利用动态建模方法建立新一代胃泌素释放肽参考区间。

IF 7.5 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Dong Zhu, Haibin Zhao, Weicheng Zhang, Xiuying Zhao
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引用次数: 0

摘要

背景:血清促胃泌素释放肽(ProGRP)水平随年龄显著变化。然而,传统的分割参考区间(RIs)不能反映与衰老相关的连续而微妙的生理变化。为了解决这一局限性,我们研究了ProGRP水平的年龄和性别特异性动态,并创新地为华北地区的成年人和老年人开发了下一代RIs。方法:对4136名经过严格筛选的20-80岁的个体进行分析。使用Mann-Whitney U检验、Spearman相关检验和Kruskal-Wallis检验评估年龄和性别对ProGRP水平的影响。Harris-Boyd方法用于评估性别或年龄划分的必要性。采用非参数方法建立年龄划分RIs。下一代RI模型是使用广义的位置、规模和形状加性模型开发的,具有与年龄相关的动态可视化。两种RI类型的临床适用性通过比较各年龄亚组的上参考值标记率来评估;接近理论2.5%的比率被认为是较好的RI准确度。结果:性别对ProGRP水平的影响很小,临床上不显著。相反,年龄有显著的影响:浓度保持稳定直到大约40岁,随后逐渐增加。划分的RIs定义为0-52.77 pg/mL(20-49岁)和0-63.68 pg/mL(≥50岁)。下一代RIs被量化并可视化。与分区RIs相比,下一代RIs在大多数年龄组中产生的参考极限标记率更接近理论的2.5%,并且表现出更大的稳定性(1.83%-3.74%比1.07%-7.10%)。结论:与分区RIs相比,用于ProGRP的下一代RIs提高了实验室结果解释的准确性。随着实验室信息学的进步,下一代RIs的临床应用有望更广泛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Establishing next-generation reference intervals for pro-gastrin-releasing peptide using a dynamic modeling approach.

Establishing next-generation reference intervals for pro-gastrin-releasing peptide using a dynamic modeling approach.

Establishing next-generation reference intervals for pro-gastrin-releasing peptide using a dynamic modeling approach.

Establishing next-generation reference intervals for pro-gastrin-releasing peptide using a dynamic modeling approach.

Background: Serum pro-gastrin-releasing peptide (ProGRP) levels significantly vary with age. However, conventional partitioned reference intervals (RIs) fail to reflect the continuous and subtle physiological changes associated with aging. To address this limitation, we investigated the age- and sex-specific dynamics of ProGRP levels and innovatively developed next-generation RIs for adults and elderly individuals in North China.

Methods: A total of 4136 rigorously screened individuals (aged 20-80 years) were analyzed. The effects of age and sex on ProGRP levels were assessed using Mann-Whitney U tests, Spearman's correlation, and Kruskal-Wallis tests. The Harris-Boyd method was used to evaluate the necessity of sex or age partitioning. Age-partitioned RIs were established using a nonparametric method. Next-generation RI models were developed using generalized additive models for location, scale, and shape, with age-related dynamics visualized. The clinical applicability of both RI types was evaluated by comparing upper reference limit flagging rates across age subgroups; rates closer to the theoretical 2.5% were considered indicative of superior RI accuracy.

Results: Sex had a minimal and clinically insignificant effect on ProGRP levels. In contrast, age had a significant effect: concentrations remained stable until approximately 40 years of age, followed by progressive increases. The partitioned RIs were defined as 0-52.77 pg/mL (20-49 years) and 0-63.68 pg/mL (≥ 50 years). Next-generation RIs were quantified and visualized. Compared with partitioned RIs, next-generation RIs yielded reference limit flagging rates more closely aligned with the theoretical 2.5% across most age groups and demonstrated significantly greater stability (1.83%-3.74% vs. 1.07%-7.10%).

Conclusions: Compared with partitioned RIs, next-generation RIs for ProGRP improve the accuracy of laboratory result interpretation. With advances in laboratory informatics, broader clinical implementation of next-generation RIs is anticipated.

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来源期刊
Journal of Translational Medicine
Journal of Translational Medicine 医学-医学:研究与实验
CiteScore
10.00
自引率
1.40%
发文量
537
审稿时长
1 months
期刊介绍: The Journal of Translational Medicine is an open-access journal that publishes articles focusing on information derived from human experimentation to enhance communication between basic and clinical science. It covers all areas of translational medicine.
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