Merhi Basma, Shireman Theresa, Carpenter Myra A, Kusek John W, Jacques Paul, Pfeffer Marc, Rao Madhumathi, Foster Meredith C, Kim S Joseph, Pesavento Todd E, Smith Stephen R, Kew Clifton E, House Andrew A, Gohh Reginald, Weiner Daniel E, Levey Andrew S, Ix Joachim H, Bostom Andrew
Division of Hypertension and Kidney Diseases, Department of Medicine, Rhode Island Hospital, Providence, RI.
Center for Gerontology and Healthcare Research, Brown University, Providence, RI.
Am J Kidney Dis. 2017 Sep;70(3):377-385. doi: 10.1053/j.ajkd.2017.04.014. Epub 2017 Jun 2.
Mild hyperphosphatemia is a putative risk factor for cardiovascular disease [CVD], loss of kidney function, and mortality. Very limited data are available from sizable multicenter kidney transplant recipient (KTR) cohorts assessing the potential relationships between serum phosphorus levels and the development of CVD outcomes, transplant failure, or all-cause mortality.
Cohort study.
SETTING & PARTICIPANTS: The Folic Acid for Vascular Outcome Reduction in Transplantation (FAVORIT) Trial, a large, multicenter, multiethnic, controlled clinical trial that provided definitive evidence that high-dose vitamin B-based lowering of plasma homocysteine levels did not reduce CVD events, transplant failure, or total mortality in stable KTRs.
Serum phosphorus levels were determined in 3,138 FAVORIT trial participants at randomization.
During a median follow-up of 4.0 years, the cohort had 436 CVD events, 238 transplant failures, and 348 deaths. Proportional hazards modeling revealed that each 1-mg/dL higher serum phosphorus level was not associated with a significant increase in CVD risk (HR, 1.06; 95% CI, 0.92-1.22), but increased transplant failure (HR, 1.36; 95% CI, 1.15-1.62) and total mortality risk associations (HR, 1.21; 95% CI, 1.04-1.40) when adjusted for treatment allocation, traditional CVD risk factors, kidney measures, type of kidney transplant, transplant vintage, and use of calcineurin inhibitors, steroids, or lipid-lowering drugs. These associations were strengthened in models without kidney measures: CVD (HR, 1.14; 95% CI, 1.00-1.31), transplant failure (HR, 1.72; 95% CI, 1.46-2.01), and mortality (HR, 1.34; 95% CI, 1.15-1.54).
We lacked data for concentrations of parathyroid hormone, fibroblast growth factor 23, or vitamin D metabolites.
Serum phosphorus level is marginally associated with CVD and more strongly associated with transplant failure and total mortality in long-term KTRs. A randomized controlled clinical trial in KTRs that assesses the potential impact of phosphorus-lowering therapy on these hard outcomes may be warranted.
轻度高磷血症被认为是心血管疾病(CVD)、肾功能丧失和死亡的危险因素。关于血清磷水平与CVD结局、移植失败或全因死亡率之间潜在关系的大规模多中心肾移植受者(KTR)队列数据非常有限。
队列研究。
移植中降低血管结局的叶酸(FAVORIT)试验,这是一项大型、多中心、多民族的对照临床试验,提供了确凿证据表明高剂量基于维生素B降低血浆同型半胱氨酸水平并不能降低稳定KTRs的CVD事件、移植失败或总死亡率。
在3138名FAVORIT试验参与者随机分组时测定血清磷水平。
在中位随访4.0年期间,该队列发生436例CVD事件、238例移植失败和348例死亡。比例风险模型显示,血清磷水平每升高1mg/dL与CVD风险显著增加无关(风险比[HR],1.06;95%置信区间[CI],0.92 - 1.22),但在调整治疗分配、传统CVD危险因素、肾脏指标、肾移植类型、移植时间以及钙调神经磷酸酶抑制剂、类固醇或降脂药物的使用后,移植失败风险增加(HR,1.36;95%CI,1.15 - 1.62),总死亡风险增加(HR,1.21;95%CI,1.04 - 1.40)。在不纳入肾脏指标的模型中,这些关联得到加强:CVD(HR,1.14;95%CI,1.00 - 1.31)、移植失败(HR,1.72;95%CI,1.46 - 2.01)和死亡率(HR,1.34;95%CI,1.15 - 1.54)。
我们缺乏甲状旁腺激素、成纤维细胞生长因子23或维生素D代谢物浓度的数据。
血清磷水平与长期KTRs的CVD存在微弱关联,与移植失败和总死亡率的关联更强。可能有必要在KTRs中进行一项随机对照临床试验,以评估降磷治疗对这些严重结局的潜在影响。