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[Congenital disorders of lipoprotein metabolism]. / Angeborene Störungen im Lipoproteinstoffwechsel.
März, W; Grammer, T B; Delgado, G; Kleber, M E.
Afiliación
  • März W; Medizinische Klinik V (Nephrologie, Hypertensiologie, Rheumatologie, Endokrinologie, Diabetologie), Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Deutschland. winfried.maerz@synlab.com.
  • Grammer TB; Klinisches Institut für Medizinische und Chemische Labordiagnostik, Medizinische Universität Graz, Graz, Österreich. winfried.maerz@synlab.com.
  • Delgado G; Synlab Akademie, synlab Holding Deutschland GmbH, P5,7, 68167, Mannheim, Deutschland. winfried.maerz@synlab.com.
  • Kleber ME; Institut für Public Health, Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Deutschland.
Herz ; 42(5): 449-458, 2017 Aug.
Article en De | MEDLINE | ID: mdl-28555288
Congenital disorders of lipid metabolism are caused by a wide range of variants of the genes for receptors, apolipoproteins, enzymes, transfer factors, and cellular cholesterol transporters. Clinically most relevant are autosomal dominant familial hypercholesterolemia (FH) and familial combined hyperlipoproteinemia (FCHL). FH has a prevalence of 1:250. It is due to mutations of the low density lipoprotein (LDL) receptor, less often to mutations of the apolipoprotein B (APOB), the proprotein convertase subtilisin/kexin type 9 (PCSK9), or the signal transducing adapter family member 1 (STAP1). FH often leads to early atherosclerosis. Its diagnosis can definitely be made only by molecular genetic testing. The detection of mutations of the LDLR, APOB, or PCSK9 is an indicator for extremely high cardiovascular risk, independently of the concentration of LDL cholesterol. FCHL is also common (1:100) and is seen in about 10% of patients with early myocardial infarction. It is produced by combinations of frequent genetic variants affecting triglycerides and LDL cholesterol. Other monogenic hyperlipoproteinemias (HLP) affect the catabolism of chylomicrons (familial chylomicronemia) or of remnants of triglyceride-rich lipoproteins (type III hyperlipoproteinemia). Multiple hereditary disorders in HDL metabolism - with a broad spectrum of clinical significance - are known. Currently, second generation sequencing methods are used to simultaneously analyze multiple disease-causing genes. This approach cost-neutrally provides additional information such as the genetic risk of atherosclerosis and predisposition to statin intolerance.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Aterosclerosis / Hiperlipoproteinemia Tipo II / Lipoproteínas Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: De Revista: Herz Año: 2017 Tipo del documento: Article Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Aterosclerosis / Hiperlipoproteinemia Tipo II / Lipoproteínas Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: De Revista: Herz Año: 2017 Tipo del documento: Article Pais de publicación: Alemania