A meta-analysis of the association between day-care attendance and childhood acute lymphoblastic leukaemia

Kevin Y Urayama, Patricia A Buffler, Emily R Gallagher, Julie M Ayoob, Xiaomei Ma, Kevin Y Urayama, Patricia A Buffler, Emily R Gallagher, Julie M Ayoob, Xiaomei Ma

Abstract

Background: Childhood acute lymphoblastic leukaemia (ALL) may be the result of a rare response to common infection(s) acquired by personal contact with infected individuals. A meta-analysis was conducted to examine the relationship between day-care attendance and risk of childhood ALL, specifically to address whether early-life exposure to infection is protective against ALL.

Methods: Searches of the PubMed database and bibliographies of publications on childhood leukaemia and infections were conducted. Observational studies of any size or location and published in English resulted in the inclusion of 14 case-control studies.

Results: The combined odds ratio (OR) based on the random effects model indicated that day-care attendance is associated with a reduced risk of ALL [OR = 0.76, 95% confidence interval (CI): 0.67, 0.87]. In subgroup analyses evaluating the influence of timing of exposure, a similarly reduced effect was observed for both day-care attendance occurring early in life (< or =2 years of age) (OR = 0.79, 95% CI: 0.65, 0.95) and day-care attendance with unspecified timing (anytime prior to diagnosis) (OR = 0.81, 95% CI: 0.70, 0.94). Similar findings were observed with seven studies in which common ALL were analysed separately. The reduced risk estimates persisted in sensitivity analyses that examined the sources of study heterogeneity.

Conclusions: This analysis provides strong support for an association between exposure to common infections in early childhood and a reduced risk of ALL. Implications of a 'hygiene'-related aetiology suggest that some form of prophylactic intervention in infancy may be possible.

Figures

Figure 1
Figure 1
Forest plot displaying ORs and 95% CIs of studies examining the association between day-care attendance and risk of childhood ALL. The risk estimates are plotted with boxes and the area of each box is inversely proportional to the variance of the estimated effect. The horizontal lines represent the 95% CIs of the risk estimate for each study. The solid vertical line at 1.0 represents a risk estimate of no effect. The dashed vertical line represents the combined risk estimate (OR = 0.76), and the width of the diamond is the 95% CI for this risk estimate (0.67–0.87).
Figure 2
Figure 2
Plot showing results of sensitivity meta-analyses evaluating the influence of potential biases within individual studies on combined risk estimates. RDD, random digit dialing.

