Baldursdóttir Theodóra Rún, Löve Þorvarður Jón, Gíslason Gauti Kjartan, Björkholm Magnus, Mellqvist Ulf-Henrik, Lund Sigrun Helga, Blimark Cecilie Hveding, Turesson Ingemar, Hultcrantz Malin, Landgren Ola, Kristinsson Sigurður Yngvi
Landspítali, National University Hospital, Reykjavík, Iceland.
Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
Eur J Haematol. 2021 Mar;106(3):380-388. doi: 10.1111/ejh.13563. Epub 2020 Dec 28.
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.
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).
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.
我们开展了一项基于人群的研究,纳入了1985年至2013年在瑞典诊断为意义未明的单克隆丙种球蛋白病(MGUS)的19303名个体,旨在确定自身免疫性疾病(一种已明确的MGUS风险因素)既往史是否为MGUS进展为多发性骨髓瘤(MM)或淋巴增殖性疾病(LP)的风险因素。利用瑞典全国患者登记系统,我们确定了MGUS诊断时伴有或不伴有自身免疫性疾病的MGUS病例,并估计了它们的进展风险。
共有5612例(29.1%)MGUS病例有自身免疫性疾病既往史。使用Cox比例风险模型,我们发现既往有自身免疫性疾病的MGUS病例进展为MM(风险比[HR]=0.83,95%置信区间[CI]0.73 - 0.94)和LP(HR = 0.84,95% CI 0.75 - 0.94)的风险显著低于(与无自身免疫性疾病的MGUS病例相比)。
在这项大型基于人群的研究中,自身免疫性疾病史与MGUS进展为MM/其他LP的风险降低相关。潜在的根本原因是由慢性抗原刺激引起的MGUS在生物学上不太可能发生触发进展的基因事件。我们的结果可能对MGUS及潜在自身免疫性疾病患者的临床咨询有影响。