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Lipid levels achieved after a first myocardial infarction and the prediction of recurrent atherosclerotic cardiovascular disease

Ohm, Joel (författare)
Karolinska Institutet
Hjemdahl, Paul (författare)
Karolinska Institutet
Skoglund, Per H. (författare)
Karolinska Inst, Dept Med Solna, Stockholm, Sweden;Stiftelsen Stockholms Sjukhem, Ctr Palliat Care, Stockholm, Sweden
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Discacciati, Andrea (författare)
Karolinska Institutet
Sundström, Johan, Professor, 1971- (författare)
Uppsala universitet,Klinisk epidemiologi
Hambraeus, Kristina (författare)
Falun Cent Hosp, Dept Cardiol, Falun, Sweden
Jernberg, Tomas (författare)
Karolinska Institutet
Svensson, Per (författare)
Karolinska Institutet
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 (creator_code:org_t)
ELSEVIER IRELAND LTD, 2019
2019
Engelska.
Ingår i: International Journal of Cardiology. - : ELSEVIER IRELAND LTD. - 0167-5273 .- 1874-1754. ; 296, s. 1-7
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Low density lipoprotein cholesterol (LDL-C) goals post-myocardial infarction (MI) are debated, and the significance of achieved blood lipid levels for predicting a first recurrent atherosclerotic cardiovascular disease (rASCVD) event post-MI is unclear.Methods: This was a cohort study on first-ever MI survivors aged <= 76 years attending 4-14 week revisits throughout Sweden 2005-2013. Personal-level data was collected from SWEDEHEART and linked national registries. Exposures were quintiles of LDL-C, high density lipoprotein cholesterol (HDL-C), total cholesterol (TC), and triglycerides (TGs) at the revisit. Group level associations with rASCVD (nonfatal MI or coronary heart disease death or fatal or nonfatal ischemic stroke) were estimated in Cox regression models. Predictive capacity was estimated by differences in C-statistic, integrated discriminatory improvement, and net reclassification improvement when adding each blood lipid to a validated risk prediction model.Results: 25,643 patients, 96.9% on statin therapy, were followed during a mean of 4.1 years. rASCVD occurred in 2173 patients (8.5%). For LDL-C and TC, moderate associations with rASCVD were observed only in the 5th vs. the lowest (referent) quintiles. For TGs and HDL-C increased risks were observed in quintiles 3-5 vs. the lowest. Minor predictive improvements were observed when lipid fractions were added to the risk model but the discrimination overall was poor (C-statistics < 0.6).Conclusions: Our data question the importance of LDL-C levels achieved at first revisit post-MI for decisions on continued treatment intensity considering the weak association with rASCVD observed in this post-MI cohort.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

Risk prediction
Lipid levels
Low density lipoprotein cholesterol (LDL-C)
Myocardial infarction
Secondary prevention
Recurrence

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