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- Kristinsson, Sigurður Yngvi
(author)
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Population-based studies on familiality and prognosis in patients with monoclonal gammopathies
- 2009
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Doctoral thesis (other academic/artistic)abstract
- Monoclonal gammopathies constitute a group of diseases which have in common an overproduction of monoclonal immunoglobulins, M-proteins. Clues to their etiology have been found in studies showing familial aggregation of these diseases. We included 2,144 patients with lymphoplasmacytic lymphoma/Waldenström s macroglobulinemia (LPL/WM) and 4,458 patients with monoclonal gammopathy of undetermined significance (MGUS), their 6,177 and 14,621 first-degree relatives respectively, and controls and their relatives. We found first-degree relatives of LPL/WM, compared to first-degree relatives of controls, to have 20-fold (95% confidence interval (CI): 4.1-98), 3.0-fold (2.0-4.4), 3.4-fold (1.7-6.6), and 5.0-fold (1.3-19) increased risks of developing LPL/WM, non-Hodgkin lymphoma (NHL), chronic lymphocytic leukemia (CLL), and MGUS, respectively. First-degree relatives of MGUS patients had increased risks of MGUS (hazard ratio (HR)=2.8; 95% CI 1.4-5.6), multiple myeloma (MM) (2.9; 1.9-4.3), LPL/WM (4.0; 1.5-11), and CLL (2.0; 1.2-2.3). These findings support shared common susceptibility genes that predispose to a variety of lymphoproliferative disorders. We included 4,259 MGUS patients and compared their survival to that of the general population by computing relative survival ratios (RSRs). One-, 5-, 10-, and 15-year RSRs were 0.98 (95% CI 0.97-0.99), 0.93 (0.91-0.95), 0.82 (0.79-0.84), and 0.70 (0.64-0.76), respectively. Younger age at MGUS diagnosis was associated with a significantly lower excess mortality compared to older age (p<0.001). The excess mortality among MGUS patients increased with longer follow-up (p<0.0001). IgM (versus IgG/A) MGUS was associated with a superior survival (p=0.038). We also compared causes of death with 16,151 matched controls and found MGUS patients to have an increased risk of dying from both malignant transformation and non-malignant causes. Our findings are of importance in the understanding and clinical management of MGUS. The underlying mechanisms of our findings may be causally related to the MGUS, but may also be explained by an underlying disease that led to the detection of MGUS. We conducted a study including 14,381 MM patients diagnosed in Sweden 1973-2003 to define survival patterns among MM patients. One-year survival improved (p<0.001) over time in all age groups. Improvement in 5-year (p<0.001) and 10-year (p<0.001) RSR was, however restricted to patients <70 years and <60 years, respectively. High dose melphalan with subsequent autologous stem cell support, thalidomide, and a continuous improvement in supportive care measures are probably the most important factors contributing to this finding. We also assessed the impact of socioeconomic status (SES) on survival in 14,744 patients with MM. Overall, higher white-collar workers had a lower mortality than other SES groups (p<0.005). No difference was observed in the first two calendar periods. However, in 1990-1999, self-employed (HR=1.18; 1.02-1.37), blue-collar workers (1.18; 1.04-1.32), and retired (1.45; 1.16-1.80) had a higher mortality compared to higher white-collar workers. In 2000-2005, blue-collar workers had a higher mortality (1.31; 1.07-1.60) compared to higher white-collar workers. Differences in co-morbidity, management and life-style, are likely factors to explain these findings. We assessed the risks of venous and arterial thrombosis in 19,391 MM and 5,395 MGUS patients compared to 76,415 and 20,761 matched controls. At 1, 5 and 10 years after MM diagnosis, there was an increased risk for venous thrombosis with HR=7.9 (6.5-9.6), 4.5 (4.0-5.1), and 3.9 (3.5-4.4), respectively. The corresponding HRs for arterial thrombosis were 2.0 (1.8-2.2), 1.5 (1.4-1.6), and 1.4 (1.4-1.5). At 1, 5 and 10 years after MGUS diagnosis, we found a 3.3-fold (2.2-5.0), 2.0-fold (1.6-2.5), and 2.0-fold (1.7-2.4) increased risk of venous thrombosis. The corresponding risks for arterial thrombosis were 1.4 (1.2-1.7), 1.2 (1.1-1.3), and 1.2 (1.1-1.3). IgG/IgA (but not IgM) MGUS patients had an increased risk for venous and arterial thrombosis. These findings are of relevance for future studies and for the improvement of thrombosis prophylaxis strategies.
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| 4. |
- Sigurbergsdottir, Adalbjorg Yr, et al.
(author)
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Disease associations with monoclonal gammopathy of undetermined significance can only be evaluated using screened cohorts: results from the population-based iStopMM study
- 2023
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In: REVISTA CHILENA DE LITERATURA. - 0718-2295. ; :108, s. 3392-3398
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Journal article (peer-reviewed)abstract
- Monoclonal gammopathy of undetermined significance (MGUS) is an asymptomatic precursor condition that precedes multiple myeloma and related disorders but has also been associated with other medical conditions. Since systematic screening is not recommended, MGUS is typically diagnosed due to underlying diseases and most cases are not diagnosed. Most previous studies on MGUS disease associations have been based on clinical cohorts, possibly resulting in selection bias. Here we estimate this selection bias by comparing clinically diagnosed and screened individuals with MGUS with re-gards to demographics, laboratory features, and comorbidities. A total of 75,422 participants in the Iceland Screens, Treats, or Prevents Multiple Myeloma (iStopMM) study were screened for MGUS by serum protein electrophoresis, immunofixation and free light chain assay (clinicaltrials gov. Identifier: NCT03327597). We identified 3,352 individuals with MGUS, whereof 240 had previously been clinically diagnosed (clinical MGUS), and crosslinked our data with large, nationwide registries for information on comorbidities. Those with clinical MGUS were more likely to have at least one comorbidity (odds ratio=2.24; 95% confidence interval: 1.30-4.19), and on average had more comorbidities than the screened MGUS group (3.23 vs. 2.36, mean difference 0.68; 95% confidence interval: 0.46-0.90). They were also more likely to have rheumato-logical disease, neurological disease, chronic kidney disease, liver disease, heart failure, or endocrine disorders. These findings indicate that individuals with clinical MGUS have more comorbidities than the general MGUS population and that previous studies have been affected by significant selection bias. Our findings highlight the importance of screening data when studying biological and epidemiological implications of MGUS.
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