Vitamin B6, Inflammation, and Cardiovascular Outcome in a Population-Based Cohort: The Prevention of Renal and Vascular End-Stage Disease (PREVEND) Study

Background: a large number of studies have linked vitamin B6 to inflammation and cardiovascular disease in the general population. However, it remains uncertain whether vitamin B6 is associated with cardiovascular outcome independent of inflammation. Methods: we measured plasma pyridoxal 5’-phosphat...

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Main Authors: Isidor Minović, Lyanne M. Kieneker, Ron T. Gansevoort, Manfred Eggersdorfer, Daan J. Touw, Albert-Jan Voerman, Margery A. Connelly, Rudolf A. de Boer, Eelko Hak, Jens Bos, Robin P. F. Dullaart, Ido P. Kema, Stephan J. L. Bakker
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Nutrients
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Online Access:https://www.mdpi.com/2072-6643/12/9/2711
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author Isidor Minović
Lyanne M. Kieneker
Ron T. Gansevoort
Manfred Eggersdorfer
Daan J. Touw
Albert-Jan Voerman
Margery A. Connelly
Rudolf A. de Boer
Eelko Hak
Jens Bos
Robin P. F. Dullaart
Ido P. Kema
Stephan J. L. Bakker
author_facet Isidor Minović
Lyanne M. Kieneker
Ron T. Gansevoort
Manfred Eggersdorfer
Daan J. Touw
Albert-Jan Voerman
Margery A. Connelly
Rudolf A. de Boer
Eelko Hak
Jens Bos
Robin P. F. Dullaart
Ido P. Kema
Stephan J. L. Bakker
author_sort Isidor Minović
collection DOAJ
description Background: a large number of studies have linked vitamin B6 to inflammation and cardiovascular disease in the general population. However, it remains uncertain whether vitamin B6 is associated with cardiovascular outcome independent of inflammation. Methods: we measured plasma pyridoxal 5’-phosphate (PLP), as an indicator of vitamin B6 status, at baseline in a population-based prospective cohort of 6249 participants of the Prevention of Renal and Vascular End-stage Disease (PREVEND) study who were free of cardiovascular disease. As indicators of low-grade systemic inflammation, we measured high-sensitivity C-reactive protein and GlycA; Results: median plasma PLP was 37.2 (interquartile range, 25.1–57.0) nmol/L. During median follow-up for 8.3 (interquartile range, 7.8–8.9) years, 409 non-fatal and fatal cardiovascular events (composite outcome) occurred. In the overall cohort, log transformed plasma PLP was associated with the composite outcome, independent of adjustment for age, sex, smoking, alcohol consumption, body mass index (BMI), estimated glomerular filtration rate (eGFR), total cholesterol:high-density lipoprotein (HDL)-cholesterol ratio, and blood pressure (adjusted hazard ratio per increment of log plasma PLP, 0.66; 95% confidence interval (CI), 0.47–0.93). However, adjustment for high-sensitivity C-reactive protein and GlycA increased the hazard ratio by 9% and 12% respectively, to non-significant hazard ratios of 0.72 (95% confidence interval, 0.51–1.01) and 0.74 (95% confidence interval, 0.53–1.05). The association of plasma PLP with cardiovascular risk was modified by gender (adjusted P<sub>interaction</sub> = 0.04). When stratified according to gender, in women the prospective association with cardiovascular outcome was independent of age, smoking, alcohol consumption, high-sensitivity C-reactive protein, and GlycA (adjusted hazard ratio, 0.50, 95% confidence interval, 0.27–0.94), while it was not in men (adjusted hazard, 0.99, 95% confidence interval, 0.65–1.51). Conclusions: in this population-based cohort, plasma PLP was associated with cardiovascular outcome, but this association was confounded by traditional risk factors and parameters of inflammation. Notably, the association of low plasma PLP with high risk of adverse cardiovascular outcome was modified by gender, with a stronger and independent association in women.
