grant

A Preliminary Elucidation of the Role of Dietary Fiber in Mitigating Sarcopenia Risk in Head and Neck Cancer

Organization UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTRLocation OKLAHOMA CITY, UNITED STATESPosted 15 Jul 2025Deadline 14 Jul 2027
NIHUS FederalResearch GrantFY202521+ years oldActive Follow-upAddressAdultAdult HumanAffectAlimentary CanalAnti-InflammatoriesAnti-Inflammatory AgentsAnti-inflammatoryAntiinflammatory EffectAttentionBiologicalCAT scanCT X RayCT XrayCT imagingCT scanCaloric IntakeCaloriesCancer BiologyCancer PrognosisCancer TreatmentCancersChromatographyClinical TrialsComplementComplement ProteinsComputed TomographyConsumptionDataData CollectionDevelopmentDiagnosisDietDietary AssessmentDietary ComponentDietary FiberDietary HistoryDigestive TractEatingEnergy IntakeEnrollmentEssential Amino AcidsFabaceaeFoodFood IntakeFood frequency questionnaireFruitFutureGI TractGasesGastrointestinal TractGastrointestinal tract structureGeneral Prognostic FactorHNC patientHead and Neck CancerHead and Neck CarcinomaHourImmunomodulationInflammationInflammatoryIngestionIntakeInterventionInterviewKnowledgeLegLegumesLeguminosaeLeguminoseaeMalignant Head and Neck NeoplasmMalignant Neoplasm TherapyMalignant Neoplasm TreatmentMalignant NeoplasmsMalignant TumorMeasuresMediatorMedicineMethodsModelingMorbidityMorbidity - disease rateMucosal InflammationMucositisMuscleMuscle AtrophyMuscle TissueMuscle functionMuscular AtrophyNCI OrganizationNational Cancer InstituteNewly DiagnosedObservation researchObservation studyObservational StudyObservational researchOutcomeParticipantPatientsPerceptionPhasePhlebotomyPreventionProceduresProductionPrognostic FactorPrognostic/Survival FactorProteinsQuestionnairesRecordsResearchRiskRisk ReductionRoleScanningShort-Chain Fatty AcidsSkeletal MuscleStructureSurvey InstrumentSurveysTimeTomodensitometryVegetablesVenous blood samplingVolatile Fatty AcidsVoluntary MuscleX-Ray CAT ScanX-Ray Computed TomographyX-Ray Computerized TomographyXray CAT scanXray Computed TomographyXray computerized tomographyabsorptionactive followupadulthoodalimentary tractanti-cancer therapyanti-inflammatory effectbehavior changebiologiccaloric dietary contentcancer therapycancer-directed therapycatscanclinical applicabilityclinical applicationcomplementationcomputed axial tomographycomputer tomographycomputerized axial tomographycomputerized tomographydesigndesigningdetermine efficacydevelopmentaldiet historydietarydietary fruitdietary vegetabledietsdigestive canalefficacy analysisefficacy assessmentefficacy determinationefficacy evaluationefficacy examinationenrollevaluate efficacyexamine efficacyfecal samplefollow upfollow-upfollowed upfollowuphead and neck cancer patienthead/neck cancerhealth beliefhealth-related beliefimmune modulationimmune regulationimmunologic reactivity controlimmunomodulatoryimmunoregulationimmunoregulatoryimprove symptomimprovedinflammation markerinflammatory markerinflammatory modulationingestinterestmalignancymalignant head and neck tumormortalitymuscle breakdownmuscle degradationmuscle deteriorationmuscle lossmuscle wastingmuscularneoplasm/cancernon-contrast CTnoncontrast CTnoncontrast computed tomographypatient prognosispea familypreventpreventingprotein intakerecruitreduce riskreduce risksreduce that riskreduce the riskreduce these risksreduces riskreduces the riskreducing riskreducing the riskresponserisk-reducingsarcopeniasarcopenicsocial rolestool samplestool specimensurvival predictionsymptom improvementsymptomatic improvementwhole grain
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Full Description

PROJECT SUMMARY/ABSTRACT
Sarcopenia remains a consequential prognostic factor that drastically affects morbidity and mortality in head and

neck cancer (HNC). Due to the catabolic state associated with sarcopenia, dietary strategies emphasizing energy

and protein intake are often encouraged. However, data suggest underlying mechanisms (e.g., inflammation)

drive the development of sarcopenia independent of energy or protein intake. Dietary fiber is notably anti-

inflammatory and has capacity to improve sarcopenia and other cancer-related outcomes, in part via production

of short chain fatty acids (SCFA) and decreased inflammation. This precise relationship is yet explored in HNC.

Moreover, it is unknown how patients perceive the feasibility of increasing their dietary fiber intake during

treatment. This study seeks to evaluate dietary fiber intake longitudinally from the time of diagnosis for a total of

six months in patients diagnosed with HNC, and to elucidate the relationship between dietary fiber intake and

measures of SCFA, inflammation, and sarcopenia. Adults newly diagnosed with HNC will be recruited and

provide iterative assessments of dietary fiber intake (National Cancer Institute Diet History Questionnaire III

[DHQIII] and 24-hour recalls), SCFA (stool samples analyzed using gas-phase chromatography), inflammatory

markers (venous blood samples and multiplex kits), skeletal muscle quantity and quality (CT scans analyzed

using SliceOMatic), muscle function (Timed Chair Stands, Leg Press Power), and perceptions regarding the

feasibility of targeting dietary fiber (semi-structured interviews [SSIs], surveys). Our central hypothesis is that

lower dietary fiber intake will significantly predict development of sarcopenia, decreased SCFA, and increased

inflammatory markers. In Aim 1, we will determine the relationship between dietary fiber intake, SCFA,

inflammatory markers, and skeletal muscle measures in patients being treated for HNC. In Aim 2, we will

characterize the feasibility (acceptability, demand, practicality, implementation) of targeting dietary fiber in

patients with HNC according to patient perceptions (SSIs, surveys) within Health Belief Model constructs and

review of study records (e.g., retention, completion of data collection). This proposal will generate fundamental

knowledge and explore the clinical application of this knowledge to support future clinical trials that have the

potential to lead to substantial paradigm shifts that could contribute to immense improvements in HNC prognosis.

Grant Number: 1R03DE035156-01
NIH Institute/Center: NIH

Principal Investigator: Ashlea Braun

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