Original Article

Molecular Psychiatry advance online publication 13 June 2017; doi: 10.1038/mp.2017.119

Prenatal fever and autism risk

M Hornig1,2, M A Bresnahan2,3, X Che1, A F Schultz1, J E Ukaigwe1, M L Eddy1, D Hirtz4, N Gunnes5, K K Lie5, P Magnus5, S Mjaaland5, T Reichborn-Kjennerud5,6, S Schjølberg5, A-S Øyen5,7, B Levin8, E S Susser2,3, C Stoltenberg5,9 and W I Lipkin1,2,10

  1. 1Center for Infection and Immunity, Mailman School of Public Health, Columbia University, New York, NY, USA
  2. 2Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA
  3. 3New York State Psychiatric Institute, New York, NY, USA
  4. 4National Institute of Neurological Disorders and Stroke, National Institutes of Health, Rockville, MD, USA
  5. 5Norwegian Institute of Public Health, Oslo, Norway
  6. 6Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway
  7. 7Lovisenberg Diakonale Sykehus, Nic Waals Institutt, Oslo, Norway
  8. 8Department of Biostatistics, Mailman School of Public Health, Columbia University, New York, NY, USA
  9. 9Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway
  10. 10Departments of Pathology and Neurology, Columbia University College of Physicians and Surgeons, New York, NY, USA

Correspondence: Dr M Hornig, Center for Infection and Immunity, Mailman School of Public Health, Columbia University, 722 West 168th Street, 17th Floor, New York, NY 10032, USA. E-mail: mady.hornig@columbia.edu

Received 25 April 2016; Revised 24 March 2017; Accepted 19 April 2017
Advance online publication 13 June 2017



Some studies suggest that prenatal infection increases risk of autism spectrum disorders (ASDs). This study was undertaken in a prospective cohort in Norway to examine whether we could find evidence to support an association of the prenatal occurrence of fever, a common manifestation of infection, with ASD risk. Prospective questionnaires provided maternal exposure data; case status was established from clinical assessments and registry linkages. In a large, prospectively ascertained cohort of pregnant mothers and their offspring, we examined infants born greater than or equal to32 weeks for associations between fever exposure in each trimester and ASD risk using logistic regression. Maternal exposure to second-trimester fever was associated with increased ASD risk, adjusting for presence of fever in other trimesters and confounders (adjusted odds ratio (aOR), 1.40; 95% confidence interval, 1.09–1.79), with a similar, but nonsignificant, point estimate in the first trimester. Risk increased markedly with exposure to three or more fever episodes after 12 weeks' gestation (aOR, 3.12; 1.28–7.63). ASD risk appears to increase with maternal fever, particularly in the second trimester. Risk magnified dose dependently with exposure to multiple fevers after 12 weeks' gestation. Our findings support a role for gestational maternal infection and innate immune responses to infection in the pathogenesis of at least some cases of ASD.



Autism spectrum disorders (ASD) are associated with prenatal exposure to a wide range of infectious agents.1, 2, 3, 4 The diversity of potential infectious triggers suggests that host factors, such as activation of maternal immunity, may have a role in the genesis of neurodevelopmental consequences.5 Consistent with this concept, some studies have demonstrated higher levels of inflammatory cytokines in amniotic fluid6 or maternal mid-gestational serum.7 Maternal responses to infection, therefore, including the timing of fever episodes relative to fetal brain development and measures to mitigate fever, may influence risk of ASD.8, 9

Maternal fever is common in pregnancy. Twenty percent of pregnant US women report one or more fever episodes.10 Primarily (though not exclusively) first-trimester fever episodes have been linked to severe brain damage and structural anomalies.9, 11 Although first-trimester exposure may also influence subsequent more subtle disruptions of brain development, some investigators have hypothesized that exposure to fever later in pregnancy should be more strongly related to more subtle disruptions—including effects on neuronal migration,12 proliferation12, 13 and myelination14—such as those reported in some studies of ASD.15, 16, 17, 18, 19 Few studies have examined the association of prenatal fever, per se, with autism outcomes, as opposed to effects of specific types of maternal infection (for example, influenza). Fever was associated with a 1.4-fold increased risk of infantile autism in a prospective Danish cohort study wherein fever reporting was restricted to the first 32 weeks of gestation.20 Fever persisting for 7 days or more was associated with a 1.6-fold increased risk for ASD and greater than threefold increase in risk for infantile autism. A retrospective case–control study in the US found a twofold increased risk of ASD or another developmental disorder with prenatal fever; risk was lower in mothers treated with antipyretics.21 However, no prospective studies have examined risk after fever across all of pregnancy or in conjunction with antipyretic use. In addition, prior work has not examined the possibility that different classes of antipyretics may differentially influence fever risk through their distinct biological effects. These include acetaminophen, an antipyretic with minimal anti-inflammatory effects that is used by over 50% of women in both Scandinavia22 and the US23 at least once during pregnancy that also affects oxidative stress,24 endocrine25 and cannabioid receptor pathways,26 and ibuprofen, a non-steroidal anti-inflammatory drug (NSAID). Understanding the influence on ASD risk of exposure to multiple fever events, and of the timing of these episodes across pregnancy, is also incomplete. Here we report results from a study in a Norwegian birth cohort where questionnaires and capture of cases through a national registry allowed us to investigate associations between prenatal fever and ASD risk. We also examined the potential for antipyretics to modify risk.


Materials and methods

Study design and participants

The Norwegian Mother and Child Cohort Study (MoBa)27 includes 114500 children born in 1999–2009. ASD cases are identified through the Autism Birth Cohort (ABC) Study,28 a case–cohort study nested within MoBa. Analyses reflect data collected through December 2014. Children from multiple births or with birth weight <2500grams or gestational age <32 weeks (6.6%, Supplementary Figure S1) were excluded. Given questionnaire design, we focused on subjects with gestational ages greater than or equal to32 weeks to ensure that all women could report fever for at least the first 4 weeks of the third trimester. Low birth weight is associated with a multitude of pre- and postnatal risk factors; thus, we also excluded subjects with low birth weight.29 This exclusion was also motivated by the nearly complete overlap in our study population of preterm and low birth weight status (887 subjects out of 892 with gestational age <32 weeks had low birth weight, or 99.44%).

Studies were approved by the Regional Committee for Medical and Health Research Ethics for Southeastern Norway and the Columbia University Medical Center Institutional Review Board.

Case diagnoses

ASD cases were identified through MoBa screening (3, 5 and 7 years), referrals and annual linkages to the Norwegian Patient Register (NPR).30 Through 2012, potential cases were invited for assessment by research clinicians using standardized diagnostic instruments.31, 32 Best-estimate ASD diagnoses were assigned using Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR)33 criteria. ASD cases among NPR-identified children not evaluated at the ABC Study Clinic were those assigned International Classification of Diseases, Tenth Revision (ICD-10) F84 diagnoses (Supplementary Methods).34 NPR ASD diagnoses have high validity: 58 out of 60 children with NPR ASD diagnoses met DSM-IV-TR ASD criteria at later ABC clinic assessment (positive predictive value: 96.7%, 95% confidence interval (CI), 87.5–99.4%; false positive rate: 3.3%, 95% CI, 0.6–12.5%).30

To explore the possibility that prenatal fever effects may be specific for certain ASD phenotypes, cases were classified as ASD with or ASD without mental retardation/intellectual disability (ID). Comorbidity with ID was based on intelligence quotient (IQ) data from ABC clinic assessments, as available (IQ<70)11 or NPR ICD-10 data consistent with a diagnosis of an ID. ASD cases without an ABC clinic IQ score <70 and who also had not received an NPR ID ICD-10 code were assigned to the ASD without ID group (Supplementary Methods).

Exposure data

Exposure timing

Data on prenatal fever and antipyretic use were obtained from questionnaires completed around gestational weeks 17 and 30, and 6 months postpartum. Mothers reported fever and medication use in 4-week intervals through 13+ and 29+ weeks’ gestation, respectively, on the 17- and 30-week questionnaires and from gestational week 30 through parturition on the 6-month postnatal questionnaire (Supplementary Table S1). An interval was considered positive for fever or antipyretic exposure if one or more exposures occurred during that interval. Trimesters were designated by gestational weeks as: first, 0–12 weeks; second, 13–28 weeks; and third, 29 weeks through birth. Overlap in timing across questionnaires was resolved as described in Supplementary Methods. Main analyses included women with at least one completed questionnaire containing prenatal data.

