首页> 外文期刊>Journal of pediatric endocrinology & metabolism: JPEM >Reevaluation of growth hormone deficiency during and after growth hormone (GH) treatment: diagnostic value of GH tests and IGF-I and IGFBP-3 measurements.
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Reevaluation of growth hormone deficiency during and after growth hormone (GH) treatment: diagnostic value of GH tests and IGF-I and IGFBP-3 measurements.

机译:重新评估生长激素(GH)治疗期间和之后的生长激素缺乏症:GH测试以及IGF-1和IGFBP-3测量的诊断价值。

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摘要

Retesting of patients with growth hormone (GH) deficiency (GHD), especially those with idiopathic GHD, has yielded normalization of the results in several studies. The aim of this study was to reevaluate patients diagnosed as GHD at completion or reconfirm the diagnosis before completion of GH treatment by retesting with provocative tests, and to evaluate the value of IGF-I and IGFBP-3 levels in the diagnosis of GHD. Fifty (33 M, 17 F) patients with GHD (peak GH level <0.46 pmol/l (10 ng/ml]) in two pharmacological tests were retested and IGF-I and IGFBP-3 levels measured. The age of the patients at retest was 15.2+/-5.0 yr. Thirteen of 50 patients (26%) normalized their GH secretion. According to the initial diagnosis, 69% of those with partial GHD (peak GH level 0.32-0.46 pmol/l [7-10 ng/ml]), 43% with isolated GHD, 33% idiopathic and 11% of those with complete GHD (peak GH level <0.32 pmol/l [7 ng/ml]) normalized their GH level at retesting. None of the patients with multiple hormone deficiency and none with small pituitary on MRI normalized GH levels at retest. The sensitivities of IGF-I and of IGFBP-3 were 70% and 67%, respectively, and the specificities were 100%, when peak GH cutoff is taken as 0.46 pmol/l (10 ng/ml) for the diagnosis of GHD. The sensitivities of IGF-I and IGFBP-3 increased to 76.5% and 73.5% when the cutoff level for GHD is taken as 0.32 pmol/l (7 ng/ml). Those patients who normalized their GH levels at retest showed a satisfactory height velocity when GH therapy was discontinued. In conclusion, reevaluation of GH status may also be undertaken while patients are still on treatment as well as at completion of treatment, especially in patients with idiopathic, partial and isolated GHD, by retesting and by IGF-I and IGFBP-3 measurements. Lowering the cutoff level of GH peak at pharmacological tests to 0.32 pmol/l (7 ng/ml) will lower the number of false positive results in the diagnosis of GHD.
机译:对生长激素缺乏症(GHD)的患者(尤其是特发性GHD的患者)进行重新测试已使一些研究的结果正常化。这项研究的目的是通过重新进行刺激性试验,重新评估在完成GH诊断或在GH治疗完成前被确诊的患者,并通过刺激性试验进行重新测试,并评估IGF-I和IGFBP-3水平在GHD诊断中的价值。在两次药理试验中,对五十名(33 M,17 F)GHD(峰值GH水平<0.46 pmol / l(10 ng / ml])的GHD患者进行了重新测试,并测量了IGF-I和IGFBP-3的水平。复检为15.2 +/- 5.0年。50名患者中有13名(26%)的GH分泌恢复正常。根据初步诊断,部分GHD(峰值GH水平为0.32-0.46 pmol / l [7-10 ng]的患者中有69% / ml]),43%的孤立GHD,33%的特发性患者和11%的完全GHD(峰值GH水平<0.32 pmol / l [7 ng / ml])的患者在重新测试时将其GH水平恢复正常。复查时,多激素缺乏且垂体检查均未见垂体小,使GH正常化,以GH峰值为截止值,IGF-I和IGFBP-3的敏感性分别为70%和67%,特异性为100%。诊断GHD为0.46 pmol / l(10 ng / ml),将GHD的临界水平定为0.32 pmol / l(7 ng / ml)时,IGF-I和IGFBP-3的敏感性增至76.5%和73.5%。 ml)。当停止GH治疗时,在重新测试时标准化的GH水平显示出令人满意的身高速度。总之,还可以通过重新测试以及通过IGF-I和IGFBP-3测量,在患者仍处于治疗期间以及治疗结束时,尤其是患有特发性,部分和孤立GHD的患者中,重新评估GH的状态。将药理学试验中GH峰的截止水平降低至0.32 pmol / l(7 ng / ml),将减少GHD诊断中假阳性结果的数量。

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