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Comparative Study
. 2009 Mar 10;6(3):e40.
doi: 10.1371/journal.pmed.1000040.

Advanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhood

Affiliations
Comparative Study

Advanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhood

Sukanta Saha et al. PLoS Med. .

Abstract

Background: Advanced paternal age (APA) is associated with an increased risk of neurodevelopmental disorders such as autism and schizophrenia, as well as with dyslexia and reduced intelligence. The aim of this study was to examine the relationship between paternal age and performance on neurocognitive measures during infancy and childhood.

Methods and findings: A sample of singleton children (n = 33,437) was drawn from the US Collaborative Perinatal Project. The outcome measures were assessed at 8 mo, 4 y, and 7 y (Bayley scales, Stanford Binet Intelligence Scale, Graham-Ernhart Block Sort Test, Wechsler Intelligence Scale for Children, Wide Range Achievement Test). The main analyses examined the relationship between neurocognitive measures and paternal or maternal age when adjusted for potential confounding factors. Advanced paternal age showed significant associations with poorer scores on all of the neurocognitive measures apart from the Bayley Motor score. The findings were broadly consistent in direction and effect size at all three ages. In contrast, advanced maternal age was generally associated with better scores on these same measures.

Conclusions: The offspring of older fathers show subtle impairments on tests of neurocognitive ability during infancy and childhood. In light of secular trends related to delayed fatherhood, the clinical implications and the mechanisms underlying these findings warrant closer scrutiny.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Primary Analyses: Model 1—Adjusted for Other Parent's Age, Mother's Race, Gestational Age, and Child Gender
Solid lines ranging from 15 to 45 y for maternal age, dotted lines ranging from 15 to 65 y for paternal age. Nonlinear model fit with 95% CIs.
Figure 2
Figure 2. Primary Analyses: Model 2—Adjusted for Other Parent's age, Mother's Race, Gestational Age, and Child Gender, Socioeconomic Index, Marital Status, and Maternal and Paternal Mental Illness
Solid lines ranging from 15 to 45 y for maternal age, dotted lines ranging from 15 to 65 y for paternal age. Nonlinear model fit with 95% CIs.

Comment in

References

    1. Toriello HV, Meck JM. Statement on guidance for genetic counseling in advanced paternal age. Genet Med. 2008;10:457–460. - PMC - PubMed
    1. Crow JF. The origins, patterns and implications of human spontaneous mutation. Nat Rev Genet. 2000;1:40–47. - PubMed
    1. Nybo Andersen AM, Hansen KD, Andersen PK, Davey Smith G. Advanced paternal age and risk of fetal death: a cohort study. Am J Epidemiol. 2004;160:1214–1222. - PubMed
    1. Kleinhaus K, Perrin M, Friedlander Y, Paltiel O, Malaspina D, et al. Paternal age and spontaneous abortion. Obstet Gynecol. 2006;108:369–377. - PubMed
    1. Rousseau F, Bonaventure J, Legeai-Mallet L, Pelet A, Rozet JM, et al. Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia. Nature. 1994;371:252–254. - PubMed

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