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Association between LDL-C and risk of myocardial infarction in CKD
Marcello Tonelli1, Paul Muntner, Anita Lloyd
1Department of Medicine, University of Alberta, Edmonton, Canada. mtonelli-admin@med.ualberta.ca
Insights
The association between high LDL cholesterol and heart attack risk is weaker in individuals with chronic kidney disease (CKD). This suggests LDL cholesterol may be a less reliable marker for heart attack risk in CKD patients.
Area of Science:
- Nephrology
- Cardiology
- Epidemiology
Background:
- Low-density lipoprotein cholesterol (LDL-C) is a key coronary risk indicator in the general population.
- Its predictive value for cardiovascular events in individuals with chronic kidney disease (CKD) remains uncertain.
Purpose of the Study:
- To investigate the association between LDL cholesterol levels and myocardial infarction risk across different stages of kidney function.
Main Methods:
- A large cohort study of 836,060 adults with baseline LDL-C, estimated glomerular filtration rate (eGFR), and proteinuria data.
- Utilized administrative data and Cox regression to assess myocardial infarction risk by LDL-C categories within eGFR strata.
Main Results:
- Myocardial infarction incidence was highest in participants with the lowest eGFR.
- The adjusted hazard ratio for myocardial infarction associated with high LDL-C (≥4.9 mmol/L) compared to referent levels (2.6-3.39 mmol/L) was greatest for eGFR ≥90 ml/min/1.73 m² (3.01) and least for eGFR 15-59.9 ml/min/1.73 m² (2.06).
Conclusions:
- The association between elevated LDL-C and myocardial infarction risk is attenuated in individuals with lower eGFR.
- LDL-C may have diminished utility as a coronary risk marker in the CKD population compared to the general population.
Abstract:
LDL cholesterol (LDL-C) is an important marker of coronary risk in the general population, but its utility in people with CKD is unclear. We studied 836,060 adults from the Alberta Kidney Disease Network with at least one measurement of fasting LDL-C, estimated GFR (eGFR), and proteinuria between 2002 and 2009. All participants were free of stage 5 CKD at cohort entry. We followed participants from first eGFR measurement to March 31, 2009; we used validated algorithms applied to administrative data to ascertain primary outcome (hospitalization for myocardial infarction) and Cox regression to calculate adjusted hazard ratios (HRs) for myocardial infarction by LDL-C categories within eGFR strata. During median follow-up of 48 months, 7762 patients were hospitalized for myocardial infarction, with incidence highest among participants with the lowest eGFR. Compared with 2.6-3.39 mmol/L (referent), the risk associated with having LDL-C above 4.9 mmol/L seemed greatest for GFR≥90 ml/min per 1.73 m(2) and least for eGFR=15-59.9 ml/min per 1.73 m(2). Specifically, the adjusted HRs (95% confidence intervals) of myocardial infarction associated with LDL-C of ≥4.9 compared with 2.6-3.39 mmol/L in participants with eGFR=15-59.9, 60-89.9, and ≥90 ml/min per 1.73 m(2) were 2.06 (1.59, 2.67), 2.30 (2.00, 2.65), and 3.01 (2.46, 3.69). In conclusion, the association between higher LDL-C and risk of myocardial infarction is weaker for people with lower baseline eGFR, despite higher absolute risk of myocardial infarction. Increased LDL-C may be less useful as a marker of coronary risk among people with CKD than the general population.
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