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William G. Herrington

Researcher at Clinical Trial Service Unit

Publications -  127
Citations -  7206

William G. Herrington is an academic researcher from Clinical Trial Service Unit. The author has contributed to research in topics: Kidney disease & Medicine. The author has an hindex of 28, co-authored 100 publications receiving 5153 citations. Previous affiliations of William G. Herrington include University of Oxford & Churchill Hospital.

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The effects of lowering LDL cholesterol with simvastatin plus ezetimibe in patients with chronic kidney disease (Study of Heart and Renal Protection): a randomised placebo-controlled trial

TL;DR: Reduction of LDL cholesterol with simvastatin 20 mg plus ezetimibe 10 mg daily safely reduced the incidence of major atherosclerotic events in a wide range of patients with advanced chronic kidney disease.
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Epidemiology of Atherosclerosis and the Potential to Reduce the Global Burden of Atherothrombotic Disease

TL;DR: Widespread changes in health behaviors and use of treatments for these risk factors are responsible for some of the dramatic declines in vascular mortality in high-income countries, and increased efforts are needed to tackle these major risk factors, particularly smoking and the emerging obesity epidemic.
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Efficacy and safety of statin therapy in older people: a meta-analysis of individual participant data from 28 randomised controlled trials

Jane Armitage, +98 more
- 02 Feb 2019 - 
TL;DR: A meta-analysis of data from all large statin trials to compare the effects of statin therapy at different ages observed a significant reduction in major vascular events in all age groups.
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Impact of renal function on the effects of LDL cholesterol lowering with statin-based regimens: a meta-analysis of individual participant data from 28 randomised trials.

TL;DR: Despite allowing for the smaller reductions in LDL cholesterol achieved by patients with more advanced chronic kidney disease, the relative reductions in major vascular events observed with statin-based treatment became smaller as eGFR declined, with little evidence of benefit in patients on dialysis.