The Childhood Vaccination Schedule and the Lack of Association With Type 1 Diabetes

Author:

Glanz Jason M.12,Clarke Christina L.1,Daley Matthew F.1,Shoup Jo Ann1,Hambidge Simon J.3,Williams Joshua T.B.3,Groom Holly C.4,Kharbanda Elyse O.5,Klein Nicola P.6,Jackson Lisa A.7,Lewin Bruno J.8,McClure David L.9,Xu Stanley8,DeStefano Frank10

Affiliation:

1. Institute for Health Research, Kaiser Permanente Colorado, Denver, Colorado

2. Department of Epidemiology, Colorado School of Public Health, University of Colorado, Aurora, Colorado

3. Denver Health and Hospital Authority, Denver, Colorado

4. Kaiser Permanente Center for Health Research, Northwest Kaiser Permanente, Portland, Oregon

5. HealthPartners Institute, Minneapolis, Minnesota

6. Kaiser Permanente Division of Research, Kaiser Permanente of Northern California, Oakland, California

7. Kaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington, Seattle, Washington

8. Kaiser Permanente Department of Research and Evaluation, Kaiser Permanente of Southern California, Pasadena, California

9. Marshfield Clinic Research Foundation Institute, Marshfield, Wisconsin

10. Immunization Safety Office, Centers for Disease Control and Prevention, Atlanta, Georgia

Abstract

OBJECTIVES Safety studies assessing the association between the entire recommended childhood immunization schedule and autoimmune diseases, such as type 1 diabetes mellitus (T1DM), are lacking. To examine the association between the recommended immunization schedule and T1DM, we conducted a retrospective cohort study of children born between 2004 and 2014 in 8 US health care organizations that participate in the Vaccine Safety Datalink. METHODS Three measures of the immunization schedule were assessed: average days undervaccinated (ADU), cumulative antigen exposure, and cumulative aluminum exposure. T1DM incidence was identified by International Classification of Disease codes. Cox proportional hazards models were used to analyze associations between the 3 exposure measures and T1DM incidence. Adjusted hazard ratios (aHRs) and 95% confidence intervals (CIs) were calculated. Models were adjusted for sex, race and ethnicity, birth year, mother’s age, birth weight, gestational age, number of well-child visits, and study site. RESULTS In a cohort of 584 171 children, the mean ADU was 38 days, the mean cumulative antigen exposure was 263 antigens (SD = 54), and the mean cumulative aluminum exposure was 4.11 mg (SD = 0.73). There were 1132 incident cases of T1DM. ADU (aHR = 1.01; 95% CI, 0.99–1.02) and cumulative antigen exposure (aHR = 0.98; 95% CI, 0.97–1.00) were not associated with T1DM. Cumulative aluminum exposure >3.00 mg was inversely associated with T1DM (aHR = 0.77; 95% CI, 0.60–0.99). CONCLUSIONS The recommended schedule is not positively associated with the incidence of T1DM in children. These results support the safety of the recommended childhood immunization schedule.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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