• <tr id="yyy80"></tr>
  • <sup id="yyy80"></sup>
  • <tfoot id="yyy80"><noscript id="yyy80"></noscript></tfoot>
  • 99热精品在线国产_美女午夜性视频免费_国产精品国产高清国产av_av欧美777_自拍偷自拍亚洲精品老妇_亚洲熟女精品中文字幕_www日本黄色视频网_国产精品野战在线观看 ?

    Risk factor analysis and clinical decision tree model construction for diabetic retinopathy in Western China

    2022-11-24 09:18:12YuanYuanZhouTaiChengZhouNanChenGuoZhongZhouHongJianZhouXingDongLiJinRuiWangChaoFangBaiRongLongYuXinXiongYingYang
    World Journal of Diabetes 2022年11期

    Yuan-Yuan Zhou,Tai-Cheng Zhou,Nan Chen,Guo-Zhong Zhou,Hong-Jian Zhou,Xing-Dong Li,Jin-Rui Wang,Chao-Fang Bai,Rong Long,Yu-Xin Xiong,Ying Yang

    Yuan-Yuan Zhou,Hong-Jian Zhou,Xing-Dong Li,Department of Endocrinology and Metabolism,The Sixth Affiliated Hospital of Kunming Medical University,The People’s Hospital of Yuxi City,Yuxi 653100,Yunnan Province,China

    Tai-Cheng Zhou,Jin-Rui Wang,Chao-Fang Bai,Rong Long,Yu-Xin Xiong,Ying Yang,Department of Endocrinology and Metabolism,Affiliated Hospital of Yunnan University,The Second People’s Hospital of Yunnan Province,Kunming 650021,Yunnan Province,China

    Nan Chen,Guo-Zhong Zhou,Department of Endocrinology and Metabolism,The Frist People’s Hospital of Anning City,Anning City 650300,Yunnan Province,China

    Abstract BACKGROUND Diabetic retinopathy (DR) is the driving force of blindness in patients with type 2 diabetes mellitus (T2DM).DR has a high prevalence and lacks effective therapeutic strategies,underscoring the need for early prevention and treatment.Yunnan province,located in the southwest plateau of China,has a high prevalence of DR and an underdeveloped economy.AIM To build a clinical prediction model that will enable early prevention and treatment of DR.METHODS In this cross-sectional study,1654 Han population with T2DM were divided into groups without (n=826) and with DR (n=828) based on fundus photography.The DR group was further subdivided into non-proliferative DR (n=403) and proliferative DR (n=425) groups.A univariate analysis and logistic regression analysis were conducted and a clinical decision tree model was constructed.RESULTS Diabetes duration ≥ 10 years,female sex,standing-or supine systolic blood pressure (SBP) ≥ 140 mmHg,and cholesterol ≥ 6.22 mmol/L were risk factors for DR in logistic regression analysis (odds ratio=2.118,1.520,1.417,1.881,and 1.591,respectively).A greater severity of chronic kidney disease (CKD) or hemoglobin A 1c increased the risk of DR in patients with T2DM.In the decision tree model,diabetes duration was the primary risk factor affecting the occurrence of DR in patients with T2DM,followed by CKD stage,supine SBP,standing SBP,and body mass index (BMI).DR classification outcomes were obtained by evaluating standing SBP or BMI according to the CKD stage for diabetes duration < 10 years and by evaluating CKD stage according to the supine SBP for diabetes duration ≥ 10 years.CONCLUSION Based on the simple and intuitive decision tree model constructed in this study,DR classification outcomes were easily obtained by evaluating diabetes duration,CKD stage,supine or standing SBP,and BMI.

    Key Words: Diabetic retinopathy;Type 2 diabetes;Western China;Decision tree

    INTRODUCTION

    Type 2 diabetes mellitus (T2DM),a common chronic disease,poses a severe threat to human health and quality of life.By 2045,an estimated 552 million people worldwide will suffer from T2DM[1].Given the socio-economic developments over the past 40 years,China has become increasingly urbanized,with a growing aging population.Moreover,obesity and overweight caused by lifestyle changes contribute to the growing burden of T2DM in China[2].As a major vascular complication of T2DM,diabetic retinopathy (DR) is currently largely responsible for blindness in the working-class[3,4].

    The two major challenges associated with DR include the high disease prevalence and lack of effective treatments.The global prevalence of DR is 34.6%.As of 2011,126.6 million people suffered from DR,and this number is estimated to reach 191.0 million in 2030 without effective and timely measures[5].The concerning prevalence and severity of DR worldwide may be modulated by racial/ethnic disparities,socio-economic status,health care systems,lifestyles,research methods,and other factors[6].Regarding Asian populations,the prevalence of DR varies according to the region.For example,the prevalence of DR is 20.1%[7],25.7%[8],and 35.0%[9] in Chinese Singaporeans,Chinese Americans,and Taiwanese Chinese,respectively.Further,the prevalence of DR in inland areas of China is 23%.It is also higher in rural areas than in urban areas and in northern areas than in southern and eastern coastal areas[10-12].

