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Fetal Origins of Mental Disorders? An Answer Based on Mendelian Randomization
The Barker hypothesis states that low birth weight (BW) is associated with higher risk of adult onset diseases, including mental disorders like schizophrenia, major depressive disorder (MDD), and attention deficit hyperactivity disorder (ADHD). The main criticism of this hypothesis is that evidence...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cambridge University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390405/ https://www.ncbi.nlm.nih.gov/pubmed/30587273 http://dx.doi.org/10.1017/thg.2018.65 |
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author | Arafat, Subhi Minică, Camelia C. |
author_facet | Arafat, Subhi Minică, Camelia C. |
author_sort | Arafat, Subhi |
collection | PubMed |
description | The Barker hypothesis states that low birth weight (BW) is associated with higher risk of adult onset diseases, including mental disorders like schizophrenia, major depressive disorder (MDD), and attention deficit hyperactivity disorder (ADHD). The main criticism of this hypothesis is that evidence for it comes from observational studies. Specifically, observational evidence does not suffice for inferring causality, because the associations might reflect the effects of confounders. Mendelian randomization (MR) — a novel method that tests causality on the basis of genetic data — creates the unprecedented opportunity to probe the causality in the association between BW and mental disorders in observation studies. We used MR and summary statistics from recent large genome-wide association studies to test whether the association between BW and MDD, schizophrenia and ADHD is causal. We employed the inverse variance weighted (IVW) method in conjunction with several other approaches that are robust to possible assumption violations. MR-Egger was used to rule out horizontal pleiotropy. IVW showed that the association between BW and MDD, schizophrenia and ADHD is not causal (all p > .05). The results of all the other MR methods were similar and highly consistent. MR-Egger provided no evidence for pleiotropic effects biasing the estimates of the effects of BW on MDD (intercept = -0.004, SE = 0.005, p = .372), schizophrenia (intercept = 0.003, SE = 0.01, p = .769), or ADHD (intercept = 0.009, SE = 0.01, p = .357). Based on the current evidence, we refute the Barker hypothesis concerning the fetal origins of adult mental disorders. The discrepancy between our results and the results from observational studies may be explained by the effects of confounders in the observational studies, or by the existence of a small causal effect not detected in our study due to weak instruments. Our power analyses suggested that the upper bound for a potential causal effect of BW on mental disorders would likely not exceed an odds ratio of 1.2. |
format | Online Article Text |
id | pubmed-6390405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63904052019-03-01 Fetal Origins of Mental Disorders? An Answer Based on Mendelian Randomization Arafat, Subhi Minică, Camelia C. Twin Res Hum Genet Articles The Barker hypothesis states that low birth weight (BW) is associated with higher risk of adult onset diseases, including mental disorders like schizophrenia, major depressive disorder (MDD), and attention deficit hyperactivity disorder (ADHD). The main criticism of this hypothesis is that evidence for it comes from observational studies. Specifically, observational evidence does not suffice for inferring causality, because the associations might reflect the effects of confounders. Mendelian randomization (MR) — a novel method that tests causality on the basis of genetic data — creates the unprecedented opportunity to probe the causality in the association between BW and mental disorders in observation studies. We used MR and summary statistics from recent large genome-wide association studies to test whether the association between BW and MDD, schizophrenia and ADHD is causal. We employed the inverse variance weighted (IVW) method in conjunction with several other approaches that are robust to possible assumption violations. MR-Egger was used to rule out horizontal pleiotropy. IVW showed that the association between BW and MDD, schizophrenia and ADHD is not causal (all p > .05). The results of all the other MR methods were similar and highly consistent. MR-Egger provided no evidence for pleiotropic effects biasing the estimates of the effects of BW on MDD (intercept = -0.004, SE = 0.005, p = .372), schizophrenia (intercept = 0.003, SE = 0.01, p = .769), or ADHD (intercept = 0.009, SE = 0.01, p = .357). Based on the current evidence, we refute the Barker hypothesis concerning the fetal origins of adult mental disorders. The discrepancy between our results and the results from observational studies may be explained by the effects of confounders in the observational studies, or by the existence of a small causal effect not detected in our study due to weak instruments. Our power analyses suggested that the upper bound for a potential causal effect of BW on mental disorders would likely not exceed an odds ratio of 1.2. Cambridge University Press 2018-12 /pmc/articles/PMC6390405/ /pubmed/30587273 http://dx.doi.org/10.1017/thg.2018.65 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is unaltered and is properly cited. The written permission of Cambridge University Press must be obtained for commercial re-use or in order to create a derivative work. |
spellingShingle | Articles Arafat, Subhi Minică, Camelia C. Fetal Origins of Mental Disorders? An Answer Based on Mendelian Randomization |
title | Fetal Origins of Mental Disorders? An Answer Based on Mendelian Randomization |
title_full | Fetal Origins of Mental Disorders? An Answer Based on Mendelian Randomization |
title_fullStr | Fetal Origins of Mental Disorders? An Answer Based on Mendelian Randomization |
title_full_unstemmed | Fetal Origins of Mental Disorders? An Answer Based on Mendelian Randomization |
title_short | Fetal Origins of Mental Disorders? An Answer Based on Mendelian Randomization |
title_sort | fetal origins of mental disorders? an answer based on mendelian randomization |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390405/ https://www.ncbi.nlm.nih.gov/pubmed/30587273 http://dx.doi.org/10.1017/thg.2018.65 |
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