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Michelle D. Failla

Researcher at Vanderbilt University Medical Center

Publications -  46
Citations -  1009

Michelle D. Failla is an academic researcher from Vanderbilt University Medical Center. The author has contributed to research in topics: Autism & Medicine. The author has an hindex of 15, co-authored 35 publications receiving 776 citations. Previous affiliations of Michelle D. Failla include New York University & Ohio State University.

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IL‐1β associations with posttraumatic epilepsy development: A genetics and biomarker cohort study

TL;DR: It is hypothesized that TBI‐induced inflammation likely contributes to seizure development, and genetic variation in the interleukin‐1beta (IL‐1 β) gene, IL‐1β levels in cerebrospinal fluid and serum, and CSF/serum IL-1β ratios would predict PTE development post‐TBI.
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S100b as a prognostic biomarker in outcome prediction for patients with severe traumatic brain injury.

TL;DR: Though CSF and serum levels were highly correlated during early time points post-TBI, this association diminished over time and Multivariate logistic regression confirmed CSF S 100b profiles in predicting GOS and DRS and showed mean and peak serum S100b as acute mortality predictors after sTBI.
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Brain-Derived Neurotrophic Factor (BDNF) in Traumatic Brain Injury-Related Mortality: Interrelationships Between Genetics and Acute Systemic and Central Nervous System BDNF Profiles.

TL;DR: BDNF levels predicted mortality, in addition to gene * age interactions, suggesting levels capture additional mortality risk, in the context of age and genetic risk.
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Acute inflammatory biomarker profiles predict depression risk following moderate to severe traumatic brain injury

TL;DR: Acute CSF IBR scores show promise for identifying individuals at risk forPTD and should explore anti-inflammatory treatments for PTD, as well as prevention and screening protocols, and link inflammatory biomarkers to symptom tracking.
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Variation in the BDNF gene interacts with age to predict mortality in a prospective, longitudinal cohort with severe TBI

TL;DR: Data suggest complex relationships between BDNF and TBI mortality that interact with age to influence survival predictions beyond clinical variables alone, and evidence supporting dynamic, temporal balances of pro-survival/pro-apoptotic target receptors may explain injury and age-related gene associations.