    Nevertheless,there is currently a paucity of effective treatments for DR.In addition to systematic interventions for controlling blood glucose levels,blood pressure,and blood lipid levels,several modern therapies have been developed,such as laser photocoagulation[13] and intravitreal injections of anti-vascular endothelial growth factor (VEGF) antibodies or glucocorticoids,which can delay the progress of proliferative DR (PDR)[14,15].However,several side effects associated with these therapies should be noted.For instance,photocoagulation may cause potential retinal damage,anti-VEGF injections are associated with relapse after drug withdrawal,and glucocorticoid use contributes to cataracts and elevated intraocular pressure in a considerable number of patients.Moreover,intraocular injections may cause complications such as endophthalmitis,intraocular hemorrhage,vitreous hemorrhage,and even retinal detachment[14,15].Therefore,the utilization of these therapeutic options in clinical practice should be based on systematic evaluation and strict indications.

    The high prevalence of DR and lack of efficient therapeutic strategies are associated with reduced quality of life of patients and pose a substantial socio-economic burden on individuals,families,and the society[16].According to an analysis of the pedigree of T2DM in Yunnan province,the prevalence of DR[17] approximates the national average[10].Therefore,the active search for associated risk factors is a fundamental priority for the prevention of DR.In this regard,a decision tree model established using identified risk factors is a useful tool.Distinct from traditional statistical methods such as logistic regression analysis,decision trees are effective machine-learning algorithms that solve classification problems.This method obtains a set of effective classification rules through systematic learning of multiple attributes of samples with known classification results.When faced with new unknown samples,the choice of classification or characteristic attributes can be quickly obtained based on the set of rules extracted from the established decision tree[18-20].Thus,a decision tree is a prediction model with a simple and intuitive flowchart structure that is particularly suitable for use in clinical practice.This study examined the risk factors associated with DR in the Han population with T2DM in Yunnan province and constructed a clinical decision tree model.

    MATERIALS AND METHODS

    Study subjects

    Patients from the Han population with T2DM were enrolled from the Department of Endocrinology,Affiliated Hospital of Yunnan University.All patients fulfilled the Chinese Diabetes Association criteria for the diagnosis of T2DM[21].The criteria for exclusion were as follows: (1) Age < 18 years;(2) positive islet autoantibodies [including islet cell autoantibodies and autoantibodies to glutamic acid decarboxylase-65,insulin,the tyrosine phosphatases islet antigen 2 (IA-2) and IA-2β,and zinc transporter 8];(3) acute complications of diabetes mellitus (including diabetic ketoacidosis or diabetic hyperosmolar state);(4) severe hepatic damage;(5) malignant tumors;(6) acute or chronic infectious diseases;(7) other eye diseases (including glaucoma,retinal vascular occlusion,and ischemic optic neuropathy);and (8) pregnancy.Finally,1654 patients with T2DM were enrolled.

    Ethical principles

    This study was approved by the Ethics Committee of Affiliated Hospital of Yunnan University (No.2021062),and written informed consent was obtained from all participants according to the principles of the Helsinki Declaration.

    This trial registration was registered at ChiCTR (ChiCTR2100 041888;registration on January 9,2021,http://www.chictr.org.cn/index.aspx).

    Clinical information collection

    Patient sex,age,diabetes duration,height,weight,waist circumference,hip circumference,waist-hip ratio (WHR),body mass index (BMI),and systolic blood pressure (SBP) and diastolic blood pressure (DBP) (both in the standing and supine positions) were recorded.

    Laboratory assessments

    All patients fasted at 22:00 the day before blood collection.At 8:00 the next day,6 mL of venous blood was collected.Fasting blood glucose (Glu0),hemoglobin A 1c (HbA1c),serum creatinine (Scr),blood urea nitrogen (BUN),uric acid (UA),triglycerides (Trig),cholesterol (Chol),high-density lipoprotein Chol (HDL-C),and low-density lipoprotein Chol (LDL-C) were measured.Based on the formula eGFR (mL/min/1.73 m2)=175 × Scr (mg/dL) -1.234 × age -0.179 × (0.790 for women)[22],the estimated glomerular filtration rate (eGFR) was calculated.

    Ophthalmological measurements

    All patients underwent non-mydriatic fundus photography and were evaluated according to the international clinical grading standards for DR established by the American Academy of Ophthalmology[23].

