Objectives:To investigate the relationship between epicardial adipose tissue(EAT)(including pericoronary adipose tissue[PCAT])with left ventricular remodeling and myocardial fibrosis in heart failure with reduced ejection fraction(HFrEF)patients.Methods:Consecutive patients diagnosed with HFrEF who underwent coronary computed tomography angiography(CCTA)and cardiac magnetic resonance imaging(CMR)examination at the First Affiliated Hospital of Air Force Medical University between May 2021 and January 2024 were included in this study(n=34).EAT CT attenuation,volume and PCAT CT attenuation of left anterior descending artery(LAD)and right coronary artery(RCA)were measured based on CCTA images.Left ventricular function parameters,late gadolinium enhancement(LGE),and extracellular volume(ECV)were evaluated based on CMR images.The correlations between EAT and PCAT with ventricular remodeling and myocardial fibrosis were evaluated in patients with HFrEF using Spearman analysis.Results:Spearman analysis showed that EAT volume were positively correlated with left ventricular end diastolic volume(LVEDV),left ventricular stroke volume(LVSV)and LGE(all P<0.05).EAT CT attenuation were positively correlated with LVEDV and left ventricular end systolic volume(LVESV),and negatively correlated with left ventricular remodeling index(LVRI),left ventricular ejection fraction(LVEF),left ventricular cardiac output(LVCO)and LGE(all P<0.05).LAD PCAT CT attenuation was positively correlated with LVESV,and negatively correlated with left ventricular maximal wall thickness,LVSV,LVEF,LVCO and LGE(all P<0.05).RCA PCAT CT attenuation were positively correlated with LVEDV and LVESV,and negatively correlated with LVEF and LGE(all P<0.05).EAT CT attenuation,volume and PCAT CT attenuation were not significantly correlated with ECV(all P>0.05).Conclusions:In HFrEF patients,both EAT and PCAT were associated with left ventricular remodeling and myocardial fibrosis.

Objectives:To investigate the relationship between epicardial adipose tissue(EAT)(including pericoronary adipose tissue[PCAT])with left ventricular remodeling and myocardial fibrosis in heart failure with reduced ejection fraction(HFrEF)patients.Methods:Consecutive patients diagnosed with HFrEF who underwent coronary computed tomography angiography(CCTA)and cardiac magnetic resonance imaging(CMR)examination at the First Affiliated Hospital of Air Force Medical University between May 2021 and January 2024 were included in this study(n=34).EAT CT attenuation,volume and PCAT CT attenuation of left anterior descending artery(LAD)and right coronary artery(RCA)were measured based on CCTA images.Left ventricular function parameters,late gadolinium enhancement(LGE),and extracellular volume(ECV)were evaluated based on CMR images.The correlations between EAT and PCAT with ventricular remodeling and myocardial fibrosis were evaluated in patients with HFrEF using Spearman analysis.Results:Spearman analysis showed that EAT volume were positively correlated with left ventricular end diastolic volume(LVEDV),left ventricular stroke volume(LVSV)and LGE(all P<0.05).EAT CT attenuation were positively correlated with LVEDV and left ventricular end systolic volume(LVESV),and negatively correlated with left ventricular remodeling index(LVRI),left ventricular ejection fraction(LVEF),left ventricular cardiac output(LVCO)and LGE(all P<0.05).LAD PCAT CT attenuation was positively correlated with LVESV,and negatively correlated with left ventricular maximal wall thickness,LVSV,LVEF,LVCO and LGE(all P<0.05).RCA PCAT CT attenuation were positively correlated with LVEDV and LVESV,and negatively correlated with LVEF and LGE(all P<0.05).EAT CT attenuation,volume and PCAT CT attenuation were not significantly correlated with ECV(all P>0.05).Conclusions:In HFrEF patients,both EAT and PCAT were associated with left ventricular remodeling and myocardial fibrosis.

