Maternal herpesvirus infections and risk of acute lymphoblastic leukemia in the offspring

被引:66
作者
Lehtinen, M
Koskela, P
Ögmundsdottir, HM
Bloigu, A
Dillner, J
Gudnadottir, M
Hakulinen, T
Kjartansdottir, A
Kvarnung, M
Pukkala, E
Tulinius, H
Lehtinen, T
机构
[1] Natl Publ Hlth Inst, Dept Infect Dis Epidemiol, SF-00300 Helsinki, Finland
[2] Natl Publ Hlth Inst, Dept Microbiol, Oulu, Finland
[3] Iceland Canc Soc, Iceland Canc Registry, Reykjavik, Iceland
[4] Univ Iceland, Sch Med, Reykjavik, Iceland
[5] Malmo Cent Hosp, Dept Clin Microbiol, Malmo, Sweden
[6] Univ Helsinki, Dept Publ Hlth, Helsinki, Finland
[7] Karolinska Inst, Ctr Microbiol & Tumor Biol, Stockholm, Sweden
[8] Finnish Canc Registry, FIN-00170 Helsinki, Finland
[9] Univ Tampere, Sch Med, FIN-33101 Tampere, Finland
关键词
antibodies; child; Epstein-Barr virus infections; herpesvirus; 4; human; leukemia; lymphocytic; acute; longitudinal studies; prospective studies;
D O I
10.1093/aje/kwg137
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
A critical role for infection in the etiology of childhood leukemia has repeatedly been suggested. The authors undertook a case-control study nested within national maternity cohorts with altogether 7 million years of follow-up to assess the relative role of three maternal herpesvirus infections in childhood acute lymphoblastic leukemia (ALL). Offspring of 550,000 mothers in Finland and Iceland formed the joint study cohort that was followed up for cancer in the offspring before age 15 years during 1975-1997 through national cancer registries. For each index mother-case pair, three or four matched control mother-control pairs were identified from national population registers. First-trimester sera were retrieved from mothers of 342 ALL and 61 other leukemia cases and from 1,216 control mothers and were tested for antibodies to cytomegalovirus, Epstein-Barr virus (EBV), and human herpesvirus 6. Serum EBV DNA was also analyzed. Conditional logistic regression-based estimates of relative risk (odds ratio) adjusted for birth order and sibship size, and population attributable fractions, were calculated. Only EBV immunoglobulin M positivity in EBV-immunoglobulin-G-positive mothers was associated with a highly significant increased risk of ALL in the offspring (adjusted odds ratio=2.9, 95% confidence interval: 1.5, 5.8). Results indicate that reactivation of maternal EBV infection is probably associated with childhood ALL.
引用
收藏
页码:207 / 213
页数:7
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