Vitamin D deficiency is associated with sudden cardiac death, combined cardiovascular events, and mortality in haemodialysis patients

被引:201
作者
Drechsler, Christiane [1 ,2 ]
Pilz, Stefan [3 ]
Obermayer-Pietsch, Barbara [3 ]
Verduijn, Marion [2 ]
Tomaschitz, Andreas [3 ]
Krane, Vera [1 ]
Espe, Katharina [4 ]
Dekker, Friedo [2 ]
Brandenburg, Vincent [5 ]
Maerz, Winfried [6 ,7 ]
Ritz, Eberhard [8 ]
Wanner, Christoph [1 ]
机构
[1] Univ Wurzburg, Div Nephrol, Dept Internal Med 1, D-97080 Wurzburg, Germany
[2] Leiden Univ Med Ctr, Dept Clin Epidemiol, Leiden, Netherlands
[3] Med Univ Graz, Div Endocrinol & Metab, Dept Internal Med, Graz, Austria
[4] Univ Potsdam, Inst Nutr Sci, Potsdam, Germany
[5] Univ Hosp, RWTH Aachen, Dept Cardiol, Aachen, Germany
[6] Synlab Ctr Lab Diagnost, Heidelberg, Germany
[7] Med Univ Graz, Clin Inst Med & Chem Lab Diagnost, Graz, Austria
[8] Ruperto Carola Univ Heidelberg, Div Nephrol, Nierenzentrum, Heidelberg, Germany
关键词
Vitamin D; Sudden cardiac death; Mortality; Dialysis; Kidney; Cardiovascular; PARATHYROID-HORMONE; D-RECEPTOR; MINERAL METABOLISM; DIALYSIS PATIENTS; RISK; 25-HYDROXYVITAMIN-D; DISEASE; SUPPLEMENTATION; EXPRESSION; OUTCOMES;
D O I
10.1093/eurheartj/ehq246
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dialysis patients experience an excess mortality, predominantly of sudden cardiac death (SCD). Accumulating evidence suggests a role of vitamin D for myocardial and overall health. This study investigated the impact of vitamin D status on cardiovascular outcomes and fatal infections in haemodialysis patients. 25-hydroxyvitamin D [25(OH)D] was measured in 1108 diabetic haemodialysis patients who participated in the German Diabetes and Dialysis Study and were followed up for a median of 4 years. By Cox regression analyses, we determined hazard ratios (HR) for pre-specified, adjudicated endpoints according to baseline 25(OH)D levels: SCD (n = 146), myocardial infarction (MI, n = 174), stroke (n = 89), cardiovascular events (CVE, n = 414), death due to heart failure (n = 37), fatal infection (n = 111), and all-cause mortality (n = 545). Patients had a mean age of 66 +/- 8 years (54% male) and median 25(OH)D of 39 nmol/L (interquartile range: 28-55). Patients with severe vitamin D deficiency [25(OH)D of < 25 nmol/L] had a 3-fold higher risk of SCD compared with those with sufficient 25(OH)D levels > 75 nmol/L [HR: 2.99, 95% confidence interval (CI): 1.39-6.40]. Furthermore, CVE and all-cause mortality were strongly increased (HR: 1.78, 95% CI: 1.18-2.69, and HR: 1.74, 95% CI: 1.22-2.47, respectively), all persisting in multivariate models. There were borderline non-significant associations with stroke and fatal infection while MI and deaths due to heart failure were not meaningfully affected. Severe vitamin D deficiency was strongly associated with SCD, CVE, and mortality, and there were borderline associations with stroke and fatal infection. Whether vitamin D supplementation decreases adverse outcomes requires further evaluation.
引用
收藏
页码:2253 / 2261
页数:9
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