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We studied the effect of freezing and thawing of serum on the determination of lipoprotein(a) Lp(a) with a commercial enzyme-linked immunosorbent assay (ELISA) and an immunoturbidimetric assay (ITA). Portions of sera from 11 apparently healthy persons and pooled sera, from an additional 10 subjects were frozen at either -20 or -70 degrees C and thawed at room temperature. Cycles of freezing and thawing were repeated during the experiments (1 month). Samples were assayed for Lp(a) after thawing. Pooled sera were subjected to quick freezing at -70 degrees C and thawing at room temperature in cycles. Results show a significant (P less than 0.05) decrease in Lp(a) concentration in sera subjected to freezing and thawing. Samples thawed from -20 degrees C gave concentrations by ELISA that were significantly lower than those of fresh samples after one freeze-thaw cycle. By ITA the decrease was significant only after two cycles. In specimens frozen at -70 degrees C, Lp(a) concentrations determined by ELISA decreased after two cycles, and by ITA after three freeze-thaw cycles. Serum samples subjected to quick freezing at -70 degrees C and thawing did not show significant decreases in Lp(a) immunoreactivity during four cycles. Immunoreactivity of Lp(a) in samples stored at 4 degrees C decreased after 6 days but fell faster in serum samples subjected to freezing and thawing before storage at 4 degrees C.
Sgoutas et al. (Tue,) studied this question.