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High homocysteine and low folate plasma concentrations are associated with cardiovascular events but not bleeding during warfarin treatment

  • Marcus Lind EMAIL logo , Jan-Håkan Jansson , Torbjörn K. Nilsson and Lars Johansson
Published/Copyright: June 11, 2016

Abstract

Background:

Previous studies have shown that homocysteine and folate levels in plasma are associated with risk for cardiovascular events and mortality. The aim of this study was to investigate if plasma concentrations of total homocysteine and folate can predict major bleeding, cardiovascular events, and all-cause mortality in patients being treated with warfarin.

Methods:

In a longitudinal cohort study, 719 patients who were taking warfarin were followed for 3001 treatment years. The following were recorded and classified: major bleeding; cardiovascular events including stroke, arterial emboli, and myocardial infarction (MI); and mortality. Blood samples collected at baseline were analysed for plasma homocysteine and folate levels.

Results:

After adjustment for age, C-reactive protein, and creatinine, high homocysteine levels were associated with cardiovascular events [hazard ratio (HR) 1.23 per standard deviation (SD); 95% confidence interval (CI): 1.03–1.47], MI (HR 1.38 per SD; 95% CI: 1.03–1.85), and all-cause mortality (HR 1.41 per SD; 95% CI: 1.19–1.68). The highest tertile of folate compared to the lowest tertile was associated with decreased risk for both cardiovascular events (HR 0.64; 95% CI: 0.43–0.91) and MI (HR 0.45; 95% CI: 0.21–0.97). There was no association between major bleeding and homocysteine or folate levels.

Conclusions:

In patients receiving warfarin treatment, high homocysteine and low folate plasma concentrations are associated with increased risk for cardiovascular events but not major bleeding. For homocysteine levels, there is also an association with all-cause mortality.


Corresponding author: Marcus Lind, MD, PhD, Department of Medicine, Skellefteå County Hospital, 931 86 Skellefteå, Sweden, Phone: +46910771100, Fax: +46910771657

  1. Author contributions: JHJ, TN designed the study; ML, JHJ, TN, LJ provided essential materials; ML performed statistical analysis; JHJ, TN, LJ interpreted the data; ML wrote the paper; JHJ, TN, LJ critically revised the paper for important intellectual content; ML and LJ had primary responsibility for the final content. All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This work was supported by grants from Visare Norr Fund and Northern County Councils, Västerbotten County Council and the Heart Foundation of Northern Sweden, the Foundation of Medical Research in Skellefteå.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2016-2-3
Accepted: 2016-5-3
Published Online: 2016-6-11
Published in Print: 2016-12-1

©2016 Walter de Gruyter GmbH, Berlin/Boston

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