The heterozygous N291S mutation in the lipoprotein lipase gene impairs whole-body insulin sensitivity and affects a distinct set of plasma metabolites in humans

• Published in: Journal of clinical lipidology 2017-03, Vol.11 (2), p.515-523.e6
• Main Authors: Berg, Sofia Mikkelsen, PhD, Havelund, Jesper, PhD, Hasler-Sheetal, Harald, PhD, Kruse, Vibeke, Thestrup Pedersen, Andreas James, MD, PhD, Bill Hansen, Aleksander, Nybo, Mads, MD, PhD, Beck-Nielsen, Henning, MD, PhD, Højlund, Kurt, MD, PhD, Færgeman, Nils Joakim, PhD
• Format: Article
• Language: English
• Subjects: Cardiovascular; Female; Gas chromatography-mass spectrometry; Gene mutation; Heterozygote; Heterozygous N291S mutation; Humans; Insulin Resistance - genetics; Insulin sensitivity; Lipoprotein Lipase - genetics; Lipoprotein lipase deficiency; Male; Middle Aged; Mutation; Plasma - metabolism; α-tocopherol
• ISSN: 1933-2874; 1876-4789
• DOI: 10.1016/j.jacl.2017.02.009

Background Mutations in the lipoprotein lipase gene causing decreased lipoprotein lipase activity are associated with surrogate markers of insulin resistance and the metabolic syndrome in humans. Objective We investigated the hypothesis that a heterozygous lipoprotein lipase mutation (N291S) induces whole-body insulin resistance and alterations in the plasma metabolome. Methods In 6 carriers of a heterozygous lipoprotein lipase mutation (N291S) and 11 age-matched and weight-matched healthy controls, we examined insulin sensitivity and substrate metabolism by euglycemic-hyperinsulinemic clamps combined with indirect calorimetry. Plasma samples were taken before and after the clamp (4 hours of physiological hyperinsulinemia), and metabolites were measured enzymatically or by gas chromatography-mass spectrometry. Results Compared with healthy controls, heterozygous carriers of a defective lipoprotein lipase allele had elevated fasting plasma levels triglycerides ( P