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Blood, 1 November 2008, Vol. 112, No. 9, pp. 3582-3586.
Prepublished online as a Blood First Edition Paper on June 17, 2008; DOI 10.1182/blood-2008-04-151076.


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Submitted April 11, 2008
Accepted June 7, 2008

Deep vein thrombosis following monoclonal gammopathy of undetermined significance (MGUS) and multiple myeloma

Sigurdur Y Kristinsson, Thomas R Fears, Gloria Gridley, Ingemar Turesson, Ulf-Henrik Mellqvist, Magnus Bjorkholm, and Ola Landgren*

Department of Medicine, Division of Hematology, Karolinska University Hospital, Stockholm, Sweden
Division of Cancer Epidemiology and Genetics, NCI, NIH, Bethesda, MD, United States
Hematology Section, Malmo University Hospital, Malmo, Sweden
Department of Medicine, Section of Hematology and Coagulation, Sahlgrenska University Hospital, Gothenburg, Sweden

* Corresponding author; email: landgreo{at}mail.nih.gov.

Patients with multiple myeloma (MM) have an increased risk of deep venous thrombosis (DVT), particularly when treated with immunomodulatory drugs. Recently, two small hospital-based studies observed individuals with the MM precursor condition, monoclonal gammopathy of undetermined significance (MGUS), to be at increased risk of developing DVT. Among 4,196,197 veterans hospitalized at least once at U.S. Veterans Affairs hospitals, we identified a total of 2,374 MGUS and 6,192 MM patients. In the entire study population, there were 39,272 persons diagnosed with a DVT (crude incidence 0.9 per 1000 person-years). A total of 31 and 151 DVTs occurred among MGUS and MM patients, respectively (crude incidence 3.1 and 8.7 per 1000 person-years, respectively; p<0.01). Compared to the entire study population, the relative risk (RR) of DVT following a diagnosis of MGUS and MM was 3.3 (2.3-4.7) and 9.2 (7.9-10.8), respectively. The most prominent excess risk of DVT was found during the first year following diagnosis of MGUS (RR=8.4, 5.7-12.2) and MM (RR=11.6, 9.2-14.5). Among 229 MGUS cases (9.5%) that progressed to MM only one individual had a DVT diagnosis prior to transformation. Our findings suggest the operation of shared underlying mechanisms causing coagulation abnormalities among patients with MGUS and MM.


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