Analysis of lipophilic fluorescent products in blood of Alzheimer's disease patients
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26991927
PubMed Central
PMC4929292
DOI
10.1111/jcmm.12824
Knihovny.cz E-zdroje
- Klíčová slova
- Alzheimer's disease, biomarkers, blood, lipofuscin-like pigments, oxidative stress,
- MeSH
- Alzheimerova nemoc krev MeSH
- erytrocyty metabolismus MeSH
- fluorescenční spektrometrie MeSH
- lidé středního věku MeSH
- lidé MeSH
- lipidy krev MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- lipidy MeSH
Alzheimer's disease (AD) is a severe neurodegenerative disorder characterized by cognitive decline. Prodromal stage of AD, also called mild cognitive impairment (MCI), especially its amnestic type (aMCI), precedes dementia stage of AD. There are currently no reliable diagnostic biomarkers of AD in the blood. Alzheimer's disease is accompanied by increased oxidative stress in brain, which leads to oxidative damage and accumulation of free radical reaction end-products. In our study, specific products of lipid peroxidation in the blood of AD patients were studied. Lipophilic extracts of erythrocytes (AD dementia = 19, aMCI = 27, controls = 16) and plasma (AD dementia = 11, aMCI = 17, controls = 16) were analysed by fluorescence spectroscopy. The level of these products is significantly increased in erythrocytes and plasma of AD dementia and aMCI patients versus controls. We concluded that oxidative stress end-products are promising new biomarkers of AD, but further detailed characterisation of these products is needed.
Zobrazit více v PubMed
Petersen RC. Mild cognitive impairment as a diagnostic entity. J Intern Med. 2004; 256: 183–94. Doi:10.1111/j.1365‐2796.2004.01388.x. PubMed DOI
Sperling RA, Aisen PS, Beckett LA, et al Toward defining the preclinical stages of Alzheimer's disease: recommendations from the National Institute on Aging‐Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimers Dement. 2011; 7: 280–92. Doi:10.1016/j.jalz.2011.03.003. PubMed DOI PMC
Skoumalová A, Hort J. Blood markers of oxidative stress in Alzheimer's disease. J Cell Mol Med. 2012; 16: 2291–300. PubMed PMC
Dalle‐Donne I, Rossi R, Colombo R, et al Biomarkers of oxidative damage in human disease. Clin Chem. 2006; 52: 601–23. PubMed
Skoumalova A, Rofina J, Schwippelova Z, et al The role of free radical in canine counterpart of senile dementia of the Alzheimer type. Exp Gerontol. 2003; 38: 711–9. PubMed
Hort J, Glosova L, Vyhnalek M, et al The liquor tau protein and beta amyloid in Alzheimer's disease. Cesk Slov Neurol N. 2007; 70: 30–6.
Hort J, Bartos A, Pirttila T, et al Use of cerebrospinal fluid biomarkers in diagnosis of dementia across Europe. Eur J Neurol. 2010; 17: 90–6. PubMed
Farrall AJ, Wardlaw JM. Blood‐brain barrier: ageing and microvaskular disease – systematic review and metaanalysis. Neurobiol Aging. 2009; 30: 337–52. PubMed
Skoumalova A, Ivica J, Santorova P, et al The lipid peroxidation products as possible markers of Alzheimer's disease in blood. Exp Gerontol. 2011; 46: 38–42. PubMed
Yesavage JA. Geriatric depression Scale. Psychopharmacol Bull. 1988; 24: 709–11. PubMed
Fazekas F, Chawluk JB, Alavi A, et al MR signal abnormalities at 1.5 T in Alzheimer's dementia and normal aging. Am J Roentgenol. 1987; 149: 351–6. PubMed
McKhann G, Drachman D, Folstein M, et al Clinical diagnosis of Alzheimer's disease: report of the NINCDS‐ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology. 1984; 34: 939–44. PubMed
Laczo J, Andel R, Vlcek K, et al Spatial navigation and APOE in amnestic mild cognitive impairment. Neurodegener Dis. 2011; 8: 169–77. Doi:10.1159/000321581. PubMed DOI
Goldstein BD, McDonagh EM. Spectrofluorescent detection of in vivo red cell lipid peroxidation in patients treated with diaminodiphenylsulphone. J Clin. Invest. 1976; 57: 1302–7. PubMed PMC
Pratico D. Evidence of oxidative stress in Alzheimer's disease brain and antioxidant therapy. Ann NY Acad. Sci. 2008; 1147: 70–8. Doi:10.1196/annals.1427.010. PubMed DOI
Montine TJ, Neely MD, Quinn JF, et al Lipid peroxidation in aging brain and Alzheimer's disease. Free Radic Biol Med. 2002; 33: 620–6. PubMed
Chio KS, Tappel AL. Synthesis and characterisation of the fluorescent products derived from malondialdehyde and amino acids. Biochemistry. 1969; 8: 155–67. PubMed
Baldeiras I, Santana I, Proenca ET, et al Peripheral oxidative damage in mild cognitive impairment and mild Alzeimer's disease. J Alzheimers Dis. 2008; 15: 117–28. PubMed
Wilhelm J, Herget J. Hypoxia induces free radical damage to rat erythrocytes and spleen: analysis of the fluorescent end‐products of lipid peroxidation. Int J Biochem Cell Biol. 1999; 31: 671–81. PubMed