of variants in HLA-DQA1-DQB1, PTPN22, INS, and CTLA4 with GAD autoantibodies and insulin secretion in nondiabetic adults of the Botnia Prospective Study.在 Botnia 前瞻性研究中,非糖尿病成年人的 HLA-DQA1-DQB1、PTPN22、INS 和 CTLA4 中的变异与 GAD 自身抗体和胰岛素分泌的关联。
Eur J Endocrinol. 2012 Jul;167(1):27-33. doi: 10.1530/EJE-12-0023. Epub 2012 Apr 16.

1 型糖尿病 HLA 易感儿童的生长情况。

Growth in Children with HLA-Conferred Susceptibility to Type 1 Diabetes.

机构信息

Department of Pediatrics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.

Children's Clinic, Tartu University Hospital, Tartu, Estonia.

出版信息

Endocrinol Metab (Seoul). 2022 Feb;37(1):175-179. doi: 10.3803/EnM.2021.1262. Epub 2022 Feb 28.

DOI:10.3803/EnM.2021.1262
PMID:35255609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8901960/
Abstract

The incidence of type 1 diabetes (T1D) is increasing throughout the world. This trend may be explained by the accelerator hypothesis. Our study investigated growth, its biochemical markers, and their associations with the development of diabetes-associated autoantibodies (DAAB) in 219 children with genetic risk for T1D. Subjects were divided into risk groups based on their human leukocyte antigen genotype. Children in the moderate- to high-risk group were significantly taller when corrected to mid-parental height and had a lower insulin-like growth factor 1 (IGF-1)/IGF-1 binding protein (IGFBP-3) molar ratio than those in the low-risk group (corrected height standard deviation score 0.22±0.93 vs. -0.04±0.84, P<0.05; molar ratio 0.199±0.035 vs. 0.211+0.039, P<0.05). Children with DAAB tended to be taller and to have a higher body mass index than those with no DAAB. Our results suggest that the accelerator hypothesis explaining the increasing incidence of T1D may not solely be dependent on environmental factors, but could be partially genetically determined.

摘要

1 型糖尿病(T1D)的发病率在全球范围内呈上升趋势。这种趋势可以用加速器假说来解释。我们的研究调查了 219 名具有 T1D 遗传风险的儿童的生长、其生化标志物及其与糖尿病相关自身抗体(DAAB)发展的关系。根据人类白细胞抗原基因型将受试者分为风险组。与低风险组相比,中高危组的儿童校正至中亲身高时明显更高,胰岛素样生长因子 1(IGF-1)/IGF-1 结合蛋白(IGFBP-3)摩尔比更低(校正身高标准差评分 0.22±0.93 与-0.04±0.84,P<0.05;摩尔比 0.199±0.035 与 0.211+0.039,P<0.05)。有 DAAB 的儿童往往比没有 DAAB 的儿童更高,体重指数也更高。我们的结果表明,解释 T1D 发病率上升的加速器假说可能不仅仅取决于环境因素,而可能部分是由遗传决定的。