996 resultados para indirizzo :: 946 :: Letterature moderne, comparate e postcoloniali
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The interplay of amyloid and mitochondrial function is considered crucial in the pathophysiology of Alzheimer's disease (AD). We tested the association of the putative marker of mitochondrial function N-acetylaspartate (NAA) as measured by proton magnetic resonance spectroscopy within the medial temporal lobe and cerebrospinal fluid amyoid-946;42 (A946;42), total Tau and pTau181. 109 patients were recruited in a multicenter study (40 mild AD patients, 14 non-AD dementia patients, 29 mild cognitive impairment (MCI) AD-type patients, 26 MCI of non-AD type patients). NAA correlated with A946;42 within the AD group. Since the NAA concentration is coupled to neuronal mitochondrial function, the correlation between NAA and A946;42 may reflect the interaction between disrupted mitochondrial pathways and amyloid production.
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Cerebrospinal fluid amyloid-beta 1-42 (A946;1-42) and phosphorylated Tau at position 181 (pTau181) are biomarkers of Alzheimer's disease (AD). We performed an analysis and meta-analysis of genome-wide association study data on A946;1-42 and pTau181 in AD dementia patients followed by independent replication. An association was found between A946;1-42 level and a single-nucleotide polymorphism in SUCLG2 (rs62256378) (P = 2.5×10(-12)). An interaction between APOE genotype and rs62256378 was detected (P = 9.5 × 10(-5)), with the strongest effect being observed in APOE-ε4 noncarriers. Clinically, rs62256378 was associated with rate of cognitive decline in AD dementia patients (P = 3.1 × 10(-3)). Functional microglia experiments showed that SUCLG2 was involved in clearance of A946;1-42.
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1899/07/25 (A3,N14).