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1型糖尿病不同临床亚型的证据:一项前瞻性研究。

Evidence for different clinical subtypes of type 1 diabetes mellitus: a prospective study.

作者信息

Schiffrin A, Ciampi A, Hendricks L, Rozen R, Weitzner G

机构信息

Division of Endocrinology and Metabolism, Montreal Children's Hospital, Quebec, Canada.

出版信息

Diabetes Res Clin Pract. 1994 Mar;23(2):95-102. doi: 10.1016/0168-8227(94)90016-7.

Abstract

The purpose of this study was to determine whether the sex, age, severity of clinical presentation, presence of ICAs, IAs, and HLA-DR and DQ types could predict, in a cohort of newly-diagnosed diabetic children: (1) the duration of beta-cell function as measured by C-peptide response to a Sustacal meal; and (2) determine if those predictors could identify disease subtypes. A cohort of 170 consecutive patients was followed for 60 months after diagnosis. We found that age (0.0029), sex (0.0136), ICA (0.0001), presence of DKA (0.0070) and C-peptide peak at diagnosis (0.0000) significantly predicted the duration of residual beta-cell function over time. Furthermore, C-peptide secretion at diagnosis, presence of ICA, age and sex allowed the identification of three different prognostic groups with varying acceleration of beta-cell loss.

摘要

本研究的目的是确定在一组新诊断的糖尿病儿童中,性别、年龄、临床表现的严重程度、胰岛细胞自身抗体(ICA)、胰岛素自身抗体(IA)的存在情况以及人类白细胞抗原-DR(HLA-DR)和-DQ类型是否能够预测:(1)通过对苏达卡尔餐的C肽反应所测量的β细胞功能持续时间;(2)确定这些预测因素是否能够识别疾病亚型。对170例连续患者在诊断后进行了60个月的随访。我们发现年龄(0.0029)、性别(0.0136)、ICA(0.0001)、糖尿病酮症酸中毒(DKA)的存在情况(0.0070)以及诊断时的C肽峰值(0.0000)显著预测了残余β细胞功能随时间的持续时间。此外,诊断时的C肽分泌、ICA的存在情况、年龄和性别能够识别出三个不同的预后组,其β细胞丢失的加速程度各不相同。

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