    Definitions

    According to the DR Preferred Practice Pattern[23].DR was clinically classified into two types-non-PDR (NPDR) and PDR;the latter was identified by neovascularization and preretinal or vitreous hemorrhage.To further study the effect of blood pressure-related indicators (SBP and DBP in both the standing and supine positions),obesity-related indicators (BMI and waist circumference),blood glucose-related indicators (Glu0 and HbA1c),blood lipid-related indicators (Chol,Trig,LDL-C,and HDL-C),and renal function related indicators (UA and eGFR) on DR,these indicators were defined according to relevant guidelines or expert consensus.Abnormal blood pressure was defined as SBP ≥ 140 mmHg and/or DBP ≥ 90 mmHg[24].Overweight was defined as BMI ≥ 24 kg/m2,obesity was defined as BMI ≥ 28 kg/m2,and abdominal obesity was defined as waist circumference ≥ 90 cm in men or ≥ 85 cm in women[25].Well-controlled blood glucose level was defined as Glu0 ≤ 7.0 mmol/L or HbA1c < 7%,generally controlled blood glucose level was defined as 7% ≤ HbA1c < 8%,and poorly controlled blood glucose level was defined as Glu0 > 7.0 mmol/L or HbA1c ≥ 8%[21].Dyslipidemia was defined as Chol ≥ 6.22 mmol/L,Trig ≥ 2.26 mmol/L,or LDL-C ≥ 4.14 mmol/L and/or HDL-C < 1.04 mmol/L[26].Hyperuricemia was defined as fasting serum UA > 420 μmol/L[27].Stages of chronic kidney disease (CKD) were determined by eGFR as follows: CKD stage 1 (G1),eGFR ≥ 90 mL/min;CKD stage 2 (G2),eGFR=60-89 mL/min;CKD stage 3 (G3),eGFR=30-59 mL/min;CKD stage 4 (G4),eGFR=15-29 mL/minl and CKD stage 5 (G5),eGFR < 15 mL/min [22].

    Statistical analysis

    Based on fundus photography,participants were divided into groups without DR (WDR group,n=826) or with DR (DR group,n=828).The DR group was further classified into the NPDR (n=403) and PDR (n=425) groups according to severity.All statistical analyses were performed using SPSS (SPSS 20.0,IBM,United States).Differences between the WDR and DR groups or the NPDR and PDR groups were assessed (Table 1).For continuous variables,Welch’st-test was used for normal distributions,while the Mann-WhitneyUtest was used for skewed distributions.For categorical variables,the chi-square test was performed.Using DR or PDR as the dependent variable,logistic regression analysis was explored to analyze DR or PDR-related risk factors.Logistic regression analysis was performed using forward selection (likelihood ratio),withP< 0.05 as the entry criterion andP> 0.1 as the removal criterion.The decision tree method was performed using the chi-squared automatic interaction detector,with 70% participants as the training dataset,and the remaining 30% as the test dataset.The variable assignments used in both logistic regression analysis and decision tree model are presented in Table 2.

    RESULTS

    Baseline clinical characteristics

    The baseline clinical characteristics of all participants are presented in Table 1.

    Univariate analysis of DR-related risk factors

    As shown in Table 1,the proportion of women,diabetes duration,supine SBP,standing SBP,supine DBP,Chol,BUN,UA,Scr,Glu0,and HbA1c were higher in the DR group than in the WDR group (allPvalues < 0.05).In contrast,the DR group had a lower BMI,hip circumference,and eGFR than the WDR group (allPvalues < 0.05).

    Univariate analysis of PDR-related risk factors

    The proportion of women,supine SBP,supine DBP,Chol,LDL-C,and BUN were significantly higher in the PDR group than in the NPDR group (allPvalues < 0.05).However,age,hip circumference,and eGFR were significantly lower in the PDR group than in the NPDR group (allPvalues < 0.05) (Table 1).

    Table 1 Univariate analysis of risk factors for diabetic retinopathy or proliferative diabetic retinopathy

    Logistic regression analysis of DR-related risk factors

    Women had a 1.520 times higher risk of DR [95% confidence interval (CI): 1.218 to 1.897] compared to men (Figure 1).Patients with diabetes duration ≥ 10 years had a 2.118-fold higher risk of DR than those with diabetes duration < 10 years (95%CI: 1.661 to 2.700).The risk of DR in patients with standing SBP ≥ 140 mmHg was 1.417 times higher than that in patients with standing SBP < 140 mmHg (95%CI: 1.046 to 1.919).Compared to patients with supine SBP < 140 mmHg,those with supine SBP ≥ 140 mmHg had a 1.881-fold higher risk of DR (95%CI: 1.399 to 2.528).Compared to patients with normal Chol,those with Chol ≥ 6.22 mmol/L had a 1.591 times higher risk of DR (95%CI: 1.104 to 2.291).The risk of DR in patients with CKD stages G2,G3,G4,and G5 was 2.206 (95%CI: 1.678 to 2.899),7.860 (95%CI: 4.573 to 13.512),9.693 (95%CI: 3.255 to 28.862),and 20.691 (95%CI: 2.540 to 168.581) times higher than that in patients with CKD stage G1.In other words,a greater severity of CKD was associated with a higher risk of DR.The risk of DR in patients with 7% ≤ HbA1c < 8% or HbA1c ≥ 8% was 1.787 (95%CI: 1.198 to 2.664) and 3.073 (95%CI: 2.225 to 4.245) times higher than that in patients with HbA1c < 7%,indicating that worse control of HbA1c was associated with a higher risk of DR.

