Objective: To explore the effects of personality and sleep quality with psychological distress of junior and senior high school stduents, so as to provide a reference basis for precise interventions of junior and senior high school students mental health. Methods: In October 2023, a convenience sampling method was used to select 9 034 students aged 12-17 from Shiyan City as the study subjects. The Pittsburgh Sleep Quality Index (PSQI) and Kessler Psychological Distress Scale (K10) were used to collect information on sleep quality and psychological distress of junior and senior high school stduents. Between group comparison was conducted by using t-test and Chi-square test. Generalized linear models were employed to analyze the interaction and joint effects of personality and sleep quality on psychological distress. Results: The generalized linear model analysis showed that the interaction between personality and sleep quality on psychological distress was statistically significant of junior and senior high school students(effect size=0.80, P <0.01). The general linear model analysis indicated that, after adjusting for variables such as age, gender, screen time, and daily sitting time with the extroverted and good sleep quality group as the reference, the introverted and poor sleep quality group had the largest mean difference in psychological distress scores (difference=0.51, P <0.05). When stratified by sleep quality, psychological distress scores were higher in the introverted and neutral personality groups with both poor and good sleep quality compared to the extroverted group (poor sleep quality: introverted difference=3.71, neutral difference=1.14; good sleep quality: introverted difference=2.23, neutral difference=0.57, all P < 0.05). When stratified by personality, psychological distress scores were higher in the poor sleep quality groups for introverted, neutral, and extroverted individuals compared to their good sleep quality counterparts (differences=8.66, 7.83, 7.34, all P < 0.05 ). Conclusions Personality and sleep quality have interactive and joint effects on psychological distress of junior and senior high school stduents. Personalized psychological interventions should be developed based on personality and sleep quality.

Objective To investigate the therapeutic effects and mechanisms of Xuefu Zhuyu Mixture(XFZY)in rats with coronary heart disease(CHD).Methods A CHD rat model was established.Successfully modeled rats were randomly divided into five groups(n=12 each):model group,Lipitor group,low-dose XFZY group(7.02 g·kg-1·d-1),high-dose XFZY group(14.04 g·kg-1·d-1),and high-dose XFZY+RS09[Toll-like receptor 4(TLR4)agonist]group(14.04 g·kg-1·d-1 XFZY+intraperitoneal RS09),with an additional normal control group(n=12).After treatment,following treatment completion,all rats underwent echocardiography to assess left ventricular end-diastolic diameter(LVDd),end-systolic diameter(LVDs),ejection fraction(LVEF),and fractional shortening(FS).Myocardial histopathology and vascular remodeling indices were evaluated via hematoxylin-eosin(HE)staining,while myocardial fibrosis was examined using Masson's trichrome staining.Enzyme-linked immunosorbent assay(ELISA)was employed to quantify inflammatory cytokine levels[tumor necrosis factorα(TNF-α),interleukin(IL)-1β,and IL-6]in myocardial tissues.Immunohistochemical analysis determined protein expression of B-cell lymphoma-2(Bc12)and Caspase 3 in myocardial tissues.Western Blot was performed to measure myocardial protein expression levels of TLR4,phosphatidylinositol 3-kinase(PI3K),phosphorylated protein kinase B(p-AKT),total AKT,phosphorylated mammalian target of rapamycin(p-mTOR),and total mTOR.Results Compared with the normal group,rats in the model group exhibited severe myocardial tissue damage,along with significantly elevated collagen volume fraction,LVDs,LVDd,myocardial levels of IL-6,TNF-α and IL-1β,cardiomyocyte apoptosis ratio,aortic media thickness,and protein expression of Caspase 3,TLR4,PI3K,p-AKT/AKT and p-mTOR/mTOR in myocardial tissue(P＜0.05).Conversely,LVEF,FS,aortic luminal diameter,and Bcl-2 protein content were significantly reduced,the difference being statistically significant(P＜0.05).Compared to the model group,both low-and high-dose XFZY groups as well as the Lipitor group demonstrated attenuated myocardial lesions,with significant reductions in collagen volume fraction,LVDs,LVDd,myocardial IL-6,TNF-α,IL-1β levels,cardiomyocyte apoptosis ratio,aortic media thickness,and protein expression of Caspase 3,TLR4,PI3K,p-AKT/AKT and p-mTOR/mTOR(P＜0.05).Concurrently,LVEF,FS,aortic luminal diameter,and Bcl-2 protein content were significantly increased,the difference being statistically significant(P＜0.05).No statistically significant differences were observed between the high-dose XFZY group and the Lipitor group for any aforementioned parameters(P＞0.05).However,rats treated with high-dose XFZY plus RS09 showed aggravated myocardial injury with manifested interstitial fibrosis,alongside significantly intensified inflammatory response,cardiomyocyte apoptosis,and vascular remodeling compared to the high-dose XFZY alone group(all P＜0.05).Conclusion XFZY alleviates CHD symptoms by suppressing TLR4/PI3K/AKT/mTOR pathway activation,thereby reducing myocardial inflammation,fibrosis,apoptosis,and vascular remodeling.

