SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Scholl M) "

Sökning: WFRF:(Scholl M)

  • Resultat 41-45 av 45
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
41.
  • Prestia, Annapaola, et al. (författare)
  • Prediction of AD dementia by biomarkers following the NIA-AA and IWG diagnostic criteria in MCI patients from three European memory clinics
  • 2015
  • Ingår i: Alzheimer's & Dementia. - : Wiley. - 1552-5260 .- 1552-5279. ; 11:10, s. 1191-1201
  • Tidskriftsartikel (refereegranskat)abstract
    • Introduction: Proposed diagnostic criteria (international working group and National Institute on Aging and Alzheimer's Association) for Alzheimer's disease (AD) include markers of amyloidosis (abnormal cerebrospinal fluid [CSF] amyloid beta [A beta]42) and neurodegeneration (hippocampal atrophy, temporo-parietal hypometabolism on [18F]-fluorodeoxyglucose-positron emission tomography (FDG-PET), and abnormal CSF tau). We aim to compare the accuracy of these biomarkers, individually and in combination, in predicting AD among mild cognitive impairment (MCI) patients. Methods: In 73 MCI patients, followed to ascertain AD progression, markers were measured. Sensitivity and specificity, positive (LR+) and negative (LR-) likelihood ratios, and crude and adjusted hazard ratios were computed. Results: Twenty-nine MCI patients progressed and 44 remained stable. Positivity to any marker achieved the lowest LR- (0.0), whereas the combination A beta 42 plus FDG-PET achieved the highest LR+ (6.45). In a survival analysis, positivity to any marker was associated with 100% conversion rate, whereas negativity to all markers was associated with 100% stability. Discussion: The best criteria combined amyloidosis and neurodegeneration biomarkers, whereas the individual biomarker with the best performance was FDG-PET.
  •  
42.
  • Prestia, Annapaola, et al. (författare)
  • Prediction of dementia in MCI patients based on core diagnostic markers for Alzheimer disease
  • 2013
  • Ingår i: Neurology. - 0028-3878 .- 1526-632X. ; 80:11, s. 1048-1056
  • Tidskriftsartikel (refereegranskat)abstract
    • Objectives: The current model of Alzheimer disease (AD) stipulates that brain amyloidosis biomarkers turn abnormal earliest, followed by cortical hypometabolism, and finally brain atrophy ones. The aim of this study is to provide clinical evidence of the model in patients with mild cognitive impairment (MCI). Methods: A total of 73 patients with MCI from 3 European memory clinics were included. Brain amyloidosis was assessed by CSF A beta 42 concentration, cortical metabolism by an index of temporoparietal hypometabolism on FDG-PET, and brain atrophy by automated hippocampal volume. Patients were divided into groups based on biomarker positivity: 1) A beta 422- FDG-PET- Hippo-, 2) A beta 42+ FDG-PET- Hippo-, 3) A beta 42+ FDG-PET + Hippo-, 4) A beta 42+ FDG-PET+ Hippo+, and 5) any other combination not in line with the model. Measures of validity were prevalence of group 5, increasing incidence of progression to dementia with increasing biological severity, and decreasing conversion time. Results: When patients with MCI underwent clinical follow-up, 29 progressed to dementia, while 44 remained stable. A total of 26% of patients were in group 5. Incident dementia was increasing with greater biological severity in groups 1 to 5 from 4% to 27%, 64%, and 100% (p for trend, 0.0001), and occurred increasingly earlier (p for trend = 0.024). Conclusions: The core biomarker pattern is in line with the current pathophysiologic model of AD. Fully normal and fully abnormal pattern is associated with exceptional and universal development of dementia. Cases not in line might be due to atypical neurobiology or inaccurate thresholds for biomarker (ab) normality. 
  •  
43.
  •  
44.
  • Uebbing, S, et al. (författare)
  • Modulation of microRNA processing by 5-lipoxygenase
  • 2021
  • Ingår i: FASEB journal : official publication of the Federation of American Societies for Experimental Biology. - 1530-6860. ; 35:2, s. e21193-
  • Tidskriftsartikel (refereegranskat)
  •  
45.
  • Wimmer, M. A., et al. (författare)
  • What are the future possibilities of eDemocracy? : A discussion paper
  • 2007
  • Ingår i: Electronic Government, Proceedings. - 9783540744436 ; , s. 401-411
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
    • This paper presents some future possibilities for eDemocracy tools and considers how these new technologies might conflict with our basic assumptions about what democracy should be. I hope this paper will contribute to discussion of under what situations different forms of eDemocracy are appropriate. The possibilities and repercussions of user profiling, voting outside of polling booths, longer decision-making periods, changeable election results and weighted voted are considered. Although none are necessarily advisable, this paper suggests they might be interesting to consider.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 41-45 av 45

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy