Autism Spectrum Disorders and Maternal Serum alpha-Fetoprotein Levels during Pregnancy

Author:

Abdallah Morsi W1,Grove Jakob2,Hougaard David M3,Nørgaard-Pedersen Bent4,Ibrahimov Fuad5,Mortensen Erik L6

Affiliation:

1. Researcher, Department of Epidemiology, Aarhus University School of Public Health, Aarhus, Denmark; Researcher, Department of Clinical Biochemistry and Immunology, Statens Serum Institute, Copenhagen, Denmark; Researcher, Institute of Public Health and Center for Healthy Aging, University of Copenhagen, Copenhagen, Denmark

2. Associate Professor, Department of Biomedicine, Faculty of Health Sciences and Bioinformatics Research Centre, Aarhus University, Aarhus, Denmark

3. Consultant, Department of Clinical Biochemistry and Immunology, Statens Serum Institute, Copenhagen, Denmark

4. Professor, Department of Clinical Biochemistry and Immunology, Statens Serum Institute, Copenhagen, Denmark

5. Health Policy Analyst [self-employed], Decatur, Georgia

6. Professor, Institute of Public Health and Center for Healthy Aging, University of Copenhagen, Copenhagen, Denmark

Abstract

Objective: Numerous studies have been trying to disentangle the complex pathophysiology of autism spectrum disorders (ASD). In our study, we explored the potential role of maternal serum (MS) alpha-fetoprotein (AFP) in the prediction and the pathophysiology of ASD. Methods: A total of 112 patients with ASD and 243 control subjects were included in a case–control study, using a historic birth cohort maintained at Statens Serum Institute. Measurements of MS-AFP were obtained from a multicentre screening program, whereas clinical data were obtained from nationwide registers. Association between MS-AFP and ASD status was analyzed using logistic regression models and nonparametric tests. Results: Crude, but not adjusted, estimates showed that MS-AFP levels were slightly, but significantly, higher in mothers of children with ASD, compared with their control subject counterparts. People with ASD had an odds ratio of 2.33, with 95% confidence intervals of 1.00 to 5.39, to have MS-AFP above 2.5 multiple of median. Excluding subjects with congenital malformation comorbidities did not alter the direction of our estimates (OR 2.60; 95% Cl 1.04 to 6.51, P = 0.04). Conclusion: Biologic plausibility of its role in the pathophysiology of ASD makes AFP a good candidate for further larger-scale studies to confirm such an association and to determine whether this pattern is unique to ASD or related to other psychiatric disorders as well.

Publisher

SAGE Publications

Subject

Psychiatry and Mental health

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