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人I型胶原羧基末端前肽和吡啶交联物作为1至18个月婴儿骨骼生长的标志物。

Carboxy-terminal propeptide of human type I collagen and pyridinium cross-links as markers of bone growth in infants 1 to 18 months of age.

作者信息

Lieuw-A-Fa M, Sierra R I, Specker B L

机构信息

Department of Pediatrics, Children's Hospital Medical Center, Cincinnati, Ohio, USA.

出版信息

J Bone Miner Res. 1995 Jun;10(6):849-53. doi: 10.1002/jbmr.5650100604.

Abstract

Serum carboxy-terminal propeptide of human type I collagen (PICP) concentrations, as a marker for bone formation, and urinary pyridinium (Pyd) cross-link concentrations, as a marker of bone resorption, were determined in 66 healthy infants aged 1-18 months who are being studied longitudinally. We hypothesized that there would be a positive correlation of growth velocity, increase in bone area, and bone mass accretion rates with PICP and Pyd cross-link concentrations. Since osteocalcin is currently used as a marker of bone formation, serum osteocalcin concentrations were also measured. Mean serum PICP and urinary Pyd cross-link concentrations were significantly greater than adult concentrations. Future growth velocity, increase in bone area, and bone mass accretion rates were not associated with PICP, Pyd cross-link, or osteocalcin concentrations. Growth velocity during the 3 months preceding sample collection correlated with serum PICP, Pyd/kg, and osteocalcin concentrations (r = 0.474, p < 0.001; r = 0.379, p < 0.001; and r = 0.516, p < 0.001, respectively). Previous increase in bone area correlated with serum PICP concentrations (r = 0.359, p = 0.01). The relationship between the infant's previous bone mass accretion rate and PICP was of borderline significance (r = 0.281, p = 0.055). In summary, normative data for PICP, Pyd cross-link concentrations, and parameters of bone growth are provided for infants 1-18 months of age and indicate that these markers reflect past and current bone metabolism and may be helpful in monitoring bone disorders in infants.

摘要

对66名年龄在1至18个月的健康婴儿进行纵向研究,测定了作为骨形成标志物的血清I型胶原羧基末端前肽(PICP)浓度以及作为骨吸收标志物的尿吡啶啉(Pyd)交联浓度。我们假设生长速度、骨面积增加和骨量增加率与PICP和Pyd交联浓度呈正相关。由于骨钙素目前被用作骨形成的标志物,因此也测定了血清骨钙素浓度。血清PICP和尿Pyd交联浓度的平均值显著高于成人浓度。未来的生长速度、骨面积增加和骨量增加率与PICP、Pyd交联或骨钙素浓度无关。样本采集前3个月的生长速度与血清PICP、Pyd/kg和骨钙素浓度相关(r分别为0.474,p<0.001;r为0.379,p<0.001;r为0.516,p<0.001)。既往骨面积增加与血清PICP浓度相关(r = 0.359,p = 0.01)。婴儿既往骨量增加率与PICP之间的关系具有临界显著性(r = 0.281,p = 0.055)。总之,提供了1至18个月龄婴儿PICP、Pyd交联浓度和骨生长参数的标准数据,表明这些标志物反映了过去和当前的骨代谢,可能有助于监测婴儿的骨疾病。

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