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Published on: February 20, 2017
Vitamin D reduces left atrial volume in patients with left ventricular hypertrophy and chronic kidney disease
Hector Tamez1, Carmine Zoccali, David Packham
1Department of Medicine, Division of Nephrology, Massachusetts General Hospital, Boston, USA.
Insights
An active vitamin D analog, paricalcitol, significantly reduced left atrial volume index (LAVi) in patients with chronic kidney disease. This therapy also attenuated the rise in brain natriuretic peptide (BNP), suggesting cardiovascular benefits.
Area of Science:
- Cardiology
- Nephrology
- Endocrinology
Background:
- Left atrial enlargement is a key indicator of diastolic dysfunction and predicts cardiovascular events.
- Vitamin D's role in cardiovascular health is under investigation, with limited evidence on its direct impact on cardiac structure.
- The PRIMO trial investigated paricalcitol's effects in patients with chronic kidney disease (CKD).
Purpose of the Study:
- To determine the effect of an activated vitamin D analog, paricalcitol, on left atrial volume index (LAVi).
- To assess paricalcitol's impact on cardiac structure and function in CKD patients.
Main Methods:
- A post hoc analysis of the PRIMO trial involving 196 patients with CKD, left ventricular hypertrophy, and preserved ejection fraction.
- Patients received either 2 μg of oral paricalcitol or placebo for 48 weeks.
- Two-dimensional echocardiography was used to measure LAVi at baseline and 24/48 weeks; brain natriuretic peptide (BNP) levels were also monitored.
Main Results:
- Paricalcitol treatment led to a significant decrease in LAVi compared to placebo (-2.79 mL/m² vs. -0.70 mL/m², P = .002).
- Paricalcitol attenuated the increase in BNP levels (10.8% vs. 21.3%, P = .02).
- Changes in BNP correlated with changes in LAVi (r = 0.17, P = .03).
Conclusions:
- Forty-eight weeks of paricalcitol therapy effectively reduces LAVi in CKD patients.
- The active vitamin D analog also mitigates the rise in BNP, a marker of cardiac strain.
- These findings suggest a potential therapeutic role for vitamin D analogs in reducing cardiovascular risk, warranting further investigation.
Background:
Left atrial enlargement, a sensitive integrator of left ventricular diastolic function, is associated with increased cardiovascular morbidity and mortality. Vitamin D is linked to lower cardiovascular morbidity, possibly modifying cardiac structure and function; however, firm evidence is lacking. We assessed the effect of an activated vitamin D analog on left atrial volume index (LAVi) in a post hoc analysis of the PRIMO trial (clinicaltrials.gov: NCT00497146).
Methods And Results:
One hundred ninety-six patients with chronic kidney disease (estimated glomerular filtration rate 15-60 mL/min per 1.73 m(2)), mild to moderate left ventricular hypertrophy, and preserved ejection fraction were randomly assigned to 2 μg of oral paricalcitol or matching placebo for 48 weeks. Two-dimensional echocardiography was obtained at baseline and at 24 and 48 weeks after initiation of therapy. Over the study period, there was a significant decrease in LAVi (-2.79 mL/m(2), 95% CI -4.00 to -1.59 mL/m(2)) in the paricalcitol group compared with the placebo group (-0.70 mL/m(2) [95% CI -1.93 to 0.53 mL/m(2)], P = .002). Paricalcitol also attenuated the rise in levels of brain natriuretic peptide (10.8% in paricalcitol vs 21.3% in placebo, P = .02). For the entire population, the change in brain natriuretic peptide correlated with change in LAVi (r = 0.17, P = .03).
Conclusions:
Forty-eight weeks of therapy with an active vitamin D analog reduces LAVi and attenuates the rise of BNP. In a population where only few therapies alter cardiovascular related morbidity and mortality, these post hoc results warrant further confirmation.
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