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Matthew F Muldoon a Center for Clinical Pharmacology,
University of Pittsburgh School of Medicine, PA 15260, Pittsburgh, USA, b Department of Psychology, University of Pittsburgh, c Department of
Epidemiology, Graduate School of Public Health, University of
Pittsburgh, d Comparative Medicine Clinical Research Center, Bowman Gray
School of Medicine, Wake Forest University, Winston-Salem, NC 27103, USA
Correspondence to: M F Muldoon, 506 Old Engineering Hall,
University of Pittsburgh, Pittsburgh, PA 15260, USA mfm10+{at}pitt.edu
Objective:
To investigate the association between
cholesterol lowering interventions and risk of death from suicide,
accident, or trauma (non-illness mortality).
Design:
Meta-analysis of the non-illness mortality outcomes of large, randomised clinical trials of cholesterol lowering treatments.
Studies reviewed:
19 out of 21 eligible trials that
had data available on non-illness mortality.
Interventions reviewed:
Dietary modification, drug
treatment, or partial ileal bypass surgery for 1-10 years
Main outcome measure:
Deaths from suicides, accidents,
and violence in treatment groups compared with control groups.
Results:
Across all trials, the odds ratio of
non-illness mortality in the treated groups, relative to control
groups, was 1.18 (95% confidence interval 0.91 to 1.52; P=0.20). The
odds ratios were 1.28 (0.94 to 1.74; P=0.12) for primary prevention trials and 1.00 (0.65 to 1.55; P=0.98) for secondary prevention trials.
Randomised clinical trials using statins did not show a treatment
related rise in non-illness mortality (0.84, 0.50 to 1.41; P=0.50),
whereas a trend toward increased deaths from suicide and violence was
observed in trials of dietary interventions and non-statin drugs (1.32, 0.98 to 1.77; P=0.06). No relation was found between the magnitude of
cholesterol reduction and non-illness mortality (P=0.23).
Conclusion:
Currently available evidence does not
indicate that non-illness mortality is increased significantly by
cholesterol lowering treatments. A modest increase may occur with
dietary interventions and non-statin drugs.
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