Effects of Vitamin D3 Supplementation on Cardiovascular and Cancer Outcomes by eGFR in VITAL

被引:3
|
作者
Limonte, Christine P. [1 ,2 ]
Zelnick, Leila R. [1 ,2 ]
Hoofnagle, Andrew N. [2 ,3 ]
Thadhani, Ravi [4 ]
Melamed, Michal L. [5 ]
Mora, Samia [6 ,7 ]
Cook, Nancy R. [7 ,8 ]
Luttmann-Gibson, Heike [7 ,9 ]
Sesso, Howard D. [7 ,8 ]
Lee, I-Min [7 ,8 ]
Buring, Julie E. [7 ,8 ]
Manson, JoAnn E. [7 ,8 ]
de Boer, Ian H. [1 ,2 ]
机构
[1] Univ Washington, Dept Med, Div Nephrol, Seattle, WA 98195 USA
[2] Univ Washington, Kidney Res Inst, Seattle, WA 98195 USA
[3] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[4] Mass Gen Brigham, Off Chief Acad Officer, Boston, MA USA
[5] Albert Einstein Coll Med, Dept Med, Div Nephrol, Bronx, NY 10467 USA
[6] Brigham & Womens Hosp, Div Cardiovasc Med, Boston, MA 02115 USA
[7] Harvard Med Sch, Brigham & Womens Hosp, Div Prevent Med, Boston, MA 02115 USA
[8] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[9] Harvard TH Chan Sch Publ Hlth, Dept Environm Hlth, Boston, MA USA
来源
KIDNEY360 | 2022年 / 3卷 / 12期
关键词
mineral metabolism; cholecalciferol; dietary supplements; neoplasms; CHRONIC KIDNEY-DISEASE; PARATHYROID-HORMONE; D METABOLISM; RISK; MORTALITY; CKD; METAANALYSIS; ASSOCIATION; ANALOGS; ADULTS;
D O I
10.34067/KID.0006472022
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background Reduced 25-hydroxyvitamin D (25[OH]D) metabolism and secondary hyperparathyroidism are common with lower estimated glomerular filtration rate (eGFR) and may contribute to cardiovascular disease and cancer risk. Methods We assessed for heterogeneity by baseline eGFR of the effects of vitamin D-3 on cardiovascular and cancer outcomes in the Vitamin D and Omega-3 Trial (VITAL). Participants were randomized to 2000 IU vitamin D(3 )and/or 1 g omega-3 fatty acids daily using a placebo-controlled, two-by-two factorial design (5.3 years follow-up). Primary study end points were incident major cardiovascular events and invasive cancer. Changes in serum 25(OH)D and parathyroid hormone (PTH) were examined. Results Baseline eGFR was available for 15,917 participants. Participants' mean age was 68 years, and 51% were women. Vitamin D3 resulted in higher serum 25(OH)D compared with placebo (difference in change 12.5 ng/ml; 95% CI, 12 to 13.1 ng/ml), without heterogeneity by eGFR (P interaction, continuous eGFR=0.2). Difference in change in PTH between vitamin D3 and placebo was larger with lower eGFR (P interaction=0.05): -6.9 (95% CI, -10.5 to -3.4), -5.8 (95% CI, -8.3 to -3.4), -4 (95% CI, -5.9 to -2.2), and -3.8 (95% CI, -5.6 to -2) pg/ml for eGFR < 60, 60-74, 75-89, and >= 90 ml/min per 1.73 m(2), respectively. Effects of vitamin D3 supplementation on cardiovascular events (P interaction=0.61) and cancer (P interaction=0.89) did not differ by eGFR: HR=1.14 (95% CI, 0.73 to 1.79), HR=1.06 (95% CI, 0.75 to 1.5), HR=0.92 (95% CI, 0.67 to 1.25), and HR=0.92 (95% CI, 0.66 to 1.27) across eGFR categories for cardiovascular events and HR=1.63 (95% CI, 1.03 to 2.58), HR=0.85 (95% CI, 0.64 to 1.11), HR=0.84 (95% CI, 0.68 to 1.03), and 1.11 (95% CI, 0.92 to 1.35) for cancer, respectively. Conclusions We observed no significant heterogeneity by baseline eGFR in the effects of vitamin D3 supplementation versus on cardiovascular or cancer outcomes, effects on 25(OH)D and PTH concentrations.
引用
收藏
页码:2095 / 2105
页数:11
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