McArthur R G, Bala R M, Rademaker A W
Clin Invest Med. 1986;9(1):6-11.
The peak levels of serum growth hormone (GH) obtained in response to administration of insulin and arginine in 26 children with constitutional delay in growth (CDG) are compared to similar test results in 7 normal children. Heights at the time of testing, and follow-up linear growth, are documented in all subjects. Most patients with constitutional delay in growth could be identified on the basis of history, physical examination, bone age radiograph, and yearly follow-up of growth. Only two patients exhibited growth of less than 4 cm per year; both had normal responses to provocative testing. In response to provocative testing, individual patients with constitutional delay in growth revealed peak levels of serum GH which were within the normal range, but the group mean peak value was less (p less than 0.05) than in normal children. One child with clinical constitutional delay in growth revealed a subnormal response to both provocative tests. The results suggest that children with constitutional delay in growth may have a diminished reserve for secreting growth hormone.
对26例体质性生长发育延迟(CDG)儿童给予胰岛素和精氨酸后血清生长激素(GH)的峰值水平,与7例正常儿童的类似检测结果进行了比较。记录了所有受试者检测时的身高以及随访期间的线性生长情况。大多数体质性生长发育延迟的患者可根据病史、体格检查、骨龄X线片及每年的生长随访来确定。只有两名患者每年生长不足4厘米;两人对激发试验的反应均正常。在激发试验中,体质性生长发育延迟的个体患者血清GH峰值水平在正常范围内,但该组的平均峰值低于正常儿童(p<0.05)。一名临床上体质性生长发育延迟的儿童对两种激发试验的反应均不正常。结果表明,体质性生长发育延迟的儿童可能分泌生长激素的储备能力下降。