Objective:To investigate the effects of long non coding RNA KCNQ1OT1(LncRNA KCNQ1OT1)on the migration and invasion of oral squamous cell carcinoma(OSCC)cells by regulating the microRNA-875-5p(miR-875-5p)/ETS like transcription factor 4(ELK4)axis.Methods:QRT-PCR was applied to detect the mRNA levels of LncRNA KCNQ1OT1,miR-875-5p,and ELK4 in OSCC cell lines(HSC-3,PE/CA-PJ15,HN13)and tissues.The dual luciferase assay was applied to detect the targeting relationship between LncRNA KCNQ1OT1 and miR-875-5p,and target relationship between miR-875-5p and ELK4.HSC-3 cells were used in control group,sh-NC group,sh-KCNQ1OT1 group,sh-KCNQ1OT1+anti-NC group,sh-KCNQ1OT1+anti-miR-875-5p group,miR-NC group,miR-875-5p mimic group,miR-875-5p mimic+pcDNA-NC group,and miR-875-5p mimic+ELK4 group.The migration and invasion abilities of HSC-3 cells were detected.Immunoblotting was applied to detect the protein expression of ELK4,MMP-2,MMP-9 and epithelial mesenchymal transition(EMT)(E-Cadherin,N-Cadherin,Vimentin).The nude mouse transplant tumor was applied to verify the effect of LncRNA KCNQ1OT1 on OSCC transplant tumors.Results:LncRNA KCNQ1OT1 and ELK4 mRNA expression increased in OSCC tissues and cancer cell lines,while miR-875-5p expression decreased(P＜0.05).Database predictions show that miR-875-5p specifically bound to LncRNAs KCNQ1OT1 and ELK4,respectively.Compared with the sh-NC group,the numbers of cell migration and cell invasion,the expression of LncRNA KCNQ1OT1,ELK4,MMP-2,MMP-9,N-Cadherin,and Vimentin in the sh-KC-NQ1OT1 group were lower,while the expression of miR-875-5p and E-Cadherin was higher(P＜0.05).Compared with the sh-KC-NQ1OT1+anti-NC group,the expression of miR-875-5p and E-Cadherin in the sh-KCNQ1OT1+anti-miR-875-5p group was lower,while the numbers of cell migration and cell invasion,the expression of ELK4,MMP-2,MMP-9,N-Cadherin,and Vimentin were higher(P＜0.05).Compared with the miR-NC group,the expression of miR-875-5p and E-Cadherin in the miR-875-5p mimic group was higher,while the numbers of cell migration and cell invasion,the expression of ELK4,MMP-2,MMP-9,N-Cadherin,and Vim-entin were lower(P＜0.05).Compared with the miR-875-5p mimic+pcDNA-NC group,the numbers of cell migration and cell inva-sion,the expression of ELK4,MMP-2,MMP-9,N-Cadherin,and Vimentin in the miR-875-5p mimic+ELK4 group were higher,while the expression of E-Cadherin was lower(P＜0.05).The transplant tumor volume and weight of the sh-KCNQ1OT1 group were smaller than those of the sh-NC group,the mRNA and protein expression levels of LncRNA KCNQ1OT1,ELK4 were lower than those of the sh-NC group,and the expression level of miR-875-5p was higher than that of the sh-NC group(P＜0.05).Conclusion:Inhibition of LncRNA KCNQ1OT1 can target the miR-875-5p/ELK4 axis to inhibit migration,invasion,and EMT of OSCC cells.