Objective: To investigate the effect of polycyclic aromatic hydrocarbons (PAHs) exposure on the level of histone H3Ser10 phosphorylation (p-H3S10) and DNA damage degree in peripheral blood lymphocyte (PBLCs). Method: 75 coke oven workers from Benxi steel plant in Liaoning Province of China (PAHs-exposed group) and local 50 hot rolling workers (control group) were recruited in this study with age, working years, labor intensity and high temperature for matching factors using cluster sampling method in 2014. HPLC-fluorescence was performed to determine the level of urinary 1-hydroxypyrene (1-OHP), DNA damage and specific histone modification were measured in PBLCs of the subjects through comet assay and ELISA assay, respectively. Linear regression model analysis was used to analyze the differences among PAHs exposure, DNA damage and p-H3S10 level in two groups. The Mediation analysis was used to analyze the regulated relationships between urinary 1-OHP, DNA damage and histone modification through the bootstrap method. Results: Age of the control and the exposed group were (45.32±8.32) and (43.87±5.67) years old (P=0.284). The concentration of urinary 1-OHP, OTM value, Tail DNA% and p-H3S10 level in exposure group were higher than that in control group, while the M (P₅-P₉₅) of p-H3S10 levels in control and exposed group were 2.21 (0.68-4.71), 4.54 (1.85-23.91) (P<0.001). The degree p-H3S10 level was increased after the subgroups which were (2.59±1.19)%, (3.24±2.81)%, (5.55±3.25)%, (8.77±7.84)%, respectively, divided by quantitated 1-OHP concentration as P₀-P₂₅, P₂₆-P₅₀, P₅₁-P₇₅ and P₇₆-P₁₀₀ (P<0.001). We also found the correlations between urinary 1-OHP and p-H3S10 level or OTM value or Tail DNA%, β (95%CI) were 0.264 (0.167-0.360), 0.500 (0.299-0.702), and 0.510 (0.384-0.671), respectively (P<0.001). Similar result was also observed between p-H3S10 level and OTM value or Tail DNA%, β (95%CI) were 0.149 (0.073-0.226) and 0.220 (0.132-0.308) (P<0.001). Moreover, the mediation effect value of DNA damage on PAHs induced p-H3S10 alteration was 0.054(P=0.040). Conclusion The results suggested that PAHs exposure could induce DNA damage and an increase in histone H3Ser10 phosphorylation in PBLCs. Particularly, the alteration of H3S10 phosphorylation may play an important role in regulating cell DNA damage repair.

Objective To investigate the effect of polycyclic aromatic hydrocarbons (PAHs) exposure on the level of histone H3Ser10 phosphorylation (p-H3S10) and DNA damage degree in peripheral blood lymphocyte (PBLCs). Method 75 coke oven workers from Benxi steel plant in Liaoning Province of China (PAHs-exposed group) and local 50 hot rolling workers (control group) were recruited in this study with age, working years, labor intensity and high temperature for matching factors using cluster sampling method in 2014. HPLC-fluorescence was performed to determine the level of urinary 1-hydroxypyrene (1-OHP), DNA damage and specific histone modification were measured in PBLCs of the subjects through comet assay and ELISA assay, respectively. Linear regression model analysis was used to analyze the differences among PAHs exposure, DNA damage and p-H3S10 level in two groups. The Mediation analysis was used to analyze the regulated relationships between urinary 1-OHP, DNA damage and histone modification through the bootstrap method. Results Age of the control and the exposed group were (45.32± 8.32) and (43.87 ± 5.67) years old (P=0.284). The concentration of urinary 1-OHP, OTM value, Tail DNA%and p-H3S10 level in exposure group were higher than that in control group,while the M (P5-P95) of p-H3S10 levels in control and exposed group were 2.21 (0.68-4.71), 4.54 (1.85-23.91) (P<0.001). The degree p-H3S10 level was increased after the subgroups which were (2.59 ± 1.19)%, (3.24 ± 2.81)%, (5.55 ± 3.25)%, (8.77 ± 7.84)%, respectively, divided by quantitated 1-OHP concentration as P0-P25, P26-P50, P51-P75 and P76-P100 (P<0.001). We also found the correlations between urinary 1-OHP and p-H3S10 level or OTM value or Tail DNA%, β (95%CI) were 0.264 (0.167-0.360), 0.500 (0.299-0.702), and 0.510 (0.384-0.671), respectively (P<0.001). Similar result was also observed between p-H3S10 level and OTM value or Tail DNA%, β (95%CI) were 0.149 (0.073-0.226) and 0.220 (0.132-0.308) (P<0.001). Moreover, the mediation effect value of DNA damage on PAHs induced p-H3S10 alteration was 0.054(P=0.040). Conclusion The results suggested that PAHs exposure could induce DNA damage and an increase in histone H3Ser10 phosphorylation in PBLCs. Particularly, the alteration of H3S10 phosphorylation may play an important role in regulating cell DNA damage repair.

