Vitamin D Therapy in Individuals With Prehypertension or Hypertension

Author:

Arora Pankaj1,Song Yanna1,Dusek Jeffery1,Plotnikoff Gregory1,Sabatine Marc S.1,Cheng Susan1,Valcour Andre1,Swales Heather1,Taylor Beth1,Carney Erin1,Guanaga Derek1,Young Joseph R.1,Karol Courtney1,Torre Michael1,Azzahir Atum1,Strachan Semerit M.1,O’Neill Dillon C.1,Wolf Myles1,Harrell Frank1,Newton-Cheh Christopher1,Wang Thomas J.1

Affiliation:

1. From the Cardiology Division, Department of Medicine, University of Alabama at Birmingham, Birmingham (P.A.); Department of Biostatistics (Y.S., F.H.) and Division of Cardiovascular Medicine, Department of Medicine (D.C.O., T.J.W.), Vanderbilt University, Nashville, TN; Integrative Health Research Center, Abbott Northwestern Hospital, Minneapolis, MN (J.D., G.P.); Division of Cardiology, Department of Medicine, Brigham & Women’s Hospital, Harvard Medical School, Boston, MA (M.S.S., S.C.);...

Abstract

Background— A large body of epidemiological and experimental evidence suggests that vitamin D deficiency may promote hypertension. This raises the possibility that vitamin D supplementation could be a simple intervention to reduce blood pressure, but data from prospective, randomized trials are limited. Methods and Results— A double-blind, randomized, controlled trial was conducted at 4 sites in the United States. We enrolled 534 individuals 18 to 50 years of age with low vitamin D status (25-hydroxyvitamin D levels ≤25 ng/mL) and systolic blood pressure of 120 to 159 mm Hg. Participants were randomized to high-dose (4000 IU/d) versus low-dose (400 IU/d) oral vitamin D 3 for 6 months. The primary end point was change in mean 24-hour systolic blood pressure. Secondary end points included change in ambulatory diastolic blood pressure and clinic systolic and diastolic blood pressures. The median age was 38 years, and 62% of participants were men. Forty-six percent of participants were white, and 48% were black. The median 25-hydroxyvitamin D level at baseline was 15.3 ng/mL. Four-hundred fifty-five participants (85%) had at least 1 follow-up blood pressure measurement; 383 participants (72%) completed the full 6-month study. At the end of the study, there was no significant difference in the primary end point (change in mean 24-hour systolic blood pressure, −0.8 versus −1.6 mm Hg in the high-dose and low-dose arms; P =0.71) or in any of the secondary end points. Furthermore, there was no evidence of association between change in 25-hydroxyvitamin D and change in 24-hour systolic blood pressure at 6 months (Spearman correlation coefficient, −0.05, P =0.34). Results were consistent across prespecified subgroups. Conclusions— Vitamin D supplementation did not reduce blood pressure in individuals with prehypertension or stage I hypertension and vitamin D deficiency. Our findings suggest that the association between vitamin D status and elevated blood pressure noted in observational studies is not causal. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifier: NCT01240512.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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