Objective To investigate the expression levels of lysophosphatidylcholine(LysoPC),microtubule associated pro-tein Tau(MAPT)and growth differentiation factor-10(GDF-10)in oral squamous cell carcinoma(SCC),and their correlation with prognosis.Methods In all,128 patients with oral squamous cell carcinoma who visited Nantong University Affiliated Hos-pital from April 2017 to April 2019 were selected as the study group,and 100 patients with benign oral lesions during the same time period were selected as the control group.The expression levels of LysoPC,Tau and GDF-10 were compared between the 2 groups of patients.The relationship between the expression levels of LysoPC,Tau,GDF-10,the clinical staging,lymph node me-tastasis,and survival of oral squamous cell carcinoma patients were analyzed,and the assessment values of these factors for prognosis were evaluated.Results The positive rate of Tau and GDF-10 in pathological tissue and LysoPC in serum of the stud-y group were lower than those of the control group(all P＜0.05).Patients with low expression levels of LysoPC,Tau and GDF-10 had a higher proportion of stage Ⅲ to Ⅳ and lymph node metastasis than those with high expression levels of LysoPC,Tau and GDF-10(all P＜0.05).The 128 patients were followed up for 5 years,86 survived(67.19％),42 died(32.81％).LysoPC,Tau and GDF-10 levels were negatively correlated with survival time(all P＜0.05,r=-0.597,-0.622,-0.656).The results of log-rank test showed that the 5-year survival rate of LysoPC,Tau and GDF-10 low expression group was lower than that of LysoPC,Tau and GDF-10 high expression group(all P＜0.05).The high expression levels of LysoPC,Tau and GDF-10 were protective factors,while lymph node metastasis and high clinical stage were risk factors(all P＜0.05).Conclusion LysoPC,Tau and GDF-10 are all low expressed in patients with oral squamous cell carcinoma,and the expression level is correlated with clinical stage and lymph node metastasis.Low expression may indicate a higher risk of death.

The clinical detection of paroxysmal atrial fibrillation(PAF)remains challenging due to its transient and stochastic characteristics,and existing dynamic mode decomposition methods have limitations in modal redundancy reduction and feature extraction when processing single-channel noisy electrocardiogram(ECG)signals.Therefore,a signal analysis method based on high-order dynamic mode decomposition is proposed.It captures high-order correlations within ECG signals through tensor decomposition techniques and decomposes complex signals into physically interpretable dynamic modes.A stability evaluation framework for signal subsystem is established based on modal interaction relationships.By incorporating quantitative indicators including proportion of modes reflecting system instability,modal distribution entropy,and eigenvalue spectrum divergence,a feature discrimination model for PAF is developed.Experimental validation using the MIT-BIH atrial fibrillation database reveals statistically significant differences(P<0.05)in stability-related features between PAF episodes and normal sinus rhythms.The classification model based on support vector machine achieves an average recognition accuracy of 96.15%.These results demonstrate that the proposed method can effectively analyze nonlinear dynamic characteristics in noisy single-lead ECG signals,thereby establishing a novel quantitative analytical framework for early detection and accurate diagnosis of PAF.

Objective To investigate the expression levels of lysophosphatidylcholine(LysoPC),microtubule associated pro-tein Tau(MAPT)and growth differentiation factor-10(GDF-10)in oral squamous cell carcinoma(SCC),and their correlation with prognosis.Methods In all,128 patients with oral squamous cell carcinoma who visited Nantong University Affiliated Hos-pital from April 2017 to April 2019 were selected as the study group,and 100 patients with benign oral lesions during the same time period were selected as the control group.The expression levels of LysoPC,Tau and GDF-10 were compared between the 2 groups of patients.The relationship between the expression levels of LysoPC,Tau,GDF-10,the clinical staging,lymph node me-tastasis,and survival of oral squamous cell carcinoma patients were analyzed,and the assessment values of these factors for prognosis were evaluated.Results The positive rate of Tau and GDF-10 in pathological tissue and LysoPC in serum of the stud-y group were lower than those of the control group(all P＜0.05).Patients with low expression levels of LysoPC,Tau and GDF-10 had a higher proportion of stage Ⅲ to Ⅳ and lymph node metastasis than those with high expression levels of LysoPC,Tau and GDF-10(all P＜0.05).The 128 patients were followed up for 5 years,86 survived(67.19％),42 died(32.81％).LysoPC,Tau and GDF-10 levels were negatively correlated with survival time(all P＜0.05,r=-0.597,-0.622,-0.656).The results of log-rank test showed that the 5-year survival rate of LysoPC,Tau and GDF-10 low expression group was lower than that of LysoPC,Tau and GDF-10 high expression group(all P＜0.05).The high expression levels of LysoPC,Tau and GDF-10 were protective factors,while lymph node metastasis and high clinical stage were risk factors(all P＜0.05).Conclusion LysoPC,Tau and GDF-10 are all low expressed in patients with oral squamous cell carcinoma,and the expression level is correlated with clinical stage and lymph node metastasis.Low expression may indicate a higher risk of death.

