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Polyclonal serum free light chain elevation is associated with increased risk of monoclonal gammopathies
Monoclonal gammopathies (MG) constitute a spectrum of disorders starting from a monoclonal gammopathy of undetermined significance (MGUS) to active disease requiring therapy such as multiple myeloma. MG are characterized by proliferation of clonal plasma cells (PC) secreting a monoclonal protein eit...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525262/ https://www.ncbi.nlm.nih.gov/pubmed/31101803 http://dx.doi.org/10.1038/s41408-019-0210-z |
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author | Kumar, Shaji Larson, Dirk R. Dispenzieri, Angela Therneau, Terry M. Murray, David L. Leif Bergsagel, P. Kyle, Robert A. Vincent Rajkumar, S. |
author_facet | Kumar, Shaji Larson, Dirk R. Dispenzieri, Angela Therneau, Terry M. Murray, David L. Leif Bergsagel, P. Kyle, Robert A. Vincent Rajkumar, S. |
author_sort | Kumar, Shaji |
collection | PubMed |
description | Monoclonal gammopathies (MG) constitute a spectrum of disorders starting from a monoclonal gammopathy of undetermined significance (MGUS) to active disease requiring therapy such as multiple myeloma. MG are characterized by proliferation of clonal plasma cells (PC) secreting a monoclonal protein either as intact immunoglobulin or free kappa or lambda free light chains (FLC). We hypothesized that a polyclonal elevation of serum FLC may indicate an inflammatory state that precedes development of MG. We studied 15,630 individuals from Olmsted county, who did not have MGUS based on baseline screening studies. At a median follow-up of 18.1 years, 264 patients had developed a clonal PC disorder; 252 with MGUS, 1 with SMM, 8 with MM, and 3 with amyloidosis, translating to an annual incidence of development of a MG of 0.1%. We examined the baseline polyclonal ΣFLC (kappa + lambda FLC) from the initial screening and grouped them into deciles. The highest decile group had a 2.6-fold (95% CI; 1.8, 3.7) increase in the risk of developing a MG, P < 0.001. We demonstrate for the first time, the increased risk of developing MG in patients with elevated serum FLC, suggesting that an underlying inflammatory state may play an etiologic role. |
format | Online Article Text |
id | pubmed-6525262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65252622019-05-20 Polyclonal serum free light chain elevation is associated with increased risk of monoclonal gammopathies Kumar, Shaji Larson, Dirk R. Dispenzieri, Angela Therneau, Terry M. Murray, David L. Leif Bergsagel, P. Kyle, Robert A. Vincent Rajkumar, S. Blood Cancer J Article Monoclonal gammopathies (MG) constitute a spectrum of disorders starting from a monoclonal gammopathy of undetermined significance (MGUS) to active disease requiring therapy such as multiple myeloma. MG are characterized by proliferation of clonal plasma cells (PC) secreting a monoclonal protein either as intact immunoglobulin or free kappa or lambda free light chains (FLC). We hypothesized that a polyclonal elevation of serum FLC may indicate an inflammatory state that precedes development of MG. We studied 15,630 individuals from Olmsted county, who did not have MGUS based on baseline screening studies. At a median follow-up of 18.1 years, 264 patients had developed a clonal PC disorder; 252 with MGUS, 1 with SMM, 8 with MM, and 3 with amyloidosis, translating to an annual incidence of development of a MG of 0.1%. We examined the baseline polyclonal ΣFLC (kappa + lambda FLC) from the initial screening and grouped them into deciles. The highest decile group had a 2.6-fold (95% CI; 1.8, 3.7) increase in the risk of developing a MG, P < 0.001. We demonstrate for the first time, the increased risk of developing MG in patients with elevated serum FLC, suggesting that an underlying inflammatory state may play an etiologic role. Nature Publishing Group UK 2019-05-17 /pmc/articles/PMC6525262/ /pubmed/31101803 http://dx.doi.org/10.1038/s41408-019-0210-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kumar, Shaji Larson, Dirk R. Dispenzieri, Angela Therneau, Terry M. Murray, David L. Leif Bergsagel, P. Kyle, Robert A. Vincent Rajkumar, S. Polyclonal serum free light chain elevation is associated with increased risk of monoclonal gammopathies |
title | Polyclonal serum free light chain elevation is associated with increased risk of monoclonal gammopathies |
title_full | Polyclonal serum free light chain elevation is associated with increased risk of monoclonal gammopathies |
title_fullStr | Polyclonal serum free light chain elevation is associated with increased risk of monoclonal gammopathies |
title_full_unstemmed | Polyclonal serum free light chain elevation is associated with increased risk of monoclonal gammopathies |
title_short | Polyclonal serum free light chain elevation is associated with increased risk of monoclonal gammopathies |
title_sort | polyclonal serum free light chain elevation is associated with increased risk of monoclonal gammopathies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525262/ https://www.ncbi.nlm.nih.gov/pubmed/31101803 http://dx.doi.org/10.1038/s41408-019-0210-z |
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