Testosterone-induced suppression of lipoprotein(a) in normal men; relation to basal lipoprotein(a) level

dc.contributor.authorBremner, William J.en_US
dc.contributor.authorBagatell, Carrie J.en_US
dc.contributor.authorMarcovina, Santica M.en_US
dc.contributor.authorLippi, Giuseppeen_US
dc.date.accessioned2008-10-17T20:43:09Z
dc.date.available2008-10-17T20:43:09Z
dc.date.issued1996-04-26en_US
dc.description.abstractThe concentration of lipoprotein(a) [Lp(a)] in human plasma is largely genetically determined and is inversely correlated to the size of apolipoprotein(a) [apo(a)]. Additionally, Lp(a) values are relatively stable within individuals and are only marginally susceptible to therapeutic treatment. The aim of our study was to evaluate the effect of exogenous testosterone on plasma Lp(a) concentration. The study was carried out on 19 healthy men who were receiving weekly intramuscular injections of 200 mg testosterone enanthate. Lp(a) values were determined at multiple time-points by a double monoclonal antibody-based enzyme immunoassay. This method is not sensitive to variation in Lp(a) size and the values are expressed in nmol/l. Apo(a) size isoforms were determined by agarose gel electrophoresis followed by immunoblotting. No correlation was found between the baseline Lp(a) values and the baseline values of testosterone or estradiol. The Lp(a) response to testosterone treatment varied widely among subjects and was dependent upon the pretreatment Lp(a) concentration. For 10 subjects with low Lp(a) values (< 25 nmol/l), no significant decrease in Lp(a) was observed while, for the nine individuals with Lp(a) values > 25 nmol/l, there was a significant and consistent reduction in Lp(a) ranging from 25 to 59%. Lp(a) levels returned to baseline values following cessation of testosterone administration. Apo(a) size polymorphism did not appear to play a role in the determination of Lp(a) response to testosterone.en_US
dc.identifier.citationAtherosclerosis. 1996 Apr 26;122(1):89-95en_US
dc.identifier.urihttp://hdl.handle.net/1773/4461
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.subjectmale contraceptionen_US
dc.subjectandrologyen_US
dc.subject5-alpha reductase inhibitorsen_US
dc.subjecttestosteroneen_US
dc.subjectgonadotropinsen_US
dc.subjectcolchicineen_US
dc.subjectklinefelter's syndromeen_US
dc.subjectreifenstein's syndromeen_US
dc.subjectspermatogenesisen_US
dc.subject.meshMaleen_US
dc.subject.meshLipoprotein(a), antagonists & inhibitors, blood, geneticsen_US
dc.subject.meshReference Valuesen_US
dc.subject.meshResearch Support, U.S. Gov't, P.H.S.en_US
dc.subject.meshPhenotypeen_US
dc.subject.meshTestosterone, pharmacologyen_US
dc.subject.meshResearch Support, U.S. Gov't, Non-P.H.S.en_US
dc.subject.meshHumansen_US
dc.subject.meshIsomerismen_US
dc.subject.meshAdulten_US
dc.titleTestosterone-induced suppression of lipoprotein(a) in normal men; relation to basal lipoprotein(a) levelen_US
dc.typeArticleen_US

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