Chromosomal damage in human diploid fibroblasts by intermittent exposure to extremely low-frequency electromagnetic fields
Bioeffects Seen
Authors not listed · 2005
Intermittent ELF-EMF at 1 mT caused a time-dependent increase in micronuclei that became significant after 10 hours and increased chromosomal aberrations up to 10-fold.
Plain English Summary
Summary written for general audiences
Researchers exposed cultured human fibroblasts to intermittent 50 Hz ELF-EMF (5 minutes on, 10 minutes off) at 1 mT for 2 to 24 hours. Micronuclei frequency increased in a time-dependent manner, becoming statistically significant after 10 hours and plateauing at roughly three times the basal level after about 15 hours. Chromosomal aberrations were also elevated, reaching up to 10-fold above baseline.
Exposure Information
Specific exposure levels were not quantified in this study.
Cite This Study
Unknown (2005). Chromosomal damage in human diploid fibroblasts by intermittent exposure to extremely low-frequency electromagnetic fields.
Show BibTeX
@article{chromosomal_damage_in_human_diploid_fibroblasts_by_intermittent_exposure_to_extremely_low_frequency_electromagnetic_fields_ce1466,
author = {Unknown},
title = {Chromosomal damage in human diploid fibroblasts by intermittent exposure to extremely low-frequency electromagnetic fields},
year = {2005},
doi = {10.1016/J.MRGENTOX.2005.04.013},
}Quick Questions About This Study
The study used intermittent 50 Hz sinusoidal ELF-EMF at 1 mT with a 5 minutes on, 10 minutes off cycle for 2 to 24 hours.
Micronuclei increased in a time-dependent manner, becoming significant after 10 hours and reaching about three times the basal level after approximately 15 hours.
Chromosomal aberrations were increased up to 10-fold above basal levels.
The authors concluded that the data strongly indicate a clastogenic potential of intermittent low-frequency electromagnetic fields, which may lead to considerable chromosomal damage in dividing cells.
They noted that environmental ELF-EMF exposure has been implicated in human cancer development and that understanding chromosomal effects is important for risk assessment.