Should we expand the concept of coronary heart disease equivalents?

Niki Katsiki1, Vasilios G Athyros, Asterios Karagiannis

  • 1aSecond Propedeutic Department of Internal Medicine, Medical School, Aristotle University of Thessaloniki, Hippokration Hospital, Thessaloniki, Greece bDepartment of Metabolic Medicine/Chemical Pathology, Guy's & St Thomas' Hospitals cDepartment of Clinical Biochemistry (Vascular Disease Prevention Clinics), Royal Free Hospital campus, University College London Medical School, University College London (UCL), London, UK.

Insights

Metabolic and inflammatory diseases, along with cancer treatments, increase coronary heart disease (CHD) risk. While not CHD equivalents, these conditions warrant further investigation for potential inclusion.

Area of Science:

  • Cardiology
  • Metabolic Diseases
  • Inflammatory Diseases
  • Oncology

Background:

  • Coronary heart disease (CHD) remains a leading cause of mortality worldwide.
  • Emerging evidence suggests links between metabolic/inflammatory conditions and cardiovascular risk.
  • The role of cancer therapies in cardiovascular health is increasingly recognized.

Purpose of the Study:

  • To review associations between metabolic and inflammatory diseases and CHD.
  • To examine the impact of radiotherapy and chemotherapy on CHD risk.
  • To evaluate the potential of these conditions as CHD equivalents.

Main Methods:

  • Narrative review of existing literature.
  • Analysis of studies on metabolic syndrome, diabetes, NAFLD, sleep apnea, erectile dysfunction, periodontitis, IBD, vasculitis, and HIV.
  • Inclusion of data on chemotherapy and radiotherapy effects.

Main Results:

  • Metabolic and inflammatory disorders are linked to increased CHD morbidity and mortality.
  • Conditions like metabolic syndrome, impaired glucose metabolism, NAFLD, and others show significant associations.
  • Chemotherapy and radiotherapy also correlate with elevated CHD risk.

Conclusions:

  • While not currently classified as CHD equivalents, these conditions significantly elevate cardiovascular risk.
  • Further research is needed to determine if specific conditions should be added to the list of CHD equivalents.
  • Identifying new CHD equivalents can refine risk stratification and prevention strategies.
Abstract

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