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      Effect of Vitamin D Supplementation on Blood Pressure : A Systematic Review and Meta-analysis Incorporating Individual Patient Data

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          Abstract

          IMPORTANCE

          Low levels of vitamin D are associated with elevated blood pressure (BP) and future cardiovascular events. Whether vitamin D supplementation reduces BP and which patient characteristics predict a response remain unclear.

          OBJECTIVE

          To systematically review whether supplementation with vitamin D or its analogues reduce BP.

          DATA SOURCES

          We searched MEDLINE, CINAHL, EMBASE, Cochrane Central Register of Controlled Trials, and http://www.ClinicalTrials.com augmented by a hand search of references from the included articles and previous reviews. Google was searched for gray literature (ie, material not published in recognized scientific journals). No language restrictions were applied. The search period spanned January 1, 1966, through March 31, 2014.

          STUDY SELECTION

          We included randomized placebo-controlled clinical trials that used vitamin D supplementation for a minimum of 4 weeks for any indication and reported BP data. Studies were included if they used active or inactive forms of vitamin D or vitamin D analogues. Cointerventions were permitted if identical in all treatment arms.

          DATA EXTRACTION AND SYNTHESIS

          We extracted data on baseline demographics, 25-hydroxyvitamin D levels, systolic and diastolic BP (SBP and DBP), and change in BP from baseline to the final follow-up. Individual patient data on age, sex, medication use, diabetes mellitus, baseline and follow-up BP, and 25-hydroxyvitamin D levels were requested from the authors of the included studies. For trial-level data, between-group differences in BP change were combined in a random-effects model. For individual patient data, between-group differences in BP at the final follow up, adjusted for baseline BP, were calculated before combining in a random-effects model.

          MAIN OUTCOMES AND MEASURES

          Difference in SBP and DBP measured in an office setting.

          RESULTS

          We included 46 trials (4541 participants) in the trial-level meta-analysis. Individual patient data were obtained for 27 trials (3092 participants). At the trial level, no effect of vitamin D supplementation was seen on SBP (effect size, 0.0 [95% CI, −0.8 to 0.8] mm Hg; P = .97; I 2 = 21%) or DBP (effect size, −0.1 [95% CI, −0.6 to 0.5] mm Hg; P = .84; I 2 = 20%). Similar results were found analyzing individual patient data for SBP (effect size, −0.5 [95% CI, −1.3 to 0.4] mm Hg; P = .27; I 2 = 0%) and DBP (effect size, 0.2 [95% CI, −0.3 to 0.7] mm Hg; P = .38; I 2 = 0%). Subgroup analysis did not reveal any baseline factor predictive of a better response to therapy.

          CONCLUSIONS AND RELEVANCE

          Vitamin D supplementation is ineffective as an agent for lowering BP and thus should not be used as an antihypertensive agent.

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          Author and article information

          Contributors
          Journal
          101589534
          40864
          JAMA Intern Med
          JAMA Intern Med
          JAMA internal medicine
          2168-6106
          2168-6114
          7 May 2018
          May 2015
          23 May 2018
          : 175
          : 5
          : 745-754
          Affiliations
          Medical Research Institute, University of Dundee, Ninewells Hospital, Dundee, Scotland
          Medical Research Institute, University of Dundee, Ninewells Hospital, Dundee, Scotland
          Medical Research Institute, University of Dundee, Ninewells Hospital, Dundee, Scotland
          Tromsø Endocrine Research Group, Institute of Clinical Medicine, UiT (Universitetet i Tromsø), The Arctic University of Norway, Tromsø, Norway
          School of Population Health, University of Auckland, Auckland, New Zealand
          School of Medicine and Dentistry, University of Aberdeen, Aberdeen, Scotland
          Division of Endocrinology, Metabolism and Lipids, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia
          Division of Geriatric Medicine, University of Colorado School of Medicine, Aurora
          Department of Medicine, University of Verona, Verona, Italy
          Division of Cardiovascular Medicine, University of Wisconsin School of Medicine and Public Health, Madison
          Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia
          Department of Medical Research, Holstebro Hospital, Holstebro, Denmark
          Department of Pediatrics and Clinical Epidemiology, Sitaram Bhartia Institute of Science and Research, New Delhi, India
          Department of Nephrology, Cambridge University Hospitals NHS (National Health Service) Foundation Trust, Cambridge, England
          Angiology Unit, Ospedale La Carità, Locarno, Switzerland
          Department of Internal Medicine, Asklepios-Paulinenklinik, Wiesbaden, Germany
          Division of Endocrinology, Metabolism and Lipids, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia
          Department of Metabolism and Nutrition, Institute of Food Science, Technology, and Nutrition, Spanish National Research Council, Madrid, Spain
          Department of Metabolism and Nutrition, Institute of Food Science, Technology, and Nutrition, Spanish National Research Council, Madrid, Spain
          Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark
          Heart and Diabetes Center North Rhine–Westphalia, Ruhr University Bochum, Bochum, Germany
          Medical Research Institute, University of Dundee, Ninewells Hospital, Dundee, Scotland
          Author notes
          Corresponding Author: Miles D. Witham, BM, BCh, PhD, Medical Research Institute, University of Dundee, Ninewells Hospital, Dundee DD1 9SY, Scotland, ( m.witham@ 123456dundee.ac.uk )
          Article
          PMC5966296 PMC5966296 5966296 nihpa956097
          10.1001/jamainternmed.2015.0237
          5966296
          25775274
          7881e05f-d5cf-407b-80c5-39f77d92e799
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