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Lassi, M.

Publications and source records attributed to Lassi, M..

2 recordsLinked to original sources

Event-Related Potential Markers of Subject Cognitive Decline and Mild Cognitive Impairment during a sustained visuo-attentive task

Subjective cognitive decline (SCD), mild cognitive impairment (MCI), or severe Alzheimers disease stages are still lacking clear electrophysiological correlates. In 178 individuals (119 SCD, 40 MCI, and 19 healthy subjects (HS)), we analysed event-related potentials recorded during a sustained visual attention task, aiming to distinguish biomarkers associated with clinical conditions and task performance. We observed condition-specific anomalies in event-related potentials (ERPs) during visual encoding (P1/N1/P2) and decision-making (P300/P600/P900): SCD individuals showed attenuated dynamics compared to HS, while MCI individuals showed amplified dynamics, except for P300, which matched clinical severity. ERP features confirmed a non-monotonic trend, with MCI showing higher neural resource recruitment. Moreover, task performance correlated with condition-specific ERP gain and latencies across early and late ERP components. These findings enhanced the understanding of the neural mechanisms underlying cognitive decline in SCD and MCI and suggested potential biomarkers for early diagnosis and intervention. HighlightsO_LIIn encoding (P1/N1/P2) and decision (P600/P900) ERPs, SCD individuals showed attenuated dynamics compared to HS, while MCI individuals exhibited amplified dynamics compared to SCD. C_LIO_LIP300 dynamics matched clinical severity. C_LIO_LIMCI individuals demonstrated higher recruitment of neural resources, indicating a non-monotonic trend in ERP features between clinical conditions. C_LIO_LITask performance correlated with condition-specific gain and latencies across multiple ERP components. C_LI

neuroscience↗

In-vivo targeted tagging of RNA isolates cell specific transcriptional responses to environmental stimuli and identifies liver-to-adipose RNA transfer

Bio-fluids contain various circulating cell-free RNA transcripts (ccfRNAs). The composition of these ccfRNAs varies between bio-fluids and constitute tantalizing biomarker candidates for several pathologies. ccfRNAs have also been demonstrated as mediators of cellular communication, yet little is known about their function in physiological and developmental settings and most works are limited to in-vitro studies. Here, we have developed iTAG-RNA, a novel method for the unbiased tagging of RNA transcripts in mice in-vivo. We used this method to isolate hepatocytes and kidney proximal epithelial cells-specific transcriptional response to a dietary challenge without interfering with the tissue architecture, and to identify multiple hepatocyte-secreted ccfRNAs in plasma. We also identified transfer of these hepatic derived ccfRNAs to adipose tissue, where they likely serve as a buffering mechanism to maintain cholesterol and lipid homeostasis. Our findings directly demonstrate in-vivo transfer of RNAs between tissues and highlight its implications for endocrine signaling and homeostasis.

molecular biology↗