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Genetic studies of Familial hypercholesterolemia: A review  [2008]

Rafiq, S. (Karachi Univ. (Pakistan). Centre for Molecular Genetics) Ahmed, N. (COMSATS Inst. of Information Technology, Islamabad (Pakistan)) Qamar, R. (COMSATS Inst. of Information Technology, Islamabad (Pakistan))

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摘要
Familial hypercholesterolemia (FH) is characterized by raised serum LDL cholesterol levels, which result in excess deposition of cholesterol in tissues, leading to accelerated atherosclerosis and increased risk of premature coronary heart disease. FH results from defects in the hepatic uptake and degradation of LDL via the LDL-receptor pathway, commonly caused by a loss-of-function mutation in the LDL-receptor gene (LDLR) or by a mutation in the gene encoding apolipoprotein B (APOB). FH is primarily an autosomal dominant disorder with a gene-dosage effect. An autosomal recessive form of FH caused by loss-of-function mutations in LDLRAPI, which encodes a protein required for clathrin-mediated internalization of the LDL receptor by liver cells, has also been documented. The most recent addition to the database of genes in which defects cause FH is one encoding a member of the proprotein convertase family, PCSK9. Rare dominant gain-of-function mutations in PCSK9 cosegregate with hypercholesterolemia, and one mutation is associated with a particularly severe FH phenotype. Expression of PCSK9 normally downregulates the LDL-receptor pathway by indirectly causing degradation of LDL-receptor protein, and loss-of-function mutations in PCSK9 result in low plasma LDL levels. Thus, PCSK9 is an attractive target for new drugs aimed at lowering serum LDL cholesterol, which should have additive lipid-lowering effects to the stains currently used.
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其它题目

  • mutation
  • genetics
  • genes
  • cholesterol
  • hyperlipidaemia

学术期刊

International Journal of Biology and Biotechnology (Pakistan)

ISSN : 1810-2719

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其他信息

类型 : Journal Article

In AGRIS since : 2009

: 5

: 3-4

Start Page : 163

End Page : 167

所有题名 :

" Genetic studies of Familial hypercholesterolemia: A review "