西班牙人口碱性磷酸酶的年龄和性别动态波动及参考区间。

Laura Castells Vilella, Paula Sánchez-Pintos, José Félix Muñiz Llama, Matías Gámez Martínez, María Luz Couce, Jordi Antón
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引用次数: 0

摘要

背景解读碱性磷酸酶(ALP)活性对诊断某些疾病至关重要。ALP 在人的一生中会发生变化,在不同人群中也会有所不同:通过一项多中心观察研究,确定西班牙人群中 ALP 活性的参考区间(RIs)和百分位图,并将 RIs 与其他国家确定的 RIs 进行比较:分析了 2020 年至 2022 年期间从西班牙 9 个三级医疗中心收集的 0 至 99 岁人群的 662 350 次 ALP 测量结果。这项研究是迄今为止发表的文献中规模最大的一项研究:根据性别和年龄建立了连续的 ALP 百分位图,可用作相关指数。生命最初几周的ALP水平较高。在青春期,男女两性的变化有所不同,男孩在 10-13 岁时达到峰值,而女孩在这个年龄段保持稳定。在成人中也观察到显著差异,如一些国家报告的那样,男性在 20 至 49 岁之间,女性在 50 至 79 岁之间,ALP 活性较高:结论:ALP 活性随年龄和性别波动,并存在地域差异。重要的是,每个人群都要有适当的参考值,以便正确诊断和早期诊断与 ALP 异常有关的疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Age- and Sex-Dynamic Fluctuations and Reference Intervals for Alkaline Phosphatase Among the Spanish Population.

Context.—: Interpretation of alkaline phosphatase (ALP) activity is essential for the diagnosis of certain diseases. ALP changes during life and may vary between different populations.

Objective.—: To establish reference intervals (RIs) and percentile charts for ALP activity in the Spanish population through a multicentric observational study and to compare the RIs to those defined in other countries.

Design.—: A total of 662 350 ALP measurements from individuals ages 0 to 99 years from 9 Spanish tertiary care centers collected between 2020 and 2022 were analyzed. This study is the largest published in the literature to date.

Results.—: Continuous percentile charts for ALP according to sex and age were established which can be used as RIs. Higher levels are reached during the first weeks of life. In puberty, a differential evolution is observed in both sexes, reaching a peak at 10 to 13 years of age in boys and remaining stable in girls at this age. Significant differences were also observed in adults, higher in men between ages 20 and 49 years and between ages 50 and 79 years in women, as reported in some countries.

Conclusions.—: ALP activity follows an age- and sex-dependent fluctuation with geographic differences. It is important to have appropriate reference values for each population in order to allow for a correct diagnostic interpretation and early diagnosis of diseases related to ALP abnormalities.

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