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Autoimmune disease is associated with a lower risk of progression in monoclonal gammopathy of undetermined significance.

Authors :
Baldursdóttir TR
Löve ÞJ
Gíslason GK
Björkholm M
Mellqvist UH
Lund SH
Blimark CH
Turesson I
Hultcrantz M
Landgren O
Kristinsson SY
Source :
European journal of haematology [Eur J Haematol] 2021 Mar; Vol. 106 (3), pp. 380-388. Date of Electronic Publication: 2020 Dec 28.
Publication Year :
2021

Abstract

Objectives and Methods: We conducted a population-based study including 19 303 individuals diagnosed with MGUS in Sweden from 1985 to 2013, with the aim to determine whether a prior history of autoimmune disease, a well-described risk factor for MGUS is a risk factor for progression of MGUS to multiple myeloma (MM) or lymphoproliferative diseases (LPs). Using the nationwide Swedish Patient registry, we identified MGUS cases with versus without an autoimmune disease present at the time of MGUS diagnosis and estimated their risk of progression.<br />Results: A total of 5612 (29.1%) MGUS cases had preceding autoimmune diseases. Using Cox proportional hazards models, we found the risk of progression from MGUS to MM (HR = 0.83, 95% CI 0.73-0.94) and LPs (HR = 0.84, 95% CI 0.75-0.94) to be significantly lower in MGUS cases with prior autoimmune disease (compared to MGUS cases without).<br />Conclusions: In this large population-based study, a history of autoimmune disease was associated with a reduced risk of progression from MGUS to MM/other LPs. Potential underlying reason is that MGUS caused by chronic antigen stimulation is biologically less likely to undergo the genetic events that trigger progression. Our results may have implications in clinical counseling for patients with MGUS and underlying autoimmune disease.<br /> (© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1600-0609
Volume :
106
Issue :
3
Database :
MEDLINE
Journal :
European journal of haematology
Publication Type :
Academic Journal
Accession number :
33295006
Full Text :
https://doi.org/10.1111/ejh.13563