    Logistic regression analysis of PDR-related risk factors

    Compared to men,women had a 2.161-fold higher risk of progression to PDR (95%CI: 1.615 to 2.890) (Figure 2).Compared to patients with diabetes duration < 10 years,patients with diabetes duration ≥ 10 years had a 1.483 times higher risk of PDR (95%CI: 1.099 to 2.001).The risk of progression to PDR in patients with CKD stages G3 and G4 was 2.109 (95%CI: 1.362 to 3.266) and 2.290 (95%CI: 1.016 to 5.165) times higher than that in patients with CKD stage G1.

    Decision tree modeling of DR-related risk factors

    As shown in Figure 3,the importance of variables in the decision tree model was presented as a root-toleaf structure,with diabetes duration being the first variable or root node,followed by CKD stage,supine SBP,standing SBP,and BMI,in order of importance.As presented in Table 3,seven “if-then” rules summarized the path from the root node to each leaf node.

    Table 2 Variable assignment

    DISCUSSION

    In this study,we attempted to reveal the DR-related risk factors in Han population with T2DM in Yunnan province and construct a predictive model for personalized DR risk assessment and early preventive effect.

    Studies have reported that various factors modulate the effects of age on DR.Although sporadic cases have been reported,the onset of DR before puberty is extremely rare[28,29].Researchers have suggested that patients with diabetes during adolescence are prone to develop serious vascular complications,including DR,compared to patients with diabetes after adolescence.This could be partly due to the characteristics of adolescent patients;for example,patients at this stage tend to be accompanied by dramatic hormone level fluctuations,and most patients present with type 1 diabetes tend to have relatively poor blood glucose self-management ability[30].Therefore,this study focused on Hanpopulation with T2DM aged ≥ 18 years in Yunnan province to exclude the potential confounding effects of adolescence and type 1 diabetes on the results.

    DR has emerged as the leading cause of blindness among 27-75 year olds worldwide[3,21].A Chinese meta-analysis reported that the prevalence of DR in patients with T2DM was age related,increasing from 12.55% in adults aged 30-39 years to 20.44% in adults aged 60-69 years and decreasing to 11.22% in those aged ≥ 80 years[12].Of the 1654 patients enrolled in this study,33.49% and 16.56% patients with DR were < 60 years of age (n=554) and ≥ 60 years of age (n=274),respectively.This suggests that the peak of DR prevalence in Han population with T2DM in Yunnan province is concentrated in the population aged < 60 years,which accounts for the majority of the social labor force.In addition,univariate analysis (Table 1) revealed no significant difference in age between the DR and WDR groups (P=0.056).However,overall age was dramatically lower in the PDR group than in the NPDR group (P< 0.001).As shown in Figures 1 and 2,age was not retained in the logistic regression equation.In conclusion,the correlation between age and DR is complex;this association depends on age stratification and may be affected by the degree of vision.This relationship warrants further exploration in future studies.

    Figure 1 Logistic regression analysis of diabetic retinopathy-related risk factors.Female sex,diabetes duration ≥ 10 years,standing systolic blood pressure (SBP) ≥ 140 mmHg,supine SBP ≥ 140 mmHg,cholesterol ≥ 6.22 mmol/L,greater severity of chronic kidney disease,and worse control of hemoglobin A 1c are associated with a higher risk of diabetic retinopathy.Values are shown using a base 10,logarithmic scale.DR: Diabetic retinopathy;OR: Odds ratio;CI: Confidence interval;BMI: Body mass index;SBP: Systolic blood pressure;Chol: Cholesterol;Trig: Triglyceride;CKD: Chronic kidney disease;HbA1c: Glycated hemoglobin A1c.

    Table 3 “If-then” rules extracted from decision tree

    The relationship between sex and DR is unclear.A study from Germany and Australia based on 120000 samples suggested that women are more likely to develop DR than men[31].Similarly,studies in the United Kingdom and Japan have reported that women are more prone to visual impairments than men[32,33].Other studies from the United States and India,however,have reported that the men have a higher risk of DR than women[6,34,35].In particular,the United Kingdom Prospective Diabetes Study (UKPDS) has proposed that DR progression is associated with the male sex[36].Therefore,it is necessary to further explore the correlation between sex and DR.Univariate analysis (Table 1) revealed that the proportion of women was significantly higher in the DR group than in the WDR group (P=0.002).Moreover,the proportion of women was significantly higher in the PDR group than in the NPDR group (P< 0.001).Indeed,further logistic regression analysis (Figures 1 and 2) re-emphasizes the importance of female sex.These findings suggest that female sex not only is a risk factor for the development of DR in patients with T2DM but also contributes to the progression of DR to PDR,at least in Yunnan province.

