The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Catabolism of lipoprotein(a) in familial hypercholesterolaemic subjects
Abstract
The in vivo turnover of autologous lipoprotein(a) (Lp(a)) was studied in four heterozygous familial hypercholesterolaemic (FH) subjects and four subjects who were hyperlipidaemic but not FH. Each of the FH subjects exhibited a much lower fractional catabolic rate (FCR) for LDL than each of the non-FH subjects. Lp(a) was purified by sequential density gradient centrifugations and was radio-iodinated. The labelled Lp(a) ran as a single band on electrophoresis in gradient polyacrylamide gels. Less than 5% of the label was in lipid, with about 40% of the remainder on apolipoprotein B (apo B) and 60% on apo(a). Labelled and unlabelled Lp(a) competed equally poorly with LDL for binding to LDL receptors on cultured fibroblasts. The FCR of Lp(a), calculated from the decay of the specific radioactivity of the Lp(a) isolated from the daily blood samples, was the same in FH subjects as in non-FH subjects. There was no consistent relationship between Lp(a) FCR and the plasma Lp(a) concentration or between FCR and the Lp(a) phenotype, at least within this sample of subjects. There was a strong association between Lp(a) concentration and production rate, with values for non-FH and FH subjects falling on the same line. The rate of decline of radioactivity in whole plasma was consistently slower than the fall in specific radioactivity of the isolated Lp(a). This difference was more marked in FH subjects than in non-FH subjects and resulted from the accumulation of radioactivity derived from…
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Other studies in humans did not find a defect in Lp(a) catabolism for patients with Familial Hypercholesterolemia.
“other studies did not37-39.”
From Functional interrogation of cellular Lp(a) uptake by genome-scale CRISPR screening (2025) · cites this paper as [38]
Citations
Cites
cDNA sequence of human apolipoprotein(a) is homologous to plasminogen
McLean, J. W., Tomlinson, J. E., Kuang, W.-J., Eaton, D. L., Chen, E. Y., Fless, G. M., Scanu, A. M., & Lawn, R. M. (1987) · Nature · doi:10.1038/330132a0 · Cited by 1,886
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The effect of nicotinic acid and acipimox on lipoprotein(a) concentration and turnover
Seed, M., O'Connor, B., Perombelon, N., O'Donnell, M., Reaveley, D., & Knight, B. L. (1993) · Atherosclerosis · doi:10.1016/0021-9150(93)90102-z · Cited by 97
Self-citationFunctional interrogation of cellular Lp(a) uptake by genome-scale CRISPR screening
Khan, T. G., Bragazzi Cunha, J., Raut, C., Burroughs, M., Vyas, H. S., Leix, K., Goonewardena, S. N., Smrcka, A. V., Speliotes, E. K., & Emmer, B. T. (2025) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2025.119174 · Cited by 6
Metadata
- Authors
- Knight, B. L., Perombelon, Y. F. N., Soutar, A. K., Wade, D. P., & Seed, M.
- Venue
- Atherosclerosis
- Publisher
- Elsevier BV
- Published
- 1991-04
- Volume
- 87
- Issue
- 2-3
- Pages
- 227-237
- ISSN
- 0021-9150
- Cited by
- 78
- References
- 1
- Language
- en
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