A rapid electrophoretic method for the detection of serum Lp(a) lipoprotein

A rapid electrophoretic method detecting serum lipoprotein(a) (Lp(a)) was described. When serum lipoproteins were electrophoresed using an agarose gel film containing 0.6% agarose and 3% sucrose, a distinct extra-band was frequently detected between beta- and prebeta-bands. This lipoprotein band was...

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Published inClinica Chimica Acta Vol. 185; no. 2; pp. 147 - 155
Main Authors Kawakami, Keiko, Tsukada, Atsuko, Okubo, Minoru, Tsukada, Toshihiko, Kobayashi, Tetsuro, Yamada, Nobuhiro, Murase, Toshio
Format Journal Article
LanguageEnglish
Published Shannon Elsevier B.V 01.11.1989
Elsevier BV
Elsevier
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ISSN0009-8981
1873-3492
DOI10.1016/0009-8981(89)90037-5

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Summary:A rapid electrophoretic method detecting serum lipoprotein(a) (Lp(a)) was described. When serum lipoproteins were electrophoresed using an agarose gel film containing 0.6% agarose and 3% sucrose, a distinct extra-band was frequently detected between beta- and prebeta-bands. This lipoprotein band was identified as Lp(a) by immunoblotting technique using anti-Lp(a) serum. Using this electrophoretic method, we studied 1353 subjects with a variety of diseases. The Lp(a)-positive subjects accounted for 8.4% of all. Neither sex nor age influenced the frequency of Lp(a) positivity. Frequencies of definite myocardial infarction in Lp(a)-positive subjects did not differ significantly from those in Lp(a)-negative ones. Those of cerebral infarction in Lp(a)-positive subjects were significantly higher than those in Lp(a)-negative ones. An electrophoretic method described herein is very useful for the rapid detection and screening of Lp(a), and hence for large-scale clinical studies of atherosclerotic risk assessment.
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ISSN:0009-8981
1873-3492
DOI:10.1016/0009-8981(89)90037-5