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Daily Early-Life Exposures to Diet Soda and Aspartame Are Associated with Autism in Males: A Case-Control Study
Since its introduction, aspartame—the leading sweetener in U.S. diet sodas (DS)—has been reported to cause neurological problems in some users. In prospective studies, the offspring of mothers who consumed diet sodas/beverages (DSB) daily during pregnancy experienced increased health problems. We hy...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10490529/ https://www.ncbi.nlm.nih.gov/pubmed/37686804 http://dx.doi.org/10.3390/nu15173772 |
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author | Fowler, Sharon Parten Gimeno Ruiz de Porras, David Swartz, Michael D. Stigler Granados, Paula Heilbrun, Lynne Parsons Palmer, Raymond F. |
author_facet | Fowler, Sharon Parten Gimeno Ruiz de Porras, David Swartz, Michael D. Stigler Granados, Paula Heilbrun, Lynne Parsons Palmer, Raymond F. |
author_sort | Fowler, Sharon Parten |
collection | PubMed |
description | Since its introduction, aspartame—the leading sweetener in U.S. diet sodas (DS)—has been reported to cause neurological problems in some users. In prospective studies, the offspring of mothers who consumed diet sodas/beverages (DSB) daily during pregnancy experienced increased health problems. We hypothesized that gestational/early-life exposure to ≥1 DS/day (DS(early)) or equivalent aspartame (ASP(early): ≥177 mg/day) increases autism risk. The case-control Autism Tooth Fairy Study obtained retrospective dietary recalls for DSB and aspartame consumption during pregnancy/breastfeeding from the mothers of 235 offspring with autism spectrum disorder (ASD: cases) and 121 neurotypically developing offspring (controls). The exposure odds ratios (ORs) for DS(early) and ASP(early) were computed for autism, ASD, and the non-regressive conditions of each. Among males, the DS(early) odds were tripled for autism (OR = 3.1; 95% CI: 1.02, 9.7) and non-regressive autism (OR = 3.5; 95% CI: 1.1, 11.1); the ASP(early) odds were even higher: OR = 3.4 (95% CI: 1.1, 10.4) and 3.7 (95% CI: 1.2, 11.8), respectively (p < 0.05 for each). The ORs for non-regressive ASD in males were almost tripled but were not statistically significant: DS(early) OR = 2.7 (95% CI: 0.9, 8.4); ASP(early) OR = 2.9 (95% CI: 0.9, 8.8). No statistically significant associations were found in females. Our findings contribute to the growing literature raising concerns about potential offspring harm from maternal DSB/aspartame intake in pregnancy. |
format | Online Article Text |
id | pubmed-10490529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104905292023-09-09 Daily Early-Life Exposures to Diet Soda and Aspartame Are Associated with Autism in Males: A Case-Control Study Fowler, Sharon Parten Gimeno Ruiz de Porras, David Swartz, Michael D. Stigler Granados, Paula Heilbrun, Lynne Parsons Palmer, Raymond F. Nutrients Article Since its introduction, aspartame—the leading sweetener in U.S. diet sodas (DS)—has been reported to cause neurological problems in some users. In prospective studies, the offspring of mothers who consumed diet sodas/beverages (DSB) daily during pregnancy experienced increased health problems. We hypothesized that gestational/early-life exposure to ≥1 DS/day (DS(early)) or equivalent aspartame (ASP(early): ≥177 mg/day) increases autism risk. The case-control Autism Tooth Fairy Study obtained retrospective dietary recalls for DSB and aspartame consumption during pregnancy/breastfeeding from the mothers of 235 offspring with autism spectrum disorder (ASD: cases) and 121 neurotypically developing offspring (controls). The exposure odds ratios (ORs) for DS(early) and ASP(early) were computed for autism, ASD, and the non-regressive conditions of each. Among males, the DS(early) odds were tripled for autism (OR = 3.1; 95% CI: 1.02, 9.7) and non-regressive autism (OR = 3.5; 95% CI: 1.1, 11.1); the ASP(early) odds were even higher: OR = 3.4 (95% CI: 1.1, 10.4) and 3.7 (95% CI: 1.2, 11.8), respectively (p < 0.05 for each). The ORs for non-regressive ASD in males were almost tripled but were not statistically significant: DS(early) OR = 2.7 (95% CI: 0.9, 8.4); ASP(early) OR = 2.9 (95% CI: 0.9, 8.8). No statistically significant associations were found in females. Our findings contribute to the growing literature raising concerns about potential offspring harm from maternal DSB/aspartame intake in pregnancy. MDPI 2023-08-29 /pmc/articles/PMC10490529/ /pubmed/37686804 http://dx.doi.org/10.3390/nu15173772 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fowler, Sharon Parten Gimeno Ruiz de Porras, David Swartz, Michael D. Stigler Granados, Paula Heilbrun, Lynne Parsons Palmer, Raymond F. Daily Early-Life Exposures to Diet Soda and Aspartame Are Associated with Autism in Males: A Case-Control Study |
title | Daily Early-Life Exposures to Diet Soda and Aspartame Are Associated with Autism in Males: A Case-Control Study |
title_full | Daily Early-Life Exposures to Diet Soda and Aspartame Are Associated with Autism in Males: A Case-Control Study |
title_fullStr | Daily Early-Life Exposures to Diet Soda and Aspartame Are Associated with Autism in Males: A Case-Control Study |
title_full_unstemmed | Daily Early-Life Exposures to Diet Soda and Aspartame Are Associated with Autism in Males: A Case-Control Study |
title_short | Daily Early-Life Exposures to Diet Soda and Aspartame Are Associated with Autism in Males: A Case-Control Study |
title_sort | daily early-life exposures to diet soda and aspartame are associated with autism in males: a case-control study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10490529/ https://www.ncbi.nlm.nih.gov/pubmed/37686804 http://dx.doi.org/10.3390/nu15173772 |
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