Fever and antipyretic exposures

Questionnaire items solicited data from mothers regarding the presence of specific conditions, including fever, along with their timing, as well as the names of medications used for fever, and the timing of that medication use. Response options for presence and timing of fever episodes and medication use varied across the three questionnaires (Supplementary Table S1). To enhance cross-questionnaire comparability, we collapsed data for 17-week questionnaire items—fever with rash and fever >38.5°C—into one category. Questionnaire-specific procedures for counting fever episodes and assigning their timing to specific trimesters are detailed further in Supplementary Methods.

We assessed use of any acetaminophen- or ibuprofen-containing medications for the reported indication of fever. Methods for addressing report of multiple medications and timing of medication use are described in Supplementary Methods, along with secondary analysis procedures for examining risk modification by antipyretic use (acetaminophen or the NSAID, ibuprofen).

Supplementary Table S2 summarizes methods for resolving discrepancies in reported fever timing and in the timing of antipyretic use in relationship to fever episodes, along with the number of affected subjects. Inconsistency in reported fever timing took on three major forms. First, some mothers indicated timing of the medication taken for fever and the name of the antipyretic, but failed to report the specific timing of fever episodes for which they reported taking an antipyretic. In these instances, maternally provided medication timing defined the fever timing. Second, when timing of fever episodes was provided but timing of the selected fever-associated antipyretics (acetaminophen, ibuprofen) was not, maternally provided fever timing defined the timing of medication use. Third, missing fever timings were imputed for the high-exposure subset of mothers who endorsed the 'fever more than three times' item on the 30-week questionnaire but failed to provide complete timing for all reported fever episodes (Supplementary Methods). Supplementary Table S2 shows that the number of affected women, and thus the scope of the problem, was small.

Potential confounders

We evaluated variables that might influence associations between primary maternal exposures (fever in all three trimesters) and ASD risk: maternal age; smoking and parity; parental education; birth month; and birth year (Supplementary Methods and Supplementary Tables S3A and S3B). Potential confounders demonstrating a significant association (P<0.05) with both the primary exposure (fever in any of the three trimesters) and the outcome (ASD) were retained in our analyses.

Statistical analysis

Main analyses

Crude and adjusted odds ratios (ORs and aORs, respectively) of ASD risk in association with maternal fever in each trimester, and for any time during pregnancy, and their associated 95% CIs were estimated by logistic regression. We first examined associations between fever and risk by fitting separate models for each time period, using all subjects responding to at least one questionnaire containing prenatal data. Analyses examining ASD risk in association with fever at any time during pregnancy included subjects responding to all questionnaires.

Subsequent analyses restricted the study sample to mothers who responded to all questionnaires addressing prenatal fever. We used three adjusted models: (1) Adjusted Model 1 (aOR1), adjusting for fever exposure in either/both of the other trimesters; (2) Adjusted Model 2 (aOR2), adjusting for all other selected confounders; and (3) Adjusted Model 3 (aOR3), adjusting for both fever in other trimesters and all confounders. This same population of respondents was used for stratified analyses comparing ASD risk in association with prenatal fever within the subgroup of ASD cases with comorbid ID and within the ASD subset without such comorbidity.

Dose–response analyses

The cumulative effect of maternal fever was estimated by counting numbers of individual time intervals wherein mothers reported fever episodes. We categorized fever exposure into three levels (0 (referent), 1–2, greater than or equal to3 episodes), with exposure periods of any time during pregnancy or >12 weeks of gestation. Using logistic regression, we estimated ORs and aORs for both exposure periods.

Fever-associated risk stratified on use of antipyretics

In exploratory analyses, we examined whether the risk effect of fever exposure was modified by acetaminophen use. Mothers reporting fever in each trimester were divided into two subgroups based on reported use or nonuse of acetaminophen specifically for fever. Crude and adjusted ORs (aOR1, aOR2 and aOR3, as above) of ASD for each subgroup (compared with the no-fever referent) were estimated by logistic regression. We performed similar secondary analyses substituting ibuprofen for acetaminophen to further examine antipyretic modification of fever-associated ASD risk. Although both agents reduce fever, as an NSAID, ibuprofen has anti-inflammatory potential that acetaminophen does not; if, as prior studies have suggested, fever-related activation of maternal immunity mediates neurodevelopmental consequences among offspring, use of ibuprofen as an antipyretic might be anticipated to be associated with greater reduction in fever-associated ASD risk than acetaminophen (Supplementary Methods).

Supplementary and sensitivity analyses

Influences of confounders on ORs of ASD were examined individually and sequentially (Supplementary Methods and Supplementary Tables S4A and S4B).

