Koch A, Dörr H G
Abteilung für Pädiatrische Endokrinologie, Klinik für Kinder und Jugendliche, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany.
Eur J Clin Chem Clin Biochem. 1997 May;35(5):379-85. doi: 10.1515/cclm.1997.35.5.379.
Serum insulin-like growth factor-I and insulin-like growth factor binding protein-3 are simply-determined screening analytes if growth hormone deficiency is suspected. The analysis of growth hormone secretion using standardised stimulation tests and secretion profiles is complicated and expensive in comparison. In retrospect, we have examined the value of insulin-like growth factor-I and its binding protein-3 for the diagnostic clarification of patients with short stature (n = 117). In 39/117 patients growth hormone secretion was investigated as ward patients. Growth hormone deficiency was diagnosed in 10 patients, for 16 patients the diagnosis was neurosecretory dysfunction. For all patients (n = 7) with lowered insulin-like growth factor binding protein-3 and insulin-like growth factor-I values (insulin-like growth factor binding protein-3 < 5th percentile, insulin-like growth factor-I < 10th percentile) a growth hormone disorder was proven. Conversely, however, only 3/10 patients with classical growth hormone deficiency (n = 3) showed a lowering of both analytes. 8/10 patients with classical growth hormone deficiency and 8/16 patients with neurosecretory dysfunction had at least one lowered value. Two patients showed normal values for insulin-like growth factor-I and insulin-like growth factor binding protein-3 despite biochemically proven growth hormone deficiency. The combined determination of insulin-like growth factor-I and insulin-like growth factor binding protein-3 can provide valuable help during preliminary diagnosis of patients of short stature, indicating a disturbance of the growth hormone secretion if the values are lowered. Normal values do not, however, exclude the possibility of a growth hormone deficiency. Inpatient endocrinological testing is indispensible if growth hormone deficiency is suspected.
如果怀疑存在生长激素缺乏,血清胰岛素样生长因子-I和胰岛素样生长因子结合蛋白-3是简单易行的筛查分析物。相比之下,使用标准化刺激试验和分泌谱来分析生长激素分泌则复杂且昂贵。回顾过去,我们研究了胰岛素样生长因子-I及其结合蛋白-3在明确身材矮小患者(n = 117)诊断方面的价值。在117例患者中,有39例作为病房患者接受了生长激素分泌情况的调查。诊断出10例生长激素缺乏患者,16例诊断为神经分泌功能障碍。对于所有胰岛素样生长因子结合蛋白-3和胰岛素样生长因子-I值降低的患者(n = 7)(胰岛素样生长因子结合蛋白-3<第5百分位数,胰岛素样生长因子-I<第10百分位数),均证实存在生长激素紊乱。然而,相反的是,在10例经典生长激素缺乏患者中只有3例(n = 3)这两种分析物的值都降低。10例经典生长激素缺乏患者中有8例,16例神经分泌功能障碍患者中有8例至少有一个值降低。尽管生化检查证实存在生长激素缺乏,但仍有2例患者的胰岛素样生长因子-I和胰岛素样生长因子结合蛋白-3值正常。联合测定胰岛素样生长因子-I和胰岛素样生长因子结合蛋白-3在身材矮小患者的初步诊断中可提供有价值的帮助,如果值降低则提示生长激素分泌紊乱。然而,正常的值并不能排除生长激素缺乏的可能性。如果怀疑存在生长激素缺乏,住院内分泌检查是必不可少的。