Relevance of class, molecular weight and isoelectric point in predicting human light chain amyloidogenicity

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Abstract
The ability to predict the amyloidogenicity of certain light chains may facilitate an earlier diagnosis of AL amyloidosis and, possibly, lead to more effective treatment. Using current methods, available in clinical chemistry laboratories, we assessed the class, the relative molecular mass (Mr) and the isoelectric point of urinary monoclonal light chains from 35 patients with AL amyloidosis (A+) and 51 without amyloidosis (A-). The light chain class (LCC) was .lambda. in 77% and 45% of A+ and A- patients, respectively. Light chain fragments (LCF) with low Mr (12-18 .times. 103) were detected in the urine of 30/.35 A+ patients and in 15/.51 A- ones. The mean (SD) isoelectric point (pI) of A+ light chains was 4.8 (1.1) while in A- patients it was 6.2 (1.6). Univariate analysis showed significant differences between the two groups for the three parameters. Discriminant analysis gave a function which allowed a correct allocation of 81% of the cases between the two groups.