OBJECTIVE To promote the industrialization process and modernization of traditional knowledge of Chinese medicine under the framework of the Regional Comprehensive Economic Partnership Agreement. METHODS It was done firstly， to sort out the framework for the protection of traditional knowledge in the international area； and secondly， to respond in the following two paths， one was the explicitization of traditional knowledge， and the other was the standardization of its carriers. RESULTS & CONCLUSIONS The goal of protecting traditional knowledge is to facilitate its modernization and accelerate its industrial utilization at the international level. As one of the countries of origin of traditional knowledge， our response is， to improve the registration provisions in the Regulations on the Protection of Traditional Knowledge of Chinese Medicine （Draft for Public Comments）， promote the synchronization of both the patent and the standard application of Chinese medicine， and strengthen the integration of Chinese standardization system with the international one， which will promote the compliance application of traditional knowledge of Chinese medicine.

OBJECTIVE To promote the industrialization process and modernization of traditional knowledge of Chinese medicine under the framework of the Regional Comprehensive Economic Partnership Agreement. METHODS It was done firstly， to sort out the framework for the protection of traditional knowledge in the international area； and secondly， to respond in the following two paths， one was the explicitization of traditional knowledge， and the other was the standardization of its carriers. RESULTS & CONCLUSIONS The goal of protecting traditional knowledge is to facilitate its modernization and accelerate its industrial utilization at the international level. As one of the countries of origin of traditional knowledge， our response is， to improve the registration provisions in the Regulations on the Protection of Traditional Knowledge of Chinese Medicine （Draft for Public Comments）， promote the synchronization of both the patent and the standard application of Chinese medicine， and strengthen the integration of Chinese standardization system with the international one， which will promote the compliance application of traditional knowledge of Chinese medicine.

Objective: To explore the associations of moderate to vigorous intensity physical activity (MVPA) and sedentary behavior (SB) among primary and secondary school students and their parents, so as to provide a scientific basis for formulating targeted physical activity promotion strategies for children and adolescents. Methods: From 2021 to 2022, basic information and 24 h movement behaviors of 2 484 pairs of students and their parents were collected from five primary and secondary schools in Haizhu District, Guangzhou City, with a convenient sampling combining with cluster sampling method. Component regression models were constructed to analyze the relationship between parental MVPA, SB and primary and secondary school students MVPA and SB, and a component isochronous substitution model was used to explore the effects of mutual substitution between parental MVPA, residual components (time use components other than SB during the 24 h period), and SB on the behavioral activities of MVPA and SB in primary and secondary school students. Results: Parental MVPA and SB of students in grade 1 to 3 were positively correlated with both students MVPA and SB ( β=0.06, 0.12, P <0.01). The component isochronous substitution model showed that substituting 10 and 20 minutes of MVPA for SB by parents in grade 1 to 3 was associated with an increase in MVPA of students, and substituting 10 and 20 minutes of residual ingredients for SB was associated with a decrease in SB of students, with mean changes of 0.8 (95% CI =0.4-1.2) and 1.4 (95% CI =0.7-2.2) and -1.4 (95% CI =-1.7 to -1.1) and -2.9 (95% CI =-3.4 to -2.3)( P <0.05). No statistically significant associations were observed between parents of students in grades 4 to 6 and 7 to 9 and students physical activity and sedentary behaviour ( P >0.05). Conclusions Parents of students in grades 1 to 3 increases MVPA and decrease SB are beneficial to increase MVPA and decrease SB of students. Parents could promote physical activity among primary and secondary school students, and the intervention gateway should be advanced, with the low grades as the optimal intervention period.

