Sepsis has a high mortality rate and a very complex pathological mechanism, in which immune dysfunction plays an important role. The lung and intestine interact physiologically and pathologically. The microflora residing on the mucosal surface of the two are closely related to immune function, which provides a theoretical and material basis for the combined treatment of lung and intestine to regulate immune dysfunction in sepsis, reduce sepsis mortality and improve long-term prognosis.

Objective:To explore the therapeutic methods and drug-symptom patterns of Traditional Chinese Medicine (TCM) for idiopathic pulmonary fibrosis (IPF) at different stages under the guidance of the " three-stage differentiated management" principle.Methods:Under the three-stage principle, 133 IPF prescriptions treated by prof. Yan Jun from 2017.2-2023.12 were analyzed. Disease and category information of each eligible case was entered into the " FangNet" platform. Association and cluster analyses were performed for core herbs, key herb pairs, and symptom-drug relationships, aiming to uncover the clinical medication characteristics and rules in the three stages.Results:(1) Early inflammatory stage: phlegm-stasis harassment, incipient but unformed masses, superficial disease location; priority was dispelling wind, dispersing pathogen, clearing lung and resolving phlegm-commonly used: ephedra, stemona, processed pinellia, peucedanum, armeniaca. (2) Mid injury stage: formed phlegm-stasis, struggle of pathogen and healthy Qi, impaired lung collaterals, obstructive phlegm-stasis, excess pathogen with intact healthy Qi; emphasis on expelling pathogen, resolving phlegm, activating blood and dredging collaterals-e.g., angelica, pheretima, bombyx, scorpio. (3) Late fibrotic stage: healthy Qi deficiency with excess pathogen, phlegm-stasis masses entrenched in collaterals; treatment focuses on tonifying lung and dissolving masses, combining dredging and tonifying to regulate Qi and blood-e.g., pinellia, rhodiola, ginseng, gecko.Conclusions:Phlegm-stasis as excess pathogen and dual deficiency of lung-kidney run through all three stages of IPF. The rise and fall of healthy Qi vs pathogen and the degree of mass formation determine stage-specific therapeutic strategies and drug-pattern adjustments.

ObjectiveTo evaluate the clinical efficacy of Maxing Loushi decoction in the treatment of acute exacerbation of chronic obstructive pulmonary disease （AECOPD） with phlegm turbidity obstructing lung syndrome， and to investigate its effects on inflammatory factors， immune function， and the programmed death-1（PD-1）/programmed death-ligand 1 （PD-L1） signaling pathway. MethodsA randomized controlled study was conducted， enrolling 90 hospitalized patients with AECOPD and phlegm turbidity obstructing lung syndrome in the Respiratory and Emergency Departments of Dongzhimen Hospital， Beijing University of Chinese Medicine， from April 2024 to December 2024. Patients were randomly assigned to a control group and an observation group using a random number table， with 45 patients in each group. The control group received conventional Western medical treatment， while the observation group received additional Maxing Loushi decoction for 14 days. Clinical efficacy， COPD Assessment Test （CAT） score， modified Medical Research Council Dyspnea Scale （mMRC）， 6-minute walk test （6MWT）， serum inflammatory factors， T lymphocyte subsets， and serum PD-1/PD-L1 levels were compared between the two groups before and after treatment. ResultsThe total clinical effective rate was 78.57% （33/42） in the control group and 95.35% （41/43） in the observation group， with the observation group showing significantly higher efficacy than that of the control group. The difference was statistically significant （χ² = 5.136， P<0.05）. After treatment， both groups showed significant reductions in CAT and mMRC scores （P<0.05， P<0.01） and significant increases in 6MWT compared to baseline （P<0.01）. The observation group demonstrated significantly greater improvements than the control group in this regard. Levels of inflammatory markers including C-reactive protein （CRP）， procalcitonin （PCT）， interleukin-6 （IL-6）， tumor necrosis factor-α （TNF-α）， monocyte chemoattractant protein-1（MCP-1）， and macrophage inflammatory protein-1α （MIP-1α） were significantly reduced in both groups （P<0.05， P<0.01）， with greater reductions in the observation group （P<0.05， P<0.01）. CD8⁺ levels were significantly reduced （P<0.01）， while CD3⁺， CD4⁺， and CD4⁺/CD8⁺ levels were significantly increased in both groups after treatment （P<0.05， P<0.01）， with more significant improvements observed in the observation group （P<0.05， P<0.01）. Serum PD-1 levels were reduced （P<0.05， P<0.01）， and PD-L1 levels were increased significantly in both groups after treatment （P<0.05， P<0.01）， with more pronounced changes in the observation group （P<0.05）. ConclusionMaxing Loushi decoction demonstrates definite therapeutic efficacy as an adjunctive treatment for patients with AECOPD and phlegm turbidity obstructing lung syndrome. It contributes to reducing serum inflammatory factors， improving immune function， and regulating the PD-1/PD-L1 signaling pathway.

