Evidence of population mixing based on the geographical distribution of childhood leukemia in Ohio

被引:11
作者
Clark, Brenda R.
Ferketich, Amy K.
Fisher, James L.
Ruymann, Frederick B.
Harris, Randall E.
Wilkins, John R., III
机构
[1] Ohio State Univ, Sch Publ Hlth, Div Hlth Behav & Hlth Promot, Columbus, OH 43210 USA
[2] Ohio State Univ, Sch Publ Hlth, Div Epidemiol, Columbus, OH 43210 USA
[3] Ohio State Univ, Ctr Comprehens Canc, Arthur G James Canc Hosp, Columbus, OH 43210 USA
[4] Ohio State Univ, Ctr Comprehens Canc, Richard J Solove Res Inst, Columbus, OH 43210 USA
[5] Columbus Childrens Hosp, Div Pediat Hematol Oncol, Columbus, OH USA
关键词
acute lymphoblastic leukemia; acute monocytic leukemia; acute myelogenous leukemia; cancer cluster; pediatric leukemia; population mixing;
D O I
10.1002/pbc.21181
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. This ecologic study examined the geographic distribution of childhood leukemias in Ohio, 1996-2000, among children aged 0-19 for evidence that population mixing may be a factor. Procedure. (1) State incidence rates were compared to Surveillance, Epidemiology and End Results (SEER) rates for each year and for the 5-year period, 1996-2000; (2) incidence rates for each of Ohio's 88 counties were compared to statewide rates; and (3) county incidence rates were compared based on population density, population growth, and rural/urban locale. SEER*Stat version 5.0 was used to derive age-specific and 0-19 age-adjusted rates. Expected values, standardized incidence ratios (SIRs), and Poisson P-values were calculated with Excel using the indirect method of standardization. Results. Of the 585 cases, 73.3% were acute lymphocytic leukemia (ALL), 16.6% acute myelogenous leukemia (AML), 3.2% acute monocytic leukemia (AMoL), and 2.6% chronic myelogenous leukemia (CML). Rates for total leukemia burden were significantly below national levels for all races (P = 0.00001), likely due to poor ascertainment of cases. Yearly incidence rates for 19962000 were stable for ALL and AML; CML rates declined over the period. Based on 2000 Census and intercensal population estimates for 1996-2000, statistically higher rates for ALL were noted for counties experiencing > 10% population change 1990-2000 (P < 0.05), especially for ages 1-4 (P < 0.03) in counties with 10-20% growth. Counties 67.9-99.2% urban experienced fewer than expected cases of AML+AMoL (P < 0.06). Conclusion. Data support Kinlen's theory of population mixing and warrant further studies in Ohio, the US and other countries. Pediatr Blood Cancer 2007;49:797-802. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:797 / 802
页数:6
相关论文
共 49 条
[1]   Genes and cancer [J].
Birch, JM .
ARCHIVES OF DISEASE IN CHILDHOOD, 1999, 80 (01) :1-3
[2]   Space–time clustering patterns in childhood leukaemia support a role for infection [J].
J M Birch ;
F E Alexander ;
V Blair ;
O B Eden ;
G M Taylor ;
R J Q McNally .
British Journal of Cancer, 2000, 82 (9) :1571-1576
[3]   Environmental and genetic risk factors for childhood leukemia: Appraising the evidence [J].
Buffler, PA ;
Kwan, ML ;
Reynolds, P ;
Urayama, KY .
CANCER INVESTIGATION, 2005, 23 (01) :60-75
[4]   Childhood acute lymphoblastic leukemia in the age of genomics [J].
Carroll, WL ;
Bhojwani, D ;
Min, DJ ;
Moskowitz, N ;
Raetz, EA .
PEDIATRIC BLOOD & CANCER, 2006, 46 (05) :570-578
[5]   The onset of the excess of childhood cancer in Seascale, Cumbria [J].
Cartwright, RA ;
Dovey, GJ ;
Kane, EV ;
Gilman, EA .
JOURNAL OF PUBLIC HEALTH MEDICINE, 2001, 23 (04) :314-322
[6]   Quantifying the effect of population mixing on childhood leukaemia risk: the Seascale cluster [J].
Dickinson, HO ;
Parker, L .
BRITISH JOURNAL OF CANCER, 1999, 81 (01) :144-151
[7]   The causes of childhood leukaemia - Delayed exposure to infection may trigger leukaemia after prenatal damage to DNA [J].
Dickinson, HO .
BRITISH MEDICAL JOURNAL, 2005, 330 (7503) :1279-1280
[8]  
Fritz A., 2000, International classification of diseases for oncology
[9]   Day care in infancy and risk of childhood acute lymphoblastic leukaemia: findings from UK case-control study [J].
Gilham, C ;
Peto, J ;
Simpson, J ;
Roman, E ;
Eden, TOB ;
Greaves, MF ;
Alexander, FE .
BMJ-BRITISH MEDICAL JOURNAL, 2005, 330 (7503) :1294-1297
[10]   In utero origins of childhood leukaemia [J].
Greaves, M .
EARLY HUMAN DEVELOPMENT, 2005, 81 (01) :123-129