Association between mineral and bone disorder in patients with acute kidney injury following cardiac surgery and adverse outcomes
Association between mineral and bone disorder in patients with acute kidney injury following cardiac surgery and adverse outcomes
复制标题
心脏手术后急性肾损伤患者矿物质和骨骼疾病之间的关联以及不良后果
DOI:
10.1186/s12882-019-1572-y
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发表时间:
2019-10
期刊:
影响因子:
--
通讯作者:
Feng Ding
中科院分区:
文献类型:
--
作者:
Tianye Yang;Wenji Wang;Xiao Tang;Peng Shi;Lulu Zhang;Wenyan Yu;Yingxin Xie;Daqiao Guo;Feng Ding
BackgroundNumerous studies have evaluated the prevalence and importance of mineral and bone disorders among patients with chronic kidney disease (CKD) and end-stage renal disease (ESRD). However, little is known about dysregulated mineral and bone metabolism in acute kidney injury (AKI).MethodsWe evaluated the association between mineral and bone metabolites and clinical outcomes in 158 patients who underwent cardiac surgery and developed AKI between June 2014 and January 2016. The baseline characteristics of the patients were recorded, and the levels of mineral and bone metabolites, including calcium, phosphate, intact parathyroid hormone (iPTH), 25-hydroxyvitamin D (25D), bone-specific alkaline phosphatase (BAP), tartrate-resistant acid phosphatase 5b (TRACP-5b) and C-terminal fibroblast growth factor 23 (cFGF23) were measured within 12 h after establishing the clinical diagnosis.ResultsThe serum phosphate, iPTH and cFGF23 levels were significantly associated with the 28-day mortality (phosphate: Hazard Ratio [HR] =2.620, 95% CI: 1.083 to 6.338,p= 0.035; iPTH: HR = 1.044, 95% CI: 1.001 to 1.090,p= 0.046; cFGF23: HR = 1.367, 95% CI: 1.168 to 1.599,p< 0.001). Moreover, higher serum cFGF23 and BAP levels were independently associated with an increased risk of adverse outcomes. Additionally, we found that the serum cFGF23 levels rose most significantly and were associated with the severity of AKI (P< 0.001).ConclusionsMineral and bone metabolites are dysregulated and are associated with adverse clinical outcomes among patients with AKI.Trial registrationwww.clinicaltrials.gov NCT 00953992. Registered 6 August 2009.
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影响因子:
13.6
作者:
Leaf, David E.;Jacob, Kirolos A.;Waikar, Sushrut S.
通讯作者:
Waikar, Sushrut S.
影响因子:
5.3
作者:
通讯作者:
--
影响因子:
3.2
作者:
Leaf DE;Waikar SS;Wolf M;Cremers S;Bhan I;Stern L
通讯作者:
Stern L
影响因子:
38.9
作者:
Druml, Wilfred;Lenz, Kurt;Laggner, Anton N.
通讯作者:
Laggner, Anton N.
影响因子:
19.6
作者:
Leaf DE;Christov M;Jüppner H;Siew E;Ikizler TA;Bian A;Chen G;Sabbisetti VS;Bonventre JV;Cai X;Wolf M;Waikar SS
通讯作者:
Waikar SS