Literature DB >> 11967775

[Respiratory diseases and genotoxicity in tobacco smoke exposed children].

G Baier1, Helga Stopper, Corinna Kopp, Ulrike Winkler, Iris Zwirner-Baier.   

Abstract

BACKGROUND: Tobacco smoke, containing more than 4800 chemical substances with a large number of mutagenic and carcinogenic compounds, is the most important indoor pollution. Aim of the study was to analyse the relationship between exposure of children (2-15 years) to environmental tobacco smoke (ETS) with the amount of respiratory diseases, the occurrence of atopic diseases and the risk for genotoxic damage. PATIENTS AND METHODS: Within the last 1.5 years 216 children were included in the study. Smoking habits of the family, environmental settings, housing, nutrition, social and economic factors were assessed by a detailed questionnaire. Two different effect markers were used to assess molecular and genetic damage. Biochemical effect of ETS was quantified by 4-aminobiphenyl-hemoglobin (4-ABP-Hb) adducts and the genotoxic damage was determined by chromosomal damage as seen in the micro nucleus test in lymphocytes.
RESULTS: Chronic rhinosinusitis and allergic rhinitis are accumulated in the ETS-exposed children. In the ETS-group atopic diseases (allergic rhinitis, extrinsic asthma or neurodermatitis) were significantly more frequent (39.5 %, p = 0.01) than in the non-exposed group (23 %). In addition the genetic predisposition was significantly decreased in the ETS-group (20.8 %, p = 0.048) compared to the non-exposed group (45 %). Until now, blood samples of 63 individuals were analysed for Hb adducts and 92 for micro nuclei. Hemoglobin adducts of 4-ABP, a human carcinogenic aromatic amine, were significantly elevated in children with smoking parents (mean: 82.2pg/g Hb, p = 0.003) compared to children with non-smoking parents (mean: 60.6 pg/g Hb). ETS-exposed children showed significantly higher micro nucleus frequencies (mean ETS: 8.0/1000 binucleate (BN) cells, p = 0.001) than non-ETS exposed children (mean: 6.2/1000 BN cells).
CONCLUSION: Our data underline the thesis, that ETS plays an important role for the development of atopic diseases. The significantly increased effect markers of tobacco smoke in exposed children give evidence, that ETS causes elevated molecular and genotoxic damage in children.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 11967775     DOI: 10.1055/s-2002-25038

Source DB:  PubMed          Journal:  Laryngorhinootologie        ISSN: 0935-8943            Impact factor:   1.057


  4 in total

Review 1.  Micronuclei in neonates and children: effects of environmental, genetic, demographic and disease variables.

Authors:  Nina Holland; Alexandra Fucic; Domenico Franco Merlo; Radim Sram; Micheline Kirsch-Volders
Journal:  Mutagenesis       Date:  2011-01       Impact factor: 3.000

Review 2.  Factors Affecting the Nuclei in Newborn and Children.

Authors:  Christos Arnaoutoglou; Anastasia Keivanidou; Georgios Dragoutsos; Ioannis Tentas; Soultana Meditskou; Paul Zarogoulidis; Dimitrios Matthaios; Chrysanthi Sardeli; Aris Ioannidis; Eleni Isidora Perdikouri; Andreas Giannopoulos
Journal:  Int J Environ Res Public Health       Date:  2022-04-01       Impact factor: 3.390

3.  Environmental Tobacco Smoke in Occupational Settings: Effect and Susceptibility Biomarkers in Workers From Lisbon Restaurants and Bars.

Authors:  Nádia Vital; Susana Antunes; Henriqueta Louro; Fátima Vaz; Tânia Simões; Deborah Penque; Maria João Silva
Journal:  Front Public Health       Date:  2021-06-04

4.  Exposure to second-hand smoke and direct healthcare costs in children - results from two German birth cohorts, GINIplus and LISAplus.

Authors:  Ariane Batscheider; Sylwia Zakrzewska; Joachim Heinrich; Christina M Teuner; Petra Menn; Carl Peter Bauer; Ute Hoffmann; Sibylle Koletzko; Irina Lehmann; Olf Herbarth; Andrea von Berg; Dietrich Berdel; Ursula Krämer; Beate Schaaf; H-Erich Wichmann; Reiner Leidl
Journal:  BMC Health Serv Res       Date:  2012-10-02       Impact factor: 2.655

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.