1. Diagnostic algorithm for familial chylomicronemia syndrome
Erik Stroes, Philippe Moulin, Klaus G. Parhofer, Vinciane Rebours, J-Matthias Löhr, Maurizio Averna 
Atherosclerosis Supplements 
Volume 23, Pages 1-7 (January 2017)
DOI: /j.atherosclerosissup
Copyright © 2016 Elsevier Ireland Ltd Terms and Conditions

2. Fig. 1
Lipoprotein lipase (LPL) is synthesized in the intracellular environment of adipose and muscle cells (1); lipase maturation factor 1 (LMF) guarantees correct homodimerization of LPL (2); glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 (GPIHBP1) is involved in the shuttling of LPL in the lumen of the capillaries (3); LPL is anchored to the capillary endothelium where it hydrolyzes the triglyceride content of chylomicrons (CM) and very low density lipoproteins (VLDL) (4); hydrolyzed free fatty acids (FFA) and monoglycerides (MG) are able to be transported inside myocytes or adipocytes where they are used for energy production or lipid storage (5).
Atherosclerosis Supplements  , 1-7DOI: ( /j.atherosclerosissup )
Copyright © 2016 Elsevier Ireland Ltd Terms and Conditions

3. Fig. 2
Risk of pancreatitis in the lipoprotein lipase deficient population. Adapted from Gaudet et al. [16]. LPLD = lipoprotein lipase deficiency; TG = triglyceridemia.
Atherosclerosis Supplements  , 1-7DOI: ( /j.atherosclerosissup )
Copyright © 2016 Elsevier Ireland Ltd Terms and Conditions

4. Fig. 3 Algorithm for diagnosis of familial chylomicronemia syndrome.
Atherosclerosis Supplements  , 1-7DOI: ( /j.atherosclerosissup )
Copyright © 2016 Elsevier Ireland Ltd Terms and Conditions