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. Author manuscript; available in PMC: 2012 Sep 1.
Published in final edited form as: Arthritis Care Res (Hoboken). 2011 Sep;63(9):1295–1306. doi: 10.1002/acr.20519

Table 2.

Subgroup analyses consisting of the pooled effect sizes of vitamin C supplementation on serum uric acid level, stratified by trial and subject characteristics.

Change in serum uric acid (mg/dL)

Sub-group N§ Effect 95% CI I2 P*
LL UL
Dose
    <500 mg/d 6 0.02 -0.21 0.26 0.0% 0.10
    ≥500 mg/d 8 -0.59 -1.05 -0.13 79.9%
Duration
    <30 days 7 -0.49 -1.20 0.22 85.2% 0.52
    ≥30 days 7 -0.25 -0.56 0.06 63.0%
Baseline Serum Ascorbic Acid
    <56.2 μmol/L 3 -0.02 -0.30 0.27 0.0% 0.20
    ≥56.2 μmol/L 4 -0.33 -0.75 0.09 53.7%
Mean Age
    <47.7 6 -0.53 -1.32 0.27 85.3% 0.55
    ≥47.7 7 -0.29 -0.61 0.04 66.1%
%Male
    <53 6 -0.26 -0.59 0.07 58.5% 0.66
    ≥53 7 -0.41 -1.06 0.24 85.6%
Baseline Serum Uric Acid
    <4.85 mg/dL 5 0.13 -0.12 0.37 0.0% 0.03
    ≥4.85 mg/dL 5 -0.78 -1.46 -0.09 85.0%
Trial Design
    Parallel 10 -0.37 -0.80 0.07 83.8% 0.91
    Crossover 4 -0.31 -0.63 0.02 0.0%
Vit C Only Intervention
    Yes 9 -0.54 -0.96 -0.11 78.1% 0.16
    No 5 0.04 -0.20 0.29 0.0%
Placebo Use
    Yes 10 -0.59 -0.95 -0.24 71.2% 0.01
    No 4 0.19 -0.07 0.45 0.0%
Allocation Concealment
    Yes 4 -0.31 -0.75 0.13 76.5% 0.89
    Not Reported 10 -0.37 -0.86 0.11 79.1%
Double-blind Design
    Yes 9 -0.50 -0.66 -0.35 0.0% 0.75
    No 5 -0.30 -1.17 0.58 90.8%
Trial Reported Compliance
    Yes 5 -0.35 -0.75 0.05 71.1% 0.92
    No 9 -0.34 -0.87 0.18 0.0%
Healthy Trial Population
    Yes 7 -0.60 -1.26 0.06 82.5% 0.20
    No 7 -0.15 -0.49 0.20 71.1%
Trial Size
    <29 5 -0.58 -1.58 0.41 87.9% 0.37
    ≥29 9 -0.23 -0.51 0.05 63.4%
*

P-values represent comparison of effects between subgroups. Category bounds were determined by the median of abstracted values.

§

N represents the number of trials. The number of trials may not always add to 13 due to the treatment of one trial as two groups (Kyllastinen et al, 1990) and due to the varying availability of subgroup data in each trial.