• J Clin Lipidol · Sep 2012

    Case Reports

    Pseudohypertriglyceridemia: two cases of probable glycerol kinase deficiency.

    • James M Backes, Thomas Dayspring, Thomas Mieras, and Patrick M Moriarty.
    • Atherosclerosis and LDL-Apheresis Center, Kansas University Medical Center, Room B440 Mail Stop 4047, Kansas City, KS 66160, USA. jbackes@kumc.edu
    • J Clin Lipidol. 2012 Sep 1; 6 (5): 469-73.

    AbstractThe National Cholesterol Educational Program Adult Treatment Panel's third report define borderline-high, high, and very high triglycerides as serum levels of 150-199 mg/dL, 200-499 mg/dL, and ≥500 mg/dL, respectively. Hypertriglyceridemia (HTG) is generally very responsive to both therapeutic lifestyle changes (TLC), and drug therapy, with niacin, omega-3 fatty acids, fibrates, and statins, each reducing levels by ~10-50%. This paper presents two cases of patients who were aggressively treated for significant HTG with little response to therapy. Although most measured triglyceride (TG) values in these patients were markedly elevated, periodic concentrations were reported as normal. When this occurs, the clinician must immediately think of the diagnosis 'pseudohypertriglyceridemia' or as it is more aptly termed 'glycerolemia' secondary to glycerol kinase deficiency (GKD).Copyright © 2012 National Lipid Association. Published by Elsevier Inc. All rights reserved.

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