The host-microbe co-metabolism system, generating diverse exogenous and endogenous bioactive molecules that influence the host's immune and metabolic functions, plays a crucial role in the pathogenesis of atherosclerosis. Recent studies have elucidated the interaction between natural medicines and this co-metabolism system. Upon oral administration, natural medicine ingredients can undergo transformation by gut microbiota, potentially enhancing their bioavailability or anti-atherogenic efficacy. Furthermore, natural medicines can exert anti-atherogenic effects via modulation of endogenous host-microbe co-metabolism. This review presents an updated understanding of the dual association between natural medicines and host-microbe co-metabolites. It explores the critical function of microbial exogenous metabolites derived from natural medicines and uncovers the mechanisms underlying natural medicines' intervention on key nodes of endogenous host-microbe co-metabolism. These insights may offer new perspectives for cardiovascular disease (CVD) treatment and guide future drug discovery efforts.
Humans ; Atherosclerosis/metabolism* ; Gastrointestinal Microbiome/drug effects* ; Biological Products/therapeutic use* ; Animals ; Host Microbial Interactions/drug effects*

Objective To investigate the relationship between the levels of peripheral blood iri-sin,myostatin(MSTN),and 25-hydroxyvitamin D[25(OH)D]and the risk and predictive value of sarcopenia in elderly patients with type 2 diabetes mellitus(T2DM)complicated by heart failure.Methods Elderly patients with T2DM complicated by heart failure who visited Xingtai Central Hospi-tal from March 2023 to March 2024 were selected as the study subjects.The sample size was calculated based on the effect size.Patients were divided into modeling set(n=140)and validation set(n=60)at a ratio of 7 to 3 using a simple randomization method.Additionally,according to the occur-rence of sarcopenia,patients in the modeling set were divided into sarcopenia group and non-sar-copenia group.Clinical data and the levels of peripheral blood irisin,MSTN,and 25(OH)D were compared between the modeling and validation sets.The receiver operating characteristic(ROC)curve was used to analyze the predictive efficacy of peripheral blood irisin,MSTN,and 25(OH)D for sarcopenia.Multivariate logistic regression analysis was employed to identify the influencing fac-tors of sarcopenia in elderly patients with T2DM complicated by heart failure,and a relevant predic-tive model was constructed using R software.Results Among 200 elderly patients with T2DM com-plicated by heart failure,71 cases developed sarcopenia,with an incidence rate of 35.50％.The proportion of regular exercise,bone mineral content,and the levels of irisin and 25(OH)D in the sarcopenia group were lower than those in the non-sarcopenia group,while the MSTN level was high-er in the sarcopenia group,and the differences were statistically significant(P＜0.05).The areas under the curve(AUCs)for predicting sarcopenia by irisin,MSTN,and 25(OH)D were 0.878(95％CI,0.812 to 0.927),0.848(95％CI,0.778 to 0.903),and 0.826(95％CI,0.753 to 0.885),respectively.The sensitivities were 74.16％,79.78％,and 88.76％,and the specifici-ties were 74.16％,79.79％,and 88.76％,respectively.The results of multivariate logistic regres-sion analysis showed that lack of exercise habits(OR=2.489,95％CI,1.665 to 3.735),de-creased bone mineral content(OR=2.340,95％CI,1.596 to 3.595),irisin ≤105.44 ng/mL(OR=3.111,95％CI,2.004 to5.147),MSTN＞19.06 μg/L(OR=2.667,95％CI,2.015 to 4.693),and25(OH)D ≤12.23 ng/mL(OR=2.547,95％CI,1.285 to 4.492)were all inde-pendent risk factors for sarcopenia in these patients(P＜0.05).The results of ROC curve analysis showed that the AUCs of the nomogram model for predicting postoperative recurrence in the modeling and validation sets were 0.875 and 0.853,respectively.The Hosmer-Lemeshow test for the model-ing and validation sets showed the following results:x2=0.715,P=0.510;x2=0.651,P=0.568.The calibration curves were basically consistent with the standard curves.The threshold probability range of decision curve analysis(DCA)was 0.1 to 0.9.Within this range,both the modeling and validation sets showed good clinical net benefits.Conclusion Peripheral blood iri-sin,MSTN,and 25(OH)D all have certain predictive values for the occurrence of sarcopenia in elderly patients with T2DM complicated by heart failure.The nomogram model constructed based on irisin,MSTN,and 25(OH)D can provide a quantitative basis for the early screening of sarcopenia in these patients.

