10 research outputs found

    Modes of Aβ toxicity in Alzheimer’s disease

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    Alzheimer’s disease (AD) is reaching epidemic proportions, yet a cure is not yet available. While the genetic causes of the rare familial inherited forms of AD are understood, the causes of the sporadic forms of the disease are not. Histopathologically, these two forms of AD are indistinguishable: they are characterized by amyloid-β (Aβ) peptide-containing amyloid plaques and tau-containing neurofibrillary tangles. In this review we compare AD to frontotemporal dementia (FTD), a subset of which is characterized by tau deposition in the absence of overt plaques. A host of transgenic animal AD models have been established through the expression of human proteins with pathogenic mutations previously identified in familial AD and FTD. Determining how these mutant proteins cause disease in vivo should contribute to an understanding of the causes of the more frequent sporadic forms. We discuss the insight transgenic animal models have provided into Aβ and tau toxicity, also with regards to mitochondrial function and the crucial role tau plays in mediating Aβ toxicity. We also discuss the role of miRNAs in mediating the toxic effects of the Aβ peptide

    Development of an Offline-Friend Addiction Questionnaire (O-FAQ): Are most people really social addicts?

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    A growing number of self-report measures aim to define interactions with social media in a pathological behavior framework; often using terminology focused on identifying those who are ‘addicted’ to engaging with others online. Specifically, measures of ‘social media addiction’ focus on motivations for online social information seeking, many of which could be motivations for offline social information seeking. It could be the case that these same measures could reveal a pattern of friend addiction in general. This study develops the Offline-Friend Addiction Questionnaire (O-FAQ) by re-wording items from highly-cited pathological social media use scales to reflect “spending time with friends”. Our methodology for validation follows literature precedent in social media addiction scales. The O-FAQ had a three-factor solution in an exploratory sample of N=807 and these factors were stable in a four-week retest (r= .72 to .86) and was validated against personality traits, and risk-taking behavior, in conceptually plausible directions. Using the same ‘polythetic classification techniques’ as pathological social media use studies, we were able to classify 69% of our sample as addicted to spending time with their friends. The discussion of our satirical research is a critical reflection on the role of measurement and human sociality in social media research. We question the extent to which connecting with others can be considered an ‘addiction’ and issues with the validation of new ‘addiction’ measures without relevant medical constructs. Readers should approach our measure with a level of skepticism that should be afforded to current social media addiction measures

    Organolead Compounds

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