Metabolic syndrome and mortality in stable coronary heart disease: relation to gender

Charlotte Kragelund1, Lars Køber, Jens Faber

  • 1Department of Cardiology, Hvidovre University Hospital, Hvidovre, Denmark. kragelund@dadlnet.dk <kragelund@dadlnet.dk>

Insights

Metabolic syndrome (MS) increases mortality risk in women with stable coronary heart disease, but not in men. This finding is independent of other cardiovascular risk factors.

Area of Science:

  • Cardiology
  • Metabolic Health
  • Epidemiology

Background:

  • Metabolic syndrome (MS) is linked to type 2 diabetes and cardiovascular disease.
  • Its impact on mortality in stable coronary heart disease (CHD) patients is unclear, as is its gender-specific association.
  • Prognostic implications of MS in stable CHD require further investigation.

Purpose of the Study:

  • To investigate the association between metabolic syndrome and all-cause mortality in patients with stable coronary heart disease.
  • To determine if this association differs between men and women.
  • To assess the prognostic value of MS independent of traditional cardiovascular risk factors.

Main Methods:

  • A cohort of 1041 patients with stable coronary heart disease undergoing elective coronary angiography was studied.
  • Baseline data included hypertension, BMI, lipids, glucose, and insulin.
  • All-cause mortality was tracked over a median of 9.2 years.

Main Results:

  • 30% of patients had metabolic syndrome (MS).
  • MS was associated with higher rates of diabetes and three-vessel coronary artery disease.
  • MS significantly increased all-cause mortality risk in women (HR=2.2, p=0.02) but not in men (HR=1.0, p=0.93).

Conclusions:

  • Metabolic syndrome provides significant prognostic information in women with stable coronary heart disease.
  • The association between MS and mortality in women is independent of conventional cardiovascular risk factors and disease severity.
  • MS does not appear to be an independent predictor of mortality in men with stable coronary heart disease.
Abstract

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