The clinical detection of paroxysmal atrial fibrillation(PAF)remains challenging due to its transient and stochastic characteristics,and existing dynamic mode decomposition methods have limitations in modal redundancy reduction and feature extraction when processing single-channel noisy electrocardiogram(ECG)signals.Therefore,a signal analysis method based on high-order dynamic mode decomposition is proposed.It captures high-order correlations within ECG signals through tensor decomposition techniques and decomposes complex signals into physically interpretable dynamic modes.A stability evaluation framework for signal subsystem is established based on modal interaction relationships.By incorporating quantitative indicators including proportion of modes reflecting system instability,modal distribution entropy,and eigenvalue spectrum divergence,a feature discrimination model for PAF is developed.Experimental validation using the MIT-BIH atrial fibrillation database reveals statistically significant differences(P<0.05)in stability-related features between PAF episodes and normal sinus rhythms.The classification model based on support vector machine achieves an average recognition accuracy of 96.15%.These results demonstrate that the proposed method can effectively analyze nonlinear dynamic characteristics in noisy single-lead ECG signals,thereby establishing a novel quantitative analytical framework for early detection and accurate diagnosis of PAF.

Objective:To investigate the effects of long non coding RNA KCNQ1OT1(LncRNA KCNQ1OT1)on the migration and invasion of oral squamous cell carcinoma(OSCC)cells by regulating the microRNA-875-5p(miR-875-5p)/ETS like transcription factor 4(ELK4)axis.Methods:QRT-PCR was applied to detect the mRNA levels of LncRNA KCNQ1OT1,miR-875-5p,and ELK4 in OSCC cell lines(HSC-3,PE/CA-PJ15,HN13)and tissues.The dual luciferase assay was applied to detect the targeting relationship between LncRNA KCNQ1OT1 and miR-875-5p,and target relationship between miR-875-5p and ELK4.HSC-3 cells were used in control group,sh-NC group,sh-KCNQ1OT1 group,sh-KCNQ1OT1+anti-NC group,sh-KCNQ1OT1+anti-miR-875-5p group,miR-NC group,miR-875-5p mimic group,miR-875-5p mimic+pcDNA-NC group,and miR-875-5p mimic+ELK4 group.The migration and invasion abilities of HSC-3 cells were detected.Immunoblotting was applied to detect the protein expression of ELK4,MMP-2,MMP-9 and epithelial mesenchymal transition(EMT)(E-Cadherin,N-Cadherin,Vimentin).The nude mouse transplant tumor was applied to verify the effect of LncRNA KCNQ1OT1 on OSCC transplant tumors.Results:LncRNA KCNQ1OT1 and ELK4 mRNA expression increased in OSCC tissues and cancer cell lines,while miR-875-5p expression decreased(P＜0.05).Database predictions show that miR-875-5p specifically bound to LncRNAs KCNQ1OT1 and ELK4,respectively.Compared with the sh-NC group,the numbers of cell migration and cell invasion,the expression of LncRNA KCNQ1OT1,ELK4,MMP-2,MMP-9,N-Cadherin,and Vimentin in the sh-KC-NQ1OT1 group were lower,while the expression of miR-875-5p and E-Cadherin was higher(P＜0.05).Compared with the sh-KC-NQ1OT1+anti-NC group,the expression of miR-875-5p and E-Cadherin in the sh-KCNQ1OT1+anti-miR-875-5p group was lower,while the numbers of cell migration and cell invasion,the expression of ELK4,MMP-2,MMP-9,N-Cadherin,and Vimentin were higher(P＜0.05).Compared with the miR-NC group,the expression of miR-875-5p and E-Cadherin in the miR-875-5p mimic group was higher,while the numbers of cell migration and cell invasion,the expression of ELK4,MMP-2,MMP-9,N-Cadherin,and Vim-entin were lower(P＜0.05).Compared with the miR-875-5p mimic+pcDNA-NC group,the numbers of cell migration and cell inva-sion,the expression of ELK4,MMP-2,MMP-9,N-Cadherin,and Vimentin in the miR-875-5p mimic+ELK4 group were higher,while the expression of E-Cadherin was lower(P＜0.05).The transplant tumor volume and weight of the sh-KCNQ1OT1 group were smaller than those of the sh-NC group,the mRNA and protein expression levels of LncRNA KCNQ1OT1,ELK4 were lower than those of the sh-NC group,and the expression level of miR-875-5p was higher than that of the sh-NC group(P＜0.05).Conclusion:Inhibition of LncRNA KCNQ1OT1 can target the miR-875-5p/ELK4 axis to inhibit migration,invasion,and EMT of OSCC cells.

