Key result
Statin therapy linked to ~37% lower coronary mortality in heterozygous familial hypercholesterolaemia.
Cohort (n=3,382)
Yes
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AIMS: To examine the changes in coronary, all-cause, and cancer mortality in patients with heterozygous familial hypercholesterolaemia (FH) before and after lipid-lowering therapy with statins. METHODS AND RESULTS: A total of 3382 patients (1650 men) aged <80 years were recruited from 21 lipid clinics in the United Kingdom and followed prospectively between 1980 and 2006 for 46 580 person-years. There were 370 deaths, including 190 from coronary heart disease (CHD) and 90 from cancer. The standardized mortality ratio (compared with the population in England and Wales) was calculated before and from 1 January 1992. In patients aged 20-79 years, CHD mortality fell significantly by 37% (95% CI = 7-56) from 3.4- to 2.1-fold excess. Primary prevention resulted in a 48% reduction in CHD mortality from 2.0-fold excess to none, with a smaller reduction of nearly 25% in patients with established disease. Coronary mortality was reduced more in women than in men. In patients without known CHD at registration, all-cause mortality from 1992 was 33% (21-43), lower than in the general population, mainly due to a 37% (21-50) lower risk of fatal cancer. CONCLUSION: The results emphasize the importance of early identification of FH and treatment with statins.
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Neil et al. (2008) conducted a cohort in Heterozygous familial hypercholesterolaemia (n=3,382). Statin lipid-lowering therapy (post-1992 era) vs. Pre-statin era (before 1 January 1992) and general population in England and Wales was evaluated on Coronary heart disease (CHD), all-cause, and cancer mortality (standardized mortality ratio) (37% reduction in CHD SMR, 95% CI 7-56). Statin therapy in heterozygous familial hypercholesterolaemia reduced coronary heart disease mortality by 37%, lowering excess risk from 3.4-fold to 2.1-fold.
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