To address possible influences relating to trends across birth years in ASD prevalence (incomplete ascertainment of cases in later birth years, given follow-up in some subjects only through age 5) and maternal fever report, we performed an analysis of fever effects stratified by early (1999–2004) and late (2005–2009) birth year periods.

We also examined fetal sex effects. Trophoblasts from male placentae are reported to respond to infection-related signals with proinflammatory cytokine production,35, 36 consistent with studies suggesting increased risk of preterm birth in males, particularly in the context of infection.36, 37, 38 Because of low numbers of girls with ASD, we pursued potential influences of sex through sensitivity analyses restricted to boys (Supplementary Methods).

Other sensitivity analyses addressed potential biases relating to gestational age at birth and fever timing imputation. Preterm births (32–36 weeks) might have obscured the ability to assess the impact of fever and antipyretic events in later pregnancy; thus, we restricted to term births (that is, gestational age >36 weeks) in sensitivity analyses. In an additional sensitivity analysis, we excluded mothers who reported high levels of fever exposure on the 30-week questionnaire (>3 fever episodes) without specifying the timing of those episodes (Supplementary Methods).



Study cohort

The study sample included 95754 children (51.4% boys) after exclusions (Supplementary Figure S1). Mean age was 9.4 years (s.d., 2.2 years; range, 5.6–15.2 years) by end of follow-up (31 December, 2014).

Table 1 shows characteristics of mothers and their pregnancies vis-à-vis prenatal fever and offspring diagnosis (ASD, non-case). The mothers of 15701 children (16.4%) reported fever in one or more 4-week intervals throughout pregnancy. Women reporting fever were more likely to have offspring at earlier gestational ages (<39 weeks), in later cohort birth years (greater than or equal to2005) and in March through August. Fever exposures were more prevalent, and ASD less prevalent, in more recent birth years (Table 1; Spearman’s rank correlation coefficient: both P<0.0001).

Autism spectrum disorder

We identified 583 cases of ASD (0.6%) through 2014. Males were overrepresented fivefold (Table 1). Mothers of ASD children were younger and less educated than non-case mothers and more likely to smoke and be first-time mothers. ASD offspring identified through end of follow-up were also more often born in earlier cohort years (<2006; higher prevalence of children not yet old enough to be diagnosed).

Main models

Table 2 shows associations between prenatal fever exposure and ASD risk for any time in pregnancy and by trimester. Women reporting fever at any time during pregnancy had increased odds of ASD in both unadjusted and adjusted models. Examining by trimester, offspring of mothers with second-trimester fever had a 1.4-fold increased risk in adjusted models (aOR, 1.40; 1.11–1.77). The first trimester showed similar, but nonsignificant, point estimates (aOR, 1.34; 0.89–2.02).

The presence of fever in the first trimester was associated with fever episodes in other trimesters. Second-trimester fever was also associated with fever in the third trimester (Pearson’s χ2-test: all associations, P<0.0001). To permit analyses that could adjust the fever-associated risk found in one trimester by accounting for fever episodes in other trimesters, we restricted to mothers completing all questionnaires containing prenatal data. As with results using all questionnaire respondents, offspring of mothers with second-trimester fever had increased risk in the crude model (OR, 1.33; 1.04–1.70; Table 3). Adjustment for fever in other trimesters had little effect. Fever-associated risk in second trimester was similar when adjusting for confounders either alone or in combination with presence of fever in other trimesters (Table 3). The first trimester showed similar but nonsignificant point estimates.

Fever-associated risk in ASD subsets with and without ID

As compared with non-cases, ASD cases with comorbid ID showed a tendency toward increased fever-associated risk in fully adjusted models both with exposure in the first (aOR3, 2.28; 0.91–5.75) and the second trimesters (aOR3, 1.64; 0.89–3.03). For ASD cases without ID, fever-associated risk was modestly but significantly increased (1.36-fold) and restricted to second-trimester exposures (Supplementary Table S5).

Dose–response models

With exposure at any time during pregnancy, risk increased 1.3-fold with one to two fever episodes (aOR, 1.31; 1.04–1.64) and more than twofold (albeit not significant) with three or more episodes (aOR, 2.15; 0.95–4.84). After gestational week 12, risk increased with higher frequency of exposure (one to two episodes: aOR, 1.30; 1.02–1.66; three or more episodes: aOR, 3.12; 1.28–7.63; Table 4).