BACKGROUND:Although traditional therapies,including drugs and surgery,cannot repair the damaged myocardial tissue,the mortality rate of myocardial infarction remains high.Stem cells provide the possibility to solve this problem due to their self-renewal and multi-directional differentiation potential. OBJECTIVE:To analyze the research progress of stem cell therapy for myocardial infarction in recent ten years by bibliometric analysis. METHODS:The related articles on stem cells and myocardial infarction published in SCI-E and SSCI from January 1,2012 to December 1,2022 in the Web of Science database were searched.EXCEL,CiteSpace and VOSviewer software were used to make statistical and visualization analyses of the data such as the number of publications,authors,institutions,journals,countries and keywords. RESULTS AND CONCLUSION:A total of 3 210 core articles were published,and the total number increased year by year.hausenloy,derek j.is the author with the largest number of publications,China is the country with the largest number of publications,and the Fourth Military Medical University is the institution with the largest number of publications.The research hotspots in this field are changing from cell experiments and animal experiments to clinical trials.In the past ten years,research in this field has been highly popular and still has great development prospects.It is necessary to promote international and inter-agency exchange and learning,and further explore the role of stem cells in the treatment of myocardial infarction.

Chemotherapy resistance in leukemia is an urgent clinical therapeutic challenge.Ferroptosis is a unique mode of cell death driven by iron-dependent phospholipid peroxidation.Leukemia is characterized by increased oxidative stress and iron overload,suggesting that leukemia cells might be susceptible to ferroptosis and indicating a possible therapeutic approach.Ferroptosis has been extensively studied in recent years and used in the treatment of various types of leukemia.Several studies have demonstrated an association between the regulatory pathways of ferroptosis and the mechanisms of leukemia drug resistance.The induction of ferroptosis through different pathways can effectively reduce the resistance of various types of leukemia cells to chemotherapeutic drugs,and thus improve their clinical efficacy.In this article,we review the regulatory mechanisms of ferroptosis and analyze the association between oxidative stress and iron metabolism pathways of ferroptosis and the mechanism of leukemia drug resistance.We also summarize the experimental studies and clinical applications of ferroptosis for the treatment of various types of drug-resistant leukemias,with the aim of providing new ideas and directions for the study of ferroptosis and a new strategy to reverse chemotherapy resistance in patients with leukemia in the future.

