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Overweight, obesity, and cardiovascular disease in heterozygous familial hypercholesterolaemia: the EAS FH Studies Collaboration registry

  • on behalf of the EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)
  • Imperial College London
  • Alexandria University
  • Hospital Universitario Virgen del Rocio
  • University of Seville
  • Ciber of Epidemiology and Public Health CIBERESP
  • University of Ioannina
  • University of Milan
  • IRCCS Multimedica - Milano
  • Masaryk University
  • CarDia
  • University of Amsterdam
  • Novo Nordisk Foundation
  • Fundación Hipercolesterolemia Familiar
  • University of the Witwatersrand
  • Universidade de São Paulo
  • Manchester University NHS Foundation Trust
  • University of Western Australia
  • Royal Perth Hospital
  • Saint Joseph University
  • Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
  • Instituto Tecnologico de Estudios Superiores de Monterrey
  • King Saud University
  • University of Al-Qadisiya
  • University of Warith Alanbiyaa
  • Cleveland Clinic Abu Dhabi
  • Prince Sultan Cardiac Centre
  • Centre for Advanced Metabolic Medicine and Nutrition
  • Sultan Qaboos University
  • Sabah Al Ahmad Cardiac Centre
  • University of Rome La Sapienza
  • P.D. Hinduja National Hospital and Medical Research Centre
  • University of Palermo
  • National Research Council of Italy
  • Medical University of Łódź
  • Institute of Polish Mother's Health Center
  • University of Zielona Gora
  • Center Hospitalier de Luxembourg
  • Medical University of Vienna
  • Instituto Nacional de Saúde Doutor Ricardo Jorge
  • University of Lisbon
  • University of British Columbia
  • Medical University of Gdańsk
  • FASTA University
  • Portuguese Atherosclerosis Society
  • Al Farabi Kazakh National University
  • Universite de Mons
  • Universitas Indonesia—Harapan Kita National Cardiovascular Center
  • RAS - USSR Cardiology Research Center
  • University Medical Centre
  • University of Ljubljana
  • Osaka Medical and Pharmaceutical University
  • University of Oslo
  • University College London
  • Ege University
  • Chulalongkorn University
  • University of Belgrade
  • Leipzig University
  • National and Kapodistrian University of Athens
  • Universidad de Oriente - Venezuela
  • Tallaght Hospital
  • University of Cape Town
  • DACH Society for the Prevention of Heart and Circulatory Diseases
  • Heidelberg University 
  • Medical University of Graz
  • SYNLAB International GmbH
  • Kyrgyz State Medical Academy
  • Korea University
  • Swiss Society for Familial Forms of Hypercholesterolemia (SSFH)
  • University of Basel
  • National Academy of Medical Sciences of Ukraine
  • Universiti Teknologi MARA
  • University of Copenhagen
  • Cyprus University of Technology
  • University of Debrecen
  • Vilnius University
  • University of Zenica
  • Medical University Sofia
  • Menoufia University
  • University of Zagreb
  • Comisión Honoraria para la Salud Cardiovascular
  • Shifa Tameer-e-Millat University
  • University of Benin
  • Technical University of Munich
  • German Centre for Cardiovascular Research
  • Ministry of Health of Republic Uzbekistan
  • Academic Medical Centre University of Amsterdam
  • National Taiwan University
  • Khoo Teck Puat Hospital
  • Russian Ministry of Health
  • Mater Dei Hospital
  • University of Malta
  • Macau University of Science and Technology
  • Phenikaa University
  • Universidad Autonoma de Guadalajara
  • Tallinn University of Technology
  • Slovak Medical University
  • Rinku General Medical Center

Research output: Contribution to journalArticlepeer-review

14 Citations (Scopus)

Abstract

Background and Overweight and obesity are modifiable risk factors for atherosclerotic cardiovascular disease (ASCVD) in the general popuAims lation, but their prevalence in individuals with heterozygous familial hypercholesterolaemia (HeFH) and whether they confer additional risk of ASCVD independent of LDL cholesterol (LDL-C) remains unclear. Methods Cross-sectional analysis was conducted in 35 540 patients with HeFH across 50 countries, in the EAS FH Studies Collaboration registry. Prevalence of World Health Organization–defined body mass index categories was investigated in adults (n = 29 265) and children/adolescents (n = 6275); and their association with prevalent ASCVD. Results Globally, 52% of adults and 27% of children with HeFH were overweight or obese, with the highest prevalence noted in Northern Africa/Western Asia. A higher overweight/obesity prevalence was found in non-high-income vs. high-income countries. Median age at familial hypercholesterolaemia diagnosis in adults with obesity was 9 years older than in normal weight adults. Obesity was associated with a more atherogenic lipid profile independent of lipid-lowering medication. Prevalence of coronary artery disease increased progressively across body mass index categories in both children and adults. Compared with normal weight, obesity was associated with higher odds of coronary artery disease in children (odds ratio 9.28, 95% confidence interval 1.77–48.77, adjusted for age, sex, lipids, and lipid-lowering medication) and coronary artery disease and stroke in adults (odds ratio 2.35, 95% confidence interval 2.10–2.63 and odds ratio 1.65, 95% confidence interval 1.27–2.14, respectively), but less consistently with peripheral artery disease. Adjusting for diabetes, hypertension and smoking modestly attenuated the associations. Conclusions Overweight and obesity are common in patients with HeFH and contribute to ASCVD risk from childhood, independent of LDL-C and lipid-lowering medication. Sustained body weight management is needed to reduce the risk of ASCVD in HeFH.

Original languageEnglish
Pages (from-to)1127-1140
Number of pages14
JournalEuropean Heart Journal
Volume46
Issue number12
DOIs
Publication statusPublished - 21 Mar 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adiposity
  • Atherosclerosis
  • Dyslipidaemia
  • Insulin resistance

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