Journal of Clinical Medicine Article Familial Hypercholesterolemia in Premature Acute Coronary Syndrome. Insights from CholeSTEMI Registry Rebeca Lorca 1,2,3, Andrea Aparicio 2, Elias Cuesta-Llavona 1,3, Isaac Pascual 2,3,* , Alejandro Junco 2 , Sergio Hevia 2, Francisco Villazón 4, Daniel Hernandez-Vaquero 2,3 , 1,2,3 1,2,3 1,3 1,3, Jose Julian Rodríguez Reguero , Cesar Moris , Eliecer Coto , Juan Gómez y and 2,3, Pablo Avanzas y 1 Reference Unit of Familiar Cardiomyopathies-HUCA, Área del Corazón y Departamento de Genética Molecular, Hospital Universitario Central Asturias, 33014 Oviedo, Spain;
[email protected] (R.L.);
[email protected] (E.C.-L.);
[email protected] (J.J.R.R.);
[email protected] (C.M.);
[email protected] (E.C.);
[email protected] (J.G.) 2 Heart Area, Hospital Universitario Central de Asturias, 33014 Oviedo, Spain;
[email protected] (A.A.);
[email protected] (A.J.);
[email protected] (S.H.);
[email protected] (D.H.-V.);
[email protected] (P.A.) 3 Instituto de Investigación Sanitaria del Principado de Asturias, ISPA, 33014 Oviedo, Spain 4 Endocrinology Department, Hospital Universitario Central Asturias, 33014 Oviedo, Spain;
[email protected] * Correspondence:
[email protected] Equal contribution of two last co-authors: Pablo Avanzas and Juan Gómez. y Received: 3 September 2020; Accepted: 26 October 2020; Published: 29 October 2020 Abstract: Familial hypercholesterolemia (FH) is an underdiagnosed genetic inherited condition that may lead to premature coronary artery disease (CAD). FH has an estimated prevalence in the general population of about 1:313. However, its prevalence in patients with premature STEMI (ST-elevation myocardial infarction) has not been widely studied.