Recent studies indicate an important role of endogenous oxidative stress in
the onset and/or in the progression of mitochondrial encephalomyopathies.
In particular, the increased production of radical species caused by altere
d mitochondrial functionality could affect both mitochondrial and nuclear D
NA integrity. We performed the micronucleus assay coupled with fluorescence
in situ hybridization (FISH) to detect chromosome damage in peripheral blo
od lymphocytes in a group of patients affected by different forms of mitoch
ondrial encephalomyopathies. Moreover the comet assay has been carried out
to detect primary and oxidative damage in the nuclear DNA. Our results show
a significant presence of both DNA and chromosome damage in patients compa
red to a matched group of controls. A reduction in DNA alterations is also
observed in patients after treatment with coenzyme-Q(10).