Antioxidant Defence, Oxidative Stress and Oxidative Damage in Saliva, Plasma and Erythrocytes of Dementia Patients. Can Salivary AGE be a Marker of Dementia?
Magdalena ChoromańskaAnna KlimiukPaula Kostecka-SochońKarolina WilczyńskaMikołaj KwiatkowskiNatalia OkuniewskaNapoleon WaszkiewiczAnna ZalewskaMaciejczyk MateuszPublished in: International journal of molecular sciences (2017)
Oxidative stress plays a crucial role in dementia pathogenesis; however, its impact on salivary secretion and salivary qualities is still unknown. This study included 80 patients with moderate dementia and 80 healthy age- and sex-matched individuals. Salivary flow, antioxidants (salivary peroxidase, catalase, superoxide dismutase, uric acid and total antioxidant capacity), and oxidative damage products (advanced oxidation protein products, advanced glycation end products (AGE), 8-isoprostanes, 8-hydroxy-2'-deoxyguanosine and total oxidant status) were estimated in non-stimulated and stimulated saliva, as well as in plasma and erythrocytes. We show that in dementia patients the concentration/activity of major salivary antioxidants changes, and the level of oxidative damage to DNA, proteins and lipids is increased compared to healthy controls. Non-stimulated and stimulated salivary secretions were significantly reduced in dementia patients. The deterioration in mini mental state examination (MMSE) score correlated with salivary AGE levels, which when considered with receiver operating characteristic (ROC) analysis, suggests their potential role in the non-invasive diagnosis of dementia. In conclusion, dementia is associated with disturbed salivary redox homeostasis and impaired secretory function of the salivary glands. Salivary AGE may be useful in the diagnosis of dementia.
Keyphrases
- mild cognitive impairment
- cognitive impairment
- oxidative stress
- end stage renal disease
- ejection fraction
- chronic kidney disease
- newly diagnosed
- uric acid
- peritoneal dialysis
- metabolic syndrome
- dna damage
- hydrogen peroxide
- fatty acid
- high intensity
- ischemia reperfusion injury
- induced apoptosis
- heat stress
- circulating tumor
- nucleic acid