Hong Peng, PhD, MBA
Director Business DevelopmentCards
About
Research
Publications
2024
Evaluating fatigue and excessive daytime sleepiness: a comparative analysis of prevalence and correlating factors in interstitial lung disease patients and healthy controls
Ouyang X, Shen Q, Zhou S, Zhou P, Song M, Guo T, Guo W, Zhang Y, Peng H. Evaluating fatigue and excessive daytime sleepiness: a comparative analysis of prevalence and correlating factors in interstitial lung disease patients and healthy controls. Annals Of Medicine 2024, 56: 2398729. DOI: 10.1080/07853890.2024.2398729.Peer-Reviewed Original ResearchInterstitial lung disease patientsInterstitial lung diseaseDiminished exercise capacityExcessive daytime sleepinessHealthy volunteersExercise capacityDaytime sleepinessEpworth Sleepiness Scale scoreQuality of lifePulmonary diffusion functionSleepiness Scale scoreFactors associated with excessive daytime sleepinessSecond Xiangya HospitalLogistic regressionLung disease patientsMultivariate logistic regressionDecreased quality of lifeCentral South UniversityCross-sectional studyPrevalence of fatigueChest painConsecutive patientsClinical characteristicsNon-ED patientsLung diseasePrevalence and prognostic value of malnutrition in patients with IPF using three scoring systems
Shen Q, Zhou S, Song M, Ouyang X, Tan Y, Peng Y, Zhou Z, Peng H. Prevalence and prognostic value of malnutrition in patients with IPF using three scoring systems. Respiratory Medicine 2024, 233: 107774. PMID: 39168392, DOI: 10.1016/j.rmed.2024.107774.Peer-Reviewed Original ResearchNutritional risk indexPrognostic nutritional indexControlling nutritional statusIPF patientsNutritional statusPrognostic valueControlling nutritional status scorePrognostic value of malnutritionModerate to severe malnutritionHigher risk of all-cause deathRisk of all-cause deathAssociated with significantly higher incidenceScoring systemDiagnosis of IPFModerate to severe riskPrevalence of malnutritionSecond Xiangya HospitalSignificantly higher incidenceAll-cause deathPredictors of mortalityAll-cause mortalityAnti-fibrotic drugsCentral South UniversitySevere malnutritionClinical associationsThe prognostic role of high-density lipoprotein cholesterol/C-reactive protein ratio in idiopathic pulmonary fibrosis
Ouyang X, Qian Y, Tan Y, Shen Q, Zhang Q, Song M, Shi J, Peng H. The prognostic role of high-density lipoprotein cholesterol/C-reactive protein ratio in idiopathic pulmonary fibrosis. QJM 2024, hcae147. PMID: 39078215, DOI: 10.1093/qjmed/hcae147.Peer-Reviewed Original ResearchIdiopathic pulmonary fibrosis patientsIdiopathic pulmonary fibrosisC-reactive proteinPrognosis of IPF patientsIPF-related deathsHigh C-reactive proteinLow HDL-CIndependent risk factorLung transplantationAll-cause deathNon-IPF controlsHDL-CReceiver operating characteristicIPF patientsPulmonary fibrosisLipid parametersEffect of lipid parametersPrognosis of idiopathic pulmonary fibrosisPredictor of clinical outcomeRisk factorsPredicting all-cause deathDevelopment of idiopathic pulmonary fibrosisCox proportional hazards modelsShorter survival timeProportional hazards model
2023
CSE regulates LINC000665/XBP-1 in the progress of pulmonary fibrosis
Song M, Shen Q, Ouyang X, Zhou Z, Luo H, Peng H. CSE regulates LINC000665/XBP-1 in the progress of pulmonary fibrosis. Tobacco Induced Diseases 2023, 21: 1-10. PMID: 38111802, PMCID: PMC10726211, DOI: 10.18332/tid/175004.Peer-Reviewed Original ResearchA novel compound heterozygous mutation in the SLC34A2 gene causes pulmonary alveolar microlithiasis
Liu Q, Ju X, Guo T, Peng H. A novel compound heterozygous mutation in the SLC34A2 gene causes pulmonary alveolar microlithiasis. QJM 2023, 117: 293-296. PMID: 38070491, DOI: 10.1093/qjmed/hcad280.Peer-Reviewed Original ResearchCoexistent Sjogren’s syndrome and Birt-Hogg-Dube´ syndrome: a case report
Lin Y, Guo T, Lei C, Yang B, Yang D, Luo H, Peng H. Coexistent Sjogren’s syndrome and Birt-Hogg-Dube´ syndrome: a case report. BMC Pulmonary Medicine 2023, 23: 460. PMID: 37993820, PMCID: PMC10664354, DOI: 10.1186/s12890-023-02680-5.Peer-Reviewed Original ResearchConceptsSjogren's syndromeBirt-HoggMultiple thin-walled cystic lesionsDiffuse cystic lung diseasesThin-walled cystic lesionsShortness of breathCystic lung diseaseLabial gland biopsyDry eyeLower lungCystic changesCystic lesionsLung diseasePhysical examinationCase reportGland biopsyDube syndromeRare caseComputed tomographyDubé syndromeInsufficient evidenceSyndromeDiagnostic algorithmLungRespiratory soundsA novel mutation of CTC1 leads to telomere shortening in a chinese family with interstitial lung disease
Liu L, Luo H, Sheng Y, Kang X, Peng H, Luo H, Fan L. A novel mutation of CTC1 leads to telomere shortening in a chinese family with interstitial lung disease. Hereditas 2023, 160: 37. PMID: 37978541, PMCID: PMC10656953, DOI: 10.1186/s41065-023-00299-4.Peer-Reviewed Original ResearchConceptsInterstitial lung diseaseLung diseaseAffected family membersHeterozygous mutationsChronic interstitial lung diseasePulmonary diffusion functionPulmonary lung diseaseWhole-exome sequencingTelomere structure integrityProgressive dyspneaReal-time PCRCTC1 geneGene mutationsInsidious onsetInterstitial pneumoniaGenetic lesionsMutation spectrumInterstitial tissueEpidemiological dataPatientsChinese familyTelomere shorteningDiseaseCTC1Family members