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Parental Age and Risk of Infant Leukaemia: A Pooled Analysis
Erin L Marcotte1,2, Todd E Druley3, Kimberly J Johnson4
1Division of Epidemiology & Clinical Research, Department of Pediatrics, University of Minnesota, Minneapolis, MN.
Insights
Young paternal age increases the risk of infant acute lymphoblastic leukaemia (ALL). Older maternal age is linked to a higher risk of infant acute myeloid leukaemia (AML).
Area of Science:
- Epidemiology
- Pediatric Oncology
- Genetics
Background:
- Infant leukaemia (IL) is a rare childhood cancer with unknown causes.
- De novo mutations are implicated in IL etiology.
- Parental age is a known risk factor for adverse offspring outcomes, including cancers.
Purpose of the Study:
- To investigate the association between parental age and infant leukaemia.
- To analyze the risk of specific infant leukaemia subtypes (ALL, AML) in relation to maternal and paternal age.
Main Methods:
- A case-control study analyzed registry data from 402 infant leukaemia cases and 45,392 controls.
- Data from five US states (New York, Minnesota, California, Texas, Washington) for births between 1981-2004 were used.
- Logistic regression calculated odds ratios (OR) and 95% confidence intervals (CI), adjusted for covariates.
Main Results:
- Maternal age of 40 years or older was associated with an increased risk of infant acute myeloid leukaemia (AML) (OR 4.80).
- Paternal age under 20 was associated with an increased risk of infant acute lymphoblastic leukaemia (ALL) (OR 3.69).
Conclusions:
- Young paternal age is a risk factor for infant ALL.
- Older maternal age is a risk factor for infant AML.
- Further research should explore parent of origin effects, de novo mutations, and environmental exposures in IL etiology.
Background:
Infant leukaemia (IL) is extremely rare with fewer than 150 cases occurring each year in the United States. Little is known about its causes. However, recent evidence supports a role of de novo mutations in IL aetiology. Parental age has been associated with several adverse outcomes in offspring, including childhood cancers. Given the role of older parental age in de novo mutations in offspring, we carried out an analysis of parental age and IL.
Methods:
We evaluated the relationship between parental age and IL in a case-control study using registry data from New York, Minnesota, California, Texas, and Washington. Records from 402 cases [219 acute lymphoblastic leukaemia (ALL), 131 acute myeloid leukaemia (AML), and 52 other] and 45 392 controls born during 1981-2004 were analysed. Odds ratios (OR) and 95% confidence intervals (CI) were calculated by logistic regression. Estimates were adjusted for infant sex, birth year category, maternal race, state, and mutually adjusted for paternal or maternal age, respectively.
Results:
Infants with mothers' age ≥40 years had an increased risk of developing AML (OR 4.80, 95% CI 1.80, 12.76). In contrast, paternal age <20 was associated with increased risk of ALL (OR 3.69, 95% CI 1.62, 8.41).
Conclusion:
This study demonstrates increased risk of infant ALL in relation to young paternal age. Given record linkage, there is little concern with recall or selection bias, although data are lacking on MLL gene status and other potentially important variables. Parent of origin effects, de novo mutations, and/or carcinogenic exposures may be involved in IL aetiology.
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