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Relation between baseline LDL-cholesterol and cardiovascular outcomes in high cardiovascular risk hypertensive
Lee S Nguyen1, Niki Procopi2, Joe-Elie Salem3
1CMC Ambroise Paré, Critical Care Medicine Department, Neuilly-sur-Seine, France; Sorbonne Université, INSERM CIC Paris-Est, AP-HP, ICAN, Pitié-Salpêtrière Hospital, Department of Pharmacology, F-75013 Paris, France.
Insights
Low-density lipoprotein cholesterol (LDL-C) levels did not significantly impact cardiovascular events in hypertensive patients over three years. This finding suggests LDL-C may not be a primary predictor for cardiovascular outcomes in this high-risk group.
Area of Science:
- Cardiology
- Clinical Research
- Epidemiology
Background:
- Hypertensive patients often present with multiple cardiovascular (CV) risk factors, including LDL-cholesterol (LDL-C), which are potential treatment targets.
- The SPRINT cohort provided a valuable dataset for investigating cardiovascular outcomes in hypertensive individuals at increased CV risk.
Purpose of the Study:
- To assess the association between LDL-C levels and major adverse cardiovascular events (MACE) in hypertensive patients at increased CV risk.
- To evaluate LDL-C as a predictor of cardiovascular outcomes within the SPRINT trial cohort.
Main Methods:
- A post-hoc analysis of the SPRINT cohort (n=9631) was conducted.
- Survival regression models were used to analyze the association between LDL-C and primary composite CV outcomes, adjusted for numerous confounding factors.
- Subgroup analyses included patients in secondary prevention, those on statin therapy, and those in primary prevention.
Main Results:
- In the overall cohort, LDL-C was not associated with the primary composite CV outcome.
- In patients undergoing secondary prevention (n=1562), LDL-C showed a marginal association with the primary outcome (aHR 1.005, p=0.005), but with poor discriminatory power (ROC AUC 0.54, p=0.087).
- No significant association between LDL-C and the primary outcome was observed in other subgroup analyses, including statin users and primary prevention groups.
Conclusions:
- This analysis suggests that LDL-C levels do not significantly influence the occurrence of cardiovascular events over a 3-year period in hypertensive patients at increased CV risk without prior cardiovascular disease history (excluding stroke).
- The findings indicate that LDL-C may not be a reliable predictor for cardiovascular events in this specific patient population.
Background:
Patients at increased cardiovascular (CV) risk, noticeably hypertensive patients, have multiple CV risk factors which may be treatment targets. LDL-cholesterol is one of such targets. Using the SPRINT cohort, studying the cardiovascular outcomes of hypertensive patients at increased CV risk, this post-hoc study aimed to assess the association of LDL-C with CV outcomes.
Methods:
Clinical outcomes were those defined in SPRINT: a composite of various CV outcomes, all-cause mortality, and CV mortality. Association between LDL-C and the primary outcome was analyzed using survival regression adjusted on confounding factors (age, sex, body-mass index, active smoking status, eGFR-estimated kidney function, history of CV disease, Framingham risk score, SPRINT treatment arm (intensive or control), baseline high-density-lipoprotein-bound cholesterol, and co-treatments by aspirin and statins).
Results:
LDL-C was not associated with the primary outcome in the overall cohort (n = 9631). Among patients in secondary prevention (i.e. with a previous history of CV disease) (n = 1562), LDL-C was marginally associated with the incidence of the primary outcome (adjusted hazard-ratio 1.005 (95% CI = 1.002-1.009), p = 0.005 (per 1 mg/dl increase)) however, discrimination was poor with a ROC AUC of 0.54, p = 0.087. There was no association between LDL-C and the primary outcome in other subgroup analyses (those under statin or not, and those in primary prevention).
Conclusion:
This post-hoc analysis of SPRINT indicates that LDL-C levels do not influence cardiovascular events over a period of 3 years in a large cohort of hypertensive patients at increased risk of cardiovascular events but without previous history of clinical cardiovascular disease other than stroke.
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