Posterior capsule opacification(PCO)is a common postoperative complication of cataract surgery, primarily caused by the proliferation and migration of residual lens epithelial cells(LECs). Although neodymium-doped yttrium aluminum garnet(Nd:YAG)laser posterior capsulotomy effectively treats PCO, it carries risks of complications such as cystoid macular edema(CME). Thus, preventing PCO formation is of critical clinical importance. Despite advancements in intraocular lens(IOL)materials and designs, achieving complete PCO eradication remains challenging. This review systematically examines recent advancements in surface-modified IOLs, including anti-biofouling IOL(reducing LECs adhesion), capsular adhesion-enhanced IOL(promoting capsular bag integration), micro-patterned IOL(physically inhibiting migration), photothermal/photodynamic IOL(inducing light-activated LECs apoptosis), and drug-eluting IOL(sustained drug release). These surface modification strategies demonstrate synergistic effects through complementary mechanisms(including physical barrier formation, chemical intervention, and bioactive regulation), effectively suppressing LECs proliferation while significantly reducing PCO incidence. Importantly, these approaches eliminate the risks associated with conventional Nd:YAG laser treatment, offering substantial advantages. By providing a comprehensive evaluation of these cutting-edge technologies, this review serves as a valuable reference for IOL design optimization. It represents a paradigm shift in cataract management strategies, transitioning from reactive therapeutic interventions to proactive preventive measures, and ultimately leads to improving long-term visual outcomes for patients.

Due to the wide variety and varying quality of medical wound dressings, as well as the current lack of unified national or industry standards for regulation, this paper proposes a research strategy for establishing a quality evaluation system for medical wound dressings‌. By developing a technical roadmap, this strategy clarifies the process flow and key points in the quality evaluation process, establishes evaluation methods for various types of medical wound dressings, and addresses important issues such as how to determine key performance indicators based on product characteristics and how to research and validate test methods for key items. This provides a detailed and feasible research strategy and evaluation method for medical wound dressing manufacturers, testing institutions, and regulatory authorities. It reduces the difficulty and cost of quality evaluation for medical wound dressings and has certain significance in standardizing and improving their quality level, ensuring their safety and effectiveness, and serving the quality and safety regulation of medical devices.‌.
Bandages/standards* ; Quality Control ; Humans ; Wounds and Injuries/therapy*

Objective To investigate the causal association between sleep disorder-related phenotypes and cerebrovascular outcomes/complications using the two-sample Mendelian randomization （MR） method， and to determine causal orientation via directionality testing. Methods Genetic variations from genome-wide association studies were used as instrumental variables to analyze eight sleep-related phenotypes （continuous sleep， snoring， napping， insomnia， morning diurnal preference， daytime sleepiness， long sleep， and short sleep） against multiple cerebrovascular outcomes and complications （cerebral infarction， unruptured cerebral artery dissection， cerebral arteritis， cerebral amyloid angiopathy， unruptured cerebral aneurysm， cerebral atherosclerosis， intracerebral hemorrhage， vascular syndrome， and sequelae of cerebrovascular disease）. The inverse-variance weighted （IVW） method was used for primary analysis， with the assistance of the sensitivity methods such as MR-Egger， weighted median， simple mode， and weighted mode， and the Estimate value was used to characterized effect direction and magnitude， with statistical significance assessed by P value. The Steiger directionality test was used to compare the extent of variance explained by instrumental variables concerning exposure and outcome and confirm causal direction. Results The IVW analysis showed that snoring was associated with an increased risk of cerebral amyloid angiopathy （Estimate=8.08， 95% CI 1.93-14.23， P=0.01）， and long sleep duration was associated with an increased risk of cerebral atherosclerosis （Estimate=14.95， 95% CI 2.44-27.46， P=0.02）. Short sleep duration was associated with an increased risk of cerebral arteritis （Estimate=13.33， 95% CI 1.54-25.12， P=0.03）； however， inconsistent directions were observed across sensitivity methods （e.g.， MR-Egger）， and therefore， it was treated as suggestive evidence rather than a robust conclusion. The Steiger test showed R2exposure>R2outcome for most exposure-outcome pairs， and the key associations did not persist under reverse-direction analyses， supporting a forward causal pathway from sleep phenotypes to cerebrovascular outcomes and reducing the likelihood of reverse causation. Conclusion Genetic evidence supports a forward causal effect of sleep-related phenotypes on cerebrovascular outcomes and complications， with the most robust findings of “snoring increases the risk of cerebral amyloid angiopathy” and “long sleep duration increases the risk of cerebral atherosclerosis”. Identification and treatment of sleep-disordered breathing and avoidance of prolonged sleep may be used as potential targets for preventing cerebrovascular disease， and multi-ethnic prospective studies and interventional trials are needed to further validate these findings and clarify the underlying biological mechanisms.