ObjectiveTo evaluate the clinical efficacy of Maxing Loushi decoction in the treatment of acute exacerbation of chronic obstructive pulmonary disease （AECOPD） with phlegm turbidity obstructing lung syndrome， and to investigate its effects on inflammatory factors， immune function， and the programmed death-1（PD-1）/programmed death-ligand 1 （PD-L1） signaling pathway. MethodsA randomized controlled study was conducted， enrolling 90 hospitalized patients with AECOPD and phlegm turbidity obstructing lung syndrome in the Respiratory and Emergency Departments of Dongzhimen Hospital， Beijing University of Chinese Medicine， from April 2024 to December 2024. Patients were randomly assigned to a control group and an observation group using a random number table， with 45 patients in each group. The control group received conventional Western medical treatment， while the observation group received additional Maxing Loushi decoction for 14 days. Clinical efficacy， COPD Assessment Test （CAT） score， modified Medical Research Council Dyspnea Scale （mMRC）， 6-minute walk test （6MWT）， serum inflammatory factors， T lymphocyte subsets， and serum PD-1/PD-L1 levels were compared between the two groups before and after treatment. ResultsThe total clinical effective rate was 78.57% （33/42） in the control group and 95.35% （41/43） in the observation group， with the observation group showing significantly higher efficacy than that of the control group. The difference was statistically significant （χ² = 5.136， P<0.05）. After treatment， both groups showed significant reductions in CAT and mMRC scores （P<0.05， P<0.01） and significant increases in 6MWT compared to baseline （P<0.01）. The observation group demonstrated significantly greater improvements than the control group in this regard. Levels of inflammatory markers including C-reactive protein （CRP）， procalcitonin （PCT）， interleukin-6 （IL-6）， tumor necrosis factor-α （TNF-α）， monocyte chemoattractant protein-1（MCP-1）， and macrophage inflammatory protein-1α （MIP-1α） were significantly reduced in both groups （P<0.05， P<0.01）， with greater reductions in the observation group （P<0.05， P<0.01）. CD8⁺ levels were significantly reduced （P<0.01）， while CD3⁺， CD4⁺， and CD4⁺/CD8⁺ levels were significantly increased in both groups after treatment （P<0.05， P<0.01）， with more significant improvements observed in the observation group （P<0.05， P<0.01）. Serum PD-1 levels were reduced （P<0.05， P<0.01）， and PD-L1 levels were increased significantly in both groups after treatment （P<0.05， P<0.01）， with more pronounced changes in the observation group （P<0.05）. ConclusionMaxing Loushi decoction demonstrates definite therapeutic efficacy as an adjunctive treatment for patients with AECOPD and phlegm turbidity obstructing lung syndrome. It contributes to reducing serum inflammatory factors， improving immune function， and regulating the PD-1/PD-L1 signaling pathway.

Objective:To explore the clinical predicting value of serum intestinal fatty acid-binding protein (I-FABP) in the development of esophageal varices (EV) in patients with chronic hepatitis B cirrhosis.Method:We used case-control study. A retrospective analysis was performed on the clinical data of 169 patients with hepatitis B cirrhosis who were admitted to the Affiliated Hospital of Yanbian University from September 2020 to October 2023. EV diagnosis and grades were based on gastroscopy. Enzyme-linked immunosorbent assay was used to measure the serum level of I-FABP on admission. Spearman correlation analysis was used to investigate the correlation among variables. Contributing factors of EV were evaluated using univariate and multivariate logistic regression analysis. Receiver operating characteristic (ROC) curves were used to evaluate the predictive performance of I-FABP for EV presence.Results:The gastroscopy showed 59 patients without EV. The median of I-FABP in the EV Group was significantly higher than that in the no-EV Group [2.01 (1.39, 2.89) μg/L vs 0.96 (0.77, 1.91) μg/L], and the difference was statistically significant ( Z=5.585, P<0.001). I-FABP showed significant positive correlations between model for end-stage liver disease sore and Von Willebrand Factor Antigen/thrombocyte Ratio ( r=0.523, 0.328, both P<0.001). Multiple logistic regression analysis identified I-FABP as the independent factor contributing to the presence of EV ( OR=1.73, P=0.045). The area under the curve of I-FABP predicting EV was 0.76. The cut-off was 1.46 μg/L. Conclusion:I-FABP is a potential marker for the formation of EV in patients with hepatitis B cirrhosis, and its increased concentration is related to reduced hepatic reserve and portal hypertension.

