Vitamin K status, all-cause mortality, and cardiovascular disease in adults with chronic kidney disease: the Chronic Renal Insufficiency Cohort

Author:

Shea M Kyla1ORCID,Barger Kathryn1,Booth Sarah L1ORCID,Wang Jifan1,Feldman Harold I2,Townsend Raymond R2,Chen Jing3,Flack John4,He Jiang5ORCID,Jaar Bernard G6,Kansal Mayank7,Rosas Sylvia E8,Weiner Daniel E9,Appel J Lawrence,Go S Alan,Lash P James,Nelson G Robert,Rahman Mahboob,Rao Panduranga S,Shah Vallabh O,Unruh Mark L,

Affiliation:

1. USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA

2. Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania School of Medicine, Philadelphia, PA, USA

3. Department of Medicine, Tulane University School of Medicine, New Orleans, LA, USA

4. Department of Internal Medicine, Southern Illinois University School of Medicine, Springfield, IL, USA

5. Department of Epidemiology, Tulane University School of Medicine, New Orleans, LA, USA

6. Department of Medicine, Johns Hopkins University, Baltimore, MD, USA

7. Department of Medicine, University of Illinois-Chicago, Chicago, IL, USA

8. Joslin Diabetes Center, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA

9. Division of Nephrology, Tufts Medical Center, Boston, MA, USA

Abstract

ABSTRACT Background Vascular calcification contributes to cardiovascular disease (CVD) and mortality in individuals with chronic kidney disease (CKD). Vitamin K-dependent proteins function as calcification inhibitors in vascular tissue. Objectives We sought to determine the association of vitamin K status with mortality and CVD events in adults with CKD. Methods Plasma dephospho-uncarboxylated matrix gla protein ((dp)ucMGP), which increases when vitamin K status is low, and plasma phylloquinone (vitamin K1), which decreases when vitamin K status is low, were measured in 3066 Chronic Renal Insufficiency Cohort participants (median age = 61 y, 45% female, 41% non-Hispanic black, median estimated glomerular filtration rate [eGFR] = 41 mL/min/1.73m2). The association of vitamin K status biomarkers with all-cause mortality and atherosclerotic-related CVD was determined using multivariable Cox proportional hazards regression. Results There were 1122 deaths and 599 atherosclerotic CVD events over the median 12.8 follow-up years. All-cause mortality risk was 21–29% lower among participants with plasma (dp)ucMGP <450 pmol/L (n = 2361) compared with those with plasma (dp)ucMGP ≥450 pmol/L (adjusted HRs [95% CIs]: <300 pmol/L = 0.71 [0.61, 0.83], 300–449 pmol/L = 0.77 [0.66, 0.90]) and 16–19% lower among participants with plasma phylloquinone ≥0.50 nmol/L (n = 2421) compared to those with plasma phylloquinone <0.50 nmol/L (adjusted HRs: 0.50, 0.99 nmol/L = 0.84 [0.72, 0.99], ≥1.00 nmol/L = 0.81 [0.70, 0.95]). The risk of atherosclerotic CVD events did not significantly differ across plasma (dp)ucMGP or phylloquinone categories. Conclusions Two biomarkers of vitamin K status were associated with a lower all-cause mortality risk but not atherosclerotic CVD events. Additional studies are needed to clarify the mechanism underlying this association and evaluate the impact of improving vitamin K status in people with CKD.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

USDA Agricultural Research Service

NIH

NCATS

Johns Hopkins University

University of Maryland

Clinical and Translational Science Collaborative of Cleveland

University of Illinois at Chicago

Clinical and Translational Research in Cardiometabolic Diseases

National Center for Research Resources

University of New Mexico School of Medicine Albuquerque

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

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