Trivedi P, Risteli J, Risteli L, Hindmarsh P C, Brook C G, Mowat A P
Department of Child Health, King's College Hospital, London, United Kingdom.
Pediatr Res. 1991 Sep;30(3):276-80. doi: 10.1203/00006450-199109000-00016.
The reproducibility and specificity of a new, rapid, simple RIA for measuring the concentration of the soluble carboxypropeptide of type I procollagen (PICP) in serum was confirmed. Serum PICP was determined in 442 healthy Caucasian subjects ranging in age from 3 wk to 18 y. Highest PICP values (mean +/- SD: 2200 +/- 350 micrograms/L) occurred in infants less than 3 mo of age, falling by 70% at 2 y and by an additional 10% at 4 y. There was no significant change in serum PICP between 4 and 16 y of age (330 +/- 130 micrograms/L), but a decrease to adult levels of less than 160 micrograms/L occurred by 18 y. In 76 children with growth disorders, serum PICP was related to linear growth velocity (p less than 0.001), although there were no significant differences in PICP among the 38 children with growth hormone insufficiency, the 21 short children with no endocrinologic abnormality, or the 17 tall children. All 15 prepubertal children treated with growth hormone for 3 mo showed significant increases in both growth velocity and serum PICP, with a significant relationship (p less than 0.01) between the degree of increases. The rise in serum PICP at 3 mo (but not baseline PICP values) predicted the increase in growth velocity after 1 y of treatment. Similar changes were observed in the concentration of the aminopropeptide of type III procollagen, except that serum aminopropeptide of type III procollagen showed a definite increase during puberty and a wider spread of values in growth disorders. We conclude that measuring serum PICP by the new, reproducible assay reflects height velocity in prepubertal children and may be a useful biochemical means of monitoring growth rates.
一种用于测定血清中I型前胶原可溶性羧基端前肽(PICP)浓度的新型快速简便放射免疫分析法(RIA)的重现性和特异性得到了证实。对442名年龄在3周龄至18岁的健康白种人受试者测定了血清PICP。3个月龄以下婴儿的PICP值最高(均值±标准差:2200±350μg/L),2岁时下降70%,4岁时再下降10%。4至16岁年龄段血清PICP无显著变化(330±130μg/L),但到18岁时降至成人水平,低于160μg/L。在76名生长障碍儿童中,血清PICP与线性生长速度相关(p<0.001),尽管在38名生长激素缺乏儿童、21名无内分泌异常的矮小儿童或17名高大儿童中,PICP无显著差异。所有15名接受生长激素治疗3个月的青春期前儿童,生长速度和血清PICP均显著增加,增加程度之间存在显著相关性(p<0.01)。治疗3个月时血清PICP的升高(而非基线PICP值)可预测治疗1年后生长速度的增加。在III型前胶原氨基端前肽浓度方面观察到类似变化,不同的是III型前胶原血清氨基端前肽在青春期有明确升高,且在生长障碍中值的分布更广泛。我们得出结论,通过这种新的可重现检测方法测定血清PICP可反映青春期前儿童的身高增长速度,可能是监测生长速率的一种有用生化手段。