Vitamin K Status and Mortality After Kidney Transplantation: A Cohort Study

被引:60
作者
Keyzer, Charlotte A. [1 ]
Vermeer, Cees [2 ]
Joosten, Michel M. [1 ,2 ,3 ]
Knapen, Marjo H. J. [2 ]
Drummen, Nadja E. A. [2 ]
Navis, Gerjan [1 ]
Bakker, Stephan J. L. [1 ,3 ]
de Borst, Martin H. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Internal Med, Div Nephrol, NL-9700 RB Groningen, Netherlands
[2] Maastricht Univ, VitaK, NL-6200 MD Maastricht, Netherlands
[3] Top Inst Food & Nutr, Wageningen, Netherlands
关键词
Desphosphorylated-uncarboxylated matrix Gla protein (dp-ucMGP); vitamin K; vitamin K insufficiency; kidney transplantation; renal transplant recipients; graft failure; mortality; vascular calcification; cardiovascular disease; MATRIX GLA-PROTEIN; CORONARY-HEART-DISEASE; C-REACTIVE PROTEIN; VASCULAR CALCIFICATION; CARDIOVASCULAR EVENTS; METABOLIC SYNDROME; RENAL-TRANSPLANTATION; HEMODIALYSIS-PATIENTS; RECIPIENTS; RISK;
D O I
10.1053/j.ajkd.2014.09.014
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Vitamin K modulates calcification by activating calcification inhibitors such as matrix Gla protein (MGP). In kidney transplant recipients, vitamin K insufficiency is common, but implications for long-term outcomes are unclear. Study Design: Single-center observational study with a longitudinal design. Setting & Participants: 518 stable kidney transplant recipients; 56% men; mean age, 51 +/- 12 (SD) years; and a median of 6 (IQR, 3-12) years after kidney transplantation. Factor: Plasma desphosphorylated-uncarboxylated MGP (dp-ucMGP) levels, reflecting vitamin K status. Outcomes: All-cause mortality and transplant failure. Results: At inclusion, median dp-ucMGP level was 1,038 (IQR, 733-1,536) pmol/L, with 473 (91%) patients having vitamin K insufficiency (defined as dp-ucMGP > 500 pmol/L). During a median follow-up of 9.8 (IQR, 8.5-10.2) years, 152 (29%) patients died and 54 (10%) developed transplant failure. Patients in the highest quartile of dp-ucMGP were at considerably higher mortality risk compared with patients in the lowest quartile (HR, 3.10; 95% CI, 1.87-5.12; P for trend < 0.001; P for quartile 1 [Q1] vs Q4 < 0.001). After adjustment for potential confounders, including kidney function and exclusion of patients treated with a vitamin K antagonist, this association remained significant. Patients in the highest quartile also were at higher risk of developing transplant failure (HR, 2.61; 95% CI, 1.22-5.57; P for trend = 0.004; P for Q1 vs Q4 = 0.01), but this association was lost after adjustment for baseline kidney function (HR, 1.20; 95% CI, 0.52-2.75; P for trend = 0.6; P for Q1 vs Q4 = 0.7). Limitations: Although MGP exists as various species, only dp-ucMGP was measured. No data were available for vascular calcification as an intermediate end point. Conclusions: Vitamin K insufficiency, that is, a high circulating level of dp-ucMGP, is highly prevalent in stable kidney transplant recipients and is associated independently with increased risk of mortality. Future studies should address whether vitamin K supplementation may lead to improved outcomes after kidney transplantation. (C) 2015 by the National Kidney Foundation, Inc.
引用
收藏
页码:474 / 483
页数:10
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