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Simple cardiovascular risk stratification by replacing total serum cholesterol with anthropometric measures: The MORGAM prospective cohort project

  • Victoria Rosberg
  • , Julie KK Vishram-Nielsen*
  • , Anna M.Dyrvig Kristensen
  • , Manan Pareek
  • , Thomas S.G. Sehested
  • , Peter M. Nilsson
  • , Allan Linneberg
  • , Luigi Palmieri
  • , Simona Giampaoli
  • , Chiara Donfrancesco
  • , Frank Kee
  • , Giuseppe Mancia
  • , Giancarlo Cesana
  • , Giovanni Veronesi
  • , Guido Grassi
  • , Kari Kuulasmaa
  • , Veikko Salomaa
  • , Tarja Palosaari
  • , Susana Sans
  • , Jean Ferrieres
  • Jean Dallongeville, Stefan Söderberg, Marie Moitry, Wojciech Drygas, Abdonas Tamosiunas, Annette Peters, Hermann Brenner, Ben Schöttker, Sameline Grimsgaard, Tor Biering-Sørensen, Michael H. Olsen
*Kontaktforfatter
  • ​Nordsjællands Hospital
  • Københavns Universitet
  • Sjællands Universitetshospital, Roskilde
  • Lund University
  • Istituto Superiore di Sanità - National Center for Epidemiology, Surveillance and Health Promotion
  • Queen's University Belfast
  • University of Milano-Bicocca
  • University of Insubria
  • National Institute for Health and Welfare
  • Catalan Department of Health
  • Institut Pasteur de Lille
  • Umeå University
  • University Hospitals of Strasbourg
  • Heidelberg University
  • German Cancer Research Center
  • UiT The Arctic University of Norway
  • Københavns Universitetshospital
  • Frederiksberg og Bispebjerg Hospital
  • Yale New Haven Hospital
  • University of Toulouse
  • National Institute of Cardiology, Warsaw, Poland.
  • Lithuanian University of Health Sciences
  • Institute of Human Genetics, Helmholtz Munich
  • Steno Diabetes Center Sjælland

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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Abstract

To assess whether anthropometric measures (body mass index [BMI], waist-hip ratio [WHR], and estimated fat mass [EFM]) are independently associated with major adverse cardiovascular events (MACE), and to assess their added prognostic value compared with serum total-cholesterol. The study population comprised 109,509 individuals (53% men) from the MORGAM-Project, aged 19–97 years, without established cardiovascular disease, and not on antihypertensive treatment. While BMI was reported in all, WHR and EFM were reported in ∼52,000 participants. Prognostic importance of anthropometric measurements and total-cholesterol was evaluated using adjusted Cox proportional-hazards regression, logistic regression, area under the receiver-operating-characteristic curve (AUCROC), and net reclassification improvement (NRI). The primary endpoint was MACE, a composite of stroke, myocardial infarction, or death from coronary heart disease. Age interacted significantly with anthropometric measures and total-cholesterol on MACE (P ≤ 0.003), and therefore age-stratified analyses (<50 versus ≥ 50 years) were performed. BMI, WHR, EFM, and total-cholesterol were independently associated with MACE (P ≤ 0.003) and resulted in significantly positive NRI when added to age, sex, smoking status, and systolic blood pressure. Only total-cholesterol increased discrimination ability (AUCROC difference; P < 0.001). In subjects < 50 years, the prediction model with total-cholesterol was superior to the model including BMI, but not superior to models containing WHR or EFM, while in those ≥ 50 years, the model with total-cholesterol was superior to all models containing anthropometric variables, whether assessed individually or combined. We found a potential role for replacing total-cholesterol with anthropometric measures for MACE-prediction among individuals < 50 years when laboratory measurements are unavailable, but not among those ≥ 50 years.

OriginalsprogEngelsk
Artikelnummer101700
TidsskriftPreventive Medicine Reports
Vol/bind26
Antal sider9
ISSN2211-3355
DOI
StatusUdgivet - apr. 2022

Bibliografisk note

Funding Information:
The MORGAM Project has received funding from EU projects MORGAM (Biomed, BMH4-CT98-3183), GenomEUtwin (FP5, QLG2-CT-2002-01254), ENGAGE (FP7, HEALTH-F4-2007-201413), CHANCES (FP7, HEALTH-F3-2010-242244), BiomarCaRE (FP7, HEALTH-F2-2011-278913), euCanSHare (Horizon 2020, No. 825903) and AFFECT-EU (Horizon 2020, No. 847770); and Medical Research Council, London (G0601463, No. 80983: Biomarkers in the MORGAM Populations). This has supported central coordination, workshops and part of the activities of the MORGAM Data Centre, the MORGAM Laboratories and the MORGAM Participating Centres. VS was supported by the Finnish Foundation for Cardiovascular Research. SSg was supported by the Swedish Heart and Lung foundation and by the County council of V?stertbotten. MP has the followings relationships ? Advisory Board and Speaking Honoraria: AstraZeneca; Speaking Honoraria: Bayer, Boehringer Ingelheim.

Publisher Copyright:
© 2022 The Author(s)

Finansiering

The MORGAM Project has received funding from EU projects MORGAM (Biomed, BMH4-CT98-3183), GenomEUtwin (FP5, QLG2-CT-2002-01254), ENGAGE (FP7, HEALTH-F4-2007-201413), CHANCES (FP7, HEALTH-F3-2010-242244), BiomarCaRE (FP7, HEALTH-F2-2011-278913), euCanSHare (Horizon 2020, No. 825903) and AFFECT-EU (Horizon 2020, No. 847770); and Medical Research Council, London (G0601463, No. 80983: Biomarkers in the MORGAM Populations). This has supported central coordination, workshops and part of the activities of the MORGAM Data Centre, the MORGAM Laboratories and the MORGAM Participating Centres. VS was supported by the Finnish Foundation for Cardiovascular Research. SSg was supported by the Swedish Heart and Lung foundation and by the County council of V?stertbotten. MP has the followings relationships ? Advisory Board and Speaking Honoraria: AstraZeneca; Speaking Honoraria: Bayer, Boehringer Ingelheim.

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