    Figure 2 Logistic regression analysis of proliferative diabetic retinopathy-related risk factors.Female sex,diabetes duration ≥ 10 years,and chronic kidney disease stage G3 or G4 are risk factors for the progression to proliferative diabetic retinopathy.Values are shown using a base 10,logarithmic scale.Abbreviations: PDR: Proliferative diabetic retinopathy;NPDR: Non-proliferative diabetic retinopathy;OR: Odds ratio;CI: Confidence interval;CKD: Chronic kidney disease.

    It is well-established that the diabetes duration majorly affects the occurrence and progression of DR[23,37].A case-control study in South Korea demonstrated that of 523 patients with T2DM,44.9% developed DR,and 13.6% developed PDR.The average diabetes duration to mild NPDR,moderatesevere NPDR,and PDR was 14.8,16.7,and 17.3 years,respectively[38].Based on the Chinese population,a meta-analysis indicated that the prevalence of DR in patients newly diagnosed with diabetes and patients with a disease course of ≥ 10 years was 9.00% and 55.52%,respectively[12].Univariate analysis (Table 1) revealed that the diabetes duration in the DR group was substantially longer than that in the WDR group (P< 0.001).In contrast,the diabetes duration did not differ significantly between the PDR and NPDR groups (P=0.221).However,logistic regression analysis (Figures 1 and 2) revealed that a diabetes duration ≥ 10 years was an extremely risk for the occurrence and progression of DR.Crucially,the diabetes duration was classified as the root node of the DR decision tree model (Table 3 and Figure 3),emphasizing that the diabetes duration is critical in DR risk assessment.

    In addition to the diabetes duration,good glycemic control is considered a key factor for reducing vascular complications of diabetes[39].This study focused on two blood-glucose-related indicators,Glu0 and HbA1c.Compared with the transient characteristics of Glu0,HbA1c reflects the overall level of blood glucose control of patients in the prior 2 to 3 months.In this study,univariate analysis (Table 1) indicated that both Glu0 and HbA1c were substantially greater in the DR group than in the WDR group (allP< 0.05).As shown in Figure 1,HbA1c but not Glu0 was retained in the logistic regression equation.These findings suggest that poor HbA1c control is associated with a higher risk of DR.In conclusion,compared to Glu0,HbA1c,which reflects long-term glucose control levels,is more relevant for the prevention of DR.However,HbA1c did not negatively affect the progression of DR.Of note,large clinical studies such as the UKPDS[40,41] and the Diabetes Control and Complications Study[42] have demonstrated that early and intensive glucose control can reduce the occurrence and progression of diabetic vascular complications,including DR.However,good glycemic control is not equivalent to excessive control.Indeed,extensive evidence indicates that recurrent hypoglycemic episodes caused by excessive strict glycemic control with insulin are associated with the early deterioration of DR,but the underlying mechanisms are unclear[43-45].

    Previous studies have demonstrated that hypertension is linked to the development and severity of DR[46,47].Since patients with diabetes are prone to have complications of postural blood pressure changes[48,49],data on standing and supine blood pressure were collected simultaneously.Univariate analysis (Table 1) revealed that standing or supine SBP and supine DBP were significantly lower in the WDR group than in the DR group (allP< 0.001),but there was no obvious difference in standing DBP between the groups (P=0.501).Although supine SBP and supine DBP were lower in the NPDR group than in the PDR group (allP< 0.05),no significant intergroup differences existed in standing SBP and standing DBP (allP> 0.05).Further logistic regression analysis (Figures 1 and 2) indicated that SBP had an effect on DR occurrence but not DR progression.In addition,supine SBP ≥ 140 mmHg was the leaf node of the decision tree model,second only to diabetes duration.Our results emphasize the detrimental effects of elevated SBP (especially supine SBP) on DR,suggesting that good blood pressure control is vital for the prevention of DR.Furthermore,the benefits of certain antihypertensive drugs,particularly angiotensin-converting enzyme inhibitors and angiotensin receptor blockers,are not limited to lowering blood pressure[50,51] and may also benefit DR through neuroprotection[52,53],increasing insulin sensitivity[54],anti-inflammatory effects[55],and inhibiting the blood-eye barrier[56,57].