Objective To investigate the expression of serum microRNA-29b(miR-29b),microRNA-199a(miR-199a),and microRNA-19a-3p(miR-19a-3p)in patients with acute cerebral infarction(ACI)and their relationship with disease severity and prognosis.Methods(1)Rats were randomly divided into a control group(Control group)and a model group(Model group),with 6 rats in each group.ACI was induced in the model group using the modified Longa suture method;the expression levels of miR-29b,miR-199a,miR-19a-3p in rat serum and brain tissue were detected and analyzed.(2)A total of 106 ACI patients diagnosed at Tangshan People's Hospital from June 2023 to June 2024 were enrolled as the study group,and 108 healthy individuals who underwent physical check-ups at the same hospital during the same period were chosen as the control group.According to the NIHSS evaluation results,the study group patients were assigned into mild(42 cases),moderate(34 cases),and severe(30 cases)groups.Based on the mRS evaluation results,the patients were assigned into good prognosis(68 cases)and poor prognosis(38 cases)groups.Real-time fluorescence quantitative PCR was applied to measure the expression levels of serum miR-29b,miR-199a,and miR-19a-3p.Pearson correlation analyzed the correlation between serum miR-29b,miR-199a,miR-19a-3p levels and NIHSS score and mRS score in ACI patients.The risk factors for poor prognosis in ACI patients were analyzed using multivariate logistic regression.ROC curves were used to analyze the predictive value of serum miR-29b,miR-199a,miR-19a-3p levels and NHISS scores in poor prognosis of ACI patients.Results(1)Compared with the Control group,the levels of miR-199a and miR-19a-3p in the serum and brain tissue of the Model group rats were significantly increased,while the level of miR-29b was significantly decreased(P<0.05);(2)Compared with the control group,as the severity of ACI patients gradually increased,the levels of serum miR-199a and miR-19a-3p unusually increased in the mild,moderate,and severe groups,while the level of miR-29b was significantly decreased(P<0.05).The NHISS score,miR-199a and miR-19a-3p levels in the poor prognosis group were significantly higher than those in the good prognosis group,while miR-29b was significantly lower than that in the good prognosis group(P<0.05).The levels of serum miR-199a and miR-19a-3p were positively correlated with NIHSS score;the level of miR-29b was negatively correlated with NIHSS score(P<0.05).Elevated serum miR-199a and miR-19a-3p levels and increased NHISS score were independent risk factors for poor prognosis in ACI patients,and elevated serum miR-29b levels were protective factors for poor prognosis in ACI patients(P<0.05).The combined prediction of poor prognosis in ACI patients using serum miR-29b,miR-199a,miR-19a-3p levels and NHISS scores yielded an ACI of 0.988,which was superior to individual predictions(Z=2.878,3.551,3.300,3.452,P<0.05).Conclusion The serum expression levels of miR-199a and miR-19a-3p were significantly up-regulated,while miR-29b levels significantly down-regulated,which were related to the disease severity and prognosis.The the combination of the three miRNAs had certain value in predicting the poor prognosis of patients.MiR-29b,miR-199a,and miR-19a-3p can be used as important predictors to evaluate the progression and prognosis of ACI patients.

