High triglyceride causes: Difference between revisions

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===Genetics===
===Genetics===
====Type I hyperlipoproteinemia====
====Type I hyperlipoproteinemia====
* [[Genetic]] deficiency or dysfunction of enzyme [[lipoprotein lipase]] (LPL) or its cofactor, apo C-II.  
* [[Genetic]] deficiency or dysfunction of enzyme [[lipoprotein lipase]] (LPL)  
* Deficiency apo C-II, that acts as a cofactor of [[lipoprotein lipase]]
* Insulin deficiency or dysfunction in diabetes type 1 and 2 can also cause this disorder as LPL requires insulin for its full function.
 
====Familial combined hyperlipidemia====  
====Familial combined hyperlipidemia====  
* [[Autosomal dominant]] disorder  
* [[Autosomal dominant]] disorder  

Revision as of 00:46, 3 October 2011

Template:Hypertriglyceridemia

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.B.B.S. [2]

Overview

Hypertriglyceridemia can occur due to various causes, including genetics, familial, metabolic and drugs

Causes

Genetics

Type I hyperlipoproteinemia

  • Genetic deficiency or dysfunction of enzyme lipoprotein lipase (LPL)
  • Deficiency apo C-II, that acts as a cofactor of lipoprotein lipase
  • Insulin deficiency or dysfunction in diabetes type 1 and 2 can also cause this disorder as LPL requires insulin for its full function.

Familial combined hyperlipidemia

  • Autosomal dominant disorder
  • Patients have either isolated triglyceride or LDL-c elevations or both.
  • Family history of premature coronary artery disease in 1 or more first-degree relatives
  • Family history for elevated triglycerides with or without elevated LDL-c levels.

Familial hypertriglyceridemia

  • Autosomal dominant trait
  • These patients and their families have isolated triglyceride elevations
  • Increased risk of premature coronary artery disease.

Metabolic

Drugs

Miscellaneous

Idiopathic (constitutional)

References


Template:WikiDoc Sources