Disparities in the prevalence, pathogenesis and progression of monoclonal gammopathy of undetermined significance and multiple myeloma between blacks and whites
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作者:
Greenberg, A. J.
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Mayo Clin & Mayo Fdn, Dept Hlth Sci Res, Div Epidemiol, Rochester, MN 55905 USAMayo Clin, Dept Internal Med, Div Hematol, Rochester, MN 55905 USA
Greenberg, A. J.
[2
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Vachon, C. M.
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Mayo Clin & Mayo Fdn, Dept Hlth Sci Res, Div Epidemiol, Rochester, MN 55905 USAMayo Clin, Dept Internal Med, Div Hematol, Rochester, MN 55905 USA
Vachon, C. M.
[2
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Rajkumar, S. V.
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Mayo Clin, Dept Internal Med, Div Hematol, Rochester, MN 55905 USAMayo Clin, Dept Internal Med, Div Hematol, Rochester, MN 55905 USA
Rajkumar, S. V.
[1
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机构:
[1] Mayo Clin, Dept Internal Med, Div Hematol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Hlth Sci Res, Div Epidemiol, Rochester, MN 55905 USA
There is marked racial disparity in the incidence of monoclonal gammopathy of undetermined significance (MGUS) and multiple myeloma, with a two to threefold increased risk in blacks compared with whites. The increased risk has been seen both in Africans and African Americans. Similarly, an increased risk of monoclonal gammopathies in blacks compared with whites has been noted after adjusting for socioeconomic and other risk factors, suggesting a genetic predisposition. The higher risk of multiple myeloma in blacks is likely a result of the higher prevalence of the premalignant MGUS stage; there are no data to suggest that blacks have a higher progression rate of MGUS to myeloma. Studies are emerging that suggest the baseline cytogenetic characteristics, and progression may differ by race. In contrast, to the increased risk noted in blacks, studies suggest that the risk may be lower in certain racial and ethnic groups, notably persons from Japan and Mexico. We review the literature on racial disparity in the prevalence, pathogenesis and progression of MGUS and multiple myeloma between blacks and whites. We also discuss future directions for research that could inform management of these conditions and positively influence patient outcomes. Leukemia (2012) 26, 609-614; doi:10.1038/leu. 2011.368; published online 23 December 2011
机构:
Univ N Carolina, Dept Med, Div Hematol & Oncol, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Med, Div Hematol & Oncol, Chapel Hill, NC 27599 USA
Guerard, Emily J.
Tuchman, Sascha A.
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Duke Canc Inst, Div Cellular Therapy & Hematol Malignancies, Durham, NC 27710 USAUniv N Carolina, Dept Med, Div Hematol & Oncol, Chapel Hill, NC 27599 USA