CHICAGO – Patients with chronic kidney disease who received the vitamin D compound paricalcitol for up to 48 weeks did not show improvement on measures of cardiac structure, function, or left ventricular mass, compared to patients who received placebo, according to a study in the February 15 issue of JAMA.
"Although primarily recommended for improving bone health, treatment with vitamin D recently has been suggested for other conditions, including cardiovascular disease (CVD)," according to background in the article. The authors add that convincing data demonstrating that vitamin D therapy improves cardiovascular health are lacking. Observational studies in patients with chronic kidney disease (CKD) report associations between vitamin D deficiency and increased risk of cardiovascular events.
Ravi Thadhani, M.D., M.P.H., of Massachusetts General Hospital, Boston, and colleagues conducted a study (PRIMO trial) to examine whether 48-weeks of treatment with paricalcitol would reduce left ventricular mass, improve diastolic function, reduce CVD events, and improve cardiac biomarkers in patients with left ventricular hypertrophy (LVH; enlargement of the left ventricle of the heart) and CKD. The randomized, placebo-controlled trial, which included 227 patients with chronic kidney disease and mild to moderate left ventricular hypertrophy, was conducted in 11 countries from July 2008 through September 2010. Participants were randomly assigned to receive oral paricalcitol (n = 115) or matching placebo (n = 112). Participants were predominantly male and had hypertension. Other CVD risk factors were frequent in both groups. The primary outcome for the study was the change in the left ventricular mass index over 48 weeks measured by cardiovascular magnetic resonance imaging.
The researchers found that after 48 weeks, there was not a significant difference in the change in the left ventricular mass index between the two groups. The change in pre-specified echocardiography measures of diastolic function also did not significantly differ between the paricalcitol and placebo groups.
The number of hospitalizations from any cause (15.7 percent of those in the paricalcitol group, and 17.0 percent of those in the placebo group) and from noncardiovascular causes (paricalcitol, 15.7 percent; placebo, 11.6 percent) did not differ between groups. However, there were fewer hospitalizations for CVD events in the paricalcitol group than in the placebo group (1 vs. 8, respectively).
There was no difference in the overall incidence of adverse events between groups (paricalcitol, 80.0 percent vs. placebo, 77.7 percent). Episodes of hypercalcemia (the presence of abnormally high levels of calcium in the blood) were more frequent in the paricalcitol group compared with the placebo group. (JAMA. 2012;307:674-684. Available pre-embargo to the media at http://www.jamamedia.org)
Editor's Note: This study was funded by an investigator-initiated grant from Abbott Laboratories. Please see the article for additional information, including other authors, author contributions and affiliations, financial disclosures, etc.
Editorial: Vitamin D in Chronic Kidney Disease - More Questions Than Answers
In an accompanying editorial, Stefan D. Anker, M.D., Ph.D., and Stephan von Haehling, M.D., Ph.D., of Charite Campus Virchow-Klinikum, Berlin, Germany, write that "the deciding factor for whether to prescribe paricalcitol (vitamin D) for patients with CKD should be based on improvement in important clinical outcomes rather than other end points."
"At this time, paricalcitol cannot be recommended for patients with CKD. The PRIMO trial needs to be followed by a larger trial adequately powered to assess clinical end points such as cardiac-related hospitalizations, dialysis events, and mortality. Considering the competition for public funding of clinical trials in CKD, the pro-vitamin D research groups may face an uphill battle to keep this treatment option viable for patients with CKD."
(JAMA. 2012;307:722-723. Available pre-embargo to the media at http://www.jamamedia.org)
Editor's Note: Both authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest and none were reported.
To contact Ravi Thadhani, M.D., M.P.H., call Ryan Donovan at 617-724-6433 or email email@example.com. To contact editorial co-author Stefan D. Anker, M.D., Ph.D., email firstname.lastname@example.org.
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