Use of Nonclonal Serum Immunoglobulin Free Light Chains to Predict Overall Survival in the General Population

Use of Nonclonal Serum Immunoglobulin Free Light Chains to Predict Overall Survival in the General Population
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DOI:
10.1016/j.mayocp.2012.03.009
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发表时间:
2012-06-01
影响因子:
8.9
通讯作者:
Rajkumar, S. Vincent
Rajkumar, S. Vincent
中科院分区:
医学2区
文献类型:
--
作者:
Dispenzieri, Angela;Katzmann, Jerry A.;Rajkumar, S. Vincent

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Objective: To determine whether the free light chain (FLC) assay provides prognostic information relevant to the general population.Methods: After excluding persons with a known plasma cell disorder, we studied 15,859 Olmsted County, Minnesota, residents 50 years or older in whom unmasked data and samples for FLC testing were available. Baseline information was obtained between March 13, 1995, and November 21, 2003, and follow-up status and cause of death were identified through June 30, 2009. The kappa and lambda FLC sum (Sigma FLC) was evaluated for its ability to predict overall survival. Specific causes of death were also investigated.Results: In 158,003 person-years of follow-up, 4348 individuals died. A high Sigma FLC was significantly predictive of worse overall survival; the risk ratio for death for those with the highest decile of Sigma FLC (ie, >= 4.72 mg/dL) was 4.4 (95% confidence interval, 4.1-4.7) relative to the remaining study participants. Multivariate analyses demonstrated that this excess risk of death was independent of age, sex, and renal insufficiency, with a corrected risk ratio of 2.1 (95% confidence interval, 1.9-2.2). The increased mortality was not restricted to any particular cause of death because the observed-to-expected risk of death from most causes was significantly higher among those individuals with an antecedent Sigma FLC of 4.72 mg/dL or higher, which is near the upper limit of normal for the test.Conclusion: A nonclonal elevation of Sigma FLC is a significant predictor of worse overall survival in the general population of persons without plasma cell disorders. (C) 2012 Mayo Foundation for Medical Education and Research Mayo Clin Proc. 2012; 87(6): 517-523