Cargando…

Aspartame Sensitivity? A Double Blind Randomised Crossover Study

BACKGROUND: Aspartame is a commonly used intense artificial sweetener, being approximately 200 times sweeter than sucrose. There have been concerns over aspartame since approval in the 1980s including a large anecdotal database reporting severe symptoms. The objective of this study was to compare th...

Descripción completa

Detalles Bibliográficos
Autores principales: Sathyapalan, Thozhukat, Thatcher, Natalie J., Hammersley, Richard, Rigby, Alan S., Pechlivanis, Alexandros, Gooderham, Nigel J., Holmes, Elaine, le Roux, Carel W., Atkin, Stephen L., Courts, Fraser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364783/
https://www.ncbi.nlm.nih.gov/pubmed/25786106
http://dx.doi.org/10.1371/journal.pone.0116212
_version_ 1782362128452157440
author Sathyapalan, Thozhukat
Thatcher, Natalie J.
Hammersley, Richard
Rigby, Alan S.
Pechlivanis, Alexandros
Gooderham, Nigel J.
Holmes, Elaine
le Roux, Carel W.
Atkin, Stephen L.
Courts, Fraser
author_facet Sathyapalan, Thozhukat
Thatcher, Natalie J.
Hammersley, Richard
Rigby, Alan S.
Pechlivanis, Alexandros
Gooderham, Nigel J.
Holmes, Elaine
le Roux, Carel W.
Atkin, Stephen L.
Courts, Fraser
author_sort Sathyapalan, Thozhukat
collection PubMed
description BACKGROUND: Aspartame is a commonly used intense artificial sweetener, being approximately 200 times sweeter than sucrose. There have been concerns over aspartame since approval in the 1980s including a large anecdotal database reporting severe symptoms. The objective of this study was to compare the acute symptom effects of aspartame to a control preparation. METHODS: This was a double-blind randomized cross over study conducted in a clinical research unit in United Kingdom. Forty-eight individual who has self reported sensitivity to aspartame were compared to 48 age and gender matched aspartame non-sensitive individuals. They were given aspartame (100mg)-containing or control snack bars randomly at least 7 days apart. The main outcome measures were acute effects of aspartame measured using repeated ratings of 14 symptoms, biochemistry and metabonomics. RESULTS: Aspartame sensitive and non-sensitive participants differed psychologically at baseline in handling feelings and perceived stress. Sensitive participants had higher triglycerides (2.05 ± 1.44 vs. 1.26 ± 0.84mmol/L; p value 0.008) and lower HDL-C (1.16 ± 0.34 vs. 1.35 ± 0.54 mmol/L; p value 0.04), reflected in (1)H NMR serum analysis that showed differences in the baseline lipid content between the two groups. Urine metabonomic studies showed no significant differences. None of the rated symptoms differed between aspartame and control bars, or between sensitive and control participants. However, aspartame sensitive participants rated more symptoms particularly in the first test session, whether this was placebo or control. Aspartame and control bars affected GLP-1, GIP, tyrosine and phenylalanine levels equally in both aspartame sensitive and non-sensitive subjects. CONCLUSION: Using a comprehensive battery of psychological tests, biochemistry and state of the art metabonomics there was no evidence of any acute adverse responses to aspartame. This independent study gives reassurance to both regulatory bodies and the public that acute ingestion of aspartame does not have any detectable psychological or metabolic effects in humans. TRIAL REGISTRATION: ISRCTN Registry ISRCTN39650237
format Online
Article
Text
id pubmed-4364783