    Figure 3 Training dataset of decision tree model for diabetic retinopathy.Based on the decision tree model constructed in this study,the diabetic retinopathy classification outcomes are obtained by evaluating standing systolic blood pressure (SBP) or body mass index according to the chronic kidney disease (CKD) stage for patients with a diabetes duration < 10 years and the evaluation of CKD stage according to the supine SBP for patients with a diabetes duration ≥ 10 years.WDR: Without diabetic retinopathy;DR: Diabetic retinopathy;CKD: Chronic kidney disease;SBP: Systolic blood pressure;BMI: Body mass index.

    To date,the complex link between dyslipidemia and DR has remained controversial[10,47,58,59].In this study,the occurrence and development of DR seemed to be more strongly affected by Chol than by Trig,HDL-C,and LDL-C Univariate analysis (Table 1) revealed that Chol was significantly higher in the DR group than in the WDR group (P< 0.001) and significantly higher in the PDR group than in the NPDR group (P=0.013).Moreover,as shown in Figures 1 and 2,Chol increased the risk of developing DR in patients with T2DM,but had no remarkable impact on DR progression.A recent meta-analysis revealed that lipid-lowering drugs exerted a protective effect on the progression of DR[60] but did not affect the deterioration of visual acuity or aggravation of hard exudate.Therefore,further large-scale clinical trials are urgently needed to substantiate the necessity of early application of lipid-lowering drugs in patients with DR.

    In parallel with the tremendous rise in the global prevalence of obesity,the prevalence of obesityrelated T2DM has also increased annually[2].However,the relationship between obesity and DR has not been fully elucidated.Reports from Wisconsin illustrated that obesity (defined by BMI) was not independently implicated in the occurrence or progression of DR in patients with T2DM within 10 years[61].Similarly,in the Hoorn study,WHR,but not BMI,was related to the occurrence of DR[62].However,data based on Asian populations have provided the opposite conclusions.For example,based on a sample of 420 Asian patients with T2DM,Manet al[63] reported that BMI was negatively correlated with mild,moderate,and severe DR,but WHR was positively correlated with DR severity.Subsequently,a Korean study demonstrated that higher BMI,increased waist circumference,and higher body fat content (measured by dual-energy X-ray) were notably correlated with a lower risk of DR[64].In this study,data regarding relevant body mass indicators were collected,including those on BMI,waist circumference,hip circumference,and WHR.Univariate analysis (Table 1) revealed that BMI and hip circumference in the DR group were remarkably lower than those in the WDR group (allP< 0.001),but waist circumference was did not differ across the groups (P=0.060).Although the PDR group had a lower hip circumference than the NPDR group (P=0.046),there were no significant intergroup differences in BMI and waist circumference (P> 0.05).In addition,an obvious difference in WHR was not noted among groups (allP> 0.05).Although the logistic regression model ultimately did not retain BMI,waist circumference,hip circumference,and WHR (Figures 1 and 2),the decision tree model (Table 3 and Figure 3) supported the protective effect of higher BMI for the assessment of DR risk.In general,although the relationship between these obesity-relevant indicators and DR is yet to be confirmed,it can be conjectured that excessively low BMI is not conducive to protection against DR in the Asian population.

    Among BUN,Scr,and UA,eGFR calculated using Scr is the gold standard for CKD staging[65].In addition,CKD staging is an essential approach to evaluating the severity of diabetic nephropathy in clinical practice.Univariate analysis (Table 1) indicated that eGFR was significantly lower in the DR group than in the WDR group (P< 0.001) and was significantly lower in the PDR group than in the NPDR group (P=0.001).Furthermore,Figures 1 and 2 highlight the importance of CKD staging in the risk assessment of DR.In this regard,the risk of occurrence and progression of DR increased stepwise with each additional risk level of CKD staging.Notably,in the decision tree model (Table 3 and Figure 3),CKD staging was second only to diabetes duration for DR risk assessment.In particular,CKD staging is a key indicator of diabetic nephropathy,and the current results also suggest that DR is often comorbid with diabetic nephropathy.This highlights the need to simultaneously screen for diabetic nephropathy in patients with DR.

    Differing from traditional statistical methods such as logistic regression analysis,decision trees are successfully employed in the field of medicine with its advantages in solving classification problems,that is,qualitatively judging the possibility of each risk factor at a specific level.Decision trees obtain a set of effective classification rules by systematically learning multiple attributes of the samples with known classification results.When faced with new unknown samples,the appropriate classification or characteristic attributes can be quickly obtained based on the set of rules extracted from the established decision tree[18-20].In other words,three basic elements compose the decision tree: root node,internal node,and leaf node.The root node is the main feature attribute in the model,the internal node is the secondary attribute judgment based on the root node,and the leaf node is the final classification outcome of the model.