OBJECTIVE: To investigate the molecular pathogenic mechanisms of a family with hereditary factor Ⅶ (FⅦ) deficiency. METHODS: A family (3 generations, 12 members) with hereditary FⅦ deficiency, in which the proband presented with menorrhagia and was admitted to the First Affiliated Hospital of Wenzhou Medical University in April 2023, was selected as the study subject. Clinical data of the family members were collected. Peripheral venous blood samples were collected from all 12 members for routine coagulation tests and genomic DNA extraction. All exons and flanking sequences of the F7 gene were amplified by PCR and analyzed by Sanger sequencing. Thrombin generation assay was performed to evaluate the coagulation potential of the proband and her parents. Multiple online bioinformatics software tools were used to analyze the conservation and pathogenicity of candidate variants identified in the proband. The pathogenicity of variant was classified according to the Standards and Guidelines for the Interpretation of Sequence Variants released by American College of Medical Genetics and Genomics (ACMG) (hereinafter referred to as ACMG guidelines). Homology modeling of the variant FⅦ protein was performed using homology modeling (SWISS-MODEL). Amino acid sequence alignment between wild-type and variant FⅦ proteins was conducted using MEGA v7, and spatial conformational differences were analyzed using PyMOL to assess the potential impact of the F7 gene variants on the structure and function of the FⅦ protein. This study was approved by the Ethics Committee of the First Affiliated Hospital of Wenzhou Medical University (Ethics No.: KY2022-R193). RESULTS: Coagulation tests showed that the proband's prothrombin time (PT) was significantly prolonged to 33.1 s, and both factor Ⅶ activity (FⅦ:C) and antigen (FⅦ:Ag) levels were reduced to 2%. Her parents, eldest sister, second sister, younger brother, and four children all showed mildly prolonged PT, with FⅦ:C and FⅦ:Ag levels approximately 50% of normal. Genetic sequencing identified compound heterozygous variants in the F7 gene of the proband: a heterozygous missense variant c.722C>A (p.Thr241Asn) in exon 7, and a heterozygous deletion variant c.1261_1261delA (p.Ile421Ser*fs75) in exon 8. Retrieval from domestic and international databases found no previous reports of the latter variant, suggesting it is novel. Familial co-segregation analysis confirmed that these variants were inherited from her father and mother, respectively. The thrombin generation assay demonstrated that the proband had a significantly decreased peak thrombin height (peak ratio: 29.5%), significantly increased thrombin lag time ratio and time-to-peak ratio (3.03 and 2.93, respectively), but only a mildly decreased endogenous thrombin potential (ETP) ratio of 90.7%. Online bioinformatics analysis indicated that threonine-241 (p.Thr241) in the FⅦ protein was not conserved, while isoleucine-421 (p.Ile421) was highly conserved. Both the p.Thr241Asn and p.Ile421Serfs*75 variant sites in the proband's F7 gene were predicted to be pathogenic. According to the ACMG guidelines, the p.Thr241Asn (PM3+PP1+PP3+PP4+PP5) and p.Ile421Ser*fs75 (PM2+PM4 +PP1+PP3+PP4) variants were both classified as "likely pathogenic". Structural analysis of the FⅦ protein indicated that the p.Ile421Ser*fs75 frameshift variant led to the substitution of Cysteine-428 by Alanine, preventing the formation of a critical disulfide bond between amino acid residues 400 and 428 present in the wild-type FVII protein. CONCLUSION The compound heterozygous variants p.Thr241Asn and p.Ile421Ser*fs75 in the F7 gene are likely the genetic etiology responsible for the reduced FⅦ levels in this hereditary FⅦ deficiency family.
Adult ; Female ; Humans ; Male ; Middle Aged ; China ; Factor VII/chemistry* ; Factor VII Deficiency/genetics* ; Heterozygote ; Mutation ; Pedigree ; East Asian People/genetics*

Objective: To investigate the comorbidity of myopia and scoliosis among primary and secondary school students in Tianjin, and to analyze the school environment risk factors contributing to these health issues, so as to provide a scientific basis for development effective prevention measures. Methods: A total of 41 654 primary and secondary school students from 16 districts of Tianjin were selected by stratified random cluster sampling from September to October 2023 to screen for myopia and scoliosis. Univariate analysis was performed to examine the data, followed by a bivariate multivariate Logistic regression model and cumulative effect analysis to explore the influencing factors of their comorbidity. Results: In 2023, the prevalence of comorbidity of screening positive myopia and scoliosis among primary and secondary school students in Tianjin was 2.65%. The prevalence was higher in suburban areas (3.26%) compared to urban areas (2.02%), higher among females (3.81%) compared to males (1.59%), and highest in high school students (6.17%) compared to middle school (4.19%) and primary school students (0.44%) (χ2=62.23, 198.69, 953.19, P<0.01). Logistic regression analysis showed that the number of physical education classes ≥3 per week, the number of eye health exercises at school ≥2 per day, outdoor activities between classes, teachers reminding to pay attention to reading and writing posture and strict eye standing posture were negatively correlated with the comorbidity of screening positive myopia and scoliosis (OR=0.66, 0.77, 0.71, 0.78, 0.74, P<0.05). Reading or electronic screen while lying or lying on the stomach was positively associated with the comorbidity of screening positive myopia and scoliosis (OR=1.77, P<0.05). Cumulative effect analysis showed that the cumulative score (4-7, 7-9, ≥10) was negatively correlated with the comorbidity of screening positive of myopia and scoliosis (OR=0.65, 0.55, 0.52, P<0.05). Conclusions The school environment support and students personal behavior habits in school are related to the comorbidity of comorbidity of screening positive myopia and scoliosis. Prevention and control of myopia and scoliosis should improve the environmental factors related to students health in school.

