Suppr超能文献

全球多中心参考值研究协调统一的统计学考量

Statistical considerations for harmonization of the global multicenter study on reference values.

作者信息

Ichihara Kiyoshi

机构信息

Department of Laboratory Sciences, Faculty of Health Sciences, Yamaguchi University Graduate School of Medicine, Ube, Japan.

出版信息

Clin Chim Acta. 2014 May 15;432:108-18. doi: 10.1016/j.cca.2014.01.025. Epub 2014 Feb 8.

Abstract

The global multicenter study on reference values coordinated by the Committee on Reference Intervals and Decision Limits (C-RIDL) of the IFCC was launched in December 2011, targeting 45 commonly tested analytes with the following objectives: 1) to derive reference intervals (RIs) country by country using a common protocol, and 2) to explore regionality/ethnicity of reference values by aligning test results among the countries. To achieve these objectives, it is crucial to harmonize 1) the protocol for recruitment and sampling, 2) statistical procedures for deriving the RI, and 3) test results through measurement of a panel of sera in common. For harmonized recruitment, very lenient inclusion/exclusion criteria were adopted in view of differences in interpretation of what constitutes healthiness by different cultures and investigators. This policy may require secondary exclusion of individuals according to the standard of each country at the time of deriving RIs. An iterative optimization procedure, called the latent abnormal values exclusion (LAVE) method, can be applied to automate the process of refining the choice of reference individuals. For global comparison of reference values, test results must be harmonized, based on the among-country, pair-wise linear relationships of test values for the panel. Traceability of reference values can be ensured based on values assigned indirectly to the panel through collaborative measurement of certified reference materials. The validity of the adopted strategies is discussed in this article, based on interim results obtained to date from five countries. Special considerations are made for dissociation of RIs by parametric and nonparametric methods and between-country difference in the effect of body mass index on reference values.

摘要

由国际临床化学与检验医学联合会(IFCC)参考区间与决策限委员会(C-RIDL)协调开展的全球多中心参考值研究于2011年12月启动,针对45种常见检测分析物,目标如下:1)使用通用方案逐国推导参考区间(RI);2)通过比对各国的检测结果探索参考值的地区性/种族差异。为实现这些目标,协调以下方面至关重要:1)招募和采样方案;2)推导RI的统计程序;3)通过共同检测一组血清来统一检测结果。为实现统一招募,鉴于不同文化背景和研究人员对健康的理解存在差异,采用了非常宽松的纳入/排除标准。在推导RI时,可能需要根据各国标准对个体进行二次排除。一种名为潜在异常值排除(LAVE)方法的迭代优化程序可用于自动优化参考个体的选择过程。为了对参考值进行全球比较,必须基于各国之间检测值的两两线性关系,对检测结果进行统一。通过对有证参考物质的协同测量间接赋予该组血清的值,可确保参考值的可追溯性。本文基于迄今从五个国家获得的中期结果,讨论了所采用策略的有效性。特别考虑了参数法和非参数法对RI的区分,以及体重指数对参考值影响的国家间差异。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验