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Association Between Aluminum Exposure From Vaccines Before Age 24 Months and Persistent Asthma at Age 24 to 59 Months

Supporting Files
File Language:
English


Details

  • Alternative Title:
    Acad Pediatr
  • Personal Author:
  • Description:
    Objective:

    To assess the association between cumulative aluminum exposure from vaccines before age 24 months and persistent asthma at age 24 to 59 months.

    Methods:

    A retrospective cohort study was conducted in the Vaccine Safety Datalink (VSD). Vaccination histories were used to calculate cumulative vaccine-associated aluminum in milligrams (mg). The persistent asthma definition required one inpatient or 2 outpatient asthma encounters, and ≥2 long-term asthma control medication dispenses. Cox proportional hazard models were used to evaluate the association between aluminum exposure and asthma incidence, stratified by eczema presence/absence. Adjusted hazard ratios (aHR) and 95% confidence intervals (CI) per 1 mg increase in aluminum exposure were calculated, adjusted for birth month/year, sex, race/ethnicity, VSD site, prematurity, medical complexity, food allergy, severe bronchiolitis, and health care utilization.

    Results:

    The cohort comprised 326,991 children, among whom 14,337 (4.4%) had eczema. For children with and without eczema, the mean (standard deviation [SD]) vaccine-associated aluminum exposure was 4.07 mg (SD 0.60) and 3.98 mg (SD 0.72), respectively. Among children with and without eczema, 6.0% and 2.1%, respectively, developed persistent asthma. Among children with eczema, vaccine-associated aluminum was positively associated with persistent asthma (aHR 1.26 per 1 mg increase in aluminum, 95% CI 1.07, 1.49); a positive association was also detected among children without eczema (aHR 1.19, 95% CI 1.14, 1.25).

    Conclusion:

    In a large observational study, a positive association was found between vaccine-related aluminum exposure and persistent asthma. While recognizing the small effect sizes identified and the potential for residual confounding, additional investigation of this hypothesis appears warranted.

  • Keywords:
  • Source:
    Acad Pediatr. 23(1):37-46
  • Pubmed ID:
    36180331
  • Pubmed Central ID:
    PMC10109516
  • Document Type:
  • Funding:
  • Volume:
    23
  • Issue:
    1
  • Collection(s):
  • Main Document Checksum:
    urn:sha256:37c0d72dd4e37f845eba218f6d15ce7f3a40ef99e271d6cca55775ffe723736b
  • Download URL:
  • File Type:
    Filetype[PDF - 334.20 KB ]
File Language:
English
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