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Conference Paper: Prenatal Antidepressant Exposure and the Risk of Autism Spectrum Disorder and Attention-Deficit Hyperactivity Disorder

TitlePrenatal Antidepressant Exposure and the Risk of Autism Spectrum Disorder and Attention-Deficit Hyperactivity Disorder
Authors
Issue Date2015
PublisherInternational Society for Pharmacoepidemiology (ISPE).
Citation
The 31st International Conference on Pharmacoepidemiology & Therapeutic Risk Management (ICPE 2015), Boston, MA., 22-26 August 2015. How to Cite?
AbstractBackground: Recent studies suggested that prenatal exposure of Selective Serotonin Reuptake Inhibitors (SSRIs) may be associated with increased risk of Autism Spectrum Disorder (ASD) and Attention Deficit Hyperactivity Disorder (ADHD). However, confounding has not been comprehensively excluded. Objectives: To investigate the association between SSRIs and ASD and ADHD in a large health-care system. Methods: 429,645 children who were delivered in public hospital were identified using the Hong Kong Population-based electronic medical records on the Clinical Data Analysis & Reporting System (2001-2014). Using a case-control study design, we evaluated the association between ASD or ADHD and prenatal exposure of SSRIs. Further analyses using disease risk score (DRS) matching (1:10) and within-patient study design, case-time-control (CTC) were conducted to address residual confounding. The Risks of ASD and ADHD were estimated using odds ratios (ORs) from logistic regression. Results: Among 429,645 children identified, 299,672 were included in the analysis. 4,208 and 2,706 children were diagnosed with ASD and ADHD respectively. 0.88% of ASD and 1.22% of ADHD children were having prenatal SSRIs exposure compared with 0.6% in controls. The adjusted OR of ASD and ADHD are 1.35 (95%CI 0.94-1.93) and 2.12 (95%CI 1.44-3.11) respectively. The findings were similar in DRS matched model. In contrasts, no association was found in CTC analysis (OR=1.12, 95%CI 0.83-1.53 for ASD; OR=0.81, 95%CI 0.58-1.12 for ADHD). Alternative analyses using non-SSRI antidepressant as exposure showed similar results. The CTC OR for ASD and ADHD were 1.08 (95%CI 0.81-1.44) and 1.02 (95%CI 0.75-1.39) respectively. In validation analysis using insulin as negative control, no association was found in CTC analyses (OR=1.13, 95%CI 0.31-4.04 for ASD; OR=1.15, 95%CI 0.25-5.28 for ADHD). Conclusions: This study does not support the hypothesis that prenatal SSRIs exposure increased the risk of ASD or ADHD in children. These results suggest that the risk of ASD and ADHD observed with prenatal SSRI exposure is likely confounded by maternal underlying medical conditions and genetic factors.
DescriptionSession: Oral Session: Neurodevelopmental Issues: Drugs and Outcomes: no. 414
Persistent Identifierhttp://hdl.handle.net/10722/217607

 

DC FieldValueLanguage
dc.contributor.authorMan, KKC-
dc.contributor.authorChan, EW-
dc.contributor.authorCoghill, DR-
dc.contributor.authorIp, P-
dc.contributor.authorSimonoff, E-
dc.contributor.authorChan, P-
dc.contributor.authorLau, WCY-
dc.contributor.authorWong, ICK-
dc.date.accessioned2015-09-18T06:06:58Z-
dc.date.available2015-09-18T06:06:58Z-
dc.date.issued2015-
dc.identifier.citationThe 31st International Conference on Pharmacoepidemiology & Therapeutic Risk Management (ICPE 2015), Boston, MA., 22-26 August 2015.-
dc.identifier.urihttp://hdl.handle.net/10722/217607-
dc.descriptionSession: Oral Session: Neurodevelopmental Issues: Drugs and Outcomes: no. 414-
dc.description.abstractBackground: Recent studies suggested that prenatal exposure of Selective Serotonin Reuptake Inhibitors (SSRIs) may be associated with increased risk of Autism Spectrum Disorder (ASD) and Attention Deficit Hyperactivity Disorder (ADHD). However, confounding has not been comprehensively excluded. Objectives: To investigate the association between SSRIs and ASD and ADHD in a large health-care system. Methods: 429,645 children who were delivered in public hospital were identified using the Hong Kong Population-based electronic medical records on the Clinical Data Analysis & Reporting System (2001-2014). Using a case-control study design, we evaluated the association between ASD or ADHD and prenatal exposure of SSRIs. Further analyses using disease risk score (DRS) matching (1:10) and within-patient study design, case-time-control (CTC) were conducted to address residual confounding. The Risks of ASD and ADHD were estimated using odds ratios (ORs) from logistic regression. Results: Among 429,645 children identified, 299,672 were included in the analysis. 4,208 and 2,706 children were diagnosed with ASD and ADHD respectively. 0.88% of ASD and 1.22% of ADHD children were having prenatal SSRIs exposure compared with 0.6% in controls. The adjusted OR of ASD and ADHD are 1.35 (95%CI 0.94-1.93) and 2.12 (95%CI 1.44-3.11) respectively. The findings were similar in DRS matched model. In contrasts, no association was found in CTC analysis (OR=1.12, 95%CI 0.83-1.53 for ASD; OR=0.81, 95%CI 0.58-1.12 for ADHD). Alternative analyses using non-SSRI antidepressant as exposure showed similar results. The CTC OR for ASD and ADHD were 1.08 (95%CI 0.81-1.44) and 1.02 (95%CI 0.75-1.39) respectively. In validation analysis using insulin as negative control, no association was found in CTC analyses (OR=1.13, 95%CI 0.31-4.04 for ASD; OR=1.15, 95%CI 0.25-5.28 for ADHD). Conclusions: This study does not support the hypothesis that prenatal SSRIs exposure increased the risk of ASD or ADHD in children. These results suggest that the risk of ASD and ADHD observed with prenatal SSRI exposure is likely confounded by maternal underlying medical conditions and genetic factors.-
dc.languageeng-
dc.publisherInternational Society for Pharmacoepidemiology (ISPE).-
dc.relation.ispartofInternational Conference on Pharmacoepidemiology & Therapeutic Risk Management, ICPE 2015-
dc.titlePrenatal Antidepressant Exposure and the Risk of Autism Spectrum Disorder and Attention-Deficit Hyperactivity Disorder-
dc.typeConference_Paper-
dc.identifier.emailMan, KKC: mkckth@hku.hk-
dc.identifier.emailChan, EW: ewchan@hku.hk-
dc.identifier.emailIp, P: patricip@hku.hk-
dc.identifier.emailWong, ICK: wongick@HKUCC-COM.hku.hk-
dc.identifier.authorityChan, EW=rp01587-
dc.identifier.authorityIp, P=rp01337-
dc.identifier.authorityWong, ICK=rp01480-
dc.identifier.hkuros253609-
dc.publisher.placeUnited States-

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