Objective:To compare the efficacy of radial forearm flap and anterolateral thigh flap in repairing soft tissue defects after oral cancer surgery and to explore their indications.Methods:A retrospective analysis was conducted on clinical data of patients with oral cancer treated at the Department of Stomatology, Affiliated Hospital of Nantong University, from May 2019 to February 2023. Patients were divided into two groups based on the repair method: the radial forearm flap group and the anterolateral thigh flap group. The groups were compared in the following aspects. (1) Surgical parameters including defect area after oral cancer resection, flap area, flap preparation time, operation time, and length of hospital stay. (2) Inflammatory markers (interleukin-6 and C-reactive protein levels) measured 1 day before surgery and 1 day after surgery. (3) Flap survival rate was calculated. (4) Complication rates was calculated in the flap donor area and infection rates in the oral recipient area within 6 months postoperatively. (5) Six months postoperatively, the patient’s oral function was assessed by a physician using the University of Washington quality of life scale (UW-QOL). The evaluation included assessments of oral opening, speech, and eating functions. Each parameter was scored on a scale of 0 to 10 (higher scores indicated better recovery). (6) Quality of life was assessed using the 36-item short form health survey scale(SF-36) at 2, 4 and 6 months postoperatively, with scores ranging from 0 to 100 (higher scores indicated better quality of life). (7) Patient satisfaction was assessed at 6 months postoperatively, with satisfaction levels categorized as satisfied, basically satisfied, and dissatisfied. The satisfaction rate was calculated as (satisfied + basically satisfied ) cases / total cases in each group × 100%. Statistical analysis was performed using SPSS 22.0. Measurement data were expressed as Mean±SD, and comparisons between groups were conducted using t-tests. Count data were expressed as cases and (or) percentages, and comparisons were made using chi-square test. P<0.05 was considered statistically significant. Results:The radial forearm flap group included 48 cases (32 males, 16 females), aged (49.3±5.0) years, with a body mass index (BMI) of (23.0±1.1) kg/m 2 and a disease course of (6.5±2.1) months. The group had 21 cases of tongue cancer, 12 of floor of mouth cancer, and 15 of buccal cancer, including 40 squamous cell carcinomas and 8 basal cell carcinomas. The anterolateral thigh flap group included 32 cases (20 males, 12 females), aged (50.1±5.0) years, with a BMI of (23.0±1.0) kg/m 2 and a disease course of (7.0±2.2) months. The group had 16 cases of tongue cancer, 7 cases of floor of mouth cancer, and 9 cases of buccal cancer, including 27 squamous cell carcinomas and 5 basal cell carcinomas. There were no significant differences in gender, age, BMI, disease course, tumor location, or pathological type between the two groups ( P>0.05). The defect area after oral cancer resection was smaller in the radial forearm flap group[ (39.0±1.3) cm 2 ] compared to the anterolateral thigh flap group[ (40.3±2.2) cm 2] ( t=3.32, P=0.001). There were no significant differences in flap area, flap preparation time, or length of hospital stay between the two groups ( P>0.05). The operation time was shorter in the radial forearm flap group [(5.1±1.1) h] compared to the anterolateral thigh flap group [(6.8±2.8) h] ( t=0.26, P<0.001). There were no significant differences in interleukin-6 and C-reactive protein levels between the two groups 1 day before surgery and 1 day after surgery ( P>0.05). The flap survival rates were 97.9% (47/48) in the radial forearm flap group and 93.8% (30/32) in the anterolateral thigh flap group, with no significant difference( P>0.05). Postoperative donor site complications mainly included infection, pigmentation, itching, etc. The overall incidence of complications in the donor site of the radial forearm flap [33.3% (16/48)] was higher than that in the anterolateral thigh