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近期发生的骨折会影响骨转换的生化标志物。

Biochemical markers of bone turnover are influenced by recently sustained fracture.

作者信息

Obrant Karl J, Ivaska Kaisa K, Gerdhem Paul, Alatalo Sari L, Pettersson Kim, Väänänen H Kalervo

机构信息

Clinical and Molecular Osteoporosis Research Unit, Department of Clinical Sciences, Malmö, Lund University, Sweden.

出版信息

Bone. 2005 May;36(5):786-92. doi: 10.1016/j.bone.2005.02.009. Epub 2005 Mar 31.

Abstract

In striving to refine the clinical utility of different markers of bone metabolism, we should take into account numerous confounders, many of which are well known, such as sampling time, fasting status, and bone density. One further confounder may be ongoing fracture healing and/or post-fracture immobilization, which at least theoretically should impose an increased bone formation and resorption. Since both recent fracture and high bone turnover are independent predictors for new fracture, we thought it of importance to define the potential influence of such fracture on markers of bone turnover. From a population-based cohort of 1604 women, all 75 years old (the OPRA-study), 1024 women attended a clinical examination. The bone metabolism was assessed in serum, by three markers of bone formation [bone-specific alkaline phosphatase (S-Bone ALP), intact and N-Mid osteocalcin (S-Total OC), and total carboxylated osteocalcin (S-cOC)], two markers of bone resorption [C-terminal cross-linked telopeptides of type I collagen (S-CTX) and tartrate-resistant acid phosphatase type 5b (S-TRACP5b)], and in urine by one marker of bone resorption [deoxypyridinoline/creatinine (U-DPD/crea)] and two putative markers of bone resorption [urinary osteocalcins (U-OC/crea)]. Current physical activity and retrospective fracture data were recorded by questionnaires. The fracture data, for the entire cohort of 1604 women, were validated with radiographic referrals and reports, saved since the beginning of the last century. All data provided, except date of occurrence of retrospectively sustained fracture, were thus obtained cross-sectionally and in all women at the age of 75. Fracture had ever been sustained by 727 of the entire cohort (n = 1604), and by 523 of the attending women (n = 1024). All markers were marginally higher (significant only for U-DPD/crea, P = 0.027) in women who had ever sustained fracture, compared to women without fracture. In women with recent retrospective fracture (since 2 years) (n = 100), the levels of all markers, except the two S-OCs, were significantly higher (r = 0.20-0.33, P = 0.049-0.001) the more recently the fracture had been sustained. Women with low current physical activity had elevated levels of U-DPD/crea (P < 0.001) and one U-OC (P = 0.014), while the other markers were unaffected.

摘要

在努力完善不同骨代谢标志物的临床应用价值时,我们应考虑到众多混杂因素,其中许多是众所周知的,如采样时间、空腹状态和骨密度。另一个混杂因素可能是正在进行的骨折愈合和/或骨折后的固定,至少从理论上讲,这会导致骨形成和骨吸收增加。由于近期骨折和高骨转换都是新发骨折的独立预测因素,我们认为确定此类骨折对骨转换标志物的潜在影响很重要。在一项基于人群的队列研究中,选取了1604名均为75岁的女性(OPRA研究),其中1024名女性参加了临床检查。通过血清中的三种骨形成标志物[骨特异性碱性磷酸酶(S-骨ALP)、完整和N-中端骨钙素(S-总OC)以及总羧化骨钙素(S-cOC)]、两种骨吸收标志物[I型胶原C末端交联端肽(S-CTX)和抗酒石酸酸性磷酸酶5b(S-TRACP5b)]来评估骨代谢,通过尿液中的一种骨吸收标志物[脱氧吡啶啉/肌酐(U-DPD/crea)]和两种假定的骨吸收标志物[尿骨钙素(U-OC/crea)]来评估骨代谢。通过问卷调查记录当前的身体活动情况和既往骨折数据。对整个1604名女性队列的骨折数据,用上世纪初以来保存的X线转诊和报告进行了验证。因此,除了回顾性发生骨折的日期外,所有提供的数据都是在所有75岁女性中横断面获取的。整个队列(n = 1604)中有727名女性曾发生过骨折,参加检查的女性(n = 1024)中有523名曾发生过骨折。与未发生过骨折的女性相比,曾发生过骨折的女性所有标志物水平略高(仅U-DPD/crea显著,P = 0.027)。在近期有回顾性骨折(过去2年)的女性(n = 100)中,除了两种S-OCs外,所有标志物水平均显著升高(r = 0.20 - 0.33,P = 0.049 - 0.001),骨折发生时间越近升高越明显。当前身体活动水平低的女性U-DPD/crea(P < 0.001)和一种U-OC(P = 0.014)水平升高,而其他标志物未受影响。

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