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. 2016 Nov 26;2016(11):CD009462. doi: 10.1002/14651858.CD009462.pub2

Summary of findings for the main comparison. Chronotherapy for the treatment of hyperlipidaemia.

Chronotherapy for the treatment of hyperlipidaemia
Participant or population: people with hyperlipidaemia
 Settings: primary care
 Intervention: evening statin dose
Comparison: morning statin dose
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No of Participants
 (studies) Quality of the evidence
 (GRADE) Comments
Assumed risk Corresponding risk
Morning statin dose Evening statin dose
Cardiovascular mortality See comment See comment Not estimable 0
 (0) See comment Included RCTs did not report on this outcome
Cardiovacular morbidity See comment See comment Not estimable 0
 (0) See comment Included RCTs did not report this outcome
At least 1 adverse event 
 Follow‐up: mean 9 weeks Study population OR 0.71 
 (0.44 to 1.15) 556
 (5 studies) ⊕⊕⊝⊝
 low1,2  
188 per 1000 141 per 1000 
 (92 to 210)
Total Cholesterol (mg/dL) 
 Follow‐up: mean 9 weeks   The mean total cholesterol (mg/dL) in the intervention groups was
 4.33 higher (1.36 lower to 10.01 higher)   514
 (5 studies) ⊕⊕⊝⊝
 low1,2  
LDL‐C (mg/dL) 
 Follow‐up: mean 9 weeks   The mean LDL‐C (mg/dL) in the intervention groups was
 4.85 higher 
 (0.87 lower to 10.57 higher)   473
 (5 studies) ⊕⊕⊝⊝
 low1,2  
HDL‐C (mg/dL) 
 Follow‐up: mean 9 weeks   The mean HDL‐C (mg/dL) in the intervention groups was
 0.54 higher 
 (1.08 lower to 2.17 higher)   514
 (5 studies) ⊕⊕⊝⊝
 low1,2  
Triglycerides (mg/dL) 
 Follow‐up: mean 9 weeks   The mean triglycerides (mg/dL) in the intervention groups was
 8.91 lower 
 (22 lower to 4.17 higher)   510
 (5 studies) ⊕⊕⊝⊝
 low1,2  
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
 CI: Confidence interval; RR: Risk ratio; OR: Odds ratio;
GRADE 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 due to study limitations (unclear or high risk of bias) in the studies included.
 2 Downgraded for imprecision due to very wide confidence interval.