Discrimination and calibration performances of non-laboratory-based and laboratory-based cardiovascular risk predictions: a systematic review.

IF 2.8 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Yihun Mulugeta Alemu, Sisay Mulugeta Alemu, Nasser Bagheri, Kinley Wangdi, Dan Chateau
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引用次数: 0

Abstract

Background and objective: This review compares non-laboratory-based and laboratory-based cardiovascular disease (CVD) risk prediction equations in populations targeted for primary prevention.

Design: Systematic review.

Methods: We searched five databases until 12 March 2024 and used prediction study risk of bias assessment tool to assess bias. Data on hazard ratios (HRs), discrimination (paired c-statistics) and calibration were extracted. Differences in c-statistics and HRs were analysed.

Protocol: PROSPERO (CRD42021291936).

Results: Nine studies (1 238 562 participants, 46 cohorts) identified six unique CVD risk equations. Laboratory predictors (eg, cholesterol and diabetes) had strong HRs, while body mass index in non-laboratory models showed limited effect. Median c-statistics were 0.74 for both models (IQR: lab 0.77-0.72; non-lab 0.76-0.70), with a median absolute difference of 0.01. Calibration measures between laboratory-based and non-laboratory-based equations were similar, although non-calibrated equations often overestimated risk.

Conclusion: The discrimination and calibration measures between laboratory-based and non-laboratory-based models show minimal differences, demonstrating the insensitivity of c-statistics and calibration metrics to the inclusion of additional predictors. However, in most reviewed studies, the HRs for these additional predictors were substantial, significantly altering predicted risk, particularly for individuals with higher or lower levels of these predictors compared with the average.

非实验室和实验室心血管风险预测的鉴别和校准性能:系统综述
背景与目的:本综述比较了非实验室和实验室心血管疾病(CVD)风险预测方程在一级预防人群中的应用。设计:系统回顾。方法:检索5个数据库,截止到2024年3月12日,使用预测研究偏倚风险评估工具进行偏倚评估。提取风险比(hr)、辨别率(配对c统计)和校准数据。分析了c统计量和hr的差异。协议:普洛斯彼罗(CRD42021291936)。结果:9项研究(1 238 562名受试者,46个队列)确定了6个独特的心血管疾病风险方程。实验室预测因子(如胆固醇和糖尿病)具有很强的hr,而非实验室模型中的体重指数显示出有限的影响。两种模型的中位c统计量均为0.74 (IQR: lab 0.77-0.72;非实验室0.76-0.70),中位绝对差为0.01。基于实验室和非基于实验室的方程之间的校准措施相似,尽管非校准方程经常高估风险。结论:基于实验室和非基于实验室的模型之间的区分和校准措施差异很小,表明c统计量和校准指标对包含额外预测因子不敏感。然而,在大多数回顾的研究中,这些额外预测因子的hr是可观的,显著改变了预测风险,特别是对于与平均水平相比这些预测因子水平较高或较低的个体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Open Heart
Open Heart CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
4.60
自引率
3.70%
发文量
145
审稿时长
20 weeks
期刊介绍: Open Heart is an online-only, open access cardiology journal that aims to be “open” in many ways: open access (free access for all readers), open peer review (unblinded peer review) and open data (data sharing is encouraged). The goal is to ensure maximum transparency and maximum impact on research progress and patient care. The journal is dedicated to publishing high quality, peer reviewed medical research in all disciplines and therapeutic areas of cardiovascular medicine. Research is published across all study phases and designs, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Opinionated discussions on controversial topics are welcomed. Open Heart aims to operate a fast submission and review process with continuous publication online, to ensure timely, up-to-date research is available worldwide. The journal adheres to a rigorous and transparent peer review process, and all articles go through a statistical assessment to ensure robustness of the analyses. Open Heart is an official journal of the British Cardiovascular Society.
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