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Diagnostic and prognostic value of short-term metabolic response to human growth hormone in short stature

机译:矮小身材对人类生长激素的短期代谢反应的诊断和预后价值

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摘要

Metabolic tests of the response to three days of administration of human growth hormone (HGH) have been done on 55 patients aged 6·2 to 20·3 years. 22 had `isolated' growth hormone deficiency (or hyposomatotrophic short stature, HS), 16 CNS tumours or multiple hormone deficiencies, 6 short stature associated with low birthweight, 3 psychosocial short stature, 4 Turner's syndrome, 1 hereditary short stature, and 3 uncertain diagnosis. Height was measured at 3-monthly intervals for a full year, then HGH was given for a full year and the difference in rate, that is the acceleration during the growth hormone year, was calculated. The height measurements were all done by one measurer in 45 of the patients.In the metabolic test there were 5 baseline days followed by 3 days of a single injection of 10 IU HGH, then 2 final days. The means for urinary nitrogen excretion, blood urea, and urinary calcium excretion were calculated for the 5 baseline days and for the last 2 HGH days plus the one subsequent day. The difference between the means is given as a percentage of baseline values.The children with isolated growth hormone (GH) deficiency had a greater decrease in nitrogen excretion (33±3%) than the low birthweight cases and small children (7±5%), but there was overlap between individuals in the isolated deficiency group (range 12 to 66%) and the rest (range -12% to 42%); 2 deficient children were below a dividing line of 20%, and 1 Turner's syndrome and 3 psychosocial short stature children were above it. The tumour and multiple deficiency patients had an average fall of 40±3% and showed no overlap with the low birthweight group. Blood urea and calcium excretion gave a worse separation. Within the isolated deficiency and the tumour and multiple deficiency groups there was no relation between any metabolic parameter and the amount of growth acceleration in the first year of HGH treatment.In the HS, though not in the tumour patients, there was a correlation (-0·60) between the decrease in percentage nitrogen excretion and peak GH level on stimulation and between per cent decrease in urinary nitrogen excretion and per cent decrease in blood urea (0·76).We conclude that the differential diagnostic value of the short-term metabolic test is very limited now that we have tests of GH response; and that in cases of isolated GH or multiple pituitary hormone deficiency the result of the metabolic test does not predict at all the height acceleration obtained on HGH treatment.
机译:已经对55名6·2至20·3岁的患者进行了三天服用人类生长激素(HGH)反应的代谢测试。 22例患有“孤立的”生长激素缺乏症(或营养不良的矮小身材,HS),16例中枢神经系统肿瘤或多种激素缺乏症,6例矮身材伴低出生体重,3例心理社会性矮身材,4特纳综合征,1例遗传性矮身材和3例不确定诊断。每隔三个月测量一次身高,测量一整年的身高,然后计算一整年的HGH,然后计算出速度差,即生长激素年的加速度。身高测量全部由一位测量者对45位患者进行。在代谢测试中,基线​​为5天,然后单次注射10 IU HGH为3天,最后2天。计算5个基线天,最后2个HGH天以及随后一日的尿氮排泄,血尿素和尿钙排泄的平均值。平均值之间的差异以基线值的百分比形式给出。孤立生长激素(GH)缺乏的儿童的氮排泄减少量(33±3%)比低出生体重儿和小孩(7±5%)大),但孤立的缺陷组(范围为12%至66%)和其他人(范围为-12%至42%)之间存在重叠; 2名缺陷儿童低于20%的分界线,其中1名特纳氏综合症和3名心理社会矮小儿童高于3%。肿瘤和多发性缺陷患者平均下降40±3%,与低出生体重组没有重叠。血液中尿素和钙的排泄导致更差的分离。在HGH治疗的第一年中,在孤立的缺陷,肿瘤和多种缺陷组中,任何代谢参数与生长加速量之间没有关系。在HS中,尽管在肿瘤患者中没有相关性(-刺激后的氮排泄百分比降低和GH峰值水平之间的百分比介于0·60之间)和尿素氮排泄的百分比降低与血尿素减少百分比之间的比例(0·76)。我们得出结论:由于我们已经进行了GH反应测试,因此术语代谢测试非常有限。并且在孤立的GH或多种垂体激素缺乏的情况下,代谢测试的结果根本无法预测HGH治疗获得的身高加速。

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