flap group [12.5% (4/32)], and the difference was statistically significant ( χ2=4.44, P=0.035). There was no significant difference in infection rates in the oral recipient area between the two groups ( P>0.05). Six months postoperatively, the average scores for oral opening, speech, and eating functions were above 7 in both groups, with no significant differences ( P>0.05). Quality of life scores improved over time in both groups, with average scores above 90 at 6 months postoperatively, and no significant differences at any time point ( P>0.05). The patient satisfaction rate was 91.7% (44/48) in the radial forearm flap group and 90.6% (29/32) in the anterolateral thigh flap group, with no significant difference ( P>0.05). Conclusion:Both radial forearm flap and anterolateral thigh flap can effectively repair soft tissue defects after oral cancer resection, significantly improving patients’oral function. The anterolateral thigh flap provides sufficient tissue volume and is suitable for patients with larger defect areas. The radial forearm flap is suitable for patients with a smaller defect area after oral cancer resection. Its surgical procedure is relatively less complex and offers an advantage in reducing surgery time. However, the donor site complications are higher with the radial forearm flap compared to the anterolateral thigh flap.

Objective:To compare the efficacy of radial forearm flap and anterolateral thigh flap in repairing soft tissue defects after oral cancer surgery and to explore their indications.Methods:A retrospective analysis was conducted on clinical data of patients with oral cancer treated at the Department of Stomatology, Affiliated Hospital of Nantong University, from May 2019 to February 2023. Patients were divided into two groups based on the repair method: the radial forearm flap group and the anterolateral thigh flap group. The groups were compared in the following aspects. (1) Surgical parameters including defect area after oral cancer resection, flap area, flap preparation time, operation time, and length of hospital stay. (2) Inflammatory markers (interleukin-6 and C-reactive protein levels) measured 1 day before surgery and 1 day after surgery. (3) Flap survival rate was calculated. (4) Complication rates was calculated in the flap donor area and infection rates in the oral recipient area within 6 months postoperatively. (5) Six months postoperatively, the patient’s oral function was assessed by a physician using the University of Washington quality of life scale (UW-QOL). The evaluation included assessments of oral opening, speech, and eating functions. Each parameter was scored on a scale of 0 to 10 (higher scores indicated better recovery). (6) Quality of life was assessed using the 36-item short form health survey scale(SF-36) at 2, 4 and 6 months postoperatively, with scores ranging from 0 to 100 (higher scores indicated better quality of life). (7) Patient satisfaction was assessed at 6 months postoperatively, with satisfaction levels categorized as satisfied, basically satisfied, and dissatisfied. The satisfaction rate was calculated as (satisfied + basically satisfied ) cases / total cases in each group × 100%. Statistical analysis was performed using SPSS 22.0. Measurement data were expressed as Mean±SD, and comparisons between groups were conducted using t-tests. Count data were expressed as cases and (or) percentages, and comparisons were made using chi-square test. P<0.05 was considered statistically significant. Results:The radial forearm flap group included 48 cases (32 males, 16 females), aged (49.3±5.0) years, with a body mass index (BMI) of (23.0±1.1) kg/m 2 and a disease course of (6.5±2.1) months. The group had 21 cases of tongue cancer, 12 of floor of mouth cancer, and 15 of buccal cancer, including 40 squamous cell carcinomas and 8 basal cell carcinomas. The anterolateral thigh flap group included 32 cases (20 males, 12 females), aged (50.1±5.0) years, with a BMI of (23.0±1.0) kg/m 2 and a disease course of (7.0±2.2) months. The group had 16 cases