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Urinary growth hormone estimation in diagnosing severe growth hormone deficiency.

机译:尿中生长激素的估计可用于诊断严重的生长激素缺乏症。

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Urinary growth hormone was measured in 54 children with short stature who had growth hormone deficiency that was initially diagnosed pharmacologically (arginine and L-dopa) and physiologically (mean growth hormone concentration during sleep evaluated twice). Based on the growth hormone response to pharmacological tests the subjects were subdivided into three groups: group A, 20 subjects with normal response (peak concentration > 8 micrograms/l); group B, 20 subjects with response between 4 and 8 micrograms/l; and group C, 14 subjects with response < 4 micrograms/l. In group A four subjects had an abnormally low nocturnal mean growth hormone concentration (< or = 3.3 micrograms/l). In group C seven subjects had multiple pituitary hormone deficiency and abnormal magnetic resonance imaging. All subjects had urine collected from 8.00 pm to 8.00 am for 4-5 consecutive nights. A positive correlation was found between serum nocturnal mean growth hormone values and urinary growth hormone in all subjects. Mean (SD) concentrations of urinary growth hormone were similar in groups A (18.0 (9.5) ng/g creatinine) and B (13.6 (5.9) ng/g creatinine), but significantly higher than that of group C (3.4 (3.7) ng/g creatinine). Considering as abnormal urinary growth hormones below the lower limit of the range in group A, specificity and sensitivity of urinary growth hormone was 100% and 35% respectively. Sensitivity for groups B and C were 5% and 78% respectively. When considering only the subjects of group C with pathological magnetic resonance findings, sensitivity increased to 100%. In the four subjects of group A with mean growth hormone concentration < or = 3.3 micrograms/l, specificity decreased to 80%. It is concluded that urinary growth hormone assay is characterised by a sensitivity too low to be regarded as improving the traditional diagnostic approach to define growth hormone deficiency, unless it is used to identify subjects with the most severe deficiencies.
机译:对54名身材矮小的儿童进行了尿中生长激素的测定,这些儿童最初是通过药理学(精氨酸和左旋多巴)和生理学(在睡眠中的平均生长激素浓度评估两次)诊断出来的。根据生长激素对药理学的反应,将受试者分为三组:A组,20名反应正常的受试者(峰值浓度> 8微克/升); B组,20名受试者的反应在4至8微克/升之间;和C组,有14位受试者的反应<4微克/升。在A组中,四名受试者的夜间平均生长激素浓度异常低(<或= 3.3微克/升)。在C组中,七名受试者患有多个垂体激素缺乏症和磁共振成像异常。所有受试者从下午8:00到上午8.00连续4-5个晚上收集尿液。在所有受试者中,血清夜间平均生长激素值与尿生长激素之间存在正相关。 A组(18.0(9.5)ng / g肌酐)和B组(13.6(5.9)ng / g肌酐)的尿液生长激素平均(SD)浓度相似,但显着高于C组(3.4(3.7)) ng / g肌酐)。考虑到异常尿生长激素低于A组范围的下限,尿生长激素的特异性和敏感性分别为100%和35%。 B组和C组的敏感度分别为5%和78%。当仅考虑具有病理磁共振结果的C组受试者时,敏感性增加到100%。在平均生长激素浓度≤或等于3.3微克/升的A组的四个受试者中,特异性降低至80%。结论是,尿生长激素测定法的特征在于灵敏度太低,以至于不能将其用于确定生长激素缺乏症的传统诊断方法,除非将其用于鉴定最严重缺陷的受试者。

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