Objective:To explore the clinical value of serum intestinal fatty acid-binding protein (I-FABP) for the formation and development of portal vein thrombosis (PVT) in patients with chronic hepatitis B (CHB) cirrhosis complicated with esophageal varices (EV).Methods:A retrospective analysis was performed for the clinical data of patients with CHB cirrhosis complicated with EV who were admitted to the Affiliated Hospital of Yanbian University from September 2020 to October 2023 in this cohort study. PVT was diagnosed and graded according to the imaging examination, and patients were divided into PVT group and non-PVT group. The thrombus recanalization of PVT in PVT group and newly occurring PVT events in non-PVT group was observed during twelve-month follow-up. Enzyme linked immunosorbent assay was used to measure the baseline level of I-FABP. Mann-Whitney U test was used for comparison between two groups. Kaplan-Meier curves and receiver operator characteristic (ROC) curves were used to evaluated the predictive performance of I-FABP for newly occurring PVT event. The cumulative incidence was compared by log-rank test. Results:A total of 161 patients with CHB cirrhosis complicated with EV were included, with an average age of (57.71±11.12) years old, including 46 patients with PVT and 115 patients without PVT. During the follow-up period, 11 PVT patients had thrombus recanalization. Meanwhile, 17 patients without PVT had newly occurring PVT events. The I-FABP level was 2.59 (1.63, 3.18) μmol/L in the PVT group and 1.94 (1.44, 2.81) μmol/L in the non-PVT group, and the difference was statistically significant ( Z=2.12, P=0.034). The baseline I-FABP level in patients with newly occurring PVT event was higher than that in patients without PVT (2.78(1.86, 3.20) μmol/L vs 1.92 (1.18, 2.74) μmol/L), while the I-FABP level in patients with thrombus recanalization was lower than that in patients without thrombus recanalization (2.06 (1.16, 2.69) μmol/L vs 2.84 (1.92, 3.27) μmol/L). The differences were both statistically significant ( Z=2.61 and 2.25, respectively, both P<0.05). The non-PVT patients were stratified according to the median level of I-FABP, and the Kaplan-Meier curve showed that patients with I-FABP<1.94 μmol/L in the non-PVT group had a significantly lower cumulative rate of newly occurring PVT during follow-up compared to those with I-FABP≥1.94 μmol/L (7.1% (4/56) vs 22.0% (13/59), χ2=5.03, P=0.025). The ROC curve showed that I-FABP had a certain predictive efficacy for the occurrence PVT. The area under the curve were 0.698 (95% confidence interval 0.606 to 0.780) and the optimal cut-off of 2.36 μmol/L, with sensitivity of 70.59% and specificity of 69.39%. Conclusion:I-FABP is not only associated with PVT recanalization in CHB cirrhosis, but also a potential biomarker for predicting PVT formation and development.

Objective:To explore the clinical predicting value of serum intestinal fatty acid-binding protein (I-FABP) in the development of esophageal varices (EV) in patients with chronic hepatitis B cirrhosis.Method:We used case-control study. A retrospective analysis was performed on the clinical data of 169 patients with hepatitis B cirrhosis who were admitted to the Affiliated Hospital of Yanbian University from September 2020 to October 2023. EV diagnosis and grades were based on gastroscopy. Enzyme-linked immunosorbent assay was used to measure the serum level of I-FABP on admission. Spearman correlation analysis was used to investigate the correlation among variables. Contributing factors of EV were evaluated using univariate and multivariate logistic regression analysis. Receiver operating characteristic (ROC) curves were used to evaluate the predictive performance of I-FABP for EV presence.Results:The gastroscopy showed 59 patients without EV. The median of I-FABP in the EV Group was significantly higher than that in the no-EV Group [2.01 (1.39, 2.89) μg/L vs 0.96 (0.77, 1.91) μg/L], and the difference was statistically significant ( Z=5.585, P<0.001). I-FABP showed significant positive correlations between model for end-stage liver disease sore and Von Willebrand Factor Antigen/thrombocyte Ratio ( r=0.523, 0.328, both P<0.001). Multiple logistic regression analysis identified I-FABP as the independent factor contributing to the presence of EV ( OR=1.73, P=0.045). The area under the curve of I-FABP predicting EV was 0.76. The cut-off was 1.46 μg/L. Conclusion:I-FABP is a potential marker for the formation of EV in patients with hepatitis B cirrhosis, and its increased concentration is related to reduced hepatic reserve and portal hypertension.

