grant

Research Core

Organization UNIVERSITY OF PENNSYLVANIALocation PHILADELPHIA, UNITED STATESPosted 1 Feb 2023Deadline 31 Dec 2027
NIHUS FederalResearch GrantFY2026AccelerationActive Follow-upAcuteAddressAnimal ExperimentsAnimalsAssayAttenuatedAutoregulationBioassayBiological AssayBody TissuesCalcanean TendonCaringCell BodyCellsCenter for Translational Science ActivitiesChemicalsChronicClinicalClinical ResearchClinical StudyClinical TrialsCommon Rat StrainsData SetDiseaseDisease ProgressionDisorderDoseEchographyEchotomographyEquityExerciseFundingFutureGait AnalysisHealthHomeostasisHospitalsHumanInequityInjectionsInsurance CarriersInsurersIntuitionInvestigatorsJointsLinkMechanicsMedical UltrasoundMedicineModelingModern ManMonitorMusculoskeletalNational Institutes of HealthOperative ProceduresOperative Surgical ProceduresOutcomePainPainfulPathogenesisPatient CarePatient Care DeliveryPatient outcomePatient-Centered OutcomesPatient-Focused OutcomesPatientsPhysiatric ProcedurePhysical Medicine ProcedurePhysical TherapeuticsPhysical therapyPhysiological HomeostasisPhysiotherapyPopulationPre-Clinical ModelPreclinical ModelsPreclinical dataProtocolProtocols documentationR-Series Research ProjectsR01 MechanismR01 ProgramRatRats MammalsRattusRegimenRegistriesReportingResearchResearch GrantsResearch PersonnelResearch Project GrantsResearch ProjectsResearchersRural CommunitySamplingScienceSurgicalSurgical InterventionsSurgical ProcedureTechniquesTendinitisTendinopathyTendon InjuriesTendon structureTendonitisTendonsTestingTherapeutic AgentsTissuesTranslatingTranslational ResearchTranslational ScienceTranslationsUltrasonic ImagingUltrasonogramUltrasonographyUltrasound DiagnosisUltrasound Medical ImagingUltrasound TestUnited States National Institutes of HealthUrban Communityachilles tendonactive followupanimal experimentattenuateattenuatescare deliverycare for patientscare of patientscaring for patientsclinical relevanceclinical translationclinically relevantclinically translatablecostdiagnostic ultrasoundearly onseteffectiveness testingexperimental animalexperimental animalsfollow upfollow-upfollowed upfollowupfundamental researchgait examinationhealinghuman tissueimprovedin vivoinnovateinnovationinnovativeintuitivemechanicmechanicalmechanical loadmetabolism measurementmetabolomicsmetabonomicsnew technologynovelnovel technologiespain symptompainful symptompatient oriented outcomespatient populationpre-clinicalpre-clinical researchpre-clinical studypreclinicalpreclinical findingspreclinical informationpreclinical researchpreclinical studyrehabilitation carerehabilitative careresearch studysonogramsonographysound measurementsuburban communitiessurgerytendon rupturetherapeutic effectivenesstooltranslationtranslation assaytranslation researchtranslational impacttranslational investigationtranslational research centertranslational sciences centerultrasoundultrasound imagingultrasound scanning
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Full Description

Research Core Summary
Achilles tendinopathy is a painful, debilitating, and chronic tendon condition. Patients receive physical

therapy as the first step in conservative treatment. These physical therapy protocols – which are the only non-

surgical treatments paid for by most insurers – prescribe mechanical loads as a therapeutic agent. However,

sixty percent of patients continue to report painful symptoms after 5 years, and fifty percent of patients seek

surgical treatment after conservative treatment fails. Therefore, maximizing the therapeutic effectiveness of

mechanical loading is critical towards improving patient outcomes and reducing the need for costly and often

ineffective surgical treatments. To meet this unmet clinical need, our proposed Research Projects will establish

the mechano-responsiveness of tendon cells throughout tendinopathy disease progression and elucidate the

mechanotransductive mechanisms that regulate cell fate and tissue homeostasis to attenuate disease

progression and improve tendon healing. To accelerate clinical translation, the overall objective of this Achilles

Tendinopathy Tissue Core is to provide patient and clinically relevant rat tendon samples, ranging from healthy

to degenerated, combined with the most complete set of longitudinal in vivo assays to maximize the translational

impact of our Research Projects proposed in this P50 application, as well as numerous NIH funded projects at

Penn aimed at improving tendon healing by our P50 team of investigators. In Aim 1, we will retrieve patient

tissues to investigate end-stage Achilles tendinopathy mechano-sensitivity. In Aim 2, we will leverage a

tendinopathy preclinical model to investigate disease pathogenesis. These 2 aims will utilize an extensive battery

of in vivo assays including gait analysis, loading monitoring, joint mechanics, ultrasound imaging, and

metabolomics to maximize research translation from our exciting Research Projects to clinical populations. In

Aim 3, we will develop novel techniques to translate preclinical findings to improve patient care. These

translational tools are necessary for follow-up animal experiments and clinical trials that will test the effectiveness

of personalized rehabilitative care at improving tendon healing and outcomes while addressing existing

inequitable care delivery for patients with Achilles tendon injuries. We will accelerate fundamental discovery

research and translation through preclinical studies to clinical populations. By establishing the Achilles

Tendinopathy Tissue Core, we will provide unique and rigorous techniques and expertise, as well as carefully

controlled and characterized study material to tendon researchers locally, and ultimately nationally, while

developing critical new technologies to improve patient care in future clinical research. We selected Achilles

tendinopathy to address a common and debilitating condition while demonstrating the proof-of-concept model

paradigm that leveraging patient tissues with preclinical models will accelerate fundamental discovery to more

effective and equitable musculoskeletal care.

Grant Number: 5P50AR080581-04
NIH Institute/Center: NIH

Principal Investigator: Josh Baxter

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