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正常妊娠羊水中及一例轻度成骨不全病例中的I型和III型前胶原前肽

Type I and type III procollagen propeptides in amniotic fluid of normal pregnancies and in a case of mild osteogenesis imperfecta.

作者信息

Kauppila S, Tekay A, Risteli L, Koivisto M, Risteli J

机构信息

University of Oulu, Oulu, Finland.

出版信息

Eur J Clin Invest. 1998 Oct;28(10):831-7. doi: 10.1046/j.1365-2362.1998.00371.x.

Abstract

BACKGROUND

The propeptides derived from type I and III procollagens, PICP, PINP and PIIINP, indicate the synthesis of the corresponding collagens. Their circulating concentrations reflect the growth velocity in infants and children

METHODS

We measured these propeptides in 145 samples of amniotic fluid of normal pregnancy. In addition, we have analysed an amniotic fluid and serum sample from a mother with osteogenesis imperfecta, and later the infant's serum sample was also collected for procollagen propeptide analysis.

RESULTS

High concentrations of propeptides, 100-1000 times higher than those in adult serum, were found in early second trimester, decreasing significantly towards term, reflecting the decreased foetal growth rate. Interestingly, the amino-terminal propeptide of type I procollagen, PINP, decreased more that the corresponding carboxy-terminal propeptide, PICP, although both are in principle derived from the same protein. At both stages of pregnancy, the discrepant ratio of PICP to PINP indicated a molar excess of PINP. Abnormally low concentrations of PICP and PINP with normal PIIINP concentrations measured in amniotic fluid and in the serum indicated decreased synthesis of type I procollagen in a foetus/infant with mild osteogenesis imperfecta.

CONCLUSIONS

Our data show a decrease in collagen synthesis with the stage of pregnancy and lower values of type I procollagen propeptides in a case of OI.

摘要

背景

源自I型和III型前胶原的前肽,即I型前胶原氨基端前肽(PINP)、I型前胶原羧基端前肽(PICP)和III型前胶原氨基端前肽(PIIINP),可指示相应胶原蛋白的合成情况。它们的循环浓度反映了婴幼儿的生长速度。

方法

我们检测了145例正常妊娠羊水样本中的这些前肽。此外,我们分析了一名患有成骨不全症母亲的羊水和血清样本,随后还采集了该婴儿的血清样本进行前胶原前肽分析。

结果

在妊娠中期早期发现前肽浓度很高,比成人血清中的浓度高100 - 1000倍,随着孕周增加显著下降,这反映了胎儿生长速度的降低。有趣的是,虽然I型前胶原的氨基端前肽(PINP)和相应的羧基端前肽(PICP)原则上都来自同一蛋白质,但PINP的下降幅度比PICP更大。在妊娠的两个阶段,PICP与PINP的差异比值表明PINP存在摩尔过量。在羊水和血清中测得的PICP和PINP浓度异常低而PIIINP浓度正常,表明患有轻度成骨不全症的胎儿/婴儿中I型前胶原的合成减少。

结论

我们的数据表明,随着妊娠进展胶原蛋白合成减少,且在成骨不全症病例中I型前胶原前肽的值较低。

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