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Generalizability of the REDUCE-IT trial to South Asians with cardiovascular disease.
Krishnaraj, Aishwarya; Bakbak, Ehab; Teoh, Hwee; Bhatt, Deepak L; Quan, Adrian; Puar, Pankaj; Lambotharan, Bhaavani; Kirubaharan, Aathmika; Firoz, Irene N; Meglis, Gus; Yanagawa, Bobby; Bari, Basel; Kirubaharan, Rajaratnam; Vijayaraghavan, Ram; Hess, David A; Demchuk, Andrew M; Mancini, G B John; Tanguay, Jean-François; Tardif, Jean-Claude; Voisine, Pierre; Leiter, Lawrence A; Verma, Subodh.
Affiliation
  • Krishnaraj A; Division of Cardiac Surgery, St. Michael's Hospital of Unity Health Toronto, 30 Bond Street, Toronto, ON M5B 1W8, Canada; Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.
  • Bakbak E; Division of Cardiac Surgery, St. Michael's Hospital of Unity Health Toronto, 30 Bond Street, Toronto, ON M5B 1W8, Canada; Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.
  • Teoh H; Division of Cardiac Surgery, St. Michael's Hospital of Unity Health Toronto, 30 Bond Street, Toronto, ON M5B 1W8, Canada; Division of Endocrinology and Metabolism, St. Michael's Hospital of Unity Health Toronto, Toronto, ON, Canada.
  • Bhatt DL; Mount Sinai Heart, Icahn School of Medicine at Mount Sinai Health System, New York, NY, USA.
  • Quan A; Division of Cardiac Surgery, St. Michael's Hospital of Unity Health Toronto, 30 Bond Street, Toronto, ON M5B 1W8, Canada.
  • Puar P; Division of Cardiac Surgery, St. Michael's Hospital of Unity Health Toronto, 30 Bond Street, Toronto, ON M5B 1W8, Canada.
  • Lambotharan B; Division of Cardiac Surgery, St. Michael's Hospital of Unity Health Toronto, 30 Bond Street, Toronto, ON M5B 1W8, Canada.
  • Kirubaharan A; Division of Cardiac Surgery, St. Michael's Hospital of Unity Health Toronto, 30 Bond Street, Toronto, ON M5B 1W8, Canada.
  • Firoz IN; Division of Cardiac Surgery, St. Michael's Hospital of Unity Health Toronto, 30 Bond Street, Toronto, ON M5B 1W8, Canada; Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.
  • Meglis G; North York Diagnostic and Cardiac Centre, Toronto, ON, Canada.
  • Yanagawa B; Division of Cardiac Surgery, St. Michael's Hospital of Unity Health Toronto, 30 Bond Street, Toronto, ON M5B 1W8, Canada; Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada; Department of Surgery, University of Toronto, Toronto, ON, Canada.
  • Bari B; Markham Health+Plex Medical Centre, Markham, ON, Canada.
  • Kirubaharan R; Fenton Medical Centre, Markham, ON, Canada.
  • Vijayaraghavan R; Scarborough Heart Health Institute, Scarborough Health Network, Scarborough, ON, Canada.
  • Hess DA; Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada; Robarts Research Institute, and Department of Physiology and Pharmacology, Western University, London, ON, Canada; Division of Vascular Surgery, St. Michael's Hospital of Unity Health Toronto, Toronto, ON, Canada.
  • Demchuk AM; Departments of Clinical Neurosciences and Radiology, Cumming School of Medicine, University of Calgary, AB, Canada.
  • Mancini GBJ; Division of Cardiology and the Centres for Cardiovascular Innovation, University of British Columbia, Vancouver, BC, Canada.
  • Tanguay JF; Montreal Heart Institute, Université de Montréal, Montréal, QC, Canada.
  • Tardif JC; Montreal Heart Institute, Université de Montréal, Montréal, QC, Canada.
  • Voisine P; Division of Cardiac Surgery, Institut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ), Université Laval, Québec City, QC, Canada.
  • Leiter LA; Division of Endocrinology and Metabolism, St. Michael's Hospital of Unity Health Toronto, Toronto, ON, Canada; Department of Medicine, University of Toronto, Toronto, ON, Canada; Department of Nutritional Sciences, University of Toronto, Toronto, ON, Canada.
  • Verma S; Division of Cardiac Surgery, St. Michael's Hospital of Unity Health Toronto, 30 Bond Street, Toronto, ON M5B 1W8, Canada; Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada; North York Diagnostic and Cardiac Centre, Toronto, ON, Canada; Department of Surgery, Unive
Med ; 4(2): 130-138.e1, 2023 02 10.
Article in En | MEDLINE | ID: mdl-36630964
BACKGROUND: South Asians (SAs) represent ∼25% of the world's population and account for >50% of global cardiovascular (CV) deaths, yet they continue to be underrepresented in contemporary clinical trials. The REDUCE-IT study demonstrated in a high-risk and predominantly White population that icosapent ethyl (IPE) lowered major adverse cardiovascular events by 25%. We sought to determine the generalizability of these results to a high-risk population of SAs with established CV disease living in Canada. METHODS: This was a cross-sectional observational study of 200 statin-treated SAs (≥45 years) with atherosclerotic CV disease (ASCVD) (NCT05271591). SA ethnicity was self-identified as being of Anglo-Indian, Bangladeshi, Bengali, Bhutanese, Goan, Gujarati, Indian, Jatt, Kashmiri, Maharashtrian, Malayali, Nepali, Pakistani, Punjabi, Sindhi, Sinhalese, Sri Lankan, Tamil, Telugu, or other SA. ASCVD was defined as the presence of coronary, carotid, or peripheral atherosclerosis. FINDINGS: Mean age of the cohort was 67 years, where 82% were men and 57% had diabetes. The predominant ASCVD phenotype was coronary artery disease (94%). Mean (SD) baseline LDL-C and triglycerides were 1.70 (0.8) mmol/L and 1.42 (1.0) mmol/L, respectively. Three-quarters were on high-intensity statin therapy. According to the Health Canada/Canadian Cardiovascular Society Guidelines and FDA-approved indication, 33% and 25% of the participants were, respectively, eligible for IPE. CONCLUSIONS: A large proportion of high-intensity, statin-treated, high-risk patients with ASCVD and of self-reported SA ethnicity are eligible for IPE. These data have important translational implications for SAs who are at a disproportionately higher risk of CV morbidity and mortality. FUNDING: This study was funded by an unrestricted grant provided by HLS Therapeutics Inc, Canada.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Atherosclerosis Type of study: Guideline / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: America do norte / Asia Language: En Journal: Med Year: 2023 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Atherosclerosis Type of study: Guideline / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: America do norte / Asia Language: En Journal: Med Year: 2023 Document type: Article Affiliation country: Country of publication: