grant

Age-related changes in skeletal muscle and lower urinary tract symptoms in older adults

Organization UNIVERSITY OF CALIFORNIA, SAN FRANCISCOLocation SAN FRANCISCO, UNITED STATESPosted 30 Sept 2021Deadline 31 May 2026
NIHUS FederalResearch GrantFY202521+ years oldAddressAdultAdult HumanAgeAgingAncillary StudyBioenergeticsBiologicalBiological MarkersBladderBladder Urinary SystemCaringCausalityCessation of lifeChronologyClinicalCreatineDataDeathDecline in mobilityDecrease in mobilityDecreased mobilityDenervationDevelopmentDiagnosisDiminished mobilityDysfunctionEpidemiologic ResearchEpidemiologic StudiesEpidemiological StudiesEpidemiologyEpidemiology ResearchEtiologyFemaleFractureFrail ElderlyFrail EldersFrail Older AdultsFrail SeniorsFrequenciesFunctional disorderFunctional impairmentFundingGait speedGenitourinaryGenitourinary systemGeroscienceGoalsGrip strengthHand StrengthHealthImpairmentIncontinenceInterventionKnowledgeLeadLegLevator AniMeasurementMeasuresMitochondriaMobility declineMobility impairmentMuscleMuscle MitochondriaMuscle TissueMuscle functionNIDDKNational Institute of Diabetes and Digestive and Kidney DiseasesNational Institutes of HealthNocturiaNycturiaOrganOutcomePathologyPb elementPelvicPelvic FloorPelvic Floor MusclePelvic RegionPelvic floor structurePelvisPersonal SatisfactionPhenotypePhysical FunctionPhysical PerformancePhysical assessmentPhysiopathologyPractice GuidelinesProspective cohortProspective, cohort studyPublic HealthQOLQOL improvementQuality of lifeReduced mobilityReduction in mobilityResearchRespirationRiskRisk FactorsRoleSarcosomesScienceSeveritiesShapesSkeletal MuscleSpinal ColumnSpineStreamSymptomsSyndromeSystemTestingThighThigh structureTimeUnited States National Institutes of HealthUrinary tractUrineUrodynamicsUrogenitalUrogenital SystemVertebral columnVoluntary MuscleWomanaccurate diagnosisadulthoodage associatedage associated alterationsage associated biomarkersage associated changesage associated declineage associated markerage correlatedage correlated alterationsage correlated changesage dependentage dependent alterationsage dependent changesage dependent declineage induced alterationsage induced changesage linkedage markerage relatedage related alterationsage related biomarkersage related changesage related declineage related markersage related pathwaysage specificage specific alterationsage specific changesagesaging associated alterationsaging associated changesaging associated mechanismaging biological markeraging biomarkeraging correlated alterationsaging correlated changesaging dependent alterationsaging dependent changesaging induced alterationsaging induced changesaging markeraging mechanismaging pathwayaging processaging related alterationsaging related changesaging related mechanismaging related pathwaysaging specific alterationsaging specific changesalterations with ageassociated symptombackbonebio-markersbiologicbiologic markerbiological markers of agebiological mechanism of agebiological pathways of agebiomarkerbiomarker identificationbiomarkers of agebone fracturecausationchanges with ageco-morbid symptomco-occuring symptomcohortcomorbid symptomconcurrent symptomcooccuring symptomcustomized therapycustomized treatmentdecline with agedecreased muscle massdevelopmentaldisease causationeffective interventionepidemiologicepidemiologic investigationepidemiologicalepidemiology studyexperiencefall riskfallsfrail older adultfrailtygenitourinary tractgeroscientifichealth related quality of lifeheavy metal Pbheavy metal leadidentification of biomarkersidentification of new biomarkersimprovedimprovements in QOLimprovements in quality of lifeindividualized medicineindividualized patient treatmentindividualized therapeutic strategyindividualized therapyindividualized treatmentinnovateinnovationinnovativelevator ani musclelow muscle masslower urinary tract symptomsmalemalleable riskmarker identificationmechanism regulating agingmechanisms involved in agingmenmitochondrialmodifiable riskmortalitymultimorbiditymultiple chronic conditionsmuscle bulkmuscle formmuscle massmuscularnovelold ageolder adultolder adulthoodolder menolder womenoxidative damageoxidative injurypathophysiologypathway involved in agingpatient specific therapiespatient specific treatmentpreventpreventingprostate enlargementprostatic enlargementquadricepsquadriceps musclequality of life improvementreduced muscle massrespiratoryrespiratory mechanismrisk/benefit ratiosexsocial rolesymptom associationsymptom comorbiditytailored medical treatmenttailored therapytailored treatmenttoolunique treatmenturinary bladderurogenital tractwalking pacewalking speedwell-beingwellbeing
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Full Description

PROJECT SUMMARY/ABSTRACT
There is a fundamental knowledge gap and missed opportunities due to the current lack of understanding of

the relationship between age-related risk factors, such as loss of both global and pelvic skeletal muscle

function, and lower urinary tract symptoms (LUTS) among older women and men. LUTS are associated with

functional impairment and poor quality of life and are at increased risk of falls, fractures, and mortality. The

current narrow focus on urinary tract pathology has led to minimal understanding of what causes these

symptoms and correspondingly few effective interventions. A new aging-focused paradigm of LUTS

pathophysiology could lead to novel interventions to treat LUTs by defining modifiable LUTS risk factors, such

as age-related changes in muscle health, and mechanisms shared across syndromes of aging.

My goals are to build an epidemiologic backbone for understanding age-related LUTS risk factors by

leveraging high-quality existing data, defining novel and modifiable risk factors and mechanisms for age-

related LUTS, and to lead subsequent translational efforts to target these risk factors and mechanisms in older

adults. The objective of this application is to evaluate longitudinal associations between multiple measures of

skeletal muscle and LUTS. My hypothesis is that age-related changes in skeletal muscle – at the system

(strength and physical performance), organ (muscle mass/volume), and cellular (mitochondrial bioenergetics)

level – are associated with LUTS severity, independent of chronological age and confounding factors.

This hypothesis will be tested by efficiently using data from the prospective cohort “Study of Muscle Mobility

and Aging” (SOMMA) to pursue the following specific aims: Aim 1) Determine how baseline and longitudinal

changes in muscle function (strength, power) and physical performance (walking speed) are associated with

change in LUTS severity; Aim 2) Determine how baseline and longitudinal changes in muscle mass and

baseline measures of both total body and pelvic floor muscle volume and shape are associated with change in

LUTS severity; and Aim 3) Determine how baseline measures of skeletal muscle mitochondrial function are

associated with change in LUTS severity. This project is innovative because it leverages the rapidly evolving

field of geroscience to improve the inadequate existing urogenital-focused paradigm of LUTS pathophysiology.

The proposed research is significant because it will produce a paradigm of age-related LUTS pathophysiology

that will result in improved care for older adults with LUTS by 1) identifying biomarkers of age-related LUTS; 2)

improving the benefit:risk ratio for existing therapies by stratifying based on novel LUTS phenotypes; 3)

distinguishing the role of changes in global versus pelvic floor muscles in the development of LUTS; 4)

facilitating the development of new treatments that target age-related LUTS mechanisms; and ultimately 5)

preventing LUTS complications (e.g., frailty, impaired mobility, falls, and poor quality of life) that may be directly

caused by LUTS or indirectly caused by shared modifiable factors for which LUTS is an early marker.

Grant Number: 5K76AG074903-05
NIH Institute/Center: NIH

Principal Investigator: Scott Bauer

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