Detection and prevalence of monoclonal gammopathy of undetermined significance: a study utilizing mass spectrometry-based monoclonal immunoglobulin rapid accurate mass measurement.


Journal

Blood cancer journal
ISSN: 2044-5385
Titre abrégé: Blood Cancer J
Pays: United States
ID NLM: 101568469

Informations de publication

Date de publication:
13 12 2019
Historique:
received: 04 06 2019
accepted: 20 11 2019
revised: 18 11 2019
entrez: 15 12 2019
pubmed: 15 12 2019
medline: 16 5 2020
Statut: epublish

Résumé

High-sensitivity mass spectrometry assays are available to detect monoclonal immunoglobulins. To better assess the prevalence of monoclonal gammopathy of undetermined significance (MGUS), we identified 300 patients diagnosed with MGUS or related gammopathy who had a prior negative work-up for monoclonal proteins as part of the Olmsted County MGUS screening study. Two mass spectrometry-based detection methods (matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) and monoclonal immunoglobulin rapid accurate mass measurements (miRAMM) along with traditional immunofixation were performed on the Olmsted baseline and MGUS diagnostics serum samples. Among the 226 patients considered negative for MGUS based on protein electrophoresis and serum-free light-chain assay, a monoclonal protein could be detected at baseline in 24 patients (10.6%) by immunofixation, 113 patients (50%) by MADLI-TOF mass spectrometry, and 149 patients (65.9%) by miRAMM mass spectrometry. In addition, using miRAMM, some patients demonstrated an oligoclonal to monoclonal transition giving insight into the origin of MGUS. Using the sensitive miRAMM, MGUS is present in 887 of 17,367 persons from the Olmsted County cohort, translating into a prevalence of 5.1% among persons 50 years of age and older. This represents the most accurate prevalence estimate of MGUS thus far.

Identifiants

pubmed: 31836698
doi: 10.1038/s41408-019-0263-z
pii: 10.1038/s41408-019-0263-z
pmc: PMC6910906
doi:

Substances chimiques

Biomarkers, Tumor 0
Immunoglobulin Light Chains 0
Myeloma Proteins 0
multiple myeloma M-proteins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

102

Subventions

Organisme : NCI NIH HHS
ID : R01 CA168762
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA186781
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA107476
Pays : United States

Références

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Auteurs

David Murray (D)

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55906, USA. Murray.david@mayo.edu.

Shaji K Kumar (SK)

Division of Hematology, Mayo Clinic, Rochester, MN, 55906, USA.

Robert A Kyle (RA)

Division of Hematology, Mayo Clinic, Rochester, MN, 55906, USA.

Angela Dispenzieri (A)

Division of Hematology, Mayo Clinic, Rochester, MN, 55906, USA.

Surendra Dasari (S)

Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55906, USA.

Dirk R Larson (DR)

Division of Biostatistics, Mayo Clinic, Rochester, MN, 55906, USA.

Celine Vachon (C)

Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55906, USA.

James R Cerhan (JR)

Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55906, USA.

S Vincent Rajkumar (SV)

Division of Hematology, Mayo Clinic, Rochester, MN, 55906, USA.

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Classifications MeSH