Clinical Significance of the Antimicrobial Peptide Cathelicidin in Acute Exacerbations of COPD
Clinical Significance of the Antimicrobial Peptide Cathelicidin in Acute Exacerbations of COPD
批准号:
9770541
负责人:
Robert M Burkes
金额:
$6.91万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-08-09 至 2020-06-30
关键词:
AcuteAddressAdmission activityAgeAwardBiological MarkersCaringChemotactic FactorsChronic Obstructive Airway DiseaseClinicalCohort AnalysisDataData AnalysesEnsureEpithelial CellsEtiologyFutureGlucocorticoidsHospitalizationHospitalsHuman Subject ResearchImmuneImmune responseIncidenceIndividualInflammationInflammatoryInhalationInnate Immune SystemInvestigationLeadLength of StayLipopolysaccharidesLungLung diseasesMeasuresMechanical ventilationMentorsMentorshipMorbidity - disease rateOutcomeParticipantPatientsPlasmaPlayPneumoniaPropertyPublicationsPulmonary Function Test/Forced Expiratory Volume 1RaceResearchResearch DesignResourcesRespiratory physiologyRiskRoleSeveritiesSignal TransductionSmokerSmoking StatusSymptomsTimeTime FactorsTobaccoTrainingTreatment ProtocolsUnited StatesVitamin Dantimicrobialantimicrobial peptidecareercathelicidincathelicidin antimicrobial peptideclinical Diagnosisclinically significantcohortcostexperiencefollow-uphealth care service utilizationhigh riskhospital readmissionmacrophagemortalityneutrophilovertreatmentpotential biomarkerprognosticprognostic significanceprognostic valueprospectivereadmission ratesresponsesexskillsspecific biomarkerstrend
中文摘要
项目摘要
COPD急性加重(AECOPD)导致该疾病的高发病率和死亡率。COPD
加重是昂贵的,与增加的医疗保健利用相关,并导致COPD的死亡率。
抗微生物肽凯萨林菌素在先天免疫系统中通过直接抗微生物杀伤起作用,
免疫细胞信号传导和脂多糖的中和。在稳定的COPD患者队列中,
对于有COPD风险的吸烟者,cathelicidin水平随着时间的推移与肺功能降低相关,
肺炎的发生率,以及需要改变常规治疗的COPD急性加重发作的增加
疗法在COPD恶化期间,血浆凯萨林菌素水平增加,可能是由于急性炎症反应。
炎症状态到目前为止,还没有研究血浆cathelicidin水平的趋势,
AECOPD或AECOPD住院期间血浆组织蛋白酶抑制素的预后意义这
提案将寻求定义COPD急性加重住院期间的抗菌肽水平和趋势,
确定COPD急性加重住院期间凯萨林菌素水平的预后意义,包括
需要提高护理和再入院率。成功完成此提案将决定
血浆cathelicidin水平在识别AECOPD高危病例中的作用
英文摘要
PROJECT ABSTRACT
Acute exacerbations of COPD (AECOPD) contribute to the high morbidity and mortality of the condition. COPD
exacerbations are costly, associated with increased healthcare utilization, and contribute to mortality in COPD.
The antimicrobial peptide cathelicidin functions in the innate immune system by direct antimicrobial killing,
immune cell signaling, and neutralization of lipopolysaccharide. In cohorts of stable COPD patients and
smokers at-risk for COPD, cathelicidin levels are associated with lower lung function over time, increased
incidence of pneumonia, and an increase in episodes of COPD exacerbations that require change in regular
therapy. During an exacerbation of COPD, plasma cathelicidin levels increase, likely due to an acute
inflammatory state. To date, there have been no investigations into the trend of plasma cathelicidin levels in
AECOPD or the prognostic implications of plasma cathelicidin during hospitalization for AECOPD. This
proposal will seek to define cathelicidin level and trend during hospitalization for COPD exacerbation and
determine prognostic implication of cathelicidin levels during hospitalization for COPD exacerbation, including
need for escalation of care and readmission rates. Successful completion of this proposal will determine the
role of plasma cathelicidin levels in identifying high-risk cases of AECOPD.
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