“Micronuclei and Disease” special issue: Aims, scope, and synthesis of outcomes

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

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“Micronuclei and Disease” special issue : Aims, scope, and synthesis of outcomes. / Fenech, Michael; Knasmueller, Siegfried; Knudsen, Lisbeth E.; Kirsch-Volders, Micheline; Deo, Permal; Franzke, Bernhard; Stopper, Helga; Andreassi, Maria Grazia; Bolognesi, Claudia; Dhillon, Varinderpal S.; Laffon, Blanca; Wagner, Karl Heinz; Bonassi, Stefano.

I: Mutation Research - Reviews in Mutation Research, Bind 788, 108384, 2021.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Fenech, M, Knasmueller, S, Knudsen, LE, Kirsch-Volders, M, Deo, P, Franzke, B, Stopper, H, Andreassi, MG, Bolognesi, C, Dhillon, VS, Laffon, B, Wagner, KH & Bonassi, S 2021, '“Micronuclei and Disease” special issue: Aims, scope, and synthesis of outcomes', Mutation Research - Reviews in Mutation Research, bind 788, 108384. https://doi.org/10.1016/j.mrrev.2021.108384

APA

Fenech, M., Knasmueller, S., Knudsen, L. E., Kirsch-Volders, M., Deo, P., Franzke, B., Stopper, H., Andreassi, M. G., Bolognesi, C., Dhillon, V. S., Laffon, B., Wagner, K. H., & Bonassi, S. (2021). “Micronuclei and Disease” special issue: Aims, scope, and synthesis of outcomes. Mutation Research - Reviews in Mutation Research, 788, [108384]. https://doi.org/10.1016/j.mrrev.2021.108384

Vancouver

Fenech M, Knasmueller S, Knudsen LE, Kirsch-Volders M, Deo P, Franzke B o.a. “Micronuclei and Disease” special issue: Aims, scope, and synthesis of outcomes. Mutation Research - Reviews in Mutation Research. 2021;788. 108384. https://doi.org/10.1016/j.mrrev.2021.108384

Author

Fenech, Michael ; Knasmueller, Siegfried ; Knudsen, Lisbeth E. ; Kirsch-Volders, Micheline ; Deo, Permal ; Franzke, Bernhard ; Stopper, Helga ; Andreassi, Maria Grazia ; Bolognesi, Claudia ; Dhillon, Varinderpal S. ; Laffon, Blanca ; Wagner, Karl Heinz ; Bonassi, Stefano. / “Micronuclei and Disease” special issue : Aims, scope, and synthesis of outcomes. I: Mutation Research - Reviews in Mutation Research. 2021 ; Bind 788.

Bibtex

@article{9f5ac96f7d3b4e6c9da4e016e61d86e9,
title = "“Micronuclei and Disease” special issue: Aims, scope, and synthesis of outcomes",
abstract = "The purpose of the “Micronuclei and Disease” special issue (SI) is to: (i) Determine the level of evidence for association of micronuclei (MN), a biomarker of numerical and structural chromosomal aberrations, with risk of specific diseases in humans; (ii) Define plausible mechanisms that explain association of MN with each disease; (iii) Identify knowledge gaps and research needed to translate MN assays into clinical practice. The “MN and Disease” SI includes 14 papers. The first is a review of mechanisms of MN formation and their consequences in humans. 11 papers are systematic reviews and/or meta-analyses of the association of MN with reproduction, child health, inflammation, auto-immune disease, glycation, metabolic diseases, chronic kidney disease, cardiovascular disease, eleven common cancers, ageing and frailty. The penultimate paper focuses on effect of interventions on MN frequency in the elderly. A road map for translation of MN data into clinical practice is the topic of the final paper. The majority of reviewed studies were case-control studies in which the ratio of mean MN frequency in disease cases relative to controls, i.e. the mean ratio (MR), was calculated. The mean of these MR values, estimated by meta-analyses, for lymphocyte and buccal cell MN in non-cancer diseases were 2.3 and 3.6 respectively, and for cancers they were 1.7 and 2.6 respectively. The highest MR values were observed in studies of cancer cases in which MN were measured in the same tissue as the tumour (MR = 4.9–10.8). This special issue is an important milestone in the evidence supporting MN as a reliable genomic biomarker of developmental and degenerative disease risk. These advances, together with results from prospective cohort studies, are helping to identify diseases in which MN assays can be practically employed in the clinical setting to better identify high risk patients and to prioritise them for preventive therapy.",
keywords = "Ageing, Cancer, Cardiovascular disease, Disease, Inflammation, Micronuclei",
author = "Michael Fenech and Siegfried Knasmueller and Knudsen, {Lisbeth E.} and Micheline Kirsch-Volders and Permal Deo and Bernhard Franzke and Helga Stopper and Andreassi, {Maria Grazia} and Claudia Bolognesi and Dhillon, {Varinderpal S.} and Blanca Laffon and Wagner, {Karl Heinz} and Stefano Bonassi",
note = "Publisher Copyright: {\textcopyright} 2021 The Authors",
year = "2021",
doi = "10.1016/j.mrrev.2021.108384",
language = "English",
volume = "788",
journal = "Mutation Research - Reviews",
issn = "1383-5742",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - “Micronuclei and Disease” special issue

T2 - Aims, scope, and synthesis of outcomes

AU - Fenech, Michael

AU - Knasmueller, Siegfried

AU - Knudsen, Lisbeth E.

AU - Kirsch-Volders, Micheline

AU - Deo, Permal

AU - Franzke, Bernhard

AU - Stopper, Helga

AU - Andreassi, Maria Grazia

AU - Bolognesi, Claudia

AU - Dhillon, Varinderpal S.

AU - Laffon, Blanca

AU - Wagner, Karl Heinz

AU - Bonassi, Stefano

N1 - Publisher Copyright: © 2021 The Authors

PY - 2021

Y1 - 2021

N2 - The purpose of the “Micronuclei and Disease” special issue (SI) is to: (i) Determine the level of evidence for association of micronuclei (MN), a biomarker of numerical and structural chromosomal aberrations, with risk of specific diseases in humans; (ii) Define plausible mechanisms that explain association of MN with each disease; (iii) Identify knowledge gaps and research needed to translate MN assays into clinical practice. The “MN and Disease” SI includes 14 papers. The first is a review of mechanisms of MN formation and their consequences in humans. 11 papers are systematic reviews and/or meta-analyses of the association of MN with reproduction, child health, inflammation, auto-immune disease, glycation, metabolic diseases, chronic kidney disease, cardiovascular disease, eleven common cancers, ageing and frailty. The penultimate paper focuses on effect of interventions on MN frequency in the elderly. A road map for translation of MN data into clinical practice is the topic of the final paper. The majority of reviewed studies were case-control studies in which the ratio of mean MN frequency in disease cases relative to controls, i.e. the mean ratio (MR), was calculated. The mean of these MR values, estimated by meta-analyses, for lymphocyte and buccal cell MN in non-cancer diseases were 2.3 and 3.6 respectively, and for cancers they were 1.7 and 2.6 respectively. The highest MR values were observed in studies of cancer cases in which MN were measured in the same tissue as the tumour (MR = 4.9–10.8). This special issue is an important milestone in the evidence supporting MN as a reliable genomic biomarker of developmental and degenerative disease risk. These advances, together with results from prospective cohort studies, are helping to identify diseases in which MN assays can be practically employed in the clinical setting to better identify high risk patients and to prioritise them for preventive therapy.

AB - The purpose of the “Micronuclei and Disease” special issue (SI) is to: (i) Determine the level of evidence for association of micronuclei (MN), a biomarker of numerical and structural chromosomal aberrations, with risk of specific diseases in humans; (ii) Define plausible mechanisms that explain association of MN with each disease; (iii) Identify knowledge gaps and research needed to translate MN assays into clinical practice. The “MN and Disease” SI includes 14 papers. The first is a review of mechanisms of MN formation and their consequences in humans. 11 papers are systematic reviews and/or meta-analyses of the association of MN with reproduction, child health, inflammation, auto-immune disease, glycation, metabolic diseases, chronic kidney disease, cardiovascular disease, eleven common cancers, ageing and frailty. The penultimate paper focuses on effect of interventions on MN frequency in the elderly. A road map for translation of MN data into clinical practice is the topic of the final paper. The majority of reviewed studies were case-control studies in which the ratio of mean MN frequency in disease cases relative to controls, i.e. the mean ratio (MR), was calculated. The mean of these MR values, estimated by meta-analyses, for lymphocyte and buccal cell MN in non-cancer diseases were 2.3 and 3.6 respectively, and for cancers they were 1.7 and 2.6 respectively. The highest MR values were observed in studies of cancer cases in which MN were measured in the same tissue as the tumour (MR = 4.9–10.8). This special issue is an important milestone in the evidence supporting MN as a reliable genomic biomarker of developmental and degenerative disease risk. These advances, together with results from prospective cohort studies, are helping to identify diseases in which MN assays can be practically employed in the clinical setting to better identify high risk patients and to prioritise them for preventive therapy.

KW - Ageing

KW - Cancer

KW - Cardiovascular disease

KW - Disease

KW - Inflammation

KW - Micronuclei

U2 - 10.1016/j.mrrev.2021.108384

DO - 10.1016/j.mrrev.2021.108384

M3 - Review

C2 - 34893149

AN - SCOPUS:85108012110

VL - 788

JO - Mutation Research - Reviews

JF - Mutation Research - Reviews

SN - 1383-5742

M1 - 108384

ER -

ID: 283735616