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Response to commentary by Li et al

Published online by Cambridge University Press:  01 January 2020

S. Andalib ,
M.S. Vafaee  and
T.M. Michel
S. Andalib*
Affiliation:
aNeuroscience Research Center, Department of Neurosurgery, Poursina Hospital, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran
M.S. Vafaee
Affiliation:
bDepartment of Nuclear Medicine, Odense University Hospital, University of Southern Denmark, Odense, Denmark cDepartment of Psychiatry, Psychiatry Region of Southern, Odense, Denmark dResearch Unit of Psychiatry, Institute of Clinical Research, University of Southern Denmark, Odense, Denmark eCenter for Applied Neuroscience, BRIDGE, Odense University Hospital, University of Southern Denmark, Psychiatry in the Region of Southern Denmark, Odense, Denmark fNeurosciences Research Center, Department of Neurology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
T.M. Michel
Affiliation:
cDepartment of Psychiatry, Psychiatry Region of Southern, Odense, Denmark dResearch Unit of Psychiatry, Institute of Clinical Research, University of Southern Denmark, Odense, Denmark eCenter for Applied Neuroscience, BRIDGE, Odense University Hospital, University of Southern Denmark, Psychiatry in the Region of Southern Denmark, Odense, Denmark
*
* Corresponding author E-mail address: [email protected]

Abstract

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Type
Commentary
Information
European Psychiatry , Volume 47 , January 2018 , pp. 49
Copyright
Copyright © European Psychiatric Association 2018

We gladly welcome the discussion in the commentary by Li et al. Reference Li and Chen[1]. While we appreciate the commentators’ interest in our work Reference Andalib, Emamhadi, Yousefzadeh-Chabok, Shakouri, Høilund-Carlsen and Vafaee[2], we would like to respond to the issues raised by them as follows.

It is clear that studies based on the same data source could be a potential source of bias in meta-analyses affecting both the pooled effect size and its standard error. Taking this into account, a sensitivity analysis was conducted to ascertain the robustness of the pooled results and related conclusion. Three separate meta-analyses were applied each time including data from only one of the Danish studies. As a result, negligible differences in OR and 95% CI were observed in the separate meta-analyses, compared with those reported when including all the three Danish studies.

The notion is attractive that every meta-analysis may be affected by potential confounders when using crude model; nonetheless, it should be noted that data source is chosen based on its availability in the literature and that is why crude model is the most applicable. In our meta-analysis, we emphasized that maternal depression was a joint adjusted confounder. However, there were a few eligible studies for inclusion and controlling all the potential confounders was impossible.

It is worth mentioning that our aim was not the assessment of trimester in the meta-analysis, but to demonstrate whether an association exists between maternal SSRI exposure and ASD offspring. Moreover, such trimester assessment was not applicable inasmuch as the required data was not available in all the included studies and more importantly, such subgroup meta-analysis with a few number of included studies does not provide sufficient power of test. We hope that the issue can be addressed in a future study when sufficient data is available.

Disclosure of interest

The authors declare that they have no competing interest.

References

Li, J., Chen, J.Comment on “Maternal SSRI exposure increases the risk of autistic offspring: a meta-analysis and systematic review”. Eur Psychiatry 2017; 45:220.CrossRefGoogle Scholar
Andalib, S., Emamhadi, M.R., Yousefzadeh-Chabok, S., Shakouri, S.K., Høilund-Carlsen, P.F., Vafaee, M.S.et al.Maternal SSRI exposure increases the risk of autistic offspring: a meta-analysis and systematic review. Eur Psychiatry 2017; 45:1611-66.CrossRefGoogle ScholarPubMed
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