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

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 longitu...

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Veröffentlicht in:American journal of kidney diseases 2015-03, Vol.65 (3), p.474-483
Hauptverfasser: Keyzer, Charlotte A., MD, Vermeer, Cees, PhD, Joosten, Michel M., PhD, Knapen, Marjo H.J., MSc, Drummen, Nadja E.A., BSc, Navis, Gerjan, MD, PhD, Bakker, Stephan J.L., MD, PhD, de Borst, Martin H., MD, PhD
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Sprache:eng
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Zusammenfassung: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.
ISSN:0272-6386
1523-6838
DOI:10.1053/j.ajkd.2014.09.014