In utero Exposure to beta-2-Adrenergic Receptor Agonist Drugs and Risk for Autism Spectrum Disorders

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In utero Exposure to beta-2-Adrenergic Receptor Agonist Drugs and Risk for Autism Spectrum Disorders. / Gidaya, Nicole B.; Lee, Brian K.; Burstyn, Igor; Michael, Yvonne; Newschaffer, Craig J.; Mortensen, Erik L.

In: Pediatrics, Vol. 137, No. 2, 20151316, 02.2016, p. 1-8.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Gidaya, NB, Lee, BK, Burstyn, I, Michael, Y, Newschaffer, CJ & Mortensen, EL 2016, 'In utero Exposure to beta-2-Adrenergic Receptor Agonist Drugs and Risk for Autism Spectrum Disorders', Pediatrics, vol. 137, no. 2, 20151316, pp. 1-8. https://doi.org/10.1542/peds.2015-1316

APA

Gidaya, N. B., Lee, B. K., Burstyn, I., Michael, Y., Newschaffer, C. J., & Mortensen, E. L. (2016). In utero Exposure to beta-2-Adrenergic Receptor Agonist Drugs and Risk for Autism Spectrum Disorders. Pediatrics, 137(2), 1-8. [20151316]. https://doi.org/10.1542/peds.2015-1316

Vancouver

Gidaya NB, Lee BK, Burstyn I, Michael Y, Newschaffer CJ, Mortensen EL. In utero Exposure to beta-2-Adrenergic Receptor Agonist Drugs and Risk for Autism Spectrum Disorders. Pediatrics. 2016 Feb;137(2):1-8. 20151316. https://doi.org/10.1542/peds.2015-1316

Author

Gidaya, Nicole B. ; Lee, Brian K. ; Burstyn, Igor ; Michael, Yvonne ; Newschaffer, Craig J. ; Mortensen, Erik L. / In utero Exposure to beta-2-Adrenergic Receptor Agonist Drugs and Risk for Autism Spectrum Disorders. In: Pediatrics. 2016 ; Vol. 137, No. 2. pp. 1-8.

Bibtex

@article{1b68a965f9414ebfa9db77ed1dc87565,
title = "In utero Exposure to beta-2-Adrenergic Receptor Agonist Drugs and Risk for Autism Spectrum Disorders",
abstract = "OBJECTIVES: The purpose of this study was to investigate associations between use of β-2-adrenergic receptor (B2AR) agonist drugs during pregnancy and risk for autism spectrum disorders (ASD).METHODS: A case-control study was conducted by using Denmark{\textquoteright}s health and population registers. Among children born between 1997 and 2006, 5200 cases with ASD admission diagnoses and 52 000 controls without ASD were identified and individually matched on month and year of birth. Conditional logistic regression models were used to estimate odds ratios (OR) and confidence intervals (CI) for any B2AR agonist exposure during pregnancy, preconception, and by trimester.RESULTS: In total, 3.7% of cases and 2.9% of controls were exposed to B2ARs during pregnancy. Use of B2ARs during pregnancy was associated with increased risk of ASD, even after adjustment for maternal asthma and other covariates (OR: 1.3, 95% CI: 1.1–1.5). The elevated risk was observed with use of B2AR during preconception (OR: 1.3, 95% CI: 1.0–1.6), first trimester (OR: 1.3, 95% CI: 1.1–1.5), second trimester (OR: 1.5, 95% CI: 1.1–1.7), and the third trimester (OR: 1.4, 95% CI: 1.1–1.7). There was some evidence that longer B2AR within-pregnancy use was associated with the increased risk.CONCLUSIONS: B2AR agonist exposure during pregnancy may be associated with an increased risk for ASD. If the effect is real, any intervention must be balanced against benefits of indicated medication use by pregnant women.",
author = "Gidaya, {Nicole B.} and Lee, {Brian K.} and Igor Burstyn and Yvonne Michael and Newschaffer, {Craig J.} and Mortensen, {Erik L.}",
year = "2016",
month = feb,
doi = "10.1542/peds.2015-1316",
language = "English",
volume = "137",
pages = "1--8",
journal = "Pediatrics",
issn = "0031-4005",
publisher = "American Academy of Pediatrics",
number = "2",

}

RIS

TY - JOUR

T1 - In utero Exposure to beta-2-Adrenergic Receptor Agonist Drugs and Risk for Autism Spectrum Disorders

AU - Gidaya, Nicole B.

