Thomas Frederick Floyd
VerifiedUniversity of Pennsylvania · Rehabilitation Medicine
Active 1981–2025
Research topics
- Medicine
- Cardiology
- Internal medicine
- Anesthesia
- Surgery
Selected publications
Journal of Cardiothoracic and Vascular Anesthesia · 2025-09-23
articleComplete debulking of the porta hepatis in low-grade appendiceal mucinous neoplasms: a case series
HPB · 2024-01-01
articleOpen accessNature Reviews Disease Primers · 2024-01-18 · 30 citations
reviewJournal of Stroke and Cerebrovascular Diseases · 2023-03-09 · 1 citations
articleCorrespondingBehavioral testing paradigms for chronic hypoxic conditions
Research Square · 2023-10-23
preprintOpen accessSenior authorAmerican Journal of Physiology-Heart and Circulatory Physiology · 2022-07-08 · 12 citations
articleOpen accessCorrespondingSupervised exercise interventions can improve symptomatology in patients with peripheral artery disease, but the underlying mechanism remains unclear. Here, MRI was used to evaluate perfusion, relative tissue oxygenation, and venous oxygen saturation in response to cuff-induced ischemia. Reactive hyperemia responses were measured before and after 3 mo of randomized supervised exercise therapy or standard medical care. Those participants who were adherent to the exercise regimen had a significant improvement in peak perfusion.
2022-01-01
articleCorrespondingUsing diffuse optics techniques, we demonstrated that exercise training increases resting calf muscle oxygen metabolism and oxygen extraction fraction in patients with peripheral artery disease. Oxygen extraction fraction increases correlated with improvement in exercise performance.
JVS Vascular Science · 2022-01-01
articleOpen accessObjective: Supervised exercise therapy (SET) is the first line treatment for intermittent claudication owing to peripheral arterial disease. Despite multiple randomized controlled trials proving the efficacy of SET, there are large differences in individual patient's responses. We used plasma metabolomics to identify potential metabolic influences on the individual response to SET. Methods: Primary metabolites, complex lipids, and lipid mediators were measured on plasma samples taken at before and after Gardner graded treadmill walking tests that were administered before and after 12 weeks of SET. We used an ensemble modeling approach to identify metabolites or changes in metabolites at specific time points that associated with interindividual variability in the functional response to SET. Specific time points analyzed included baseline metabolite levels before SET, dynamic metabolomics changes before SET, the difference in pre- and post-SET baseline metabolomics, and the difference (pre- and post-SET) of the dynamic (pre- and post-treadmill). Results: High levels of baseline anandamide levels pre- and post-SET were associated with a worse response to SET. Increased arachidonic acid (AA) and decreased levels of the AA precursor dihomo-γ-linolenic acid across SET were associated with a worse response to SET. Participants who were able to tolerate large increases in AA during acute exercise had longer, or better, walking times both before and after SET. Conclusions: We identified two pathways of relevance to individual response to SET that warrant further study: anandamide synthesis may activate endocannabinoid receptors, resulting in worse treadmill test performance. SET may train patients to withstand higher levels of AA, and inflammatory signaling, resulting in longer walking times. Clinical Relevance: This manuscript describes the use of metabolomic techniques to measure the interindividual effects of SET in patients with peripheral artery disease (PAD). We identified high levels of AEA are linked to CB1 signaling and activation of inflammatory pathways. This alters energy expenditure in myoblasts by decreasing glucose uptake and may induce an acquired skeletal muscle myopathy. SET may also help participants tolerate increased levels of AA and inflammation produced during exercise, resulting in longer walking times. This data will enhance understanding of the pathophysiology of PAD and the mechanism by which SET improves walking intolerance.
Cells · 2022-01-26 · 14 citations
articleOpen accessSenior authorCorrespondingAltered hypoxia-inducible factor-alpha (HIF-α) activity may have significant consequences in the hippocampus, which mediates declarative memory, has limited vascularization, and is vulnerable to hypoxic insults. Previous studies have reported that neurovascular coupling is reduced in aged brains and that diseases which cause hypoxia increase with age, which may render the hippocampus susceptible to acute hypoxia. Most studies have investigated the actions of HIF-α in aging cortical structures, but few have focused on the role of HIF-α within aged hippocampus. This study tests the hypothesis that aging is associated with impaired hippocampal HIF-α activity. Dorsal hippocampal sections from mice aged 3, 9, 18, and 24 months were probed for the presence of HIF-α isoforms or their associated gene products using immunohistochemistry and fluorescent in situ hybridization (fISH). A subset of each age was exposed to acute hypoxia (8% oxygen) for 3 h to investigate changes in the responsiveness of HIF-α to hypoxia. Basal mean intensity of fluorescently labeled HIF-1α protein increases with age in the hippocampus, whereas HIF-2α intensity only increases in the 24-month group. Acute hypoxic elevation of HIF-1α is lost with aging and is reversed in the 24-month group. fISH reveals that glycolytic genes induced by HIF-1α (lactose dehydrogenase-a, phosphoglycerate kinase 1, and pyruvate dehydrogenase kinase 1) are lower in aged hippocampus than in 3-month hippocampus, and mRNA for monocarboxylate transporter 1, a lactose transporter, increases. These results indicate that lactate, used in neurotransmission, may be limited in aged hippocampus, concurrent with impaired HIF-α response to hypoxic events. Therefore, impaired HIF-α may contribute to age-associated cognitive decline during hypoxic events.
Journal of Clinical and Experimental Neuropsychology · 2022-09-14 · 3 citations
articleOpen access= 2.12. Preoperative cognitive measures reflecting temporal and parietal lobe functions predicted postoperative clinical stroke/TIA within 1 week of SAVR and mortality within 1 year of SAVR. As such, cognitive measures may offer objective and timely indicators of preoperative health, specifically vulnerabilities in cerebral hypoperfusion, which may inform intervention and/or intensive postoperative monitoring and follow-up after SAVR.
Recent grants
NIH · $3.8M · 2013
NIH · $130k · 2006
The Microcirculation in Claudication and Exercise Rehabilitation
NIH · $5.0M · 2003–2016
NIH · $8.8M · 2015
NIH · $6.1M · 2016–2024
Frequent coauthors
- 64 shared
Sarah J. Ratcliffe
Society for Vascular Surgery
- 59 shared
Emile R. Mohler
- 55 shared
Joseph E. Bavaria
University of Pennsylvania
- 53 shared
Michael A. Acker
- 50 shared
Molly Fanning
University of Pennsylvania
- 48 shared
Scott E. Kasner
Hospital of the University of Pennsylvania
- 46 shared
Wilson Y. Szeto
City of Hope
- 45 shared
Tania Giovannetti
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