尿igf - 1测定及其临床应用。

N Hizuka, K Takano, K Asakawa, I Sukegawa, R Horikawa, Y Yoshizawa, S Saito, K Shizume
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引用次数: 0

摘要

在人类尿液中发现了免疫反应性和受体反应性igf - 1;尿液中30%的igf - 1免疫反应性为游离形式,其余为高分子量形式(约40000 MW)。用Sep-Pak C18药筒提取尿液IGF-I后,用放射免疫法定量,该方法仅测量IGF-I的游离形式。测定3例垂体功能低下儿童和16例矮个子正常儿童每日(24小时)尿IGF-I排泄量。24小时尿样中IGF-I水平与血浆IGF-I水平和24小时平均血浆GH浓度相关。然而,24小时平均血浆生长激素浓度与24小时尿液样本中的生长激素水平和血浆IGF-I水平的相关性优于与尿液IGF-I值的相关性。正常人单次尿液样本中igf - 1的平均水平介于肢端肥大症患者(较高)和垂体功能减退症患者(较低)之间。然而,在正常和垂体功能低下患者之间的个体值有重叠。这些数据表明尿IGF-I值被生长激素分泌状态改变,尽管尿IGF-I测量的临床应用可能有限。
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Urinary IGF-I measurement and its clinical application.

Immunoreactive and receptor-reactive IGF-I was found to be present in human urine; 30% of the IGF-I immunoreactivity in urine was in its free form and the remainder was a high molecular weight form (approximately 40,000 MW). Urinary IGF-I was quantified by radioimmunoassay after extraction by Sep-Pak C18 cartridge, a method that measures only the free form of IGF-I. Daily (24-hour) urinary IGF-I excretion was measured in 3 hypopituitary children and 16 short normal children. The IGF-I level in the 24-hour urine samples correlated with the plasma IGF-I level and the mean 24-hour plasma GH concentration. The mean 24-hour plasma GH concentration, however, correlated better with the GH level in the 24-hour urine samples and the plasma IGF-I level than with the urinary IGF-I value. The mean IGF-I levels in single urine samples from normal subjects lay between those from patients with acromegaly (which were high) and those from patients with hypopituitarism (which were low). There were overlaps, however, in individual values between the normal and hypopituitary patients. These data indicate that urinary IGF-I values are altered by the GH secretion state, though the clinical application of urinary IGF-I measurement may be limited.

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11th International Symposium on Growth and Growth Disorders. Proceedings of a meeting, Stockholm, Sweden, 26-27 April 1991. 12th International Symposium on Growth and Growth Disorders. Geneva, 25-26 October 1991. The carbohydrate-deficient glycoprotein syndrome. A new inherited multisystemic disease with severe nervous system involvement. Growth hormone treatment in short children with chronic renal failure and after renal transplantation: combined data from European clinical trials. The European Study Group. Growth response in prepubertal children with idiopathic growth hormone deficiency during the first two years of treatment with human growth hormone. Analysis of the Kabi Pharmacia International Growth Study.
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