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本文引用的文献

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ISPAD Clinical Practice Consensus Guidelines 2022: Definition, epidemiology, and classification of diabetes in children and adolescents.《国际儿童青少年糖尿病研究学会(ISPAD)2022临床实践共识指南:儿童和青少年糖尿病的定义、流行病学及分类》
Pediatr Diabetes. 2022 Dec;23(8):1160-1174. doi: 10.1111/pedi.13454.
2
2. Classification and Diagnosis of Diabetes: Standards of Care in Diabetes-2023.2. 糖尿病的分类和诊断:2023 年糖尿病护理标准。
Diabetes Care. 2023 Jan 1;46(Suppl 1):S19-S40. doi: 10.2337/dc23-S002.
3
ISPAD Clinical Practice Consensus Guidelines 2022: Type 2 diabetes in children and adolescents.ISPAD 临床实践共识指南 2022:儿童和青少年 2 型糖尿病。
Pediatr Diabetes. 2022 Nov;23(7):872-902. doi: 10.1111/pedi.13409. Epub 2022 Sep 25.
4
Type 2 diabetes mellitus: pathogenesis and genetic diagnosis.2型糖尿病:发病机制与基因诊断
J Diabetes Metab Disord. 2020 Sep 22;19(2):1959-1966. doi: 10.1007/s40200-020-00641-x. eCollection 2020 Dec.
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Pediatric Type 2 Diabetes: Not a Mini Version of Adult Type 2 Diabetes.儿童 2 型糖尿病:并非成人 2 型糖尿病的缩影。
Endocrinol Metab Clin North Am. 2020 Dec;49(4):679-693. doi: 10.1016/j.ecl.2020.08.003. Epub 2020 Oct 14.
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Diagnosis, Therapy and Follow-Up of Diabetes Mellitus in Children and Adolescents.儿童和青少年糖尿病的诊断、治疗及随访
Exp Clin Endocrinol Diabetes. 2019 Dec;127(S 01):S39-S72. doi: 10.1055/a-1018-8963. Epub 2019 Dec 20.
7
ISPAD Clinical Practice Consensus Guidelines 2018: Type 2 diabetes mellitus in youth.《国际儿童青少年糖尿病学会(ISPAD)2018年临床实践共识指南:青少年2型糖尿病》
Pediatr Diabetes. 2018 Oct;19 Suppl 27:28-46. doi: 10.1111/pedi.12719.
8
Type 2 Diabetes in Children and Adolescents.儿童和青少年2型糖尿病
Can J Diabetes. 2018 Apr;42 Suppl 1:S247-S254. doi: 10.1016/j.jcjd.2017.10.037.
9
The Time Is Right for a New Classification System for Diabetes: Rationale and Implications of the β-Cell-Centric Classification Schema.糖尿病新分类系统时机已到:以β细胞为中心的分类模式的基本原理及影响
Diabetes Care. 2016 Feb;39(2):179-86. doi: 10.2337/dc15-1585.
10
Tyrosine phosphatase-related islet antigen 2(256-760) autoantibodies, the only marker of islet autoimmunity that increases by increasing the degree of BMI in obese subjects with type 2 diabetes.酪氨酸磷酸酶相关胰岛抗原 2(256-760)自身抗体是胰岛自身免疫的唯一标志物,在肥胖的 2 型糖尿病患者中,随着 BMI 程度的增加而增加。
Diabetes Care. 2015 Mar;38(3):513-20. doi: 10.2337/dc14-1638. Epub 2015 Jan 7.

抗β细胞自身抗体预测临床诊断为2型糖尿病的儿科患者早期胰岛素需求。

Autoantibodies against beta cells to predict early insulin requirements in pediatric patients with clinically diagnosed type 2 diabetes.

作者信息

Molina Jorge M, Medina Patricia G, Gomez Rita A, Herrera Julia R, Martínez Nancy L, Hernández Brenda, García Yesenia

机构信息

Department of Endocrinology, Children's Hospital Federico Gomez, Mexico 06720, Mexico.

National Medical Center "Siglo XXI", UMAE Hosp Especialidades, Unidad Invest Med Epidemiol Clin, Mexican Social Security Institute, Mexico 06720, Mexico.

