| Literature DB >> 30527143 |
Liam R Brunham1, Isabelle Ruel2, Sumayah Aljenedil2, Jean-Baptiste Rivière2, Alexis Baass3, Jack V Tu4, G B John Mancini5, Paolo Raggi6, Milan Gupta7, Patrick Couture8, Glen J Pearson6, Jean Bergeron8, Gordon A Francis9, Brian W McCrindle10, Katherine Morrison11, Julie St-Pierre12, Mélanie Henderson13, Robert A Hegele14, Jacques Genest15, Jeannette Goguen16, Daniel Gaudet17, Guillaume Paré18, Jacques Romney19, Thomas Ransom20, Sophie Bernard21, Pamela Katz22, Tisha R Joy23, David Bewick24, James Brophy15.
Abstract
Familial hypercholesterolemia (FH) is the most common monogenic disorder causing premature atherosclerotic cardiovascular disease. It affects 1 in 250 individuals worldwide, and of the approximately 145,000 Canadians estimated to have FH, most are undiagnosed. Herein, we provide an update of the 2014 Canadian Cardiovascular Society position statement on FH addressing the need for case identification, prompt recognition, and treatment with statins and ezetimibe, and cascade family screening. We provide a new Canadian definition for FH and tools for clinicians to make a diagnosis. The risk of atherosclerotic cardiovascular disease in patients with "definite" FH is 10- to 20-fold that of a normolipidemic individual and initiating treatment in youth or young adulthood can normalize life expectancy. Target levels for low-density lipoprotein cholesterol are proposed and are aligned with the Canadian Cardiovascular Society guidelines on dyslipidemia. Recommendation for the use of inhibitors of proprotein convertase kexin/subtilisin type 9 are made in patients who cannot achieve therapeutic low-density lipoprotein cholesterol targets on maximally tolerated statins and ezetimibe. The writing committee used the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) methodology in the preparation of the present document, which offers guidance for practical evaluation and management of patients with FH. This position statement also aims to raise awareness of FH nationally, and to mobilize patient support, promote knowledge translation, and availability of treatment and health care resources for this under-recognized, but important medical condition.Entities:
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Year: 2018 PMID: 30527143 DOI: 10.1016/j.cjca.2018.09.005
Source DB: PubMed Journal: Can J Cardiol ISSN: 0828-282X Impact factor: 5.223