Fever-associated risk stratified on use of antipyretics

In secondary stratified analyses, we examined whether use of acetaminophen for fever modified fever-associated ASD risk. Risk tended to be lower within each trimester in febrile women who took acetaminophen for fever than in febrile women who did not (compared to the referent group of afebrile women; Supplementary Table S6A). The risk was similar both for women febrile in the second trimester who did and who did not specifically report taking acetaminophen for fever.

Additional secondary stratified analyses examined the potential for modification of fever-associated risk through the use of the NSAID, ibuprofen, given that, unlike acetaminophen, it has anti-inflammatory properties in addition to its antipyretic effects. These analyses were compromised by overall small numbers and cells with zero values. Among febrile women whose offspring were later diagnosed with ASD, none had taken ibuprofen for fever in any trimester (Supplementary Table S6B).

Supplementary and sensitivity analyses

Accounting for confounders slightly increased ORs in main models. Birth year, introduced either individually or sequentially into the models, had the most marked influence on ORs in the second trimester compared with other confounders; however, the magnitude of these effects was quite modest (Supplementary Materials; Supplementary Tables S4A and S4B).

We pursued a series of sensitivity analyses to determine whether effects differed in early vs late birth years (1999–2004 vs 2005–2009), as well as for boys, term births (excluding children born at gestational weeks 32–36) or offspring of mothers providing complete, or nearly complete, fever timing on the 30-week questionnaire. In fully adjusted analyses stratified on birth year period, we found that the association of second-trimester fever with increased odds of ASD was only observed in the earlier part of the cohort (1999–2004 births, children aged 10–15 years at end of follow-up: aOR3, 1.86; 1.37–2.52; 2005–2009 births, children aged 5–9 years at end of follow-up: aOR3, 0.88; 0.57–1.37). We also found a first-trimester effect restricted to the later birth year period (2004–2009: aOR3, 1.89; 1.02–3.50; Supplementary Tables S7A and S7B).

For the remaining sensitivity analyses, we found minimal differences in ORs (Supplementary Materials and Supplementary results).



Prenatal fever was associated with increased ASD risk among offspring in the ABC. Effects were strongest in the second trimester but followed similar patterns in the first. Risks were minimally mitigated in women taking acetaminophen for fever in the second trimester. Risks increased markedly and dose dependently with fever frequency, with particularly strong effects after 12 weeks’ gestation.

The strengths of our study are its basis in a large, prospective, population-based birth cohort with exposure data collected in 4-week intervals and linkage to a patient registry for case ascertainment. Maternal self-reporting and differences across the three questionnaires may contribute to some exposure misclassification; however, differential reporting is minimized by our study design, as fever reporting precedes the diagnosis of autism. Maternal self-report may also detect fevers that healthcare records might miss. In addition, the overall rate of maternally reported fever in our cohort across pregnancy (16.4%) was similar to that reported in a retrospective study in the US (20.5%) for any fever with infection during pregnancy.10

Our findings complement prior literature on prenatal fever and ASD risk.20, 21 Prospective examination of fever exposures through birth revealed that fever-associated risk, most prominent in second trimester, was not influenced by the presence of fever in the other two trimesters. Similar patterns pertained for the first trimester but not the third. The only prior prospective study found an association with prolonged fever in the first and second trimesters but could not exclude a possible third-trimester effect, as no data were collected after 32 weeks’ gestation.20

To our knowledge, there are no other prospective studies examining maternally reported use of antipyretics for fever and ASD. A retrospective study reporting an association of first- and second-trimester fever with increased ASD risk found that acetaminophen and NSAIDs mitigated fever-associated risks.21 Data were not separately reported for antipyretics with and without anti-inflammatory potential. Here we found only small risk reduction with use of acetaminophen for fever in conjunction with a small increase in risk among febrile women who did not take acetaminophen. In contrast, none of the women with offspring later diagnosed with ASD used ibuprofen for fever in pregnancy, although these findings must be interpreted with extreme caution, given the low overall frequency of ibuprofen use in this population.

ASD is associated with increased prevalence of autoimmune disorders in mothers and first-degree relatives.39 Microglial activation40, 41, 42, 43 and elevated brain chemokine levels42 are also reported. Animal models of maternal gestational infection or exposure to noninfectious mimics of bacterial (lipopolysaccharide)44, 45 or viral (polyinosinic:polycytidylic acid)46, 47 infection result in neurodevelopmental damage reminiscent of ASD. Evidence from these models suggests that maternal fever-associated immune responses mediate consequences in offspring47, 48, 49, 50, 51, 52 and are abrogated by NSAIDs.47 As in ASD, effects are most prominent in males.53 Our results are consistent with these models in that fever is associated with increased risk, risk is accentuated in males and antipyretics tend to decrease fever-associated risk.