of tongue cancer, 7 cases of floor of mouth cancer, and 9 cases of buccal cancer, including 27 squamous cell carcinomas and 5 basal cell carcinomas. There were no significant differences in gender, age, BMI, disease course, tumor location, or pathological type between the two groups ( P>0.05). The defect area after oral cancer resection was smaller in the radial forearm flap group[ (39.0±1.3) cm 2 ] compared to the anterolateral thigh flap group[ (40.3±2.2) cm 2] ( t=3.32, P=0.001). There were no significant differences in flap area, flap preparation time, or length of hospital stay between the two groups ( P>0.05). The operation time was shorter in the radial forearm flap group [(5.1±1.1) h] compared to the anterolateral thigh flap group [(6.8±2.8) h] ( t=0.26, P<0.001). There were no significant differences in interleukin-6 and C-reactive protein levels between the two groups 1 day before surgery and 1 day after surgery ( P>0.05). The flap survival rates were 97.9% (47/48) in the radial forearm flap group and 93.8% (30/32) in the anterolateral thigh flap group, with no significant difference( P>0.05). Postoperative donor site complications mainly included infection, pigmentation, itching, etc. The overall incidence of complications in the donor site of the radial forearm flap [33.3% (16/48)] was higher than that in the anterolateral thigh flap group [12.5% (4/32)], and the difference was statistically significant ( χ2=4.44, P=0.035). There was no significant difference in infection rates in the oral recipient area between the two groups ( P>0.05). Six months postoperatively, the average scores for oral opening, speech, and eating functions were above 7 in both groups, with no significant differences ( P>0.05). Quality of life scores improved over time in both groups, with average scores above 90 at 6 months postoperatively, and no significant differences at any time point ( P>0.05). The patient satisfaction rate was 91.7% (44/48) in the radial forearm flap group and 90.6% (29/32) in the anterolateral thigh flap group, with no significant difference ( P>0.05). Conclusion:Both radial forearm flap and anterolateral thigh flap can effectively repair soft tissue defects after oral cancer resection, significantly improving patients’oral function. The anterolateral thigh flap provides sufficient tissue volume and is suitable for patients with larger defect areas. The radial forearm flap is suitable for patients with a smaller defect area after oral cancer resection. Its surgical procedure is relatively less complex and offers an advantage in reducing surgery time. However, the donor site complications are higher with the radial forearm flap compared to the anterolateral thigh flap.

Objective:To analyze the expression of pentraxin-3 (PTX-3) and cyclooxygenase-2 (COX-2) in patients with polycystic ovary syndrome (PCOS) and their relationship with insulin resistance.Methods::A total of 150 PCOS patients diagnosed and treated in our hospital from Dec. 2020 to Mar. 2023 were collected as the study subjects. According to the insulin resistance index (HOMA-IR), 68 cases were in the insulin resistance group and 82 cases in the non insulin resistance group. 150 healthy individuals who underwent physical examination were included into the control group; Enzyme linked immunosorbent assay (ELISA) was applied to detect serum levels of PTX-3 and COX-2; Pearson method was applied to analyze the correlation between serum PTX-3 and COX-2 levels, and their correlation with general data; Logistic regression was applied to analyze the influencing factors of insulin resistance in PCOS patients; Receiver operating characteristic (ROC) curve was applied to analyze the diagnostic value of serum PTX-3 and COX-2 for insulin resistance in PCOS patients.Results::Fasting blood sugar (FBG) [ (5.46±1.12), (4.71±1.03) mmol/L] in insulin-resistant and non-insulin-resistant groups, fasting insulin (FINS), HOMA-IR, testosterone (T), estradiol (E2), total cholesterol (TC), triglycerides (TG), LDL cholesterol (LDL-C), PTX-3, and COX-2 were