    This study extended traditional statistical analysis by building a DR decision model using machine learning based on the attributes of T2DM samples.In the decision tree model,diabetes duration was demonstrated to primarily affect the occurrence of DR in patients with T2DM,namely,the root node.The extraction rules were interpreted as follows: for patients with diabetes duration < 10 years,if they met the criteria of: (1) CKD stage=G3/G4/G5;(2) CKD stage=G2 and BMI < 24 kg/m2;or (3) CKD stage=G1 and standing SBP ≥ 140 mmHg,then DR was prone to occur.In contrast,for patients with diabetes duration ≥ 10 years,if they met the criteria of: (1) Supine SBP < 140 mmHg and CKD stage=G2/G3/G4;or (2) supine SBP ≥ 140 mmHg and CKD stage=G3/G4/G5,then DR was prone to occur.This model may assist clinicians in Yunnan province (particularly primary medical staff who lack relevant DR detection approaches such as ophthalmoscope) to make more effective clinical predictions of DR risk in patients with T2DM.Our decision tree model is simple and intuitive,highlighting its potential for application in clinical practice.

    However,there are several limitations that should be noted.First of all,this study did not record in detail the medication of patients,especially the use of anti-diabetic,lipid-lowering and antihypertensive drugs.Secondly,Yunnan province is located in the western plateau of China,and its climate,cultural and economic conditions are very different from those of plain areas.Therefore,these confounding factors should be included in the future to enhance the integrity and reliability of research conclusions.

    CONCLUSION

    Female sex,diabetes duration ≥ 10 years,standing or supine SBP ≥ 140 mmHg,Chol ≥ 6.22 mmol/L,deterioration of CKD stage,and HbA1c are key DR-related risk factors in the Han population with T2DM in Yunnan province.The concise and intuitive DR prediction model developed through machine learning in this study could help clinicians quickly predict DR outcomes based on patients' potential risk factors and conduct early individualized interventions.

    ARTICLE HIGHLIGHTS

    Research background

    Yunnan province has a high prevalence of diabetic retinopathy (DR).Accordingly,it is of great significance to explore the DR-related factors and to construct an economic and intuitive clinical prediction model.

    Research motivation

    The research motivation is early intervention using the DR-related risk factors from the perspective of a predictive model to reduce the prevalence of DR in patients with type 2 diabetes mellitus (T2DM).

    Research objectives

    The research intends to establish a prediction model that allows clinically early prevention and treatment of DR.

    Research methods

    A total of 1654 Han population with T2DM were recruited in this study and were grouped in the without DR and DR groups.The DR group was further subgrouped according to the severity of DR.Then,univariate analysis,logistic regression analysis,and clinical decision tree models of clinical data were performed.

    Research results

    Based on the decision tree model constructed in this study,DR classification outcomes were obtained by evaluating diabetes duration followed by stages of chronic kidney disease,supine systolic blood pressure (SBP),standing SBP,and body mass index.

    Research conclusions

    Personalized interventions for DR-related risk factors based on a decision tree model may potentially reduce the prevalence of DR.

    Research perspectives

    In this study,patients with T2DM in Western China were taken as samples to analyze the influencing factors of DR and build a clinical prediction model.In the future,it is hoped that the prediction model can produce certain social and economic benefits in clinical practice.In addition,when comparing with other clinical studies on DR,we found some controversies,such as the impact of sex and body mass index on DR,which opened up a new direction for future research.

    FOOTNOTES

    Author contributions:Zhou YY contributed to the conception and design,acquisition of data or analysis and interpretation of data,and drafting the article or revising it critically for important intellectual content;Yang Y and Zhou TC were responsible for supervision,project administration,and funding acquisition;Chen N and Zhou GZ were responsible for literature and formal analysis;Wang JR,Bai CF,Long R,Xiong YX,Zhou HJ,and Li XD were responsible for patient recruitment and clinical data curation;all authors gave final approval of the version to be published.

    Supported bythe Natural Science Foundation of China,No.82 160159;Natural Science Foundation of Yunnan Province,No.202101AY070001-199;Scientific Research Fund of Yunnan Education Department,No.2021J0303;and Postgraduate Innovation Fund of Kunming Medical University,No.2020D009.

    Institutional review board statement:The study was reviewed and approved by the Ethics Committee of Affiliated Hospital of Yunnan University (Approval No.2021062).

    Informed consent statement:Written informed consent was obtained from all participants.

    Conflict-of-interest statement:All the authors report no relevant conflicts of interest for this article.

    Data sharing statement:No additional data are available.

    STROBE statement:The authors have read the STROBE Statement-checklist of items,and the manuscript was prepared and revised according to the STROBE Statement-checklist of items.

    Open-Access:This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers.It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BYNC 4.0) license,which permits others to distribute,remix,adapt,build upon this work non-commercially,and license their derivative works on different terms,provided the original work is properly cited and the use is noncommercial.See: https://creativecommons.org/Licenses/by-nc/4.0/

    Country/Territory of origin:China

    ORCID number:Yuan-Yuan Zhou 0000-0003-2608-4866;Chao-Fang Bai 0000-0003-4724-6537;Ying Yang 0000-0001-5753-7106.

