TY - JOUR
T1 - Human micronucleus project
T2 - International database comparison for results with the cytokinesis-block micronucleus assay in human lymphocytes: I. Effect of laboratory protocol, scoring criteria, and host factors on the frequency of micronuclei
AU - Bonassi, Stefano
AU - Fenech, Michael
AU - Lando, Cecilia
AU - Lin, Yi ping
AU - Ceppi, Marcello
AU - Peter Chang, Wushou
AU - Holland, Nina
AU - Kirsch-Volders, Micheline
AU - Zeiger, E.
AU - Ban, Sadayuki
AU - Barale, Roberto
AU - Bigatti, Maria Paola
AU - Bolognesi, Claudia
AU - Jia, Cao
AU - Di Giorgio, Marina
AU - Ferguson, Lynnette R.
AU - Fucic, Aleksandra
AU - Lima, Omar Garcia
AU - Hrelia, P.
AU - Krishnaja, Ayyathan P.
AU - Lee, Tung Kwang
AU - Migliore, Lucia
AU - Mikhalevich, Ludmilla
AU - Mirkova, Ekaterina
AU - Mosesso, Pasquale
AU - Müller, Wolfgang Ulrich
AU - Odagiri, Youichi
AU - Scarffi, Maria Rosaria
AU - Szabova, Elena
AU - Vorobtsova, Irena
AU - Vral, Anne
AU - Zijno, Andrea
PY - 2001
Y1 - 2001
N2 - Micronucleus (MN) expression in peripheral blood lymphocytes is well established as a standard method for monitoring chromosome damage in human populations. The first results of an analysis of pooled data from laboratories using the cytokinesis-block micronucleus (CBMN) assay and participating in the HUMN (HUman MicroNucleus project) international collaborative study are presented. The effects of laboratory protocol, scoring criteria, and host factors on baseline micronucleated binucleate cell (MNC) frequency are evaluated, and a reference range of "normal" values against which future studies may be compared is provided. Primary data from historical records were submitted by 25 laboratories distributed in 16 countries. This resulted in a database of nearly 7000 subjects. Potentially significant differences were present in the methods used by participating laboratories, such as in the type of culture medium, the concentration of cytochalasin-B, the percentage of fetal calf serum, and in the culture method. Differences in criteria for scoring micronuclei were also evident. The overall median MNC frequency in nonexposed (i.e., normal) subjects was 6.5‰ and the interquartile range was between 3 and 12‰. An increase in MNC frequency with age was evident in all but two laboratories. The effect of gender, although not so evident in all databases, was also present, with females having a 19% higher level of MNC frequency (95% confidence interval: 14-24%). Statistical analyses were performed using random-effects models for correlated data. Our best model, which included exposure to genotoxic factors, host factors, methods, and scoring criteria, explained 75% of the total variance, with the largest contribution attributable to laboratory methods.
AB - Micronucleus (MN) expression in peripheral blood lymphocytes is well established as a standard method for monitoring chromosome damage in human populations. The first results of an analysis of pooled data from laboratories using the cytokinesis-block micronucleus (CBMN) assay and participating in the HUMN (HUman MicroNucleus project) international collaborative study are presented. The effects of laboratory protocol, scoring criteria, and host factors on baseline micronucleated binucleate cell (MNC) frequency are evaluated, and a reference range of "normal" values against which future studies may be compared is provided. Primary data from historical records were submitted by 25 laboratories distributed in 16 countries. This resulted in a database of nearly 7000 subjects. Potentially significant differences were present in the methods used by participating laboratories, such as in the type of culture medium, the concentration of cytochalasin-B, the percentage of fetal calf serum, and in the culture method. Differences in criteria for scoring micronuclei were also evident. The overall median MNC frequency in nonexposed (i.e., normal) subjects was 6.5‰ and the interquartile range was between 3 and 12‰. An increase in MNC frequency with age was evident in all but two laboratories. The effect of gender, although not so evident in all databases, was also present, with females having a 19% higher level of MNC frequency (95% confidence interval: 14-24%). Statistical analyses were performed using random-effects models for correlated data. Our best model, which included exposure to genotoxic factors, host factors, methods, and scoring criteria, explained 75% of the total variance, with the largest contribution attributable to laboratory methods.
KW - Biomarkers
KW - Cytokinesis-block micronucleus assay
KW - DNA damage
KW - Peripheral blood lymphocytes
KW - Pooled reanalysis
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U2 - 10.1002/1098-2280(2001)37:1<31::AID-EM1004>3.0.CO;2-P
DO - 10.1002/1098-2280(2001)37:1<31::AID-EM1004>3.0.CO;2-P
M3 - Article
C2 - 11170240
AN - SCOPUS:0035144198
SN - 0893-6692
VL - 37
SP - 31
EP - 45
JO - Environmental and Molecular Mutagenesis
JF - Environmental and Molecular Mutagenesis
IS - 1
ER -