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维生素 D 补充与心血管疾病和癌症预防的芬兰维生素 D 试验:一项随机对照试验。

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

机构信息

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

Independent scientist, Kangasala, Finland.

出版信息

Am J Clin Nutr. 2022 May 1;115(5):1300-1310. doi: 10.1093/ajcn/nqab419.

Abstract

BACKGROUND

Vitamin D insufficiency is associated with risks 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 incidences.

METHODS

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 3 arms: placebo, 1600 IU/day, or 3200 IU/day vitamin D3. Follow-up was by annual study questionnaires and national registry data. A representative subcohort 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 (compared with placebo: 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 subcohort, the mean baseline serum 25-hydroxyvitamin D concentration was 75 nmol/L (SD, 18 nmol/L). After 12 months, the concentrations were 73 nmol/L (SD, 18 nmol/L), 100 nmol/L (SD, 21 nmol/L), and 120 nmol/L (SD, 22 nmol/L) in the placebo, 1600 IU/d, and 3200 IU/d arms, respectively.

CONCLUSIONS

Vitamin D3 supplementation did not lower the incidences of major CVD events or invasive cancer among older adults, possibly due to sufficient vitamin D status in most participants at baseline.

摘要

背景

维生素 D 不足与心血管疾病 (CVD) 和癌症的风险相关,但维生素 D 补充的益处证据有限。

目的

研究维生素 D3 补充对 CVD 和癌症发病率的影响。

方法

这是一项为期 5 年的、随机、安慰剂对照试验,参与者为来自一般芬兰人群的 2495 名年龄≥60 岁的男性和年龄≥65 岁的绝经后女性,他们无 CVD 或癌症病史。该研究有 3 个组:安慰剂、1600 IU/天或 3200 IU/天的维生素 D3。随访通过年度研究问卷和国家登记数据进行。一个由 551 名参与者组成的代表性亚组进行了更详细的面对面调查。主要终点是主要 CVD 和侵袭性癌症的发病情况。次要终点包括主要 CVD 终点的各个组成部分(心肌梗死、中风和 CVD 死亡率)、特定部位癌症和癌症死亡。

结果

在随访期间,安慰剂组、1600 IU/d 组(与安慰剂相比:HR:0.97;95%CI:0.63-1.49;P=0.89)和 3200 IU/d 组(HR:0.84;95%CI:0.54-1.31;P=0.44)分别有 41 例(4.9%)、42 例(5.0%)和 36 例(4.3%)发生主要 CVD 事件。在安慰剂组、1600 IU/d 组(HR:1.14;95%CI:0.75-1.72;P=0.55)和 3200 IU/d 组(HR:0.95;95%CI:0.61-1.47;P=0.81)分别有 41 例(4.9%)、48 例(5.8%)和 40 例(4.8%)被诊断为侵袭性癌症。次要终点或总死亡率无显著差异。在亚组中,平均基线血清 25-羟维生素 D 浓度为 75 nmol/L(标准差 18 nmol/L)。12 个月后,安慰剂组、1600 IU/d 组和 3200 IU/d 组的浓度分别为 73 nmol/L(标准差 18 nmol/L)、100 nmol/L(标准差 21 nmol/L)和 120 nmol/L(标准差 22 nmol/L)。

结论

维生素 D3 补充剂并不能降低老年人主要 CVD 事件或侵袭性癌症的发病率,这可能是由于大多数参与者在基线时的维生素 D 状态已经足够。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e16b/9071497/78d0c9210bb9/nqab419fig1g.jpg

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