References

    1. Greaves M. Infection, immune responses and the aetiology of childhood leukaemia. Nat Rev Cancer. 2006;6:193–203.
    1. McNally RJ, Eden TO. An infectious aetiology for childhood acute leukaemia: a review of the evidence. Br J Haematol. 2004;127:243–63.
    1. O'C;onnor SM, Boneva RS. Infectious etiologies of childhood leukemia: plausibility and challenges to proof. Environ Health Perspect. 2007;115:146–50.
    1. Kinlen L. Evidence for an infective cause of childhood leukaemia: comparison of a Scottish new town with nuclear reprocessing sites in Britain. Lancet. 1988;2:1323–27.
    1. Alexander FE, Boyle P, Carli PM, et al. Spatial clustering of childhood leukaemia: summary results from the EUROCLUS project. Br J Cancer. 1998;77:818–24.
    1. Kinlen L. Childhood leukaemia and ordnance factories in west Cumbria during the Second World War. Br J Cancer. 2006;95:102–6.
    1. Kinlen L, Doll R. Population mixing and childhood leukaemia: Fallon and other US clusters. Br J Cancer. 2004;91:1–3.
    1. Kinlen LJ. Epidemiological evidence for an infective basis in childhood leukaemia. Br J Cancer. 1995;71:1–5.
    1. Kinlen LJ. Infection and childhood leukemia. Cancer Caus Cont. 1998;9:237–39.
    1. Kinlen LJ, Balkwill A. Infective cause of childhood leukaemia and wartime population mixing in Orkney and Shetland, UK. Lancet. 2001;357:858.
    1. Kinlen LJ, Dickson M, Stiller CA. Childhood leukaemia and non-Hodgkin's; lymphoma near large rural construction sites, with a comparison with Sellafield nuclear site. BMJ. 1995;310:763–68.
    1. MacKenzie J, Greaves MF, Eden TO, et al. The putative role of transforming viruses in childhood acute lymphoblastic leukemia. Haematologica. 2006;91:240–43.
    1. Greaves MF. Speculations on the cause of childhood acute lymphoblastic leukemia. Leukemia. 1988;2:120–25.
    1. Greaves MF, Pegram SM, Chan LC. Collaborative group study of the epidemiology of acute lymphoblastic leukaemia subtypes: background and first report. Leuk Res. 1985;9:715–33.
    1. Greaves MF, Wiemels J. Origins of chromosome translocations in childhood leukaemia. Nat Rev Cancer. 2003;3:639–49.
    1. Greaves MF, Alexander FE. An infectious etiology for common acute lymphoblastic leukemia in childhood? Leukemia. 1993;7:349–60.
    1. Hepworth SJ, Feltbower RG, McKinney PA. Childhood leukaemias and CNS tumours: correlation of international incidence rates. Eur J Cancer. 2006;42:509–13.
    1. Urayama K, Ma X, Buffler PA. Exposure to infections through day-care attendance and risk of childhood leukemia. Rad Protec Dos. 2008;132:259–66.
    1. Osterholm MT. Infectious disease in child day care: an overview. Pediatrics. 1994;94:987–90.
    1. Alexander FE, McKinney PM, Cartwright RA. Migration patterns of children with leukaemia and non-Hodgkin's; lymphoma in three areas of northern England. J Public Health Med. 1993;15:9–15.
    1. Holmes SJ, Morrow AL, Pickering LK. Child-care practices: effects of social change on the epidemiology of infectious diseases and antibiotic resistance. Epidemiol Rev. 1996;18:10–28.
    1. Dockerty JD, Skegg DC, Elwood JM, Herbison GP, Becroft DM, Lewis ME. Infections, vaccinations, and the risk of childhood leukaemia. Br J Cancer. 1999;80:1483–89.
    1. Petridou E, Kassimos D, Kalmanti M, et al. Age of exposure to infections and risk of childhood leukaemia. BMJ. 1993;307:774.
    1. Petridou E, Trichopoulos D, Kalapothaki V, et al. The risk profile of childhood leukaemia in Greece: a nationwide case-control study. Br J Cancer. 1997;76:1241–47.
    1. Schuz J, Kaatsch P, Kaletsch U, Meinert R, Michaelis J. Association of childhood cancer with factors related to pregnancy and birth. Int J Epidemiol. 1999;28:631–39.
    1. Shaw G, Lavey R, Jackson R, Austin D. Association of childhood leukemia with maternal age, birth order, and paternal occupation. A case–control study. Am J Epidemiol. 1984;119:788–95.
    1. Smith M, Ries L, Gurney J, Ross J. Leukemia. In: Ries L, Smith M, Gurney J, et al., editors. Cancer Incidence and Survival among Children and Adolescents: United States SEER Program 1975-1995. Pub. No. 99-4649 ed. Bethesda, MD: National Cancer Institute, SEER Program, 1999, pp.17–34.
    1. Charalampopoulou A, Petridou E, Spyridopoulos T, et al. An integrated evaluation of socioeconomic and clinical factors in the survival from childhood acute lymphoblastic leukaemia: a study in Greece. Eur J Cancer Prev. 2004;13:397–401.
    1. Ma X, Buffler PA, Selvin S, et al. Daycare attendance and risk of childhood acute lymphoblastic leukaemia. Br J Cancer. 2002;86:1419–24.
    1. MacArthur AC, McBride ML, Spinelli JJ, Tamaro S, Gallagher RP, Theriault GP. Risk of childhood leukemia associated with vaccination, infection, and medication use in childhood: the Cross-Canada Childhood Leukemia Study. Am J Epidemiol. 2008;167:598–606.
    1. Rosenbaum PF, Buck GM, Brecher ML. Allergy and infectious disease histories and the risk of childhood acute lymphoblastic leukaemia. Paediatr Perinat Epidemiol. 2005;19:152–64.
    1. Chan LC, Lam TH, Li CK, et al. Is the timing of exposure to infection a major determinant of acute lymphoblastic leukaemia in Hong Kong? Paediatr Perinat Epidemiol. 2002;16:154–65.
    1. Gilham C, Peto J, Simpson J, et al. Day care in infancy and risk of childhood acute lymphoblastic leukaemia: findings from UK case-control study. BMJ. 2005;330:1294.
