Tangier disease: update for 2020

被引:27
|
作者
Hooper, Amanda J. [1 ,2 ,3 ]
Hegele, Robert A. [4 ,5 ,6 ]
Burnett, John R. [1 ,2 ,3 ]
机构
[1] Royal Perth Hosp, Dept Clin Biochem, PathWest Lab Med WA, Perth, WA, Australia
[2] Fiona Stanley Hosp Network, Perth, WA, Australia
[3] Univ Western Australia, Fac Hlth & Med Sci, Sch Med, Perth, WA, Australia
[4] Western Univ, Schulich Sch Med, Dept Med, London, ON, Canada
[5] Western Univ, Schulich Sch Med, Dept Biochem, London, ON, Canada
[6] Western Univ, Robarts Res Inst, London, ON, Canada
关键词
ABCA1; low HDL-cholesterol; tangier disease; CHOLESTEROL EFFLUX; ABCA1; MUTATION;
D O I
10.1097/MOL.0000000000000669
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose of reviewTo appraise recent advances in our knowledge of the severe genetic HDL deficiency disorder, Tangier disease.Recent findingsWhile Tangier disease can cause premature atherosclerotic cardiovascular disease (ASCVD), new evidence suggests that heterozygous ABCA1 variant carriers are also at increased risk. Advances have been made in the study of the neurological abnormalities observed in Tangier disease, both in their assessment and the identification of potential new therapies.SummaryTangier disease is an extremely rare condition and, as such, the published literature around its range of clinical manifestations, including peripheral neuropathy, premature ASCVD and platelet abnormalities is limited. Patient registries may assist in this regard.
引用
收藏
页码:80 / 84
页数:5
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