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Multi-omics to predict changes during cold pressor test.
Kogelman, Lisette J A; Ernst, Madeleine; Falkenberg, Katrine; Mazzoni, Gianluca; Courraud, Julie; Lundgren, Li Peng; Laursen, Susan Svane; Cohen, Arieh; Olesen, Jes; Hansen, Thomas Folkmann.
Afiliação
  • Kogelman LJA; Danish Headache Center, Department of Neurology, Copenhagen University Hospital, 2600, Glostrup, Denmark. Lisette.kogelman@regionh.dk.
  • Ernst M; Section for Clinical Mass Spectrometry, Danish Center for Neonatal Screening, Department of Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Falkenberg K; Danish Headache Center, Department of Neurology, Copenhagen University Hospital, 2600, Glostrup, Denmark.
  • Mazzoni G; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Courraud J; Section for Clinical Mass Spectrometry, Danish Center for Neonatal Screening, Department of Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Lundgren LP; Section for Clinical Mass Spectrometry, Danish Center for Neonatal Screening, Department of Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Laursen SS; Section for Clinical Mass Spectrometry, Danish Center for Neonatal Screening, Department of Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Cohen A; Section for Clinical Mass Spectrometry, Danish Center for Neonatal Screening, Department of Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Olesen J; Danish Headache Center, Department of Neurology, Copenhagen University Hospital, 2600, Glostrup, Denmark.
  • Hansen TF; Danish Headache Center, Department of Neurology, Copenhagen University Hospital, 2600, Glostrup, Denmark.
BMC Genomics ; 23(1): 759, 2022 Nov 19.
Article em En | MEDLINE | ID: mdl-36402977
ABSTRACT

BACKGROUND:

The cold pressor test (CPT) is a widely used pain provocation test to investigate both pain tolerance and cardiovascular responses. We hypothesize, that performing multi-omic analyses during CPT gives the opportunity to home in on molecular mechanisms involved. Twenty-two females were phenotypically assessed before and after a CPT, and blood samples were taken. RNA-Sequencing, steroid profiling and untargeted metabolomics were performed. Each 'omic level was analyzed separately at both single-feature and systems-level (principal component [PCA] and partial least squares [PLS] regression analysis) and all 'omic levels were combined using an integrative multi-omics approach, all using the paired-sample design.

RESULTS:

We showed that PCA was not able to discriminate time points, while PLS did significantly distinguish time points using metabolomics and/or transcriptomic data, but not using conventional physiological measures. Transcriptomic and metabolomic data revealed at feature-, systems- and integrative- level biologically relevant processes involved during CPT, e.g. lipid metabolism and stress response.

CONCLUSION:

Multi-omics strategies have a great potential in pain research, both at feature- and systems- level. Therefore, they should be exploited in intervention studies, such as pain provocation tests, to gain knowledge on the biological mechanisms involved in complex traits.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metabolômica / Transcriptoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Dinamarca

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metabolômica / Transcriptoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Dinamarca