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骨转换标志物(包括低羧化骨钙素)与老年男性的死亡风险相关。

Bone Turnover Markers Including Undercarboxylated Osteocalcin Are Associated With Mortality Risk in Older Men.

机构信息

Medical School, University of Western Australia, Perth, Australia.

Department of Endocrinology and Diabetes, Fiona Stanley Hospital, Perth, Australia.

出版信息

J Bone Miner Res. 2022 Aug;37(8):1464-1472. doi: 10.1002/jbmr.4631. Epub 2022 Jul 8.

Abstract

Osteocalcin in its undercarboxylated form (ucOC) may influence diabetes risk; however, its relationship with all-cause and cause-specific mortality is unclear. Whether other bone turnover markers (BTMs) are associated with mortality risk differently from ucOC also remains uncertain. Our aim was to determine associations of serum ucOC with all-cause and cause-specific mortality and compare these with the corresponding associations of serum total osteocalcin (TOC), procollagen type I N-propeptide (PINP), and collagen type 1 C-terminal cross-linked telopeptide (CTX) in older men. We conducted a prospective cohort study of 3871 community-dwelling men, aged 77.0 ± 3.6 years at baseline, followed for a median of 12.3 years. Exposure variables were ucOC, TOC, PINP, and CTX concentrations assayed in serum. Outcomes were incidence of all deaths and deaths due to cardiovascular disease (CVD) or cancer, ascertained using death registry data. Cox regression analyses adjusted for cardiovascular risk factors and prevalent CVD and for prevalent cancer in analyses of cancer-related mortality. Higher concentrations of ucOC, PINP, and CTX were associated with all-cause mortality (hazard ratio [HR] per 1 standard deviation increase: ucOC 1.12, 95% confidence interval [CI] 1.06-1.18, p < 0.001; PINP HR = 1.06, 95% CI 1.01-1.11, p = 0.009; CTX HR = 1.13, 95% CI 1.08-1.19, p < 0.001), but TOC was not associated. Similar results were found after excluding men with an incident fracture during follow-up. Higher ucOC and CTX were associated with CVD mortality (ucOC HR per 1 SD increase 1.13, 95% CI 1.05-1.22, p = 0.001; CTX HR = 1.12, 95% CI 1.04-1.20, p = 0.003), but this result was not significant in competing risks analysis. Higher CTX was also associated with cancer mortality (HR = 1.12, 95% CI 1.01-1.23, p = 0.024). In conclusion, in older men, higher bone turnover, assessed by BTMs including ucOC, is a biomarker for all-cause mortality risk. Undercarboxylated osteocalcin was a more informative biomarker for this outcome than TOC. Higher CTX was associated with all-cause and cancer-related mortality. Further evaluation of causality and potential underlying mechanisms is warranted. © 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

摘要

非羧化骨钙素(ucOC)可能会影响糖尿病风险;然而,其与全因和特定原因死亡率的关系尚不清楚。其他骨转换标志物(BTMs)与死亡率的关联是否与 ucOC 不同也尚不确定。我们的目的是确定血清 ucOC 与全因和特定原因死亡率的相关性,并将其与老年男性血清总骨钙素(TOC)、I 型前胶原 N 端前肽(PINP)和 I 型胶原 C 端交联肽(CTX)的相应相关性进行比较。我们对 3871 名居住在社区的男性进行了前瞻性队列研究,这些男性在基线时的年龄为 77.0±3.6 岁,中位随访时间为 12.3 年。暴露变量为血清中 ucOC、TOC、PINP 和 CTX 的浓度。使用死亡登记数据确定所有死亡和心血管疾病(CVD)或癌症导致的死亡的发生率作为结局。在分析与癌症相关的死亡率时,使用 Cox 回归分析调整了心血管危险因素、现患 CVD 和癌症。ucOC、PINP 和 CTX 浓度的升高与全因死亡率相关(每增加一个标准差的风险比[HR]:ucOC 1.12,95%置信区间[CI]1.06-1.18,p<0.001;PINP HR=1.06,95%CI 1.01-1.11,p=0.009;CTX HR=1.13,95%CI 1.08-1.19,p<0.001),但 TOC 没有关联。在随访期间发生骨折的男性被排除后,也得到了类似的结果。ucOC 和 CTX 浓度的升高与 CVD 死亡率相关(ucOC 每增加一个标准差的 HR 为 1.13,95%CI 为 1.05-1.22,p=0.001;CTX HR=1.12,95%CI 为 1.04-1.20,p=0.003),但在竞争风险分析中这一结果并不显著。较高的 CTX 也与癌症死亡率相关(HR=1.12,95%CI 为 1.01-1.23,p=0.024)。总之,在老年男性中,骨转换标志物(包括 ucOC)评估的较高骨转换是全因死亡率风险的生物标志物。非羧化骨钙素是该结局更具信息性的生物标志物。较高的 CTX 与全因和癌症相关死亡率相关。需要进一步评估因果关系和潜在的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60c4/9540459/5843c6ae1f5b/JBMR-37-1464-g001.jpg

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