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参考区间的再探讨:一种基于小样本量和生物学变异数据的新型人群参考区间模型。

Reference Intervals Revisited: A Novel Model for Population-Based Reference Intervals, Using a Small Sample Size and Biological Variation Data.

机构信息

Acibadem Labmed Clinical Laboratories, Acibadem Mehmet Ali Aydinlar University, Istanbul, Turkey.

Department of Medical Biochemistry, School of Medicine, Acibadem Mehmet Ali Aydinlar University, Istanbul, Turkey.

出版信息

Clin Chem. 2024 Oct 3;70(10):1279-1290. doi: 10.1093/clinchem/hvae109.

Abstract

BACKGROUND

Conventional population-based reference intervals (popRIs) are established on the ranking of single measurement results from at least 120 reference individuals. In this study, we aimed to explore a new model for popRIs, utilizing biological variation (BV) data to define the reference interval (RI) limits and compared BV-based popRI from different sample sizes with previously published conventional popRIs from the same population.

METHODS

The model is based on defining the population set point (PSP) from single-measurement results of a group of reference individuals and using the total variation around the PSP, derived from the combination of BV and analytical variation, to define the RI limits. Using data from 143 reference individuals for 48 clinical chemistry and hematology measurands, BV-based popRIs were calculated for different sample sizes (n = 16, n = 30, and n = 120) and considered acceptable if they covered 90% of the population. In addition, simulation studies were performed to estimate the minimum number of required reference individuals.

RESULTS

The median ratio of the BV-based to conventional RI ranges was 0.98. The BV-based popRIs calculated from the different samples were similar, and most met the coverage criterion. For 25 measurands ≤16 reference individuals and for 23 measurands >16 reference individuals were required to estimate the PSP.

CONCLUSIONS

The BV-based popRI model delivered robust RIs for most of the included measurands. This new model requires a smaller group of reference individuals than the conventional popRI model and can be implemented if reliable BV data are available.

摘要

背景

传统的基于人群的参考区间(popRIs)是基于至少 120 名参考个体的单一测量结果的排序来建立的。在这项研究中,我们旨在探索一种新的 popRI 模型,利用生物变异(BV)数据来定义参考区间(RI)的界限,并比较来自不同样本量的基于 BV 的 popRI 与来自同一人群的先前发表的传统 popRI。

方法

该模型基于从一组参考个体的单次测量结果中定义人群设定点(PSP),并使用源自 BV 和分析变异组合的 PSP 周围的总变异来定义 RI 界限。使用来自 143 名参考个体的 48 个临床化学和血液学测量值的数据,计算了不同样本量(n=16、n=30 和 n=120)的基于 BV 的 popRI,如果它们涵盖了 90%的人群,则认为是可接受的。此外,还进行了模拟研究来估计所需参考个体的最小数量。

结果

基于 BV 的 RI 范围与传统 RI 范围的中位数比值为 0.98。从不同样本计算的基于 BV 的 popRI 相似,并且大多数满足覆盖标准。对于 25 个测量值≤16 名参考个体,以及对于 23 个测量值>16 名参考个体,需要估计 PSP。

结论

基于 BV 的 popRI 模型为大多数包含的测量值提供了稳健的 RI。与传统的 popRI 模型相比,这种新模型需要较少的参考个体群体,如果有可靠的 BV 数据,则可以实施。

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