A screening method for abnormally high lipoprotein(a) concentrations by agarose lipoprotein electrophoresis

A routine electrophoretic method detecting plasma lipoprotein(a) (Lp(a)) is described. Plasma lipoproteins were electrophoresed using an agarose gel film containing cations which retard migration of beta-, prebeta- and alpha-bands. When present, the Lp(a)-band was detected between prebeta- and alpha-bands. This extra-band lipoprotein has been demonstrated to be Lp(a), by an immunofixation technique using anti-Lp(a) antibodies. This original procedure allows a distinct separation of Lp(a) from prebeta even after samples have been stored at 4 degrees C for several days, or in cases of hyperlipemic samples with increased prebeta lipoproteins. The reliability of this detection test has been tested in comparison with an Lp(a) electroimmunoassay. Both these techniques have been performed on 719 randomly selected subjects. With electrophoresis, the Lp(a)-positive subjects accounted for 34.2% of the subjects and although this method does not distinguish between different levels of positivity (depending on the sample), the presence of Lp(a)-band was always perceptible at concentrations that belong to the upper 15th percentile of values as determined by electroimmunodiffusion; inversely, all Lp(a)-positive plasma was measurable. In consequence, since it is reliable and relatively inexpensive, this detection test on modified agarose gel appears very useful for revealing the presence of abnormally high values of Lp(a) in populations.