Objective:To investigate the regulatory effect of transient receptor potential cation channel subfamily C member 3 (TRPC3) on the retina in oxygen-induced retinopathy (OIR) mice and biological behavior of human retinal vascular endothelial cells (HREC).Methods:A total of 32 healthy SPF grade 7-day-old C57BL/6 mice were selected and randomly divided into a control group and an OIR group by the random number table method, with 16 mice in each group.The control group received no special treatment, and the OIR model was established in the OIR group.On postnatal day 17 (PN17), the success of the model establishment was verified by immunofluorescence staining of the retinal patch.The in vitro cultured HREC were divided into a normal control group, a transfection reagent group, and a si-TRPC3 group.The normal control group received no special treatment, while the transfection reagent group and the si-TRPC3 group were transfected with transfection reagent or transfection reagent + si-TRPC3.The relative expression of TRPC3 mRNA was detected by real-time quantitative fluorescence PCR.The relative expressions of TRPC3, transcription factor NF-E2 related factor (Nrf2), and superoxide dismutase (SOD) proteins were determined by Western blot.HREC were further divided into a normal control group, a vascular endothelial growth factor (VEGF) group, a si-TRPC3 group, and a Pyr3 (TRPC3 channel inhibitor) group, which were cultured in complete medium, medium containing 20 ng/ml VEGF recombinant protein, medium containing 20 ng/ml VEGF recombinant protein (si-TRPC3 transfection for 72 hours), and medium containing 20 ng/ml VEGF recombinant protein+ 1 μmol/L Pyr3 for 48 hours, respectively.The proliferation ability of HREC was detected using cell counting kit 8 (CCK-8). The horizontal and vertical migration ability of cells were detected by cell scratch assay and transwell assay, respectively.This study followed the 3R principles of animal welfare and was approved by the Ethics Committee of Hebei Eye Hospital (No.2023LW04). Results:Pathological neovascular clusters with strong fluorescent staining appeared in the retina of OIR mice on PN17.The relative expressions of TRPC3 mRNA and protein in the retina of OIR mice were 2.057±0.244 and 1.517±0.290, respectively, significantly higher than 0.983±0.033 and 0.874±0.052 of control group ( t=6.165, 3.094; both at P<0.05). The relative expression levels of TRPC3 mRNA and protein were significantly lower, and the relative expression levels of Nrf2 and SOD proteins were higher in the si-TRPC3 group than in the normal control and transfection reagent groups, and the differences were statistically significant (all at P<0.05). The CCK-8 experiment results showed that the cell absorbance value was higher in the VEGF group than in the normal control group, and lower in the si-TRPC3 and Pyr3 groups than in the VEGF group, with statistically significant differences (all at P<0.05). The results of the cell scratch experiment showed that the lateral migration rate of VEGF group cells was higher than that of normal control group, while the lateral migration rate of si-TRPC3 group and Pyr3 group cells was lower than that of VEGF group, and the differences were statistically significant (all at P<0.05). The transwell experiment results showed that the number of stained cells in the VEGF group was higher than that in the normal control group, and the number of stained cells in the si-TRPC3 group and Pyr3 group was lower than that in the VEGF group, with statistically significant differences (all at P<0.05). Conclusions:Hypoxia induces increased TRPC3 expression in OIR mouse retina, and downregulation of TRPC3 inhibits HREC proliferation and migration.The mechanism is related to the activation of the Nrf2-related oxidative stress pathway.