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spelling doaj.art-f14ed925c83845dcb91b6dae9b1284142023-11-20T12:38:39ZengMDPI AGNutrients2072-66432020-09-01129271110.3390/nu12092711Vitamin B6, Inflammation, and Cardiovascular Outcome in a Population-Based Cohort: The Prevention of Renal and Vascular End-Stage Disease (PREVEND) StudyIsidor Minović0Lyanne M. Kieneker1Ron T. Gansevoort2Manfred Eggersdorfer3Daan J. Touw4Albert-Jan Voerman5Margery A. Connelly6Rudolf A. de Boer7Eelko Hak8Jens Bos9Robin P. F. Dullaart10Ido P. Kema11Stephan J. L. Bakker12Department of Laboratory Medicine, University of Groningen, University Medical Center Groningen, 9700RB Groningen, The NetherlandsDepartment of Internal Medicine, University of Groningen, University Medical Center Groningen, 9700RB Groningen, The NetherlandsDepartment of Internal Medicine, University of Groningen, University Medical Center Groningen, 9700RB Groningen, The NetherlandsDSM Nutritional Products, CH-4303 Kaiseraugst, SwitzerlandDepartment of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, 9700RB Groningen, The NetherlandsDepartment of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, 9700RB Groningen, The NetherlandsLaboratory Corporation of America® Holdings (LabCorp), Morrisville, NC 27560, USADepartment of Cardiology, University of Groningen, University Medical Center Groningen, 9700RB Groningen, The NetherlandsUnit of Pharmacotherapy, Epidemiology and Economics, University of Groningen, 9712CP Groningen, The NetherlandsUnit of Pharmacotherapy, Epidemiology and Economics, University of Groningen, 9712CP Groningen, The NetherlandsDepartment of Internal Medicine, University of Groningen, University Medical Center Groningen, 9700RB Groningen, The NetherlandsDepartment of Laboratory Medicine, University of Groningen, University Medical Center Groningen, 9700RB Groningen, The NetherlandsDepartment of Internal Medicine, University of Groningen, University Medical Center Groningen, 9700RB Groningen, The NetherlandsBackground: a large number of studies have linked vitamin B6 to inflammation and cardiovascular disease in the general population. However, it remains uncertain whether vitamin B6 is associated with cardiovascular outcome independent of inflammation. Methods: we measured plasma pyridoxal 5’-phosphate (PLP), as an indicator of vitamin B6 status, at baseline in a population-based prospective cohort of 6249 participants of the Prevention of Renal and Vascular End-stage Disease (PREVEND) study who were free of cardiovascular disease. As indicators of low-grade systemic inflammation, we measured high-sensitivity C-reactive protein and GlycA; Results: median plasma PLP was 37.2 (interquartile range, 25.1–57.0) nmol/L. During median follow-up for 8.3 (interquartile range, 7.8–8.9) years, 409 non-fatal and fatal cardiovascular events (composite outcome) occurred. In the overall cohort, log transformed plasma PLP was associated with the composite outcome, independent of adjustment for age, sex, smoking, alcohol consumption, body mass index (BMI), estimated glomerular filtration rate (eGFR), total cholesterol:high-density lipoprotein (HDL)-cholesterol ratio, and blood pressure (adjusted hazard ratio per increment of log plasma PLP, 0.66; 95% confidence interval (CI), 0.47–0.93). However, adjustment for high-sensitivity C-reactive protein and GlycA increased the hazard ratio by 9% and 12% respectively, to non-significant hazard ratios of 0.72 (95% confidence interval, 0.51–1.01) and 0.74 (95% confidence interval, 0.53–1.05). The association of plasma PLP with cardiovascular risk was modified by gender (adjusted P<sub>interaction</sub> = 0.04). When stratified according to gender, in women the prospective association with cardiovascular outcome was independent of age, smoking, alcohol consumption, high-sensitivity C-reactive protein, and GlycA (adjusted hazard ratio, 0.50, 95% confidence interval, 0.27–0.94), while it was not in men (adjusted hazard, 0.99, 95% confidence interval, 0.65–1.51). Conclusions: in this population-based cohort, plasma PLP was associated with cardiovascular outcome, but this association was confounded by traditional risk factors and parameters of inflammation. Notably, the association of low plasma PLP with high risk of adverse cardiovascular outcome was modified by gender, with a stronger and independent association in women.https://www.mdpi.com/2072-6643/12/9/2711vitamin B6pyridoxal 5’-phosphateinflammationGlycAcardiovascular
spellingShingle Isidor Minović
Lyanne M. Kieneker
Ron T. Gansevoort
Manfred Eggersdorfer
Daan J. Touw
Albert-Jan Voerman
Margery A. Connelly
Rudolf A. de Boer
Eelko Hak
Jens Bos
Robin P. F. Dullaart
Ido P. Kema
Stephan J. L. Bakker
Vitamin B6, Inflammation, and Cardiovascular Outcome in a Population-Based Cohort: The Prevention of Renal and Vascular End-Stage Disease (PREVEND) Study
Nutrients
vitamin B6
pyridoxal 5’-phosphate
inflammation
GlycA
cardiovascular
title Vitamin B6, Inflammation, and Cardiovascular Outcome in a Population-Based Cohort: The Prevention of Renal and Vascular End-Stage Disease (PREVEND) Study
title_full Vitamin B6, Inflammation, and Cardiovascular Outcome in a Population-Based Cohort: The Prevention of Renal and Vascular End-Stage Disease (PREVEND) Study
title_fullStr Vitamin B6, Inflammation, and Cardiovascular Outcome in a Population-Based Cohort: The Prevention of Renal and Vascular End-Stage Disease (PREVEND) Study
title_full_unstemmed Vitamin B6, Inflammation, and Cardiovascular Outcome in a Population-Based Cohort: The Prevention of Renal and Vascular End-Stage Disease (PREVEND) Study
title_short Vitamin B6, Inflammation, and Cardiovascular Outcome in a Population-Based Cohort: The Prevention of Renal and Vascular End-Stage Disease (PREVEND) Study
title_sort vitamin b6 inflammation and cardiovascular outcome in a population based cohort the prevention of renal and vascular end stage disease prevend study
topic vitamin B6
pyridoxal 5’-phosphate
inflammation
GlycA
cardiovascular
url https://www.mdpi.com/2072-6643/12/9/2711
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