AU - Lee, Brian K.

AU - Burstyn, Igor

AU - Michael, Yvonne

AU - Newschaffer, Craig J.

AU - Mortensen, Erik L.

PY - 2016/2

Y1 - 2016/2

N2 - OBJECTIVES: The purpose of this study was to investigate associations between use of β-2-adrenergic receptor (B2AR) agonist drugs during pregnancy and risk for autism spectrum disorders (ASD).METHODS: A case-control study was conducted by using Denmark’s health and population registers. Among children born between 1997 and 2006, 5200 cases with ASD admission diagnoses and 52 000 controls without ASD were identified and individually matched on month and year of birth. Conditional logistic regression models were used to estimate odds ratios (OR) and confidence intervals (CI) for any B2AR agonist exposure during pregnancy, preconception, and by trimester.RESULTS: In total, 3.7% of cases and 2.9% of controls were exposed to B2ARs during pregnancy. Use of B2ARs during pregnancy was associated with increased risk of ASD, even after adjustment for maternal asthma and other covariates (OR: 1.3, 95% CI: 1.1–1.5). The elevated risk was observed with use of B2AR during preconception (OR: 1.3, 95% CI: 1.0–1.6), first trimester (OR: 1.3, 95% CI: 1.1–1.5), second trimester (OR: 1.5, 95% CI: 1.1–1.7), and the third trimester (OR: 1.4, 95% CI: 1.1–1.7). There was some evidence that longer B2AR within-pregnancy use was associated with the increased risk.CONCLUSIONS: B2AR agonist exposure during pregnancy may be associated with an increased risk for ASD. If the effect is real, any intervention must be balanced against benefits of indicated medication use by pregnant women.

AB - OBJECTIVES: The purpose of this study was to investigate associations between use of β-2-adrenergic receptor (B2AR) agonist drugs during pregnancy and risk for autism spectrum disorders (ASD).METHODS: A case-control study was conducted by using Denmark’s health and population registers. Among children born between 1997 and 2006, 5200 cases with ASD admission diagnoses and 52 000 controls without ASD were identified and individually matched on month and year of birth. Conditional logistic regression models were used to estimate odds ratios (OR) and confidence intervals (CI) for any B2AR agonist exposure during pregnancy, preconception, and by trimester.RESULTS: In total, 3.7% of cases and 2.9% of controls were exposed to B2ARs during pregnancy. Use of B2ARs during pregnancy was associated with increased risk of ASD, even after adjustment for maternal asthma and other covariates (OR: 1.3, 95% CI: 1.1–1.5). The elevated risk was observed with use of B2AR during preconception (OR: 1.3, 95% CI: 1.0–1.6), first trimester (OR: 1.3, 95% CI: 1.1–1.5), second trimester (OR: 1.5, 95% CI: 1.1–1.7), and the third trimester (OR: 1.4, 95% CI: 1.1–1.7). There was some evidence that longer B2AR within-pregnancy use was associated with the increased risk.CONCLUSIONS: B2AR agonist exposure during pregnancy may be associated with an increased risk for ASD. If the effect is real, any intervention must be balanced against benefits of indicated medication use by pregnant women.

U2 - 10.1542/peds.2015-1316

DO - 10.1542/peds.2015-1316

M3 - Journal article

C2 - 26738885

VL - 137

SP - 1

EP - 8

JO - Pediatrics

JF - Pediatrics

SN - 0031-4005

IS - 2

M1 - 20151316

ER -

ID: 167479903