Why the study?
Does the latex immunoturbidimetric assay kit provide reliable measurement of serum Lp(a) compared to ELISA?
Does the latex immunoturbidimetric assay kit provide reliable measurement of serum Lp(a) compared to ELISA?
The latex immunoturbidimetric assay kit on COBAS MIRA provides a reliable and reproducible method for measuring serum Lp(a) with excellent correlation to ELISA.
We had an opportunity to test a reagent kit for serum lipoprotein (a) [Lp(a)] assay, which was based on the latex immunoturbidimetric assay method, and applied it to COBAS MIRA (Roche). Reproducibility of the assay procedure was 0.92-4.0% CV of three samples which contained 12.58-60.4 mg/dl of Lp(a). Minimum detectable concentration was 1.5-2.0 mg/dl. It was confirmed that interference of co-existing substances, i.e. hemoglobin, bilirubin, and intralipid, was negligible. No cross reactivity was seen with plasminogen. Correlation with a ELISA method was excellent. Frequency distribution of Lp(a) in healthy Japanese was similar to that found in white population.
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Fujita et al. (1994) studied this question.
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