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Lp(a) assembles inside the cell from newly made LDL and apo(a), a stable-isotope kinetic study of 9 healthy people (Atherosclerosis 2012)

Original title: In vivo stable-isotope kinetic study suggests intracellular assembly of lipoprotein(a)

Atherosclerosis · · 7

Frischmann ME, Ikewaki K, Trenkwalder E, Lamina C, Dieplinger B, Soufi M, Schweer H, Schaefer JR, König P, Kronenberg F, Dieplinger H

This study investigated Lp(a) assembly mechanisms using in vivo stable-isotope kinetics of apolipoprotein(a) [apo(a)] and apoB-100 from Lp(a) and LDL in 9 healthy volunteers, calculating fractional synthesis rate, production rate and retention time via multicompartmental modelling. Mean production rate was similar for apo(a) (1.15 nmol/kg/day) and apoB-100 from Lp(a) (1.31 nmol/kg/day), but significantly different from apoB-100 production from LDL (32.6 nmol/kg/day), with matching fractional synthesis rate and retention time patterns for Lp(a)-apo(a) and Lp(a)-apoB that differed from LDL-apoB. The findings suggest two distinct kinetic apoB pools within Lp(a) and LDL, consistent with intracellular assembly of Lp(a) from apo(a) and newly synthesised LDL.

Read the paper (DOI)PubMed

Original abstract

Objective: Lipoprotein(a) [Lp(a)] consists of apolipoprotein B-100 (apoB-100) as part of an LDL-like particle and the covalently linked glycoprotein apolipoprotein(a) [apo(a)]. Detailed mechanisms of its biosynthesis, assembly, secretion and catabolism are still poorly understood. To address the Lp(a) assembly mechanism, we studied the in vivo kinetics of apo(a) and apoB-100 from Lp(a) and LDL apoB-100 in nine healthy probands using stable-isotope methodology.

Methods: The level of isotope enrichment was used to calculate the fractional synthesis rate (FSR), production rate (PR) and retention time (RT) using SAAMII software and multicompartmental modeling.

Results: We observed a similar mean PR for apo(a) (1.15 nmol/kg/d) and apoB-100 (1.31 nmol/kg/d) from Lp(a), which differed significantly from the PR for apoB-100 from LDL (32.6 nmol/kg/d). Accordingly, mean FSR and RT values for Lp(a)-apo(a) were similar to those of Lp(a)-apoB and different from those for LDL-apoB.

Conclusion: Two different kinetic apoB pools within Lp(a) and LDL suggest intracellular Lp(a) assembly from apo(a) and newly synthesized LDL.

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Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.