Reductions in all-cause, cancer, and coronary mortality in statin-treated patients with heterozygous familial hypercholesterolaemia: a prospective registry study

被引:344
作者
Neil, Andrew [1 ]
Cooper, Jackie [2 ]
Betteridge, John [3 ]
Capps, Nigel [4 ]
McDowell, Ian [5 ]
Durrington, Paul [6 ]
Seed, Mary [7 ]
Humphries, Steve E. [2 ]
机构
[1] Univ Oxford, Div Publ Hlth & Primary Hlth Care, NIHR Sch Primary Care Res, Oxford OX3 7LF, England
[2] Royal Free & Univ Coll Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JJ, England
[3] Royal Free & Univ Coll Med Sch, Dept Med, London WC1E 6JJ, England
[4] Princess Royal Hosp, Shrewsbury & Telford Hosp NHS Trust, Dept Clin Biochem, Telford TF6 6TF, Shrops, England
[5] Univ Wales Hosp, Dept Med Biochem & Immunol, Cardiff CF4 4XW, S Glam, Wales
[6] Univ Manchester, Sch Clin & Lab Sci, Cardiovasc Res Grp, Manchester, Lancs, England
[7] Univ London, Charing Cross Hosp, Imperial Coll Fac Med, Dept Med, London, England
关键词
D O I
10.1093/eurheartj/ehn422
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. 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. The results emphasize the importance of early identification of FH and treatment with statins.
引用
收藏
页码:2625 / 2633
页数:9
相关论文
共 40 条
[1]  
ALONSO R, 2008, ATHEROSCLEROSIS, DOI DOI 10.1016/J.ATHEROSCLEROSIS2007.12.024
[2]  
[Anonymous], 1991, BMJ, V303, P893
[3]  
[Anonymous], 2007, HYPERLIPIDAEMIA DIAG
[4]  
[Anonymous], 2003, DIET NUTR PREV CHRON
[5]   Statin treatment for children and adolescents with heterozygous familial hypercholesterolaemia: A systematic review and meta-analysis [J].
Arambepola, C. ;
Farmer, A. J. ;
Perera, R. ;
Neil, H. A. W. .
ATHEROSCLEROSIS, 2007, 195 (02) :339-347
[6]   Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90,056 participants in 14 randomised trials of statins [J].
Baigent, C ;
Keech, A ;
Kearney, PM ;
Blackwell, L ;
Buck, G ;
Pollicino, C ;
Kirby, A ;
Sourjina, T ;
Peto, R ;
Collins, R ;
Simes, J .
LANCET, 2005, 366 (9493) :1267-1278
[7]   ISCHEMIC DISEASE IN MEN AND WOMEN WITH FAMILIAL HYPERCHOLESTEROLEMIA AND XANTHOMATOSIS - COMPARATIVE-STUDY OF GENETIC AND ENVIRONMENTAL-FACTORS IN 274 HETEROZYGOUS CASES [J].
BEAUMONT, V ;
JACOTOT, B ;
BEAUMONT, JL .
ATHEROSCLEROSIS, 1976, 24 (03) :441-450
[8]   Sequence variations in PCSK9, low LDL, and protection against coronary heart disease [J].
Cohen, JC ;
Boerwinkle, E ;
Mosley, TH ;
Hobbs, HH .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (12) :1264-1272
[9]   COHORT STUDY ANALYSIS WITH A FORTRAN COMPUTER-PROGRAM [J].
COLEMAN, M ;
DOUGLAS, A ;
HERMON, C ;
PETO, J .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 1986, 15 (01) :134-137
[10]   The relationship of molecular genetic to clinical diagnosis of familial hypercholesterolemia in a Danish population [J].
Damgaard, D ;
Larsen, ML ;
Nissen, PH ;
Jensen, JA ;
Jensen, HK ;
Soerensen, VR ;
Jensen, LG ;
Faergeman, O .
ATHEROSCLEROSIS, 2005, 180 (01) :155-160