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出生后第一年茶碱代谢的变化。

Alterations in theophylline metabolism during the first year of life.

作者信息

Kraus D M, Fischer J H, Reitz S J, Kecskes S A, Yeh T F, McCulloch K M, Tung E C, Cwik M J

机构信息

Department of Pharmacy Practice, University of Illinois at Chicago 60612.

出版信息

Clin Pharmacol Ther. 1993 Oct;54(4):351-9. doi: 10.1038/clpt.1993.160.

Abstract

Maturational changes in theophylline disposition were evaluated in 52 infants (gestational age, 24 to 40 weeks; postnatal age, 2 to 69 weeks) receiving maintenance theophylline therapy. Theophylline and metabolites were measured in serum and urine at steady state, and the influence of clinical parameters on the maturational changes was analyzed by multiple stepwise linear regression. Theophylline clearance and urine metabolite pattern reached adult values at 55 weeks' postconceptional age. Serum caffeine concentrations greater than 1 microgram/ml occurred in infants up to 50 weeks' postconceptional age. Disappearance of serum caffeine concentrations and maturation of theophylline clearance were primarily related (p < 0.001) to development of the demethylation pathway to 3-methylxanthine. Postconceptional age was the major factor (p < 0.001) explaining the interpatient variability in theophylline clearance (r2 = 0.57), serum caffeine to theophylline ratio (r2 = 0.46), and urinary excretion of theophylline (r2 = 0.51), caffeine (r2 = 0.49), 1,3-methyluric acid (r2 = 0.32), 1-methyluric acid (r2 = 0.53), and 3-methylxanthine (r2 = 0.58). Our findings indicate that postconceptional age rather than postnatal age should be used as a maturational marker during theophylline therapy in infancy.

摘要

对52例接受氨茶碱维持治疗的婴儿(胎龄24至40周;出生后年龄2至69周)的氨茶碱处置成熟变化进行了评估。在稳态下测定血清和尿液中的氨茶碱及其代谢产物,并通过多元逐步线性回归分析临床参数对成熟变化的影响。氨茶碱清除率和尿液代谢产物模式在孕龄55周时达到成人水平。在孕龄50周之前的婴儿中,血清咖啡因浓度大于1微克/毫升。血清咖啡因浓度的消失和氨茶碱清除率的成熟主要与向3 - 甲基黄嘌呤的去甲基化途径的发育有关(p < 0.001)。孕龄是解释氨茶碱清除率(r2 = 0.57)、血清咖啡因与氨茶碱比值(r2 = 0.46)以及氨茶碱、咖啡因、1,3 - 甲基尿酸、1 - 甲基尿酸和3 - 甲基黄嘌呤的尿排泄(r2分别为0.51、0.49、0.32、0.53和0.58)的患者间变异性的主要因素(p < 0.001)。我们的研究结果表明,在婴儿期氨茶碱治疗期间,应使用孕龄而非出生后年龄作为成熟标志物。

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