Summary
Oxidative
stress is involved in many pathophysiological processes, aging and
cancer. Assessment and amelioration of oxidative stress are
invaluable components of preventive approaches to optimizing health
and longevity.
8-OHdG
Urinary
8-hydroxy-2’-deoxyguanosine (8-OHdG) is an excellent biomarker of
oxidative stress and a risk factor for a variety of diseases
including cancer. Reactive oxygen species (ROS) are produced as a
result of normal oxygen metabolism or exposure to toxins. Excessive
levels are associated with oxidative damage to fats, proteins and
DNA. 8-OHdG is the most frequently detected and studied oxidized
part of DNA that is considered to be pre-cancerous due to its
potential for initiation and promotion of cancer. Bladder and
prostate cancers have been associated with elevated levels of
8-OHdG.
Oxidative
Stress and High 8-OHdG
Oxidative
stress and elevations of 8-OHdG have been associated with numerous
pathological processes including cystic fibrosis, eczema, rheumatoid
arthritis, pancreatitis, chronic hepatitis, inflammatory bowel
disease, and neurological diseases such as Parkinson’s, Alzheimer’s
and Huntington’s. Elevated levels of 8-OHdG also have been
associated with hyperglycemia and have been positively correlated
with HbA1c and the severity of nephropathy and retinopathy in
diabetics. Environmental factors, lifestyle choices (e.g. smoking,
recreational drugs), and some pharmaceuticals also have been
associated with elevated urine levels of 8-OHdG. Known environmental
factors include exposure to ionizing radiation (e.g. indoor radon),
asbestos, toxic metals and metal fumes (e.g. manganese, chromium and
vanadium), diesel exhaust, benzene, styrene, toluene and zylenes. In
grade school children, exposure to toxic/carcinogenic metals
released from coal-fired power plants as assessed by measurement of
elements in urine was significantly correlated with urine levels of
8-OHdG.
Oxidative
Stress and Moderate 8-OHdG
Moderately
elevated levels of 8-OHdG have been associated with inadequate
intake of carotinoids, antioxidant-rich foods and supplemental
antioxidants. A finding of an elevated level of 8-OHdG in a first
morning urine void warrants identification of the source(s) of
oxidative stress/inflammation and assessment of the primary
intracellular antioxidant glutathione. The efficacy of therapeutic
intervention to ameliorate oxidative stress should be monitored by
subsequent re-testing of urine 8-OHdG and glutathione levels.
Talk to your
health care provider about having a DNA Oxidative Damage Assay
today!
**Description
courtesy of Doctor’s Data In