Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/31330
Title: Apolipoprotein(a) Kinetics in Statin-Treated Patients With Elevated Plasma Lipoprotein(a) Concentration
Contributor(s): Ma, Louis (author); Chan, Dick C (author); Ooi, Esther M M (author); Marcovina, Santica M (author); Barrett, P Hugh R  (author)orcid ; Watts, Gerald F (author)
Publication Date: 2019-12
Open Access: Yes
DOI: 10.1210/jc.2019-01382Open Access Link
Handle Link: https://hdl.handle.net/1959.11/31330
Abstract: 

Background: Lipoprotein(a) [Lp(a)] is a low-density lipoprotein‒like particle containing apolipoprotein(a) [apo(a)]. Patients with elevated Lp(a), even when treated with statins, are at increased risk of cardiovascular disease. We investigated the kinetic basis for elevated Lp(a) in these patients.

Objectives: Apo(a) production rate (PR) and fractional catabolic rate (FCR) were compared between statin-treated patients with and without elevated Lp(a).

Methods: The kinetics of apo(a) were investigated in 14 patients with elevated Lp(a) and 15 patients with normal Lp(a) levels matched for age, sex, and body mass index using stable isotope techniques and compartmental modeling. All 29 patients were on background statin treatment. Plasma apo(a) concentration was measured using liquid chromatography–mass spectrometry.

Results: The plasma concentration and PR of apo(a) were significantly higher in patients with elevated Lp(a) than in patients with normal Lp(a) concentration (all P < 0.01). The FCR of apo(a) was not significantly different between the groups. In univariate analysis, plasma concentration of apo(a) was significantly associated with apo(a) PR in both patient groups (r = 0.699 and r = 0.949, respectively; all P < 0.01). There was no significant association between plasma apo(a) concentration and FCR in either of the groups (r = 0.160 and r = −0.137, respectively).

Conclusion: Elevated plasma Lp(a) concentration is a consequence of increased hepatic production of Lp(a) particles in these patients. Our findings provide a kinetic rationale for the use of therapies that target the synthesis of apo(a) and production of Lp(a) particles in patients with elevated Lp(a).

Publication Type: Journal Article
Source of Publication: Journal of Clinical Endocrinology and Metabolism, 104(12), p. 6247-6255
Publisher: Oxford University Press
Place of Publication: United States of America
ISSN: 1945-7197
0021-972X
Fields of Research (FoR) 2020: 320101 Cardiology (incl. cardiovascular diseases)
320803 Systems physiology
Socio-Economic Objective (SEO) 2020: 200105 Treatment of human diseases and conditions
Peer Reviewed: Yes
HERDC Category Description: C1 Refereed Article in a Scholarly Journal
Publisher/associated links: https://research-repository.uwa.edu.au/en/publications/fae54593-5651-4ee5-bc0d-5c6b6a8e830c
Appears in Collections:Journal Article

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