Vitamin D supplementation and prevention of cardiovascular disease and cancer in the Finnish Vitamin D Trial—a randomized controlled trial

Author:

Virtanen Jyrki K1ORCID,Nurmi Tarja1,Aro Antti2,Bertone-Johnson Elizabeth R3,Hyppönen Elina4,Kröger Heikki15,Lamberg-Allardt Christel6ORCID,Manson JoAnn E7,Mursu Jaakko1,Mäntyselkä Pekka18,Suominen Sakari9,Uusitupa Matti1,Voutilainen Ari1,Tuomainen Tomi-Pekka1,Hantunen Sari1

Affiliation:

1. From the University of Eastern Finland, Institute of Public Health and Clinical Nutrition, Kuopio, Finland

2. Independent scientist, Kangasala, Finland

3. Departments of Biostatistics and Epidemiology and Health Promotion and Policy, School of Public Health and Health Sciences, University of Massachusetts, Amherst, MA, USA

4. Australian Centre for Precision Health, Unit of Clinical and Health Sciences, University of South Australia, and South Australian Health and Medical Research Institute, Adelaide, Australia

5. Department of Orthopaedics, Traumatology and Hand Surgery, Kuopio University Hospital, Kuopio, Finland

6. University of Helsinki, Department of Food and Nutrition, Helsinki, Finland

7. Department of Medicine, Brigham and Women's Hospital Harvard Medical School and the Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA

8. Primary Health Care Unit, Kuopio University Hospital, Kuopio, Finland

9. Department of Public Health, University of Turku, Turku University Hospital, and School of Health Sciences, University of Skövde, Sweden

Abstract

Abstract Background Vitamin D insufficiency is associated with risk of cardiovascular diseases (CVD) and cancer in observational studies, but evidence for benefits with vitamin D supplementation is limited. Objectives To investigate the effects of vitamin D3 supplementation on CVD and cancer incidence. Design The study was a 5-year randomized placebo-controlled trial among 2495 male participants ≥ 60 years and post-menopausal female participants ≥ 65 years from a general Finnish population who were free of prior CVD or cancer. The study had three arms: placebo, 1600 IU/day or 3200 IU/day vitamin D3. Follow-up was by annual study questionnaires and national registry data. A representative sub-cohort of 551 participants had more detailed in-person investigations. The primary endpoints were incident major CVD and invasive cancer. Secondary endpoints included the individual components of the primary CVD endpoint (myocardial infarction, stroke, and CVD mortality), site-specific cancers and cancer death. Results During the follow-up, there were 41 (4.9%), 42 (5.0%) and 36 (4.3%) major CVD events in the placebo, 1600 IU/d (vs. placebo: hazard ratio (HR), 0.97;95% CI, 0.63,1.49; P = 0.89), and 3200 IU/d (HR, 0.84;95% CI, 0.54,1.31; P = 0.44) arms, respectively. Invasive cancer was diagnosed in 41 (4.9%), 48 (5.8%) and 40 (4.8%) participants in the placebo, 1600 IU/d (HR, 1.14;95% CI, 0.75,1.72; P = 0.55), and 3200 IU/d (HR, 0.95;95% CI, 0.61,1.47; P = 0.81) arms, respectively. There were no significant differences in the secondary endpoints or total mortality. In the sub-cohort, the mean (standard deviation) baseline serum 25-hydroxyvitamin D concentration was 75 (18) nmol/L. After 12 months, the concentrations were 73 (18) nmol/L, 100 (21) nmol/L and 120 (22) nmol/L in the placebo, 1600 IU/d and 3200 IU/d arms, respectively. Conclusions Vitamin D3 supplementation did not lower the incidence of major CVD events or invasive cancer among older adults, possibly due to sufficient vitamin D status in most participants at baseline. Clinical Trial Registry number: ClinicalTrials.gov: NCT01463813, https://clinicaltrials.gov/ct2/show/NCT01463813.

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

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