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用于预测 2 型糖尿病的非侵入性风险评分(EPIC-InterAct):对现有模型的验证。

Non-invasive risk scores for prediction of type 2 diabetes (EPIC-InterAct): a validation of existing models.

机构信息

University Medical Center Utrecht, Utrecht, Netherlands; University of Cape Town and South African Medical Research Council, Cape Town, South Africa; The George Institute for Global Health, Sydney, NSW, Australia.

University Medical Center Utrecht, Utrecht, Netherlands.

出版信息

Lancet Diabetes Endocrinol. 2014 Jan;2(1):19-29. doi: 10.1016/S2213-8587(13)70103-7. Epub 2013 Oct 8.

DOI:10.1016/S2213-8587(13)70103-7
PMID:24622666
Abstract

BACKGROUND

The comparative performance of existing models for prediction of type 2 diabetes across populations has not been investigated. We validated existing non-laboratory-based models and assessed variability in predictive performance in European populations.

METHODS

We selected non-invasive prediction models for incident diabetes developed in populations of European ancestry and validated them using data from the EPIC-InterAct case-cohort sample (27,779 individuals from eight European countries, of whom 12,403 had incident diabetes). We assessed model discrimination and calibration for the first 10 years of follow-up. The models were first adjusted to the country-specific diabetes incidence. We did the main analyses for each country and for subgroups defined by sex, age (<60 years vs ≥60 years), BMI (<25 kg/m(2)vs ≥25 kg/m(2)), and waist circumference (men <102 cm vs ≥102 cm; women <88 cm vs ≥88 cm).

FINDINGS

We validated 12 prediction models. Discrimination was acceptable to good: C statistics ranged from 0·76 (95% CI 0·72-0·80) to 0·81 (0·77-0·84) overall, from 0·73 (0·70-0·76) to 0·79 (0·74-0·83) in men, and from 0·78 (0·74-0·82) to 0·81 (0·80-0·82) in women. We noted significant heterogeneity in discrimination (pheterogeneity<0·0001) in all but one model. Calibration was good for most models, and consistent across countries (pheterogeneity>0·05) except for three models. However, two models overestimated risk, DPoRT by 34% (95% CI 29-39%) and Cambridge by 40% (28-52%). Discrimination was always better in individuals younger than 60 years or with a low waist circumference than in those aged at least 60 years or with a large waist circumference. Patterns were inconsistent for BMI. All models overestimated risks for individuals with a BMI of <25 kg/m(2). Calibration patterns were inconsistent for age and waist-circumference subgroups.

INTERPRETATION

Existing diabetes prediction models can be used to identify individuals at high risk of type 2 diabetes in the general population. However, the performance of each model varies with country, age, sex, and adiposity.

FUNDING

The European Union.

摘要

背景

目前尚未对现有预测 2 型糖尿病模型在不同人群中的表现进行比较。我们验证了现有的非实验室模型,并评估了在欧洲人群中预测性能的可变性。

方法

我们选择了基于欧洲人群的非侵入性预测模型,并使用来自欧洲八国的 EPIC-InterAct 病例队列样本的数据(27779 名个体,其中 12403 名患有糖尿病)对其进行验证。我们评估了前 10 年随访的模型区分度和校准情况。首先,根据各国糖尿病发病率调整了模型。我们对每个国家和按性别、年龄(<60 岁与≥60 岁)、BMI(<25 kg/m2 与≥25 kg/m2)和腰围(男性<102 cm 与≥102 cm;女性<88 cm 与≥88 cm)划分的亚组进行了主要分析。

结果

我们验证了 12 种预测模型。区分度可接受至良好:C 统计量总体范围为 0.76(95%CI 0.72-0.80)至 0.81(0.77-0.84),男性为 0.73(0.70-0.76)至 0.79(0.74-0.83),女性为 0.78(0.74-0.82)至 0.81(0.80-0.82)。除了一个模型外,所有模型的区分度均存在显著异质性(p<0.0001)。大多数模型的校准情况良好,且在各国间一致(p>0.05),除了 3 个模型外。然而,有 2 个模型高估了风险,DPoRT 模型高估了 34%(95%CI 29-39%),剑桥模型高估了 40%(28-52%)。在年龄小于 60 岁或腰围较小的个体中,区分度始终优于年龄至少 60 岁或腰围较大的个体。对于 BMI,模式不一致。所有模型均高估了 BMI<25 kg/m2 的个体的风险。对于年龄和腰围亚组,校准模式不一致。

解释

现有的糖尿病预测模型可用于识别普通人群中 2 型糖尿病高危个体。然而,每个模型的性能因国家、年龄、性别和肥胖程度而异。

资助

欧盟。

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