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[Preprint]. 2020 Nov 25:2020.07.14.20152728. [Version 3] doi: 10.1101/2020.07.14.20152728

Table 2: Placebo controlled RCTs:

Proportion of participants experiencing at least one acute respiratory infection, overall and stratified by potential effect-modifiers

Potential effect-modifier No of trials Proportion with ≥1 ARI, intervention group (%) Proportion with ≥1 ARI, control group (%) Odds ratio (95% CI) I2 % P for heterogeneity
Overall 36 13685/22288 (61.4) 13565/21721 (62.5) 0.91 (0.84 to 0.99) 37.2 0.01
Baseline 25(OH)D, nmol/L[a]
<25 19 1348/1798 (75.0) 1388/1819 (76.3) 0.78 (0.53 to 1.16) 47.2 0.01
25 – 49.9 28 3439/4666 (73.7) 3347/4501 (74.4) 1.03 (0.92 to 1.15) 0.4 0.46
50 – 74.9 29 1679/2839 (59.1) 1565/2578 (60.7) 0.90 (0.76 to 1.06) 11.2 0.29
≥75 25 945/1543 (61.2) 908/1471 (61.7) 0.97 (0.81 to 1.16) 0.0 0.78
Dosing frequency
Daily 18 1056/2134 (49.5) 1020/1871 (54.5) 0.75 (0.61 to 0.93) 52.5 0.005
Weekly 6 4482/6421 (69.8) 4447/6335 (70.2) 0.97 (0.88 to 1.06) 0.0 0.48
Monthly or less frequently 12 8147/13733 (59.3) 8098/13515 (59.9) 0.98 (0.93 to 1.03) 0.0 0.57
Daily dose equivalent, IU[b]
<400 2 482/1175 (41.0) 511/1133 (45.1) 0.65 (0.31 to 1.37) 86.3 0.007
400–1000 10 656/1236 (53.1) 627/1069 (58.7) 0.70 (0.55 to 0.89) 31.2 0.16
1001–2000 15 9946/15885 (62.6) 10022/15817 (63.4) 0.97 (0.92 to 1.03) 1.0 0.44
>2000 7 2291/3462 (66.2) 2250/3444 (65.3) 1.05 (0.84 to 1.31) 37.1 0.15
Trial duration, months
≤12 29 1977/4887 (40.5) 1866/4368 (42.7) 0.82 (0.72 to 0.93) 38.1 0.02
>12 7 11708/17401 (67.3) 11699/17353 (67.4) 0.99 (0.95 to 1.04) 0.0 0.91
Age, yrs[a]
<1 5 875/2901 (30.2) 839/2796 (30.0) 0.95 (0.82 to 1.10) 18.7 0.30
1–15.9 15 4297/5994 (71.7) 4303/5877 (73.2) 0.71 (0.57 to 0.90) 46.0 0.03
16–64.9 21 3137/4876 (64.3) 3087/4727 (65.3) 0.97 (0.93 to 1.09) 11.5 0.31
≥65 16 5376/8589 (62.6) 5352/8394 (63.4) 0.96 (0.90 to 1.02) 0.0 0.67
Airway disease
Asthma only 4 203/404 (50.2) 202/391 (51.7) 0.73 (0.36 to 1.49) 71.7 0.01
COPD only 2 106/208 (51.0) 104/207 (50.2) 1.01 (0.68 to 1.51) 0.0 0.71
Unrestricted 30 13376/21676 (61.7) 13259/21123 (62.8) 0.91 (0.84 to 0.99) 35.0 0.03
[a]

The number of trials in each category for this variable adds up to more than 36, since this is a participant-level variable, i.e. some trials contributed data from participants who fell into more than one category

[b]

Data from two trials that included higher-dose, lower-dose and placebo arms18,47 are excluded from this sub-group analysis, since the higher-dose and lower-dose arms spanned the 1,000 IU/day cut-off, rendering them unclassifiable