Pulmonary impairment after tuberculosis in Georgia: Enhancing clinical research capacity to address the intersection of non-communicablediseases and tuberculosis
Pulmonary impairment after tuberculosis in Georgia: Enhancing clinical research capacity to address the intersection of non-communicablediseases and tuberculosis
批准号:
10002119
负责人:
Maia Kipiani
金额:
$16.98万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-08-01 至 2022-06-30
关键词:
AddressAftercareAnti-Inflammatory AgentsAreaAutomobile DrivingBiologicalBiological FactorsBiological MarkersCessation of lifeChronicClinicalClinical ResearchCollagenCommunicable DiseasesCountryDataDiagnosisDiagnostic radiologic examinationDiseaseDrug resistanceEmission-Computed TomographyEnrollmentEnzymesEpidemicEpidemiologistExhalationFutureGoalsHealthHigh PrevalenceImpairmentIndividualInflammationInflammatory ResponseInfrastructureInstitutesIntegration Host FactorsInterventionLaboratoriesLeadLongevityLungLung InflammationLung diseasesMatrix Metalloproteinase InhibitorMatrix MetalloproteinasesMeasuresMentorsMicrobiologyMissionModelingMorbidity - disease rateMultidrug-Resistant TuberculosisMycobacterium tuberculosisNitric OxidePathway interactionsPatientsPharmaceutical PreparationsPoliciesPositron-Emission TomographyPrevalencePreventionPrevention strategyProspective StudiesPublic HealthPulmonary TuberculosisPulse OximetryQuality of lifeRehabilitation therapyResearchResearch InfrastructureResearch PersonnelResidual stateResourcesRiskSeveritiesSmokingSpecialistSpirometryStructureStructure of parenchyma of lungSurvivorsTimeTissuesTrainingTranslational ResearchTuberculosisWorkX-Ray Computed Tomographybaseclinical predictorscohortcomorbiditydisabilityevidence baseexperienceextensive drug resistanceimprovedinflammatory markerinnovationinsightinternational centerlow and middle-income countrieslung injurymortalitymultidisciplinarynovelpathogenpreventprogramsprospectiveradiologistrespiratorytreatment strategytuberculosis treatment
中文摘要
项目总结
英文摘要
PROJECT SUMMARY
The intersection of tuberculosis (TB) disease with non-communicable disease, including chronic pulmonary
impairment, has emerged as a critical clinical and public health obstacle. Rapidly expanding non-communicable
disease epidemics threaten TB control in low- and middle-income countries, including Georgia, where preventing
and treating TB disease remains a great burden. However, to date, the notion that TB disease may increase the
risk of chronic non-communicable disease has not been well explored. We will determine the extent to which
multidrug-resistant (MDR) TB, smoking, and biomarkers of lung inflammation contribute to increased prevalence
of pulmonary impairment post-TB in the country of Georgia. This research will advance understanding of dual
burdens of communicable and non-communicable diseases and build individual and institutional research capacity
in Georgia.
The long-term objective of this research is to elucidate the relationship between TB patient and TB pathogen factors
with post-TB chronic pulmonary impairment, and strengthen research capacity for future work to identify treatment
and prevention strategies that reduce the risk of chronic non-communicable diseases after TB treatment
completion. The specific aims of this proposal are to: (1) determine the burden, predictors, and trajectory of
pulmonary impairment post-TB treatment; (2) explore the relationship between biomarkers of lung inflammation
and lung destruction at time of TB treatment completion with severity of pulmonary impairment; and (3) build
increased research infrastructure and capacity for Georgia that is focused on the intersection of TB and chronic
pulmonary impairment. The aims of this project will be achieved by enrolling a cohort of patients (n=130) at the
time of TB treatment completion and following them prospectively for one year. At both time points this study will
measure spirometry, pulse oximetry, and quality of life among patients who were treated for drug susceptible TB
(n=65) and among patients treated for MDR TB (n=65). The analysis will include multiple modeling strategies to
assess the relationship between patient and host factors and the risk of chronic pulmonary impairment.
The proposed study will help to characterize the extent to which TB contributes to chronic pulmonary impairment
and will identify which existing clinical respiratory rehabilitation interventions may be used to improve quality of life
throughout the lifespan among patients with TB. In addition, this R21 will leverage a cadre of current and former
Fogarty-supported trainees and provide invaluable mentored training experiences in the areas of TB and chronic
pulmonary diseases. A long term goal of the proposed work is to prepare for prospective studies that follow patient
cohorts beginning at the time of TB diagnosis, during TB treatment, and several years after TB treatment.
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