Metabolic syndrome predicts cardiovascular risk and mortality in familial hypercholesterolemia

Martine Paquette1, Sophie Bernard2, Bertrand Cariou3

  • 1Lipids, Nutrition, and Cardiovascular Prevention Clinic of the Montreal Clinical Research Institute, Montreal, Québec H2W 1R7, Canada (Drs Paquette, Bernard, and Baass).

Insights

Metabolic syndrome (MetS) significantly increases cardiovascular risk in familial hypercholesterolemia (FH) patients. This risk is independent of LDL-C and other traditional factors, highlighting the need for targeted management strategies.

Area of Science:

  • Cardiology
  • Genetics
  • Metabolic Disorders

Background:

  • Familial hypercholesterolemia (FH) is strongly linked to premature atherosclerotic cardiovascular disease (ASCVD).
  • Other risk factors beyond LDL-C influence FH phenotype severity.
  • The impact of metabolic syndrome (MetS) on ASCVD risk in FH patients requires further investigation.

Purpose of the Study:

  • To investigate the association between MetS and the incidence of ASCVD endpoints.
  • To examine the relationship between MetS and all-cause mortality in FH patients.

Main Methods:

  • Prospective follow-up study utilizing data from 5 independent FH cohorts in Europe and North America.
  • Analysis of 2401 adult heterozygous FH patients without prior ASCVD events, with 21,139 person-years of follow-up.
  • Multivariate Cox proportional hazards regression to assess the association between MetS and endpoint incidence.

Main Results:

  • MetS prevalence was 14% in the study population.
  • MetS significantly predicted incident 10-year ASCVD (HR 2.07), 10-year MACE (HR 4.59), 10-year MI (HR 4.29), and 30-year all-cause mortality (HR 4.87), independent of traditional risk factors.
  • Hazard ratios (HR) and 95% confidence intervals (CI) were reported for key outcomes.

Conclusions:

  • FH patients with MetS exhibit elevated cardiovascular risk, independent of LDL-C and other conventional risk factors.
  • Further research is needed to establish optimal strategies for mitigating cardiovascular risk associated with MetS in this population.
Abstract

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