Optimized GFR Estimation Equations for Chinese Neonates and Children: Development of New Models and Comparison With Existing Ones

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Biopharmaceutics & Drug Disposition Pub Date : 2026-09-30 Epub Date: 2026-06-03 DOI:10.1002/bdd.70032
Hiotong Lam, Yahui Zhang, Zhe Hou, Jinfang Yuan, Zihan Lei, Haiyan Li, Xueting Yao, Tongyan Han, Dongyang Liu
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引用次数: 0

Abstract

Glomerular filtration rate (GFR) maturation is critical for drug dosing in neonates and children. Current equations face dual limitations: they are primarily derived from Caucasian populations and fail to account for the fundamental physiological differences between neonates and children. This study aimed to develop Chinese-specific GFR equations and to characterize how the key predictors of GFR differ between these two developmental stages. Creatinine clearance as measured GFR (mGFR) in 58 hospitalized neonates (gestational age range, 30.3–41.0 weeks, postnatal age range, 0 to 26 days, mGFR = 3.08 ± 1.86 mL/min) without renal impairment were enrolled. Moreover, a published database of Chinese children (N = 87, age range, 1 to 18 years, mGFR = 97.0 ± 31.9 mL/min/1.73 m2) was applied. Demographic and renal function markers were included to develop equations using the stepwise regression method in allometric form. The GFR prediction equation of serum cystatin C, blood urea nitrogen and postmenstrual age of Chinese neonates was established. In children, GFR is associated with cystatin C, creatinine, weight and age. In an internal comparison with 16 published equations, our newly developed models showed favorable performance within our cohorts, with correlation (R2 of 0.617 and 0.578) and accuracy (P20 of 46.6% and 70.1%, P50 of 93.1% and 100%), respectively. The equations would provide scientific basis for aiding diagnosis of renal function of Chinese neonates and children, and supporting better precision medicine of drugs mainly excreted by kidney.

中国新生儿和儿童GFR估算方程的优化:新模型的建立及与现有模型的比较。
肾小球滤过率(GFR)成熟对新生儿和儿童的药物剂量至关重要。目前的方程面临双重限制:它们主要来自高加索人群,无法解释新生儿和儿童之间基本的生理差异。本研究旨在建立中国特异性的GFR方程,并表征GFR的关键预测因子在这两个发育阶段之间的差异。研究纳入58例无肾损害住院新生儿(胎龄30.3 ~ 41.0周,出生后0 ~ 26天,mGFR = 3.08±1.86 mL/min)的肌酐清除率测定GFR (mGFR)。此外,应用已发表的中国儿童数据库(N = 87,年龄范围1 ~ 18岁,mGFR = 97.0±31.9 mL/min/1.73 m2)。纳入人口统计学指标和肾功能指标,采用异速形态逐步回归方法建立方程。建立中国新生儿血清胱抑素C、血尿素氮与经后年龄的GFR预测方程。在儿童中,GFR与胱抑素C、肌酐、体重和年龄有关。在与16个已发表方程的内部比较中,我们新开发的模型在我们的队列中显示出良好的性能,相关性(R2为0.617和0.578)和准确性(P20分别为46.6%和70.1%,P50为93.1%和100%)。该方程可为我国新生儿及儿童肾脏功能的辅助诊断提供科学依据,为肾脏排泄为主药物的精准医疗提供支持。
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
CiteScore
3.60
自引率
0.00%
发文量
35
审稿时长
6-12 weeks
期刊介绍: Biopharmaceutics & Drug Dispositionpublishes original review articles, short communications, and reports in biopharmaceutics, drug disposition, pharmacokinetics and pharmacodynamics, especially those that have a direct relation to the drug discovery/development and the therapeutic use of drugs. These includes: - animal and human pharmacological studies that focus on therapeutic response. pharmacodynamics, and toxicity related to plasma and tissue concentrations of drugs and their metabolites, - in vitro and in vivo drug absorption, distribution, metabolism, transport, and excretion studies that facilitate investigations related to the use of drugs in man - studies on membrane transport and enzymes, including their regulation and the impact of pharmacogenomics on drug absorption and disposition, - simulation and modeling in drug discovery and development - theoretical treatises - includes themed issues and reviews and exclude manuscripts on - bioavailability studies reporting only on simple PK parameters such as Cmax, tmax and t1/2 without mechanistic interpretation - analytical methods
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