Severe/Extreme Hypertriglyceridemia and LDL Apheretic Treatment: Review of the Literature, Original Findings
Author(s) -
Olga Diakoumakou,
Georgios Hatzigeorgiou,
Nikos Gontoras,
Maria Boutsikou,
Vana Kolovou,
Sophie Mavrogeni,
Vassiliki Giannakopoulou,
Genovefa Kolovou
Publication year - 2014
Publication title -
cholesterol
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.876
H-Index - 20
eISSN - 2090-1291
pISSN - 2090-1283
DOI - 10.1155/2014/109263
Subject(s) - medicine , hypertriglyceridemia , metabolic syndrome , disease , diabetes mellitus , coronary artery disease , atherosclerotic cardiovascular disease , bioinformatics , intensive care medicine , pediatrics , triglyceride , endocrinology , cholesterol , biology
Hypertriglyceridemia (HTG) is a feature of numerous metabolic disorders including dyslipidemias, metabolic syndrome, and diabetes mellitus type 2 and can increase the risk of premature coronary artery disease. HTG may also be due to genetic factors (called primary HTG) and particularly the severe/extreme HTG (SEHTG), which is a usually rare genetic disorder. Even rarer are secondary cases of SEHTG caused by autoimmune disease. This review considers the causes of SEHTG, and their management including treatment with low density lipoprotein apheresis and analyzes the original findings.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom