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2.
Mutat Res ; 319(4): 317-23, 1993 Dec.
Article in English | MEDLINE | ID: mdl-7504206

ABSTRACT

By analogy to the techniques applied for monitoring biological effects of exposure to genotoxic agents in occupational populations, we have carried out cytogenetic monitoring in a group of inhabitants of a village (Mellery, Belgium) suspected to have been exposed to a variety of toxic environmental pollutants. These pollutants probably originated from a neighboring chemical wastes site. A group of 51 environmentally exposed and 52 reference persons (including children) were examined for the frequency of sister-chromatid exchanges (SCE) in their peripheral blood lymphocytes. The technique was further refined by using a high frequency cells (HFC) analysis. Analysis of the reference subgroups showed a significant difference between non-smoking adults and children. The influence of tobacco was clear, too. In the exposed group, no significant differences could be demonstrated between either the smokers or the non-smokers or the children. Furthermore, not only were the mean frequencies of SCE higher than in the respective reference subgroups but comparison between the two groups also showed a higher number of individuals presenting a HFC level above the background in the exposed group. Surprisingly, the difference was more pronounced for the children. A follow-up of the same exposed population carried out 18 months later and after remediation of the atmospheric chemical release, the previously observed tendencies in the exposure parameter remained unmodified.


Subject(s)
Environmental Monitoring/methods , Environmental Pollutants/adverse effects , Sister Chromatid Exchange/drug effects , Adult , Belgium , Cells, Cultured , Child , Female , Humans , Lymphocytes/ultrastructure , Male , Reference Values
3.
Article in English | MEDLINE | ID: mdl-8348059

ABSTRACT

Since the mid-eighties, a sand pit located at the boundary of Mellery, a small village in Belgium, has been used as a dumping ground for industrial waste. After a particularly dry summer, many people complained of very foul smells coming from the dumping ground. An analysis of the environmental atmosphere detected alkanes and chlorinated saturated and unsaturated hydrocarbons in various concentrations. Consequently, the Belgian Ministry of the Environment requested additional measurements from the dumping site and the surrounding regions. Given the hazards and possible ill health effects associated with simultaneous exposure to low levels of many chemicals, biomarkers of personal exposure were measured in a representative group of people living in this village. The cytogenetic consequences of daily exposure to a mixture of genotoxicants were measured by the Sister Chromatid Exchange assay. The study included a group of 51 environmentally exposed persons (including 11 children) and 52 controls. A significant increase in Sister Chromatid Exchange frequency was detected among the inhabitants of the village compared to that of the control group, especially among the children living in Mellery as compared to the matched control children.


Subject(s)
Hazardous Waste/adverse effects , Industrial Waste/adverse effects , Sister Chromatid Exchange , Adolescent , Adult , Air Pollutants/analysis , Belgium , Carcinogens/analysis , Carcinogens/pharmacology , Child , Child, Preschool , Cohort Studies , Cycloparaffins/analysis , Environmental Exposure , Female , Hazardous Waste/analysis , Humans , Hydrocarbons, Chlorinated/analysis , Industrial Waste/analysis , Male , Middle Aged , Mutagens/adverse effects , Mutagens/analysis , Polycyclic Compounds/analysis , Sister Chromatid Exchange/drug effects , Sister Chromatid Exchange/genetics , Smoking/genetics
5.
Humangenetik ; 26(3): 223-30, 1975.
Article in French | MEDLINE | ID: mdl-1132879

ABSTRACT

The lymphocytic transformation in vitro has been studied in 2 cases of ataxia-telangiectasia and compared to that of 2 controls. Significant difference was found between the two groups in the behavior of lymphocytes for two different times of culture. After 48 hrs culturing, important individual variability in RNA synthesis and lower per cent of cells in mitosis was found in the first group. After 120 hrs culturing less important DNA synthesis was found in the first group and about the same per cent of cells in mitosis. After 48 hrs cultures, cellular damage was found in the first group and after 120 hrs cultures, chromosome anomalies were found in the first group.


Subject(s)
Ataxia Telangiectasia/immunology , Chromosome Aberrations , Lymphocyte Activation , Ataxia Telangiectasia/genetics , Autoradiography , Cell Survival , Cells, Cultured , Child , DNA/biosynthesis , Humans , In Vitro Techniques , Mitosis , RNA/biosynthesis , Time Factors
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