Cargando…
Blood Metabolite Signatures of Metabolic Syndrome in Two Cross-Cultural Older Adult Cohorts
Metabolic syndrome (MetS) affects an increasing number of older adults worldwide. Cross-cultural comparisons can provide insight into how factors, including genetic, environmental, and lifestyle, may influence MetS prevalence. Metabolomics, which measures the biochemical products of cell processes,...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072935/ https://www.ncbi.nlm.nih.gov/pubmed/32079087 http://dx.doi.org/10.3390/ijms21041324 |
_version_ | 1783506522256441344 |
---|---|
author | Mahajan, Uma V. Varma, Vijay R. Huang, Chiung-Wei An, Yang Tanaka, Toshiko Ferrucci, Luigi Takebayashi, Toru Harada, Sei Iida, Miho Legido-Quigley, Cristina Thambisetty, Madhav |
author_facet | Mahajan, Uma V. Varma, Vijay R. Huang, Chiung-Wei An, Yang Tanaka, Toshiko Ferrucci, Luigi Takebayashi, Toru Harada, Sei Iida, Miho Legido-Quigley, Cristina Thambisetty, Madhav |
author_sort | Mahajan, Uma V. |
collection | PubMed |
description | Metabolic syndrome (MetS) affects an increasing number of older adults worldwide. Cross-cultural comparisons can provide insight into how factors, including genetic, environmental, and lifestyle, may influence MetS prevalence. Metabolomics, which measures the biochemical products of cell processes, can be used to enhance a mechanistic understanding of how biological factors influence metabolic outcomes. In this study we examined associations between serum metabolite concentrations, representing a range of biochemical pathways and metabolic syndrome in two older adult cohorts: The Tsuruoka Metabolomics Cohort Study (TMCS) from Japan (n = 104) and the Baltimore Longitudinal Study of Aging (BLSA) from the United States (n = 146). We used logistic regression to model associations between MetS and metabolite concentrations. We found that metabolites from the phosphatidylcholines-acyl-alkyl, sphingomyelin, and hexose classes were significantly associated with MetS and risk factor outcomes in both cohorts. In BLSA, metabolites across all classes were uniquely associated with all outcomes. In TMCS, metabolites from the amino acid, biogenic amines, and free fatty acid classes were uniquely associated with MetS, and metabolites from the sphingomyelin class were uniquely associated with elevated triglycerides. The metabolites and metabolite classes we identified may be relevant for future studies exploring disease mechanisms and identifying novel precision therapy targets for individualized medicine. |
format | Online Article Text |
id | pubmed-7072935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70729352020-03-19 Blood Metabolite Signatures of Metabolic Syndrome in Two Cross-Cultural Older Adult Cohorts Mahajan, Uma V. Varma, Vijay R. Huang, Chiung-Wei An, Yang Tanaka, Toshiko Ferrucci, Luigi Takebayashi, Toru Harada, Sei Iida, Miho Legido-Quigley, Cristina Thambisetty, Madhav Int J Mol Sci Article Metabolic syndrome (MetS) affects an increasing number of older adults worldwide. Cross-cultural comparisons can provide insight into how factors, including genetic, environmental, and lifestyle, may influence MetS prevalence. Metabolomics, which measures the biochemical products of cell processes, can be used to enhance a mechanistic understanding of how biological factors influence metabolic outcomes. In this study we examined associations between serum metabolite concentrations, representing a range of biochemical pathways and metabolic syndrome in two older adult cohorts: The Tsuruoka Metabolomics Cohort Study (TMCS) from Japan (n = 104) and the Baltimore Longitudinal Study of Aging (BLSA) from the United States (n = 146). We used logistic regression to model associations between MetS and metabolite concentrations. We found that metabolites from the phosphatidylcholines-acyl-alkyl, sphingomyelin, and hexose classes were significantly associated with MetS and risk factor outcomes in both cohorts. In BLSA, metabolites across all classes were uniquely associated with all outcomes. In TMCS, metabolites from the amino acid, biogenic amines, and free fatty acid classes were uniquely associated with MetS, and metabolites from the sphingomyelin class were uniquely associated with elevated triglycerides. The metabolites and metabolite classes we identified may be relevant for future studies exploring disease mechanisms and identifying novel precision therapy targets for individualized medicine. MDPI 2020-02-16 /pmc/articles/PMC7072935/ /pubmed/32079087 http://dx.doi.org/10.3390/ijms21041324 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mahajan, Uma V. Varma, Vijay R. Huang, Chiung-Wei An, Yang Tanaka, Toshiko Ferrucci, Luigi Takebayashi, Toru Harada, Sei Iida, Miho Legido-Quigley, Cristina Thambisetty, Madhav Blood Metabolite Signatures of Metabolic Syndrome in Two Cross-Cultural Older Adult Cohorts |
title | Blood Metabolite Signatures of Metabolic Syndrome in Two Cross-Cultural Older Adult Cohorts |
title_full | Blood Metabolite Signatures of Metabolic Syndrome in Two Cross-Cultural Older Adult Cohorts |
title_fullStr | Blood Metabolite Signatures of Metabolic Syndrome in Two Cross-Cultural Older Adult Cohorts |
title_full_unstemmed | Blood Metabolite Signatures of Metabolic Syndrome in Two Cross-Cultural Older Adult Cohorts |
title_short | Blood Metabolite Signatures of Metabolic Syndrome in Two Cross-Cultural Older Adult Cohorts |
title_sort | blood metabolite signatures of metabolic syndrome in two cross-cultural older adult cohorts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072935/ https://www.ncbi.nlm.nih.gov/pubmed/32079087 http://dx.doi.org/10.3390/ijms21041324 |
work_keys_str_mv | AT mahajanumav bloodmetabolitesignaturesofmetabolicsyndromeintwocrossculturalolderadultcohorts AT varmavijayr bloodmetabolitesignaturesofmetabolicsyndromeintwocrossculturalolderadultcohorts AT huangchiungwei bloodmetabolitesignaturesofmetabolicsyndromeintwocrossculturalolderadultcohorts AT anyang bloodmetabolitesignaturesofmetabolicsyndromeintwocrossculturalolderadultcohorts AT tanakatoshiko bloodmetabolitesignaturesofmetabolicsyndromeintwocrossculturalolderadultcohorts AT ferrucciluigi bloodmetabolitesignaturesofmetabolicsyndromeintwocrossculturalolderadultcohorts AT takebayashitoru bloodmetabolitesignaturesofmetabolicsyndromeintwocrossculturalolderadultcohorts AT haradasei bloodmetabolitesignaturesofmetabolicsyndromeintwocrossculturalolderadultcohorts AT iidamiho bloodmetabolitesignaturesofmetabolicsyndromeintwocrossculturalolderadultcohorts AT legidoquigleycristina bloodmetabolitesignaturesofmetabolicsyndromeintwocrossculturalolderadultcohorts AT thambisettymadhav bloodmetabolitesignaturesofmetabolicsyndromeintwocrossculturalolderadultcohorts |