TY - JOUR
T1 - Congenital abnormalities and acute leukemia among children with Down syndrome
T2 - A children's oncology group study
AU - Linabery, Amy M.
AU - Blair, Cindy K.
AU - Gamis, Alan S.
AU - Olshan, Andrew F.
AU - Heerema, Nyla A.
AU - Ross, Julie A.
PY - 2008/10
Y1 - 2008/10
N2 - Children with Down syndrome, due to their heightened risk of leukemia and increased prevalence of congenital abnormalities, comprise a valuable population in which to study etiology. A Children's Oncology Group study investigated the causes of childhood leukemia in children with Down syndrome diagnosed at ages 0 to 19 years during the period 1997-2002. Telephone interviews were completed with mothers of 158 cases [n = 97 acute lymphoblastic leukemia (ALL) and n = 61 acute myeloid leukemia (AML)] and 173 controls. Odds ratios (OR) and 95% confidence intervals (95% CI) were computed via unconditional logistic regression to evaluate the association between congenital abnormalities and acute leukemia overall, and ALL and AML analyzed separately. The results do not provide evidence for an association among the index children (OR Combined, 0.74; 95% CI, 0.45-1.23; ORALL, 0.67; 95% CI, 0.38-1.20; ORAML,1.03; 95% CI, 0.49-2.16) or their siblings (OR Combined, 1.23; 95% CI, 0.71-2.13; ORALL, 1.12; 95% CI, 0.60-2.09; ORAML, 1.60; 95% CI, 0.66-3.86), suggesting congenital malformations do not confer additional risk of leukemia beyond the risk attributable to trisomy 21 in this population.
AB - Children with Down syndrome, due to their heightened risk of leukemia and increased prevalence of congenital abnormalities, comprise a valuable population in which to study etiology. A Children's Oncology Group study investigated the causes of childhood leukemia in children with Down syndrome diagnosed at ages 0 to 19 years during the period 1997-2002. Telephone interviews were completed with mothers of 158 cases [n = 97 acute lymphoblastic leukemia (ALL) and n = 61 acute myeloid leukemia (AML)] and 173 controls. Odds ratios (OR) and 95% confidence intervals (95% CI) were computed via unconditional logistic regression to evaluate the association between congenital abnormalities and acute leukemia overall, and ALL and AML analyzed separately. The results do not provide evidence for an association among the index children (OR Combined, 0.74; 95% CI, 0.45-1.23; ORALL, 0.67; 95% CI, 0.38-1.20; ORAML,1.03; 95% CI, 0.49-2.16) or their siblings (OR Combined, 1.23; 95% CI, 0.71-2.13; ORALL, 1.12; 95% CI, 0.60-2.09; ORAML, 1.60; 95% CI, 0.66-3.86), suggesting congenital malformations do not confer additional risk of leukemia beyond the risk attributable to trisomy 21 in this population.
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U2 - 10.1158/1055-9965.EPI-08-0284
DO - 10.1158/1055-9965.EPI-08-0284
M3 - Article
C2 - 18829445
AN - SCOPUS:54249124252
SN - 1055-9965
VL - 17
SP - 2572
EP - 2577
JO - Cancer Epidemiology Biomarkers and Prevention
JF - Cancer Epidemiology Biomarkers and Prevention
IS - 10
ER -