Associations of maternal antidepressant use during the first trimester of pregnancy with preterm birth, small for gestational age, autism spectrum disorder, and attention-deficit/hyperactivity disorder in offspring
Open accessAbstract
Importance: Prenatal antidepressant exposure has been associated with adverse outcomes. Previous studies, however, may not have adequately accounted for confounding. Objective: To evaluate alternative hypotheses for associations between first-trimester antidepressant exposure and birth and neurodevelopmental problems. Design, Setting, and Participants: This retrospective cohort study included Swedish offspring born between 1996 and 2012 and followed up through 2013 or censored by death or emigration. Analyses controlling for pregnancy, maternal and paternal covariates, as well as sibling comparisons, timing of exposure comparisons, and paternal comparisons, were used to examine the associations. Exposures: Maternal self-reported first-trimester antidepressant use and first-trimester antidepressant dispensations. Main Outcomes and Measures: Preterm birth (<37 gestational weeks), small for gestational age (birth weight <2 SDs below the mean for gestational age), and first inpatient or outpatient clinical diagnosis of autism spectrum disorder and attention-deficit/hyperactivity disorder in offspring. Results: Among 1 580 629 offspring (mean gestational age, 279 days; 48.6% female; 1.4% [n = 22 544] with maternal first-trimester self-reported antidepressant use) born to 943 776 mothers (mean age at childbirth, 30 years), 6.98% of exposed vs 4.78% of unexposed offspring were preterm, 2.54% of exposed vs 2.19% of unexposed were small for gestational age, 5.28% of exposed vs 2.14% of unexposed were diagnosed with autism spectrum disorder by age 15 years, and 12.63% of exposed vs 5.46% of unexposed were diagnosed with attention-deficit/hyperactivity disorder by age 15 years. At the population level, first-trimester exposure was associated with all outcomes compared with unexposed offspring (preterm birth odds ratio [OR], 1.47 [95% CI, 1.40-1.55]; small for gestational age OR, 1.15 [95% CI, 1.06-1.25]; autism spectrum disorder hazard ratio [HR], 2.02 [95% CI, 1.80-2.26]; attention-deficit/hyperactivity disorder HR, 2.21 [95% CI, 2.04-2.39]). However, in models that compared siblings while adjusting for pregnancy, maternal, and paternal traits, first-trimester antidepressant exposure was associated with preterm birth (OR, 1.34 [95% CI, 1.18-1.52]) but not with small for gestational age (OR, 1.01 [95% CI, 0.81-1.25]), autism spectrum disorder (HR, 0.83 [95% CI, 0.62-1.13]), or attention-deficit/hyperactivity disorder (HR, 0.99 [95% CI, 0.79-1.25]). Results from analyses assessing associations with maternal dispensations before pregnancy and with paternal first-trimester dispensations were consistent with findings from the sibling comparisons. Conclusions and Relevance: Among offspring born in Sweden, after accounting for confounding factors, first-trimester exposure to antidepressants, compared with no exposure, was associated with a small increased risk of preterm birth but no increased risk of small for gestational age, autism spectrum disorder, or attention-deficit/hyperactivity disorder.
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The null result for prenatal SSRIs and ASD agrees with multiple large population studies designed to handle confounding by indication.
“Our findings of no association between prenatal SSRI exposure and ASD are consistent with the conclusions of several large, population-based studies that specifically address confounding by indication (19–26, 42).”
From Maternal Psychiatric Conditions, Treatment With Selective Serotonin Reuptake Inhibitors, and Neurodevelopmental Disorders (2021) · cites this paper as [25]
The DD-prenatal SSRI pattern resembled the ASD pattern and matched earlier null findings for ADHD, DD, and ID.
“Relationships between DD and prenatal SSRIs were overall similar to those observed with ASD, and in agreement with previous null reports of prenatal SSRI use and ADHD (21, 25, 42), DD (32, 57), and ID (27, 58).”
From Maternal Psychiatric Conditions, Treatment With Selective Serotonin Reuptake Inhibitors, and Neurodevelopmental Disorders (2021) · cites this paper as [25]
Two observational studies reported results for paternal antidepressant exposure during the maternal pregnancy period vs. all unexposed women for ASD.
“two observational studies reported results for paternal antidepressant exposure during the maternal pregnancy period vs. all unexposed women [33, 34]”
Three included studies used the same data source and related patients from Denmark, and three from Sweden.
“Three studies used the same data source and related patients from Denmark [28, 30, 33] and three from Sweden [32, 34, 35].”
Three observational studies reported results from sibling analyses for ADHD.
“Three observational studies reported results from sibling analyses [34, 37, 38]”
Adjustment for use of other medicines during pregnancy occurred in five studies assessing ASD and four studies assessing ADHD.
“Adjustment for use of other medicines during pregnancy occurred in five studies assessing ASD as the outcome and four studies assessing ADHD as the outcome [19, 25, 31, 34–37].”
One study reported estimates for paternal antidepressant exposure during pregnancy for ADHD.
“one study reported estimates for paternal antidepressant exposure during pregnancy [34]”
A total of seven observational studies measuring ADHD as an outcome were identified.
“a total of seven observational studies measuring ADHD as an outcome [17, 18, 31, 34, 36–38] were identified”
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References 37 · Cited by 226
- Authors
- Sujan, A. C., Rickert, M. E., Öberg, A. S., Quinn, P. D., Hernández-Díaz, S., Almqvist, C., Lichtenstein, P., Larsson, H., & D’Onofrio, B. M.
- Affiliations
- Indiana University Bloomington (US)
- Harvard University (US)
- Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts
- Karolinska Institutet (SE)
- Örebro University (SE)
- Department of Psychological and Brain Sciences, Indiana University, Bloomington2Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden
- ORCID
- Venue
- JAMA
- Publisher
- American Medical Association (AMA)
- Published
- 2017-04-18
- Volume
- 317
- Issue
- 15
- Pages
- 1553
- ISSN
- 0002-9955 (ISSN-L)
- 0098-7484
- PMC
- PMC5875187
- OpenAlex
- W2606395855
- Cited by
- 226
- References
- 37
- Citations by year
- 2026: 15 · 2025: 13 · 2024: 19 · 2023: 12 · 2022: 27 · 2021: 23 · 2020: 31 · 2019: 33 · 2018: 30 · 2017: 23
- FWCI
- 30.05
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- JAMA (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Figshare (submittedVersion, cc-by)
- Open Archive (Karolinska Institutet) (submittedVersion)
- Funders
- National Institute of Mental Health (T32MH103213)
- National Institute on Drug Abuse (K99DA040727)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Pregnancy and Medication Impact
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Prenatal Substance Exposure Effects
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Maternal Mental Health During Pregnancy and Postpartum
- Keywords
- prenatal antidepressant exposure, first trimester, maternal antidepressant use, preterm birth, small for gestational age, autism spectrum disorder, attention deficit hyperactivity disorder, neurodevelopmental outcomes, birth weight, confounding adjustment, Swedish cohort, offspring outcomes, sibling comparison, exposure timing, confounding by indication
- MeSH terms
- Autism Spectrum Disorder, Adolescent, Adult, Antidepressive Agents, Attention Deficit Disorder with Hyperactivity, Female, Humans, Infant, Newborn, Infant, Small for Gestational Age, Male, Pregnancy, Pregnancy Trimester, First, Prenatal Exposure Delayed Effects, Retrospective Studies, Sweden, Time Factors, Logistic Models, Odds Ratio, Selective Serotonin Reuptake Inhibitors, Maternal Exposure, Paternal Exposure, Siblings, Premature Birth, Young Adult
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