Objective:To explore the clinical value of serum intestinal fatty acid-binding protein (I-FABP) for the formation and development of portal vein thrombosis (PVT) in patients with chronic hepatitis B (CHB) cirrhosis complicated with esophageal varices (EV).Methods:A retrospective analysis was performed for the clinical data of patients with CHB cirrhosis complicated with EV who were admitted to the Affiliated Hospital of Yanbian University from September 2020 to October 2023 in this cohort study. PVT was diagnosed and graded according to the imaging examination, and patients were divided into PVT group and non-PVT group. The thrombus recanalization of PVT in PVT group and newly occurring PVT events in non-PVT group was observed during twelve-month follow-up. Enzyme linked immunosorbent assay was used to measure the baseline level of I-FABP. Mann-Whitney U test was used for comparison between two groups. Kaplan-Meier curves and receiver operator characteristic (ROC) curves were used to evaluated the predictive performance of I-FABP for newly occurring PVT event. The cumulative incidence was compared by log-rank test. Results:A total of 161 patients with CHB cirrhosis complicated with EV were included, with an average age of (57.71±11.12) years old, including 46 patients with PVT and 115 patients without PVT. During the follow-up period, 11 PVT patients had thrombus recanalization. Meanwhile, 17 patients without PVT had newly occurring PVT events. The I-FABP level was 2.59 (1.63, 3.18) μmol/L in the PVT group and 1.94 (1.44, 2.81) μmol/L in the non-PVT group, and the difference was statistically significant ( Z=2.12, P=0.034). The baseline I-FABP level in patients with newly occurring PVT event was higher than that in patients without PVT (2.78(1.86, 3.20) μmol/L vs 1.92 (1.18, 2.74) μmol/L), while the I-FABP level in patients with thrombus recanalization was lower than that in patients without thrombus recanalization (2.06 (1.16, 2.69) μmol/L vs 2.84 (1.92, 3.27) μmol/L). The differences were both statistically significant ( Z=2.61 and 2.25, respectively, both P<0.05). The non-PVT patients were stratified according to the median level of I-FABP, and the Kaplan-Meier curve showed that patients with I-FABP<1.94 μmol/L in the non-PVT group had a significantly lower cumulative rate of newly occurring PVT during follow-up compared to those with I-FABP≥1.94 μmol/L (7.1% (4/56) vs 22.0% (13/59), χ2=5.03, P=0.025). The ROC curve showed that I-FABP had a certain predictive efficacy for the occurrence PVT. The area under the curve were 0.698 (95% confidence interval 0.606 to 0.780) and the optimal cut-off of 2.36 μmol/L, with sensitivity of 70.59% and specificity of 69.39%. Conclusion:I-FABP is not only associated with PVT recanalization in CHB cirrhosis, but also a potential biomarker for predicting PVT formation and development.

Sepsis has a high mortality rate and a very complex pathological mechanism, in which immune dysfunction plays an important role. The lung and intestine interact physiologically and pathologically. The microflora residing on the mucosal surface of the two are closely related to immune function, which provides a theoretical and material basis for the combined treatment of lung and intestine to regulate immune dysfunction in sepsis, reduce sepsis mortality and improve long-term prognosis.

Objective:To explore the therapeutic methods and drug-symptom patterns of Traditional Chinese Medicine (TCM) for idiopathic pulmonary fibrosis (IPF) at different stages under the guidance of the " three-stage differentiated management" principle.Methods:Under the three-stage principle, 133 IPF prescriptions treated by prof. Yan Jun from 2017.2-2023.12 were analyzed. Disease and category information of each eligible case was entered into the " FangNet" platform. Association and cluster analyses were performed for core herbs, key herb pairs, and symptom-drug relationships, aiming to uncover the clinical medication characteristics and rules in the three stages.Results:(1) Early inflammatory stage: phlegm-stasis harassment, incipient but unformed masses, superficial disease location; priority was dispelling wind, dispersing pathogen, clearing lung and resolving phlegm-commonly used: ephedra, stemona, processed pinellia, peucedanum, armeniaca. (2) Mid injury stage: formed phlegm-stasis, struggle of pathogen and healthy Qi, impaired lung collaterals, obstructive phlegm-stasis, excess pathogen with intact healthy Qi; emphasis on expelling pathogen, resolving phlegm, activating blood and dredging collaterals-e.g., angelica, pheretima, bombyx, scorpio. (3) Late fibrotic stage: healthy Qi deficiency with excess pathogen, phlegm-stasis masses entrenched in collaterals; treatment focuses on tonifying lung and dissolving masses, combining dredging and tonifying to regulate Qi and blood-e.g., pinellia, rhodiola, ginseng, gecko.Conclusions:Phlegm-stasis as excess pathogen and dual deficiency of lung-kidney run through all three stages of IPF. The rise and fall of healthy Qi vs pathogen and the degree of mass formation determine stage-specific therapeutic strategies and drug-pattern adjustments.