Questionnaire analysis did not indicate an association between risk and maternally reported symptoms of infection in individual organ systems that might implicate specific infectious agents. Nonetheless, we are testing the possibility that risk is associated with specific infectious agents through sequence-based and serological assays of samples collected mid-pregnancy and at birth from cases and controls. Linkage to patient register data, including hospitalization records, may also be used in future work to confirm timing and severity of illness episodes. Other evidence relating to severity of illness, such as degree of fever, may also prove informative; however, study questionnaires did not ask mothers to report this information for all time periods in pregnancy.

We acknowledge that our findings are limited by small numbers, particularly for first- and third-trimester exposures to fever and antipyretics; replication in other populations will also be critical before determining the implications of this work for management of fever in pregnancy. However, factors besides small numbers may have contributed to the wider CI we obtained for the first-trimester effect across all birth years, including shorter length of follow-up for ASD outcomes among younger cohort children, heterogeneity in the composition of the ASD group, or both. Our analyses stratified on earlier vs later birth year periods—despite even smaller numbers than in analyses including all birth years—provide evidence within the later birth year group of a more robust first-trimester effect (1.89-fold, with CIs excluding 1). Although the difference between aORs by birth year are not statistically significant in either trimester comparison, precision is lacking for testing such an interaction, and birth-year-dependent differences in the composition of the ASD group (DSM-IV-TR subsets) may have influenced our trimester-based results.

It is also important to bear in mind that causality cannot be definitively established through observational research. Nonetheless, we found consistently increased risk with higher levels of fever exposure. Opposing patterns of prevalence of ASD and fever exposure in our study sample—decreased prevalence of ASD but increased prevalence of fever exposure in later cohort years—may have biased results. However, our age-specific ASD prevalence patterns are similar to those reported in other work in Norway54 as well as other Nordic countries, where diagnoses are often registered at ages far exceeding those at which symptoms typically begin.55 Follow-up studies may resolve whether ASD underascertainment in younger cohort children diminished effect sizes. Birth in later cohort years had a greater influence on ascertainment of higher-functioning cases, as these subsets are typically diagnosed at older ages, as well as more generally for younger members of the cohort, based on reduced length of follow-up. The case sample is thus perhaps weighted toward more severe cases. However, the rate of ID comorbidity did not vary substantially between early and late birth year periods (15.30 vs 13.99%, respectively). Although ID is not a simple proxy for ASD severity, our key finding—an increase in risk for ASD in association with maternal second-trimester fever—was restricted to ASD without ID, suggesting a degree of specificity. Prenatal fever increased risk in the ASD group with ID in the first but not the second trimester, consistent with previous work indicating a relationship of first-trimester fever exposure with severe structural defects of the central nervous and other organ systems.9 More conclusive analysis awaits detection of additional cases with extended follow-up.

Our findings support the hypothesis that fever and associated immune disturbances are implicated in a subset of ASD cases. Although acetaminophen was associated with a small decrease in risk in the context of fever, prior studies reporting ablation of fever-associated risk with use of a diverse range of medications with antipyretic properties, including NSAIDs as well as acetaminophen—along with our own limited data on ibuprofen—suggest that the choice of antipyretic warrants scrutiny. We have not addressed microbial causes of maternal fever and immune activation. Accordingly, future work should focus on identifying and preventing prenatal infections and inflammatory responses that may contribute to ASD pathogenesis.


Conflict of interest

The authors declare no conflict of interest.



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This study was funded by the National Institute of Neurological Disorders and Stroke of the National Institutes of Health U01 NS47537 (WIL) and R56 NS086122 (MH/WIL), Jane Botsford Johnson Foundation (WIL/MH), Simons Foundation Autism Research Initiative (SFARI) (WIL/MH) and the Norwegian Ministry of Health and Care Services, the Norwegian Ministry of Education and Research, and the following grants from the Research Council of Norway providing general support to the ABC: 189457, 190694 and 196452. We thank Ms Eleanor Kahn for administrative support. MH and WIL dedicate this work to the memory of Jerome Hornig and Evelyn Lipkin.

Supplementary Information accompanies the paper on the Molecular Psychiatry website

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