Implications of the new American College of Cardiology/American Heart Association cholesterol guidelines for primary atherosclerotic cardiovascular disease event prevention in a multi ethnic cohort: Multi-Ethnic Study of Atherosclerosis (MESA)

被引:22
|
作者
Yeboah, Joseph [1 ]
Sillau, Stefan [2 ]
Delaney, Joseph C. [2 ]
Blaha, Michael J. [3 ]
Michos, Erin D. [3 ]
Young, Rebekah [2 ]
Qureshi, Waqas T. [1 ]
McClelland, Robyn [2 ]
Burke, Gregory L. [4 ]
Psaty, Bruce M. [5 ,6 ,7 ]
Herrington, David M. [1 ]
机构
[1] Wake Forest Sch Med, Heart & Vasc Ctr Excellence, Winston Salem, NC 27157 USA
[2] Univ Washington, Dept Biostat, Sch Med, Seattle, WA 98195 USA
[3] Johns Hopkins Univ, Sch Med, Ciccarone Ctr Prevent Heart Dis, Baltimore, MD USA
[4] Wake Forest Univ, Sch Med, Div Publ Hlth Sci, Winston Salem, NC 27109 USA
[5] Univ Washington, Cardiovasc Hlth Res Unit, Dept Med, Seattle, WA 98195 USA
[6] Univ Washington, Cardiovasc Hlth Res Unit, Dept Epidemiol & Hlth Serv, Seattle, WA 98195 USA
[7] Grp Hlth Cooperat Puget Sound, Grp Hlth Res Unit, Seattle, WA USA
关键词
STATIN THERAPY; ADHERENCE; RISK; DISCONTINUATION; VALIDATION;
D O I
10.1016/j.ahj.2014.12.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The impact of replacing the National Cholesterol Education Program (NCEP)/Adult Treatment Program (ATP) Ill cholesterol guidelines with the new 2013 American College of Cardiology (ACC)/American Heart Association (AHA) guidelines for primary prevention of cardiovascular disease is unclear. Methods We used risk factor and 10-year clinical event rate data from MESA, combined with estimates of efficacy of moderate and high-intensity statin therapy from meta-analyses of statin primary prevention trials to estimate (a) the change in number of subjects eligible for drug therapy and (2) the anticipated reduction in atherosclerotic cardiovascular disease (ASCVD) events and increment in type 2 diabetes mellitus (T2DM) associated with the change in cholesterol guidelines. Results Of the 6,814 MESA participants, 5,437 were not on statins at baseline and had complete data for analysis (mean age 61.4 +/- 10.3). Using the NCEP/ATP III guidelines, 1,334 (24.5%) would have been eligible for statin therapy compared with 3,015 (55.5%) under the new ACC/AHA guidelines. Among the subset of newly eligible, 127/1,742 (7.3%) had an ASCVD event during 10 years of follow-up. Assuming 10 years of moderate-intensity statin therapy, the estimated absolute reduction in ASCVD events for the newly eligible group was 2.06% (number needed to treat [NNT] 48.6) and the estimated absolute increase in T2DM was 0.90% (number needed to harm [NNH] 110.7). Assuming 10 years of high-intensity statin therapy, the corresponding estimates for reductions in ASCVD and increases in T2DM were as follows: ASCVD 2.70% (NNT 37.5) and T2DM 2.60% (NNH 38.6). The estimated effects of moderate-intensity statins on 10-year risk for ASCVD and T2DM in participants eligible for statins under the NCEP/ATP III were as follows: 3.20% (NNT 31.5) and 1.06% (NNH 94.2), respectively. Conclusion Substituting the NCEP/ATP III cholesterol guidelines with the 2013 ACC/AHA cholesterol guidelines in MESA more than doubled the number of participants eligible for statin therapy. If the new ACC/AHA cholesterol guidelines are adopted and extend the primary prevention population eligible for treatment, the risk-benefit profile is much better for moderate-intensity than high-intensity statin treatment.
引用
收藏
页码:387 / 395
页数:9
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