    1. Infante-Rivard C, Fortier I, Olson E. Markers of infection, breast-feeding and childhood acute lymphoblastic leukaemia. Br J Cancer. 2000;83:1559–64.
    1. Jourdan-Da, Silva N, Perel Y, et al. Infectious diseases in the first year of life, perinatal characteristics and childhood acute leukaemia. Br J Cancer. 2004;90:139–45.
    1. Kamper-Jorgensen M, Woodward A, Wohlfahrt J, et al. Childcare in the first 2 years of life reduces the risk of childhood acute lymphoblastic leukemia. Leukemia. 2008;22:189–93.
    1. Ma X, Buffler PA, Wiemels JL, et al. Ethnic difference in daycare attendance, early infections, and risk of childhood acute lymphoblastic leukemia. Cancer Epidemiol Biomarkers Prev. 2005;14:1928–34.
    1. Neglia JP, Linet MS, Shu XO, et al. Patterns of infection and day care utilization and risk of childhood acute lymphoblastic leukaemia. Br J Cancer. 2000;82:234–40.
    1. Perrillat F, Clavel J, Auclerc MF, et al. Day-care, early common infections and childhood acute leukaemia: a multicentre French case-control study. Br J Cancer. 2002;86:1064–69.
    1. Roman E, Watson A, Bull D, Baker K. Leukaemia risk and social contact in children aged 0–4 years in southern England. J Epidemiol Community Health. 1994;48:601–602.
    1. Rosenbaum PF, Buck GM, Brecher ML. Early child-care and preschool experiences and the risk of childhood acute lymphoblastic leukemia. Am J Epidemiol. 2000;152:1136–44.
    1. Schuz J, Kaletsch U, Meinert R, Kaatsch P, Michaelis J. Association of childhood leukaemia with factors related to the immune system. Br J Cancer. 1999;80:585–90.
    1. Roman E, Simpson J, Ansell P, et al. Childhood acute lymphoblastic leukemia and infections in the first year of life: a report from the United Kingdom Childhood Cancer Study. Am J Epidemiol. 2007;165:496–504.
    1. Deeks JJ, Altman DG, Bradburn MJ. Statistical methods for examining heterogeneity and combining results from several studies in meta-analysis. In: Egger M Davey, Smith G, Altman DG., editors. Systematic Rewiews in Health Care: Meta-Analysis in Context. London: BMJ Publishing Group; 2001. pp. 285–312.
    1. DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7:177–88.
    1. Greenland S. Quantitative methods in the review of epidemiologic literature. Epidemiol Rev. 1987;9:1–30.
    1. Sterne JA, Egger M. Funnel plots for detecting bias in meta-analysis: guidelines on choice of axis. J Clin Epidemiol. 2001;54:1046–55.
    1. Begg CB, Mazumdar M. Operating characteristics of a rank correlation test for publication bias. Biometrics. 1994;50:1088–101.
    1. 2005. Stata Statistical Software: Release 9 [program] College Station, TX: StataCorp LP.
    1. Greenberg ER. Random digit dialing for control selection. A review and a caution on its use in studies of childhood cancer. Am J Epidemiol. 1990;131:1–5.
    1. Ma X, Buffler PA, Layefsky M, Does MB, Reynolds P. Control selection strategies in case–control studies of childhood diseases. Am J Epidemiol. 2004;159:915–21.
    1. Wiemels JL, Pagnamenta A, Taylor GM, Eden OB, Alexander FE, Greaves MF. A lack of a functional NAD(P)H:quinone oxidoreductase allele is selectively associated with pediatric leukemias that have MLL fusions. United Kingdom Childhood Cancer Study Investigators. Cancer Res. 1999;59:4095–99.
    1. Wiemels JL, Smith RN, Taylor GM, Eden OB, Alexander FE, Greaves MF. Methylenetetrahydrofolate reductase (MTHFR) polymorphisms and risk of molecularly defined subtypes of childhood acute leukemia. Proc Natl Acad Sci USA. 2001;98:4004–4009.
    1. Alexander FE, Patheal SL, Biondi A, et al. Transplacental chemical exposure and risk of infant leukemia with MLL gene fusion. Cancer Res. 2001;61:2542–46.
    1. Greaves MF. Aetiology of acute leukaemia. Lancet. 1997;349:344–49.
    1. Ross JA, Davies SM, Potter JD, Robison LL. Epidemiology of childhood leukemia, with a focus on infants. Epidemiol Rev. 1994;16:243–72.
    1. Bethesda, MD: National Cancer Institute, SEER Program; 1999. Ries LAG. Cancer Incidence and Survival among Children and Adolescents: United States SEER Program 1975–1995.
    1. Simpson J, Smith A, Ansell P, Roman E. Childhood leukaemia and infectious exposure: A report from the United Kingdom Childhood Cancer Study (UKCCS) Eur J Cancer. 2007;43:2396–403.
    1. Greaves M, Buffler PA. Infections in early life and risk of childhood ALL. Br J Cancer. 2009;100:863.
    1. Chang JS, Metayer C, Fear NT, et al. Parental social contact in the work place and the risk of childhood acute lymphoblastic leukaemia. Br J Cancer. 2007;97:1315–21.
    1. Kwan ML, Buffler PA, Abrams B, Kiley VA. Breastfeeding and the risk of childhood leukemia: a meta-analysis. Public Health Rep. 2004;119:521–35.
    1. Ma X, Does MB, Metayer C, Russo C, Wong A, Buffler PA. Vaccination history and risk of childhood leukaemia. Int J Epidemiol. 2005;34:1100–1109.
    1. Dorak MT, Lawson T, Machulla HK, Darke C, Mills KI, Burnett AK. Unravelling an HLA-DR association in childhood acute lymphoblastic leukemia. Blood. 1999;94:694–700.
    1. Taylor GM, Dearden S, Ravetto P, et al. Genetic susceptibility to childhood common acute lymphoblastic leukaemia is associated with polymorphic peptide-binding pocket profiles in HLA-DPB1*0201. Hum Mol Genet. 2002;11:1585–97.
    1. Zaccone P, Burton OT, Cooke A. Interplay of parasite-driven immune responses and autoimmunity. Trends Parasitol. 2008;24:35–42.

Source: PubMed

3
Subskrybuj