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. 2021 Aug 10;2021(8):CD010037. doi: 10.1002/14651858.CD010037.pub3

Summary of findings 1. Calcium supplementation/fortification compared to control for prevention of primary hypertension.

Calcium supplementation/fortification compared to control for prevention of primary hypertension
Patient or population: People who may be at risk for primary hypertension
Settings: US (8), New Zealand (3), and one each in The Netherlands, Belgium and Denmark, Guatemala and Iran
Intervention: Calcium supplementation/fortification
Comparison: Placebo
Outcomes Illustrative blood pressure in control group b Mean difference in mmHg (95% CIa) No of participants
(studies) Quality of the evidence
(GRADE)c Comments
Systolic blood pressure (range of follow‐up from 4 weeks to 4 years) 115.62 1.37 lower (2.08 lower to 0.66 lower) 3140
(18 studies) ⊕⊕⊕⊕
high Women: ‐1.25 mmHg [95% CI: ‐2.53, 0.03; 8 studies]
Men: ‐2.07 mmHg [95% CI: ‐3.56, ‐0.59; 5 studies]
Both: ‐1.11 mmHg [95% CI: ‐2.15, ‐0.08; 6 studies]
Diastolic blood pressure (range of follow‐up from 4 weeks to 4 years) 78.17 1.45 lower (2.23 lower to 0.67 lower)
 
 
3039
(17 studies) ⊕⊕⊕⊕
high Women: ‐1.03 mmHg [95% CI: ‐1.80, ‐0.26; 8 studies]
Men: ‐1.91 mmHg [95% CI: ‐2.80, ‐1.02; 5 studies]
Both: ‐0.25 mmHg [95% CI: ‐1.08, 0.57; 5 studies]
Systolic blood pressure. Dose less than 1000 mg a day (range of follow‐up from 12 weeks to 2 years) 103.74 0.02 lower (2.23 lower to 2.20 higher) 302
(3 studies) ⊕⊕⊕⊝
moderate1 Subgroup analysis by dose
Systolic blood pressure. Dose between 1000 mg a day and less than 1500 mg a day (range from 4 weeks to 2 years) 116.29 1.05 lower (1.91 lower to 0.19 lower) 2488
(9 studies) ⊕⊕⊕⊕
high Subgroup analysis by dose
Systolic blood pressure. Dose 1500 mg a day or more (range of follow‐up from 4 weeks to 4 years) 112.85 2.79 lower (4.71 lower to 0.86 lower) 350
(7 studies) ⊕⊕⊕⊝
moderate1 Subgroup analysis by dose
Systolic blood pressure. Less than 35 years of age (range of follow‐up from 4 weeks to 22 weeks) 113.23 1.79 lower (3.20 lower to 0.38 lower) 452
(9 studies) ⊕⊕⊕⊝
moderate1 Subgroup analysis by age
Systolic blood pressure. 35 years or older (range of follow‐up from 4 weeks to 4 years) 124.20 0.97 lower (1.83 lower to 0.10 lower) 2688
(10 studies) ⊕⊕⊕⊕
high Subgroup analysis by age
Adverse events (secondary outcome)         One study evaluated side effects, but none were reported. A further two studies mentioned that the supplements were well tolerated. No trials reported any incidence of kidney stone formation, iron deficiency anaemia, anaemia, cardiovascular events, myocardial infarction, stroke or mortality.
aCI: Confidence interval; bEstimated using Comprehensive Meta‐Analysis Software Software; cGRADE Working Group grades of evidence  
 
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.
 

1. Downgraded one level for imprecision due to small number of participants.