出版信息

World J Diabetes. 2024 Aug 15;15(8):1717-1725. doi: 10.4239/wjd.v15.i8.1717.

DOI:10.4239/wjd.v15.i8.1717
PMID:39192864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11346091/
Abstract

BACKGROUND

Autoimmunity has emerged as a probable disease modifier in patients with clinically diagnosed type 2 diabetes mellitus (T2DM), that is, patients who have insulin resistance, obesity, and other cardiovascular risk factors, suggesting that the presence of glutamic acid decarboxylase (anti-GAD65), islet antigen 2 (anti-IA2), and zinc transporter 8 (anti-Zn8T) antibodies could have deleterious effects on beta cell function, causing failure and earlier requirement for insulin treatment.

AIM

To evaluate anti-GAD65, anti-IA2 and anti-Zn8T as predictors of early insulin requirement in adolescents with a clinical diagnosis of T2DM.

METHODS

This was a case-control study in patients with clinically diagnosed with T2DM (68 cases and 64 controls with and without early insulin dependence respectively), male and female, aged 12-18 years. Somatometry, blood pressure, glucose, insulin, C-peptide, glycated hemoglobin A1c, and lipid profiles were assessed. ELISA was used to measure anti-GAD65, anti-IA2, and anti-Zn8T antibodies. Descriptive statistics, Pearson's test, Student's test, and logistic regression was performed. < 0.05 was considered statistically significant.

RESULTS

There were 132 patients (53.8% female), with a mean age was 15.9 ± 1.3 years, and there was a disease evolution time of 4.49 ± 0.88 years. The presence of anti-GAD65, anti-IA2, and anti-Zn8T positivity was found in 29.5%, 18.2%, and 15.9%, respectively. Dividing the groups by early or no insulin dependence showed that the group with insulin had a higher frequency of antibody positivity: anti-GAD65 odds ratio (OR): 2.42 (1.112-5.303, 0.026); anti-IA2: OR: 1.55 (0.859-2.818, = 0.105); and anti-Zn8T: OR: 7.32 (2.039-26.279, = 0.002).

CONCLUSION

Anti-GAD65 positivity was high in our study. Anti-GAD65 and anti-Zn8T positivity showed a significantly depleted beta cell reserve phenotype, leading to an increased risk of early insulin dependence.

摘要

背景

自身免疫已成为临床诊断为2型糖尿病(T2DM)患者中一种可能的疾病修饰因素,即那些存在胰岛素抵抗、肥胖和其他心血管危险因素的患者,这表明谷氨酸脱羧酶(抗GAD65)、胰岛抗原2(抗IA2)和锌转运体8(抗Zn8T)抗体的存在可能对β细胞功能产生有害影响,导致β细胞功能衰竭以及更早需要胰岛素治疗。

目的

评估抗GAD65、抗IA2和抗Zn8T作为临床诊断为T2DM的青少年早期胰岛素需求预测指标的价值。

方法

这是一项病例对照研究,纳入临床诊断为T2DM的患者(68例病例组和64例对照组,分别为有和无早期胰岛素依赖的患者),年龄在12 - 18岁,男女均有。评估了体格测量、血压、血糖、胰岛素、C肽、糖化血红蛋白A1c和血脂谱。采用酶联免疫吸附测定法(ELISA)检测抗GAD65、抗IA2和抗Zn8T抗体。进行了描述性统计、Pearson检验、Student检验和逻辑回归分析。P < 0.05被认为具有统计学意义。

结果

共有132例患者(53.8%为女性),平均年龄为15.9 ± 1.3岁,疾病进展时间为4.49 ± 0.88年。抗GAD65、抗IA2和抗Zn8T阳性率分别为29.5%、18.2%和15.9%。根据是否早期胰岛素依赖对分组进行分析,结果显示胰岛素依赖组抗体阳性率更高:抗GAD65优势比(OR):2.42(1.112 - 5.303,P = 0.026);抗IA2:OR:1.55(0.859 - 2.818,P = 0.105);抗Zn8T:OR:7.32(2.039 - 26.279,P = 0.002)。

结论

在我们的研究中,抗GAD65阳性率较高。抗GAD65和抗Zn8T阳性表明β细胞储备表型明显减少,导致早期胰岛素依赖风险增加。