Title of article :
A novel four base-pair deletion within the A-GLOBin gene promoter associated with slight increase of A expression in adult
Author/Authors :
Huang، Xiao-Dong نويسنده , , Yang، Xuexian O. نويسنده , , Huang، Rui-Bin نويسنده , , Zhang، Hong-Yuan نويسنده , , Zhao، Hua-Lu نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2000
Abstract :
To assess the cancer risk of monoclonal gammopathy of undetermined significance (MGUS) we identified 1229 cases of MGUS in the period 1978 to 1993. Data on cancer occurrence in the MGUS cohort were obtained from the Danish Cancer Registry. The expected numbers of cancer cases were calculated from age-, sex-, county-, and period-specific cancer incidence rates. In the MGUS cohort 64 new cancers with a known association with M-components were diagnosed versus 5.0 expected giving a standardized incidence ratio (SIR) of 12.9 (95% confidence interval, 9.9-16.5). The relative risks of developing multiple myeloma (SIR 34.3), Waldenstr?mʹs macroglobulinemia (SIR 63.8), and non-Hodgkinʹs lymphoma (SIR 5.9) were significantly increased and independent of time passed from detection of the M-component. The relative risk of chronic lymphocytic leukemia was not significantly increased, SIR 2.7 (0.5-7.7). Among cancer sites without known association with M-components 141 cases were observed versus 94.6 expected giving a SIR of 1.5 (1.3-1.8). This enhanced risk was seen for several non-hematological cancer sites but for most cancer sites the risk was dependent on time passed from detection of the M-component, indicating a bias rather than a causal role of MGUS. Am. J. Hematol. 63:1-6, 2000.
Keywords :
hereditary persistance of fetal hemoglobin , human fetal globin gene , small deletion , promoter mutation
Journal title :
American Journal of Hematology
Journal title :
American Journal of Hematology