Familial hypercholesterolemia (FH) is a frequently undiagnosed genetic disease characterized by substantial elevations of low-density lipoprotein cholesterol (LDL-C). The prevalence of heterozygous FH (HeFH) in the general population is 1:500 inhabitants, while the prevalence of homozygous FH (HoFH) is 1:1,000,000. If FH is not identified and aggressively treated at an early age, affected individuals have a 20-fold increased lifetime risk of coronary heart disease compared with the general population. This narrative review provide a concise overview of recommendations for diagnosis and treatment of adults and children with FH, and discuss the utility of considering FH as a comorbidity at the entry of cardiac rehabilitation programmes
Familial hypercholesterolemia in cardiac rehabilitation: a new field of interest / Ambrosetti, M; Malfatto, G; Maria Cremona, A; Arca, M; Faggiano, P. - In: MONALDI ARCHIVES FOR CHEST DISEASE. - ISSN 1122-0643. - 2:82(2014), pp. 87-92. [10.4081/monaldi.2014.49]
Familial hypercholesterolemia in cardiac rehabilitation: a new field of interest
Ambrosetti MPrimo
Writing – Original Draft Preparation
;Arca MPenultimo
Writing – Original Draft Preparation
;
2014
Abstract
Familial hypercholesterolemia (FH) is a frequently undiagnosed genetic disease characterized by substantial elevations of low-density lipoprotein cholesterol (LDL-C). The prevalence of heterozygous FH (HeFH) in the general population is 1:500 inhabitants, while the prevalence of homozygous FH (HoFH) is 1:1,000,000. If FH is not identified and aggressively treated at an early age, affected individuals have a 20-fold increased lifetime risk of coronary heart disease compared with the general population. This narrative review provide a concise overview of recommendations for diagnosis and treatment of adults and children with FH, and discuss the utility of considering FH as a comorbidity at the entry of cardiac rehabilitation programmesFile | Dimensione | Formato | |
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