Cargando…
Metabolite-related dietary patterns and the development of islet autoimmunity
The role of diet in type 1 diabetes development is poorly understood. Metabolites, which reflect dietary response, may help elucidate this role. We explored metabolomics and lipidomics differences between 352 cases of islet autoimmunity (IA) and controls in the TEDDY (The Environmental Determinants...
Autores principales: | , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794249/ https://www.ncbi.nlm.nih.gov/pubmed/31616039 http://dx.doi.org/10.1038/s41598-019-51251-4 |
_version_ | 1783459249397956608 |
---|---|
author | Johnson, Randi K. Vanderlinden, Lauren DeFelice, Brian C. Kechris, Katerina Uusitalo, Ulla Fiehn, Oliver Sontag, Marci Crume, Tessa Beyerlein, Andreas Lernmark, Åke Toppari, Jorma Ziegler, Anette-G. She, Jin-Xiong Hagopian, William Rewers, Marian Akolkar, Beena Krischer, Jeffrey Virtanen, Suvi M. Norris, Jill M. |
author_facet | Johnson, Randi K. Vanderlinden, Lauren DeFelice, Brian C. Kechris, Katerina Uusitalo, Ulla Fiehn, Oliver Sontag, Marci Crume, Tessa Beyerlein, Andreas Lernmark, Åke Toppari, Jorma Ziegler, Anette-G. She, Jin-Xiong Hagopian, William Rewers, Marian Akolkar, Beena Krischer, Jeffrey Virtanen, Suvi M. Norris, Jill M. |
author_sort | Johnson, Randi K. |
collection | PubMed |
description | The role of diet in type 1 diabetes development is poorly understood. Metabolites, which reflect dietary response, may help elucidate this role. We explored metabolomics and lipidomics differences between 352 cases of islet autoimmunity (IA) and controls in the TEDDY (The Environmental Determinants of Diabetes in the Young) study. We created dietary patterns reflecting pre-IA metabolite differences between groups and examined their association with IA. Secondary outcomes included IA cases positive for multiple autoantibodies (mAb+). The association of 853 plasma metabolites with outcomes was tested at seroconversion to IA, just prior to seroconversion, and during infancy. Key compounds in enriched metabolite sets were used to create dietary patterns reflecting metabolite composition, which were then tested for association with outcomes in the nested case-control subset and the full TEDDY cohort. Unsaturated phosphatidylcholines, sphingomyelins, phosphatidylethanolamines, glucosylceramides, and phospholipid ethers in infancy were inversely associated with mAb+ risk, while dicarboxylic acids were associated with an increased risk. An infancy dietary pattern representing higher levels of unsaturated phosphatidylcholines and phospholipid ethers, and lower sphingomyelins was protective for mAb+ in the nested case-control study only. Characterization of this high-risk infant metabolomics profile may help shape the future of early diagnosis or prevention efforts. |
format | Online Article Text |
id | pubmed-6794249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67942492019-10-21 Metabolite-related dietary patterns and the development of islet autoimmunity Johnson, Randi K. Vanderlinden, Lauren DeFelice, Brian C. Kechris, Katerina Uusitalo, Ulla Fiehn, Oliver Sontag, Marci Crume, Tessa Beyerlein, Andreas Lernmark, Åke Toppari, Jorma Ziegler, Anette-G. She, Jin-Xiong Hagopian, William Rewers, Marian Akolkar, Beena Krischer, Jeffrey Virtanen, Suvi M. Norris, Jill M. Sci Rep Article The role of diet in type 1 diabetes development is poorly understood. Metabolites, which reflect dietary response, may help elucidate this role. We explored metabolomics and lipidomics differences between 352 cases of islet autoimmunity (IA) and controls in the TEDDY (The Environmental Determinants of Diabetes in the Young) study. We created dietary patterns reflecting pre-IA metabolite differences between groups and examined their association with IA. Secondary outcomes included IA cases positive for multiple autoantibodies (mAb+). The association of 853 plasma metabolites with outcomes was tested at seroconversion to IA, just prior to seroconversion, and during infancy. Key compounds in enriched metabolite sets were used to create dietary patterns reflecting metabolite composition, which were then tested for association with outcomes in the nested case-control subset and the full TEDDY cohort. Unsaturated phosphatidylcholines, sphingomyelins, phosphatidylethanolamines, glucosylceramides, and phospholipid ethers in infancy were inversely associated with mAb+ risk, while dicarboxylic acids were associated with an increased risk. An infancy dietary pattern representing higher levels of unsaturated phosphatidylcholines and phospholipid ethers, and lower sphingomyelins was protective for mAb+ in the nested case-control study only. Characterization of this high-risk infant metabolomics profile may help shape the future of early diagnosis or prevention efforts. Nature Publishing Group UK 2019-10-15 /pmc/articles/PMC6794249/ /pubmed/31616039 http://dx.doi.org/10.1038/s41598-019-51251-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Johnson, Randi K. Vanderlinden, Lauren DeFelice, Brian C. Kechris, Katerina Uusitalo, Ulla Fiehn, Oliver Sontag, Marci Crume, Tessa Beyerlein, Andreas Lernmark, Åke Toppari, Jorma Ziegler, Anette-G. She, Jin-Xiong Hagopian, William Rewers, Marian Akolkar, Beena Krischer, Jeffrey Virtanen, Suvi M. Norris, Jill M. Metabolite-related dietary patterns and the development of islet autoimmunity |
title | Metabolite-related dietary patterns and the development of islet autoimmunity |
title_full | Metabolite-related dietary patterns and the development of islet autoimmunity |
title_fullStr | Metabolite-related dietary patterns and the development of islet autoimmunity |
title_full_unstemmed | Metabolite-related dietary patterns and the development of islet autoimmunity |
title_short | Metabolite-related dietary patterns and the development of islet autoimmunity |
title_sort | metabolite-related dietary patterns and the development of islet autoimmunity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794249/ https://www.ncbi.nlm.nih.gov/pubmed/31616039 http://dx.doi.org/10.1038/s41598-019-51251-4 |
work_keys_str_mv | AT johnsonrandik metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT vanderlindenlauren metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT defelicebrianc metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT kechriskaterina metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT uusitaloulla metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT fiehnoliver metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT sontagmarci metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT crumetessa metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT beyerleinandreas metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT lernmarkake metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT topparijorma metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT ziegleranetteg metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT shejinxiong metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT hagopianwilliam metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT rewersmarian metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT akolkarbeena metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT krischerjeffrey metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT virtanensuvim metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT norrisjillm metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity AT metaboliterelateddietarypatternsandthedevelopmentofisletautoimmunity |