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Association of lipid profile biomarkers with breast cancer by molecular subtype: analysis of the MEND study

  • H3 Africa Kidney Research Network
  • University of Kansas
  • Duke University
  • Duke University
  • University of North Carolina
  • University of North Carolina at Chapel Hill
  • Lagos University Teaching Hospital
  • Obafemi Awolowo University
  • University College Hospital, Ibadan
  • Federal Medical Centre
  • Our Lady of Apostle Catholic Hospital
  • University of Alabama at Birmingham
  • College of Public Health
  • College of Medicine, University of Ibadan
  • University of Ilorin
  • University of Ghana
  • University of Nigeria
  • National Cancer Institute at Frederick
  • University of Michigan, Ann Arbor
  • University of Cape Coast Ghana
  • Kwame Nkrumah University of Science and Technology
  • University of Abuja
  • Loyola University Chicago
  • National Human Genome Research Institute (NHGRI)
  • Boston Medical Center
  • National Institutes of Health
  • University of Toronto
  • Duke University Medical Center
  • University of the Western Cape
  • Harvard Medical School
  • Nnamdi Azikiwe University
  • Aminu Kano Teaching Hospital
  • Delta State University Teaching Hospital
  • Lagos State University
  • Usmanu Danfodiyo University
  • University of Illinois at Chicago
  • Université de Yaoundé I
  • University of Cape Town
  • New York University
  • Duke University
  • Technion-Israel Institute of Technology
  • Duke Cancer Institute

Research output: Contribution to journalArticlepeer-review

10 Citations (Scopus)

Abstract

There is conflicting evidence on the role of lipid biomarkers in breast cancer (BC), and no study to our knowledge has examined this association among African women. We estimated odds ratios (ORs) and 95% confidence intervals (95% CI) for the association of lipid biomarkers—total cholesterol, high-density lipoprotein (HDL), low-density lipoprotein (LDL), and triglycerides—with odds of BC overall and by subtype (Luminal A, Luminal B, HER2-enriched and triple-negative or TNBC) for 296 newly diagnosed BC cases and 116 healthy controls in Nigeria. Each unit standard deviation (SD) increase in triglycerides was associated with 39% increased odds of BC in fully adjusted models (aOR: 1.39; 95% CI: 1.03, 1.86). Among post-menopausal women, higher total cholesterol (aOR: 1.65; 95% CI: 1.06, 2.57), LDL cholesterol (aOR: 1.59; 95% CI: 1.04, 2.41), and triglycerides (aOR: 1.91; 95% CI: 1.21, 3.01) were associated with increased odds of BC. Additionally, each unit SD increase in LDL was associated with 64% increased odds of Luminal B BC (aOR 1.64; 95% CI: 1.06, 2.55). Clinically low HDL was associated with 2.7 times increased odds of TNBC (aOR 2.67; 95% CI: 1.10, 6.49). Among post-menopausal women, higher LDL cholesterol and triglycerides were significantly associated with increased odds of Luminal B BC and HER2 BC, respectively. In conclusion, low HDL and high LDL are associated with increased odds of TN and Luminal B BC, respectively, among African women. Future prospective studies can definitively characterize this association and inform clinical approaches targeting HDL as a BC prevention strategy.

Original languageEnglish
Article number10631
JournalScientific Reports
Volume12
Issue number1
DOIs
Publication statusPublished - Dec 2022

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

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