Coronary Heart Disease, Peripheral Arterial Disease, and Stroke in Familial Hypercholesterolaemia: Insights From the SAFEHEART Registry (Spanish Familial Hypercholesterolaemia Cohort Study)

OBJECTIVE—Heterozygous familial hypercholesterolemia (FH) is the most common premature atherosclerotic cardiovascular disease (ASCVD)–related monogenic disorder, and it is associated with ischemic heart disease. There is limited information whether FH increases the risk of peripheral arterial and ce...

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Veröffentlicht in:Arteriosclerosis, thrombosis, and vascular biology thrombosis, and vascular biology, 2016-09, Vol.36 (9), p.2004-2010
Hauptverfasser: Pérez de Isla, Leopoldo, Alonso, Rodrigo, Mata, Nelva, Saltijeral, Adriana, Muñiz, Ovidio, Rubio-Marin, Patricia, Diaz-Diaz, José L, Fuentes, Francisco, de Andrés, Raimundo, Zambón, Daniel, Galiana, Jesús, Piedecausa, Mar, Aguado, Rocio, Mosquera, Daniel, Vidal, José I, Ruiz, Enrique, Manjón, Laura, Mauri, Marta, Padró, Teresa, Miramontes, José P, Mata, Pedro
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Sprache:eng
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Zusammenfassung:OBJECTIVE—Heterozygous familial hypercholesterolemia (FH) is the most common premature atherosclerotic cardiovascular disease (ASCVD)–related monogenic disorder, and it is associated with ischemic heart disease. There is limited information whether FH increases the risk of peripheral arterial and cerebrovascular disease. Our aim was to analyze ASCVD prevalence and characteristics in different arterial territories in a large FH population, to compare them with an unaffected control population and to determine which factors are associated to ASCVD. APPROACH AND RESULTS—SAFEHEART (Spanish Familial Hypercholesterolaemia Cohort Study) is an ongoing registry of molecularly defined patients with heterozygous FH in Spain. ASCVD in the different arterial territories was analyzed, as well as individual characteristics, genetic variables, and lipid-lowering therapies. The study recruited 4132 subjects (3745 ≥18 years); 2,752 of those enrolled were molecularly diagnosed FH cases. Median age was 44.0 years (45.9% men) and 40 years (46.6% men) in FH patients and unaffected relatives (P
ISSN:1079-5642
1524-4636
DOI:10.1161/ATVBAHA.116.307514