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The need for reliable biomarkers for monitoring potential treatments in Alzheimer's disease (CROSBI ID 605179)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Šimić, Goran The need for reliable biomarkers for monitoring potential treatments in Alzheimer's disease // Conference proceedings INTERDISCIPLINARY CHEMICAL APPROACHES FOR NEUROPATHOLOGY CM1103 \4th Neuroscience Day University of Malta XJENZA Journal of the Malta Chamber of Scientists 2013, Vol. 1 (Suppl. 1) / Giuseppe Di Giovani and Rona R. Ramsay (ur.). Valletta: Malta Chamber of Scientists and Malta Physiological Society, 2013. str. 106-106

Podaci o odgovornosti

Šimić, Goran

engleski

The need for reliable biomarkers for monitoring potential treatments in Alzheimer's disease

The search for predictive biomarkers for Alzheimer’s disease (AD) is a high priority in neurodegenerative disease research underlined by the lack of significant progress in identifying new treatments for the past 12 years. Despite major efforts and considerable investments the only treatments approved for AD are only palliative. They include the cholinesterase inhibitors (donepezil, galantamine, and rivastigmine) that act on the cholinergic deficit, and the NMDA receptor antagonist, memantine, which has neuroprotective effects. These agents are generally considered to have marginal efficacy. As it can be logically assumed that a late therapeutic intervention would be less efficient than an early one, development of biomarkers for AD both to diagnose the disease early and to follow-up its progression, remains a major challenge. Currently, it is comprised of 6 main approaches: 1) behavioral assessment, including measurement of cognitive status using various neuropsychological scales (MMSE, ADAS-Cog, etc.) ; 2) changes in brain structure (mainly volume of the cerebral cortex, particularly entorhinal cortex and hippocampus) ; 3) alterations in brain metabolism (most notably within the default mode network) by using FDG-PET and fMRI ; 4) measurement of β-amyloid load within the brain by PIB-PET ; 5) cerebrospinal fluid (CSF) biomarker profiles (the three main CSF biomarkers of AD being β-amyloid, total tau, and phosphorylated forms of tau proteins) ; and 6) post-mortem confirmation of characteristic AD histopathology. In my talk I will attempt to describe new developments within each of these biomarker approaches by analyzing their pathological specificity, early diagnostic sensitivity, and correlation with AD progression. Finally, I will argue that, despite numerous publications and recommendation criteria, the predictive usefulness of these various biomarker approaches, individually or collectively, has yet to be established.

Alzheimer's disease; amyloid beta; default mode network; energy metabolism; pathogenesis; tau protein

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Podaci o prilogu

106-106.

2013.

objavljeno

Podaci o matičnoj publikaciji

Conference proceedings INTERDISCIPLINARY CHEMICAL APPROACHES FOR NEUROPATHOLOGY CM1103 \4th Neuroscience Day University of Malta XJENZA Journal of the Malta Chamber of Scientists 2013, Vol. 1 (Suppl. 1)

Giuseppe Di Giovani and Rona R. Ramsay

Valletta: Malta Chamber of Scientists and Malta Physiological Society

1818-7250

Podaci o skupu

Interdisciplinary Chemical Approaches for Neuropathology with 4th Neuroscience Day at University of Malta

predavanje

22.10.2013-25.10.2013

Valletta, Malta

Povezanost rada

Temeljne medicinske znanosti, Kliničke medicinske znanosti, Psihologija