Objective To explore the effects of Tanganjianwan(TGJW)combined with abdominal massage(AM)on glucose and lipid metabolism and inflammatory factors in obesity and type 2 diabetes mellitus(OT2DM)patients with metformin treatment.Methods Patients with OT2DM diagnosed in Wuhan Hospital of Traditional Chinese Medicine from June 2021 to June 2023 were included as study subjects,and were divided into the AM group(metformin combined with AM)and the TGJW group(metformin combined with AM+TGJW)according to the random number table method.The treatment efficacy and safety were assessed by continuous intervention for 3 months.Obesity-related indices[waist-hip ratio(WHR)and body mass index(BMI)],glycemic and lipid metabolic indices[glycosylated hemoglobin(HbA1c),fasting blood glucose(FBG),postprandial 2-hour glucose(P2hG),total cholesterol(TC),triglycerides(TG),high-density lipoprotein cholesterol(HDL-C)and low-density lipoprotein cholesterol(LDL-C)],insulin sensitivity indexes[homeostasis model insulin resistance index(HOMA-IR)and homeostasis model pancreaticβ-cell function index(HOMA-β)],and inflammation indexes[interleukin-6(IL-6),tumor necrosis factor α(TNF-α),and C-reactive protein(CRP)]changes were compared before and after treatment between the TGJW group and the AM group.Results A total of 100 OT2DM patients were included in the study,with 50 cases each in the TGJW group and AM group.After the intervention,the treatment efficiency of the TGJW group was significantly higher than that of the AM group(P＜0.05),and no malignant adverse events occurred during treatment.Compared with the pre-treatment period,the levels of WHR,BMI,FBG,P2hG,HbA1c,TC,TG,LDL-C,HOMA-IR,IL-6,TNF-α,and CRP decreased in both groups(P＜0.05),while the levels of HDL-C and HOMA-β increased significantly(P＜0.05).After the intervention,the levels of WHR,BMI,FBG,P2hG,HbA1c,TC,TG,LDL-C,HOMA-IR,IL-6,TNF-α,and CRP in the TGJW group were lower than those in the AM group(P-＜0.05),while the levels of HDL-C and HOMA-β were higher than those in the AM group(P＜0.05).Conclusion Compared with AM treatment alone,TGJW combined with AM can improve glucose-lipid metabolism,insulin sensitivity and inflammation indexes in OT2DM patients,enhance the therapeutic effect of metformin treatment in OT2DM patients,and is safe,it has certain clinical promotion significance.

Objective:To investigate key differential expressed genes(DEGs),enriched biological functions and signaling pathways in exosomes derived from angiosarcoma cells ISOHAS and angiosarcoma stem-like cells Sphere by bioinformatics analysis,to provide new therapeutic targets for angiosarcoma.Methods:Transcriptome sequencing of exosomes derived from ISOHAS and Sphere were performed to screen for DEGs by|log2FC|>2 and FDR<0.05 as criteria.Bioinformatics analysis was used to enrich GO and KEGG pathways of DEGs to identify biological functions and signaling pathways of enriched DEGs.STRING database was used to screen key DEGs,and iPath was used to visualize to identify metabolic pathways enriched by DEGs.Results:Transcriptome sequencing results showed that 91 DEGs were identified in exosomes derived from ISOHAS and Sphere.GO and KEGG pathway enrichment analysis demonstrated that main biological functions and signaling pathways enriched by DEGs were response to glucocorticoid and TNF signaling pathway,respectively.STRING database demonstrated that TNF and IL-6 were key DEGs.iPath metabolic network analysis demonstrated that DEGs were mainly identified in lipid metabolism and nucleotide metabolism.Conclusion:Sphere-derived exosomes may influence occurrence and development of angiosarcoma by carrying key genes TNF and IL-6 to interfere with glucocorticoid response,TNF signaling pathway,lipid metabolism,nucleotide metabolism and other biological functions and signaling pathways,providing new ideas for therapeutic targets for angiosarcoma.