Chen Po-Cheng, Chang Shu-Wei, Hsieh Chih-Yu, Liou Jian-Chiun, Chang Jia-Feng, Wang Ting-Ming
Department of Urology, En Chu Kong Hospital, New Taipei City 237, Taiwan.
Department of Civil Engineering, National Taiwan University, Taipei 106, Taiwan.
Diagnostics (Basel). 2021 Jul 13;11(7):1254. doi: 10.3390/diagnostics11071254.
The risk of skeletal events is rising in parallel with the burden of chronic kidney disease and mineral bone disorder (CKD-MBD), whilst the role of the fat-bone axis in CKD-MBD remains elusive. Adiponectin derived from adipocytes has emerged as a valid biomarker of low bone mineral density and increased marrow adiposity. We aimed to explore the association between adiponectin and bone fracture (BF) risks in patients with maintenance hemodialysis (MHD).
Serum concentrations of adiponectin and bio-clinical data were determined at study entry. The Cox proportional hazard regression analyses were used to assess unadjusted and adjusted hazard ratios (aHRs) of adiponectin and various clinical predictors for BF risks. The predictive accuracy of adiponectin for BF events was evaluated by receiver operating characteristic (ROC) curve analysis.
Age and serum concentrations of adiponectin, phosphate, and intact parathyroid hormone were significantly associated with higher risks of BF. With respect to the risk of BF events, the cumulative event-free survival curves differed significantly between the high and low concentration groups of adiponectin ( = 0.02). In multivariable analysis, higher adiponectin levels were associated with an incremental risk of BF (adjusted hazard ratios (aHRs): 1.08 (95% confidence interval (CI): 1.01-1.15, < 0.05). The ROC analysis of adiponectin cutoff point concentration (18.15 ug/mL) for prediction of BF showed 0.66 (95% CI = 0.49 to 0.84).
Adiponectin was associated with an incremental risk of BF that could serve as a potential predictor of BF in MHD patients. In the high-risk population with hyperphosphatemia, an elevated adiponectin level could alert clinicians to the urgent need to correct mineral dysregulation and undertake further bone survey.
骨骼事件的风险随着慢性肾脏病和矿物质骨代谢紊乱(CKD-MBD)负担的增加而上升,而脂肪-骨骼轴在CKD-MBD中的作用仍不明确。脂肪细胞分泌的脂联素已成为低骨矿物质密度和骨髓脂肪增多的有效生物标志物。我们旨在探讨维持性血液透析(MHD)患者脂联素与骨折(BF)风险之间的关联。
在研究开始时测定血清脂联素浓度和生物临床数据。采用Cox比例风险回归分析评估脂联素和各种临床预测因素对BF风险的未调整和调整风险比(aHRs)。通过受试者工作特征(ROC)曲线分析评估脂联素对BF事件的预测准确性。
年龄以及血清脂联素、磷酸盐和完整甲状旁腺激素浓度与较高的BF风险显著相关。关于BF事件的风险,脂联素高浓度组和低浓度组的累积无事件生存曲线存在显著差异(P = 0.02)。在多变量分析中,较高的脂联素水平与BF风险增加相关(调整风险比(aHRs):1.08(95%置信区间(CI):1.01-1.15,P < 0.05)。脂联素预测BF的截断点浓度(18.15 ug/mL)的ROC分析显示为0.66(95%CI = 0.49至0.84)。
脂联素与BF风险增加相关,可作为MHD患者BF的潜在预测指标。在高磷血症的高危人群中,脂联素水平升高可提醒临床医生迫切需要纠正矿物质失调并进行进一步的骨骼检查。