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绝经后骨质疏松症研究中的骨形成生化标志物

Biochemical markers of bone formation in the study of postmenopausal osteoporosis.

作者信息

Dominguez Cabrera C, Sosa Henríquez M, Traba M L, Alvarez Villafañe E, de la Piedra C

机构信息

Unidad Metabólica, Hospital Insular de Canarias, Las Palmas, Spain.

出版信息

Osteoporos Int. 1998;8(2):147-51. doi: 10.1007/BF02672511.

Abstract

A comparative study was performed on the sensitivity of the determination of the available biochemical markers of bone formation--total and bone alkaline phosphatase (TAP and bAP, respectively), osteocalcin (BGP), procollagen I aminoterminal propeptide (PINP) and procollagen I carboxyterminal propeptide (PICP)--in the study of postmenopausal osteoporosis. The comparison between PINP and PICP, due to the recent development of the amino-terminal assay, is of special interest. The study included 26 untreated osteoporotic postmenopausal women, age 59 +/- 6 years (range 46-69 years) and 17 healty control postmenopausal women, age 56 +/- 7 years (range 48-70 years). We found a significant increase in the levels of bAP (p = 0.0021), BGP (p = 0.041), PINP (p = 0.0001) and PCIP (p = 0.0073), but not in the levels of TAP (p = 0.3389), in osteoporotic patients with respect to the control group. Serum PINP and bAP showed the highest diagnostic accuracy among the markers of bone formation studies, as can be deduced from the receiver operating characteristics (ROC) curves. In spite of their similar origin (amino-terminal and carboxy-terminal release from a procollagen molecule), the results obtained by measuring levels of PINP are significantly better than those found with PICP.

摘要

对绝经后骨质疏松症研究中骨形成的可用生化标志物——总碱性磷酸酶和骨碱性磷酸酶(分别为TAP和bAP)、骨钙素(BGP)、I型前胶原氨基端前肽(PINP)和I型前胶原羧基端前肽(PICP)测定的敏感性进行了一项比较研究。由于氨基端检测方法的最新发展,PINP和PICP之间的比较特别令人关注。该研究纳入了26名未经治疗的绝经后骨质疏松症女性,年龄为59±6岁(范围46 - 69岁)以及17名健康的绝经后对照女性,年龄为56±7岁(范围48 - 70岁)。我们发现,与对照组相比,骨质疏松症患者的bAP(p = 0.0021)、BGP(p = 0.041)、PINP(p = 0.0001)和PCIP(p = 0.0073)水平显著升高,但TAP水平未升高(p = 0.3389)。血清PINP和bAP在骨形成研究标志物中显示出最高的诊断准确性,这可从受试者工作特征(ROC)曲线推导得出。尽管PINP和PICP起源相似(从原胶原分子的氨基端和羧基端释放),但通过测量PINP水平获得的结果明显优于PICP。

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