significantly higher than those in the control group ( P<0.05), HDL cholesterol (HDL-C) were significantly lower than those in the control group ( P<0.05), and the insulin-resistant group FBG, FINS, HOMA-IR, T, E2, TC, TG, LDL-C, PTX-3 and COX-2 levels were significantly higher than those in the non-insulin-resistant group ( P<0.05), and HDL-C levels were significantly lower than those in the non-insulin-resistant group ( P<0.05). According to Pearson correlation analysis, serum PTX-3 and COX-2 levels were positively correlated ( r=0.587, P<0.05), both of which were positively correlated with FBG, FINS, HOMA-IR, E2, T, TC, TG and LDL-C, and negatively correlated with HDL-C. According to Logistic regression analysis, the elevated levels of PTX-3, COX-2, FBG, FINS, and HOMA-IR were risk factors affecting insulin resistance in PCOS patients ( P<0.05). According to the ROC curve, the AUC of insulin resistance in PCOS patients diagnosed by the combination of the two was better than that diagnosed separately by PTX-3 and COX-2 (Z combination vs PTX-3=2.205, Z combination vs COX-2=2.703, P<0.05) . Conclusions::The expression levels of PTX-3 and COX-2 in the serum of PCOS patients are obviously increased, and they are closely related to insulin resistance. The combination of the two can improve the diagnostic value of insulin resistance in PCOS patients.

Objective:To analyze the expression of pentraxin-3 (PTX-3) and cyclooxygenase-2 (COX-2) in patients with polycystic ovary syndrome (PCOS) and their relationship with insulin resistance.Methods::A total of 150 PCOS patients diagnosed and treated in our hospital from Dec. 2020 to Mar. 2023 were collected as the study subjects. According to the insulin resistance index (HOMA-IR), 68 cases were in the insulin resistance group and 82 cases in the non insulin resistance group. 150 healthy individuals who underwent physical examination were included into the control group; Enzyme linked immunosorbent assay (ELISA) was applied to detect serum levels of PTX-3 and COX-2; Pearson method was applied to analyze the correlation between serum PTX-3 and COX-2 levels, and their correlation with general data; Logistic regression was applied to analyze the influencing factors of insulin resistance in PCOS patients; Receiver operating characteristic (ROC) curve was applied to analyze the diagnostic value of serum PTX-3 and COX-2 for insulin resistance in PCOS patients.Results::Fasting blood sugar (FBG) [ (5.46±1.12), (4.71±1.03) mmol/L] in insulin-resistant and non-insulin-resistant groups, fasting insulin (FINS), HOMA-IR, testosterone (T), estradiol (E2), total cholesterol (TC), triglycerides (TG), LDL cholesterol (LDL-C), PTX-3, and COX-2 were significantly higher than those in the control group ( P<0.05), HDL cholesterol (HDL-C) were significantly lower than those in the control group ( P<0.05), and the insulin-resistant group FBG, FINS, HOMA-IR, T, E2, TC, TG, LDL-C, PTX-3 and COX-2 levels were significantly higher than those in the non-insulin-resistant group ( P<0.05), and HDL-C levels were significantly lower than those in the non-insulin-resistant group ( P<0.05). According to Pearson correlation analysis, serum PTX-3 and COX-2 levels were positively correlated ( r=0.587, P<0.05), both of which were positively correlated with FBG, FINS, HOMA-IR, E2, T, TC, TG and LDL-C, and negatively correlated with HDL-C. According to Logistic regression analysis, the elevated levels of PTX-3, COX-2, FBG, FINS, and HOMA-IR were risk factors affecting insulin resistance in PCOS patients ( P<0.05). According to the ROC curve, the AUC of insulin resistance in PCOS patients diagnosed by the combination of the two was better than that diagnosed separately by PTX-3 and COX-2 (Z combination vs PTX-3=2.205, Z combination vs COX-2=2.703, P<0.05) . Conclusions::The expression levels of PTX-3 and COX-2 in the serum of PCOS patients are obviously increased, and they are closely related to insulin resistance. The combination of the two can improve the diagnostic value of insulin resistance in PCOS patients.