Objective To investigate the effect of polycyclic aromatic hydrocarbons (PAHs) exposure on the level of histone H3Ser10 phosphorylation (p-H3S10) and DNA damage degree in peripheral blood lymphocyte (PBLCs). Method 75 coke oven workers from Benxi steel plant in Liaoning Province of China (PAHs-exposed group) and local 50 hot rolling workers (control group) were recruited in this study with age, working years, labor intensity and high temperature for matching factors using cluster sampling method in 2014. HPLC-fluorescence was performed to determine the level of urinary 1-hydroxypyrene (1-OHP), DNA damage and specific histone modification were measured in PBLCs of the subjects through comet assay and ELISA assay, respectively. Linear regression model analysis was used to analyze the differences among PAHs exposure, DNA damage and p-H3S10 level in two groups. The Mediation analysis was used to analyze the regulated relationships between urinary 1-OHP, DNA damage and histone modification through the bootstrap method. Results Age of the control and the exposed group were (45.32± 8.32) and (43.87 ± 5.67) years old (P=0.284). The concentration of urinary 1-OHP, OTM value, Tail DNA%and p-H3S10 level in exposure group were higher than that in control group,while the M (P5-P95) of p-H3S10 levels in control and exposed group were 2.21 (0.68-4.71), 4.54 (1.85-23.91) (P<0.001). The degree p-H3S10 level was increased after the subgroups which were (2.59 ± 1.19)%, (3.24 ± 2.81)%, (5.55 ± 3.25)%, (8.77 ± 7.84)%, respectively, divided by quantitated 1-OHP concentration as P0-P25, P26-P50, P51-P75 and P76-P100 (P<0.001). We also found the correlations between urinary 1-OHP and p-H3S10 level or OTM value or Tail DNA%, β (95%CI) were 0.264 (0.167-0.360), 0.500 (0.299-0.702), and 0.510 (0.384-0.671), respectively (P<0.001). Similar result was also observed between p-H3S10 level and OTM value or Tail DNA%, β (95%CI) were 0.149 (0.073-0.226) and 0.220 (0.132-0.308) (P<0.001). Moreover, the mediation effect value of DNA damage on PAHs induced p-H3S10 alteration was 0.054(P=0.040). Conclusion The results suggested that PAHs exposure could induce DNA damage and an increase in histone H3Ser10 phosphorylation in PBLCs. Particularly, the alteration of H3S10 phosphorylation may play an important role in regulating cell DNA damage repair.

Objective To explore the effects of moist exposed burn ointment ( MEBO) and in situ skin regeneration technology in the treatment of pressure ulcers in elderly patients in community. Methods A total of 31 elderly patients with pressure ulcers in community were treated with MEBO and in situ skin regeneration technology. The amount of wound exudate, histological types and area change were observed dynamically to evaluate the condition of wound healing. Results There were 14 elderly patients with StageⅠ-Ⅱ pressure ulcers healed within two weeks after treatment, and other 17 patients were healed without skin-grafting within 120 days. Conclusions The application of MEBO and in situ skin regeneration technology can effectively promote healing of pressure ulcers in elderly patients in community and is worthy of clinical promotion and application.