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Nidadavolu, L.

Publications and source records attributed to Nidadavolu, L..

2 recordsLinked to original sources

Monocytes are biological sensors of aging and frailty in humans

Among older adults, frailty is clinically identifiable and characterized by increased vulnerability to adverse health outcomes. Although various tools exist to identify frailty, diagnosis often depends on late-stage clinical symptoms, which typically limit proactive intervention options. We considered whether aging and frailty information may be encoded in the single-cell behaviors and dynamic responses of primary human monocytes. Combining high-content imaging, single-cell behavior profiling, and machine learning, we demonstrated unique age- and frailty-dependent monocyte behaviors at baseline and following exposure to inflammatory stressors. Using these single-cell behaviors, we developed a deep learning neural network model called scTRAIT. scTRAIT accurately predicts the frailty status of older donors, including the capability to track and forecast longitudinal changes in frailty status. Collectively, these findings demonstrate that aging and frailty information are robustly encoded within single-cell behaviors, establishing monocytes as significant biological sensors of aging and frailty in humans. TeaserSingle-cell monocyte responses enable robust prediction of aging and frailty in humans

bioengineering↗

Characterizing Post-Mortem Brain Molecular Taxonomy of Cognitive Resilience and Translating it to Living Humans

Here, we define cognitive resilience as slower or faster cognitive decline after we regress out the effects of common brain neuropathologies. Its understanding could provide important insights into the biology underlying cognitive health, enabling the development of more effective strategies to prevent cognitive decline and dementia. However, this requires the development of a practical method to quantify resilience and measure it in living individuals, as well as identifying heterogenous pathways associated with resilience in different individuals. Here, we approach this problem by using a data-driven framework to quantify and characterize molecular signatures underlying cognitive resilience. Using multimodal contrastive trajectory inference (mcTI) on bulk RNA sequencing and tandem mass tag (TMT) proteomic data from 898 post- mortem brain samples from the Religious Orders Study and the Rush Memory and Aging Project (ROSMAP), we derived individual-level molecular pseudotime values reflecting the molecular path from high to low resilience across individuals. Additionally, we identified two distinct molecular subtypes of resilience, each characterized by unique transcriptomic and proteomic signatures, and differing associations with several phenotypes. To translate our brain-derived pseudotime and subtypes to living individuals, we developed prediction models with paired genetics, ante-mortem blood omics, clinical, psychosocial, imaging and device data from the same individuals, demonstrating the potential to predict brain molecular resilience profiles in living persons. Our findings establish a framework for quantifying resilience based on multi- level molecular signatures, identify molecularly distinct resilience subtypes, and demonstrate the feasibility of translating brain-derived molecular profiles to living individuals--laying the groundwork for the development of targeted resilience-promoting interventions in cognitive aging.

neuroscience↗