J 2021

Towards a comprehensive characterisation of the human internal chemical exposome: Challenges and perspectives

DAVID, Arthur, Jade CHAKER, Elliott James PRICE, Vincent BESSONNEAU, Andrew J. CHETWYND et. al.

Basic information

Original name

Towards a comprehensive characterisation of the human internal chemical exposome: Challenges and perspectives

Authors

DAVID, Arthur, Jade CHAKER, Elliott James PRICE, Vincent BESSONNEAU, Andrew J. CHETWYND, Chiara Maria VITALE, Jana KLÁNOVÁ, Douglas I. WALKER, Jean-Philippe ANTIGNAC, Robert BAROUKI and Gary W. MILLER

Edition

Environment International, OXFORD, PERGAMON-ELSEVIER SCIENCE LTD, 2021, 0160-4120

Other information

Language

English

Type of outcome

Article in a journal

Country of publisher

United Kingdom of Great Britain and Northern Ireland

Confidentiality degree

is not subject to a state or trade secret

References:

URL

Organization

Přírodovědecká fakulta – Repository – Repository

DOI

http://dx.doi.org/10.1016/j.envint.2021.106630

UT WoS

000685539700011

EID Scopus

2-s2.0-85106328122

Keywords in English

Exposome; High-Resolution Mass Spectrometry; Internal chemical exposome; Non-targeted analysis; Suspect screening; EWAS

Links

EF16_027/0008360, research and development project. EF20_079/0017045, research and development project.
Changed: 29/3/2022 03:55, RNDr. Daniel Jakubík

Abstract

V originále

The holistic characterisation of the human internal chemical exposome using high-resolution mass spectrometry (HRMS) would be a step forward to investigate the environmental AE tiology of chronic diseases with an unprecedented precision. HRMS-based methods are currently operational to reproducibly profile thousands of endogenous metabolites as well as externally-derived chemicals and their biotransformation products in a large number of biological samples from human cohorts. These approaches provide a solid ground for the discovery of unrecognised biomarkers of exposure and metabolic effects associated with many chronic diseases. Nevertheless, some limitations remain and have to be overcome so that chemical exposomics can provide unbiased detection of chemical exposures affecting disease susceptibility in epidemiological studies. Some of these limitations include (i) the lack of versatility of analytical techniques to capture the wide diversity of chemicals; (ii) the lack of analytical sensitivity that prevents the detection of exogenous (and endogenous) chemicals occurring at (ultra) trace levels from restricted sample amounts, and (iii) the lack of automation of the annotation/identification process. In this article, we discuss a number of technological and methodological limitations hindering applications of HRMS-based methods and propose initial steps to push towards a more comprehensive characterisation of the internal chemical exposome. We also discuss other challenges including the need for harmonisation and the difficulty inherent in assessing the dynamic nature of the internal chemical exposome, as well as the need for establishing a strong international collaboration, high level networking, and sustainable research infrastructure. A great amount of research, technological development and innovative bio-informatics tools are still needed to profile and characterise the "invisible" (not profiled), "hidden" (not detected) and "dark" (not annotated) components of the internal chemical exposome and concerted efforts across numerous research fields are paramount.
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