Application of the comet assay in human biomonitoring: An hCOMET perspective.
Comet assay
DNA damage
Fpg-sensitive sites
Human biomonitoring
Statistical analysis
Journal
Mutation research. Reviews in mutation research
ISSN: 1388-2139
Titre abrégé: Mutat Res Rev Mutat Res
Pays: Netherlands
ID NLM: 101632211
Informations de publication
Date de publication:
Historique:
received:
01
07
2019
revised:
29
10
2019
accepted:
07
11
2019
entrez:
21
3
2020
pubmed:
21
3
2020
medline:
10
7
2020
Statut:
ppublish
Résumé
The comet assay is a well-accepted biomonitoring tool to examine the effect of dietary, lifestyle, environmental and occupational exposure on levels of DNA damage in human cells. With such a wide range of determinants for DNA damage levels, it becomes challenging to deal with confounding and certain factors are inter-related (e.g. poor nutritional intake may correlate with smoking status). This review describes the effect of intrinsic (i.e. sex, age, tobacco smoking, occupational exposure and obesity) and extrinsic (season, environmental exposures, diet, physical activity and alcohol consumption) factors on the level of DNA damage measured by the standard or enzyme-modified comet assay. Although each factor influences at least one comet assay endpoint, the collective evidence does not indicate single factors have a large impact. Thus, controlling for confounding may be necessary in a biomonitoring study, but none of the factors is strong enough to be regarded a priori as a confounder. Controlling for confounding in the comet assay requires a case-by-case approach. Inter-laboratory variation in levels of DNA damage and to some extent also reproducibility in biomonitoring studies are issues that have haunted the users of the comet assay for years. Procedures to collect specimens, and their storage, are not standardized. Likewise, statistical issues related to both sample-size calculation (before sampling of specimens) and statistical analysis of the results vary between studies. This review gives guidance to statistical analysis of the typically complex exposure, co-variate, and effect relationships in human biomonitoring studies.
Identifiants
pubmed: 32192646
pii: S1383-5742(19)30045-6
doi: 10.1016/j.mrrev.2019.108288
pii:
doi:
Substances chimiques
Escherichia coli Proteins
0
DNA-Formamidopyrimidine Glycosylase
EC 3.2.2.23
DNA-formamidopyrimidine glycosylase, E coli
EC 3.2.2.23
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
108288Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.