Low vitamin D status: a contributing factor in the pathogenesis of congestive heart failure?

A Zittermann, SS Schleithoff, G Tenderich… - Journal of the American …, 2003 - jacc.org
A Zittermann, SS Schleithoff, G Tenderich, HK Berthold, R Körfer, P Stehle
Journal of the American College of Cardiology, 2003jacc.org
Objectives: This study was designed to evaluate the association between vitamin D status
and congestive heart failure (CHF). Background: Impaired intracellular calcium metabolism
is an important factor in the pathogenesis of CHF. The etiology of CHF, however, is not well
understood. Methods: Twenty patients age< 50 years and 34 patients age≥ 50 years with
New York Heart Association classes≥ 2 and 34 control subjects age≥ 50 years were
recruited. N-terminal pro-atrial natriuretic peptide (NT-proANP), a predictor of CHF severity; …
Objectives
This study was designed to evaluate the association between vitamin D status and congestive heart failure (CHF).
Background
Impaired intracellular calcium metabolism is an important factor in the pathogenesis of CHF. The etiology of CHF, however, is not well understood.
Methods
Twenty patients age <50 years and 34 patients age ≥50 years with New York Heart Association classes ≥2 and 34 control subjects age ≥50 years were recruited. N-terminal pro-atrial natriuretic peptide (NT-proANP), a predictor of CHF severity; vitamin D metabolites; and parameters of calcium metabolism were measured in fasting blood samples collected between November 2000 and March 2001.
Results
Both groups of CHF patients had markedly increased serum levels of NT-proANP (p < 0.001), increased serum phosphorus levels (p < 0.001), and reduced circulating levels of both 25-hydroxyvitamin D (p < 0.001) and calcitriol (p < 0.001). Albumin-corrected calcium levels were reduced and parathyroid hormone levels were increased in the younger CHF patients compared with the controls (both p values <0.001). Moreover, parathyroid hormone levels tended to be higher in the elderly CHF patients than in the controls (p = 0.074). In a nonlinear regression analysis 25-hydroxyvitamin D and calcitriol were inversely correlated with NT-proANP (r2= 0.16; p < 0.001 and r2= 0.12; p < 0.01, respectively). The vitamin D genotype at the BmsI restriction site did not differ between the study groups.
Conclusions
The low vitamin D status can explain alterations in mineral metabolism as well as myocardial dysfunction in the CHF patients, and it may therefore be a contributing factor in the pathogenesis of CHF.
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