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-43647832015-03-23 Aspartame Sensitivity? A Double Blind Randomised Crossover Study Sathyapalan, Thozhukat Thatcher, Natalie J. Hammersley, Richard Rigby, Alan S. Pechlivanis, Alexandros Gooderham, Nigel J. Holmes, Elaine le Roux, Carel W. Atkin, Stephen L. Courts, Fraser PLoS One Research Article BACKGROUND: Aspartame is a commonly used intense artificial sweetener, being approximately 200 times sweeter than sucrose. There have been concerns over aspartame since approval in the 1980s including a large anecdotal database reporting severe symptoms. The objective of this study was to compare the acute symptom effects of aspartame to a control preparation. METHODS: This was a double-blind randomized cross over study conducted in a clinical research unit in United Kingdom. Forty-eight individual who has self reported sensitivity to aspartame were compared to 48 age and gender matched aspartame non-sensitive individuals. They were given aspartame (100mg)-containing or control snack bars randomly at least 7 days apart. The main outcome measures were acute effects of aspartame measured using repeated ratings of 14 symptoms, biochemistry and metabonomics. RESULTS: Aspartame sensitive and non-sensitive participants differed psychologically at baseline in handling feelings and perceived stress. Sensitive participants had higher triglycerides (2.05 ± 1.44 vs. 1.26 ± 0.84mmol/L; p value 0.008) and lower HDL-C (1.16 ± 0.34 vs. 1.35 ± 0.54 mmol/L; p value 0.04), reflected in (1)H NMR serum analysis that showed differences in the baseline lipid content between the two groups. Urine metabonomic studies showed no significant differences. None of the rated symptoms differed between aspartame and control bars, or between sensitive and control participants. However, aspartame sensitive participants rated more symptoms particularly in the first test session, whether this was placebo or control. Aspartame and control bars affected GLP-1, GIP, tyrosine and phenylalanine levels equally in both aspartame sensitive and non-sensitive subjects. CONCLUSION: Using a comprehensive battery of psychological tests, biochemistry and state of the art metabonomics there was no evidence of any acute adverse responses to aspartame. This independent study gives reassurance to both regulatory bodies and the public that acute ingestion of aspartame does not have any detectable psychological or metabolic effects in humans. TRIAL REGISTRATION: ISRCTN Registry ISRCTN39650237 Public Library of Science 2015-03-18 /pmc/articles/PMC4364783/ /pubmed/25786106 http://dx.doi.org/10.1371/journal.pone.0116212 Text en © 2015 Sathyapalan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sathyapalan, Thozhukat
Thatcher, Natalie J.
Hammersley, Richard
Rigby, Alan S.
Pechlivanis, Alexandros
Gooderham, Nigel J.
Holmes, Elaine
le Roux, Carel W.
Atkin, Stephen L.
Courts, Fraser
Aspartame Sensitivity? A Double Blind Randomised Crossover Study
title Aspartame Sensitivity? A Double Blind Randomised Crossover Study
title_full Aspartame Sensitivity? A Double Blind Randomised Crossover Study
title_fullStr Aspartame Sensitivity? A Double Blind Randomised Crossover Study
title_full_unstemmed Aspartame Sensitivity? A Double Blind Randomised Crossover Study
title_short Aspartame Sensitivity? A Double Blind Randomised Crossover Study
title_sort aspartame sensitivity? a double blind randomised crossover study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364783/
https://www.ncbi.nlm.nih.gov/pubmed/25786106
http://dx.doi.org/10.1371/journal.pone.0116212
work_keys_str_mv AT sathyapalanthozhukat aspartamesensitivityadoubleblindrandomisedcrossoverstudy
AT thatchernataliej aspartamesensitivityadoubleblindrandomisedcrossoverstudy
AT hammersleyrichard aspartamesensitivityadoubleblindrandomisedcrossoverstudy
AT rigbyalans aspartamesensitivityadoubleblindrandomisedcrossoverstudy
AT pechlivanisalexandros aspartamesensitivityadoubleblindrandomisedcrossoverstudy
AT gooderhamnigelj aspartamesensitivityadoubleblindrandomisedcrossoverstudy
AT holmeselaine aspartamesensitivityadoubleblindrandomisedcrossoverstudy
AT lerouxcarelw aspartamesensitivityadoubleblindrandomisedcrossoverstudy
AT atkinstephenl aspartamesensitivityadoubleblindrandomisedcrossoverstudy
AT courtsfraser aspartamesensitivityadoubleblindrandomisedcrossoverstudy