Lipoprotein characterization in Quaker parrots (Myiopsitta monachus) using gel‐permeation high‐performance liquid chromatography

Background Lipid accumulation disorders, such as atherosclerosis and hepatic lipidosis, are common in psittacine birds and associated with various dyslipidemias. Gel‐permeation high‐performance liquid chromatography (GP‐HPLC) is a reference method for advanced lipoprotein profiling based on particle...

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Veröffentlicht in:Veterinary clinical pathology 2020-09, Vol.49 (3), p.417-427
Hauptverfasser: Beaufrère, Hugues, Gardhouse, Sara, Ammersbach, Mélanie
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Sprache:eng
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Zusammenfassung:Background Lipid accumulation disorders, such as atherosclerosis and hepatic lipidosis, are common in psittacine birds and associated with various dyslipidemias. Gel‐permeation high‐performance liquid chromatography (GP‐HPLC) is a reference method for advanced lipoprotein profiling based on particle size separation, followed by an analysis of lipid contents. Objectives The objectives were to (a) characterize Quaker parrot lipoproteins using a commercial GP‐HPLC method (Liposearch panel), and (b) obtain preliminary information on the reliability of the Friedewald formula for low‐density lipoprotein‐cholesterol (LDL‐C) measurements. Methods Plasma samples were collected from 12 fasted healthy Quaker parrots. Cholesterol concentrations, triglyceride concentrations, particle sizes, and particle numbers were determined by GP‐HPLC for four classes and 20 sub‐fractions of lipoproteins. The LDL‐C concentrations obtained using the Friedewald formula and direct measurements were compared with Bland‐Altman plots. Alternate formulas were determined using multiple linear regression. Results High‐density lipoprotein (HDL) was the predominant lipoprotein in Quaker parrots, and most particles were of medium‐to‐small sizes belonging to two sub‐fractions (average size, 10.6 nm). LDL was the second most common lipoprotein and included large‐to‐small particles belonging to three sub‐fractions (average size, 24.9 nm). Very‐low‐density lipoproteins (VLDL) and portomicrons were present in low concentrations. The Friedewald formula underestimated LDL‐C concentrations with a significant bias of 0.44 mmol/L. An alternate formula was proposed: LDL‐C = 0.75*Non‐HDL‐C. Conclusions GP‐HPLC allowed unprecedented characterization of plasma lipoproteins in Quaker parrots. Characterizing psittacine lipoprotein is useful for validation and interpretation of routine clinical tests as well as for use in epidemiologic and experimental research on psittacine lipid accumulation disorders.
ISSN:0275-6382
1939-165X
DOI:10.1111/vcp.12895