    S-Editor:Chen YL

    L-Editor:A

    P-Editor:Chen YL

    国产国语露脸激情在线看| av有码第一页| 色94色欧美一区二区| 99国产精品一区二区蜜桃av | 夫妻午夜视频| 国产片特级美女逼逼视频| 国产欧美日韩一区二区三区在线| 午夜福利,免费看| 大陆偷拍与自拍| 99国产精品一区二区蜜桃av | 人妻人人澡人人爽人人| 亚洲色图综合在线观看| 少妇猛男粗大的猛烈进出视频| 秋霞在线观看毛片| 欧美+亚洲+日韩+国产| av天堂在线播放| 久久精品熟女亚洲av麻豆精品| 国产主播在线观看一区二区 | 精品第一国产精品| netflix在线观看网站| 老司机在亚洲福利影院| 免费看av在线观看网站| 亚洲第一av免费看| www.999成人在线观看| 国产男女超爽视频在线观看| 母亲3免费完整高清在线观看| 中文欧美无线码| 黄色片一级片一级黄色片| 免费不卡黄色视频| 成人三级做爰电影| 男女国产视频网站| 欧美日韩视频高清一区二区三区二| 91精品伊人久久大香线蕉| 无限看片的www在线观看| 亚洲欧美中文字幕日韩二区| 亚洲精品一卡2卡三卡4卡5卡 | 亚洲精品日韩在线中文字幕| 考比视频在线观看| 一个人免费看片子| 999久久久国产精品视频| 欧美精品高潮呻吟av久久| 日韩精品免费视频一区二区三区| 80岁老熟妇乱子伦牲交| 欧美日韩中文字幕国产精品一区二区三区| 国产色视频综合| 变态另类成人亚洲欧美熟女| а√天堂www在线а√下载| 精品一区二区三区四区五区乱码| 高潮久久久久久久久久久不卡| 午夜两性在线视频| 国产av不卡久久| 好男人在线观看高清免费视频 | 亚洲久久久国产精品| 给我免费播放毛片高清在线观看| 99国产精品99久久久久| 国产野战对白在线观看| 色播亚洲综合网| 精品久久久久久成人av| 亚洲午夜精品一区,二区,三区| 精华霜和精华液先用哪个| 午夜亚洲福利在线播放| 很黄的视频免费| 精品第一国产精品| 欧美不卡视频在线免费观看 | 久久狼人影院| 一个人免费在线观看的高清视频| www.www免费av| 久久久精品国产亚洲av高清涩受| 日本一本二区三区精品| 久热爱精品视频在线9| 欧美av亚洲av综合av国产av| 色综合亚洲欧美另类图片| 日本精品一区二区三区蜜桃| 中文字幕另类日韩欧美亚洲嫩草| 免费在线观看成人毛片| 色婷婷久久久亚洲欧美| 久久中文看片网| 桃红色精品国产亚洲av| 91老司机精品| 欧美+亚洲+日韩+国产| 亚洲av电影在线进入| 日本撒尿小便嘘嘘汇集6| 一本综合久久免费| 久久99热这里只有精品18| www.www免费av| 男女那种视频在线观看| 悠悠久久av| 欧美av亚洲av综合av国产av| 香蕉av资源在线| 色综合站精品国产| 亚洲五月天丁香| 欧美日韩福利视频一区二区| 久久久国产成人精品二区| 国产精品永久免费网站| 看黄色毛片网站| 老司机在亚洲福利影院| 熟女少妇亚洲综合色aaa.| 淫妇啪啪啪对白视频| 国产亚洲精品av在线| 色老头精品视频在线观看| 国产午夜福利久久久久久| 黄色 视频免费看| 久久久国产欧美日韩av| 久久精品国产亚洲av香蕉五月| 亚洲精品美女久久久久99蜜臀| 欧美日韩亚洲综合一区二区三区_| 久久亚洲真实| 久久久国产成人免费| 欧美黄色淫秽网站| 看片在线看免费视频| 曰老女人黄片| 亚洲专区中文字幕在线| av视频在线观看入口| 久久精品国产99精品国产亚洲性色| 天天一区二区日本电影三级| 男人舔女人下体高潮全视频| 亚洲精华国产精华精| 亚洲欧洲精品一区二区精品久久久| 一边摸一边做爽爽视频免费| 国产精品一区二区三区四区久久 | 日本成人三级电影网站| 欧美激情极品国产一区二区三区| 非洲黑人性xxxx精品又粗又长| 成人永久免费在线观看视频| 搡老岳熟女国产| 久久亚洲真实| 免费一级毛片在线播放高清视频| 亚洲精品在线观看二区| 免费人成视频x8x8入口观看| 正在播放国产对白刺激| 国产爱豆传媒在线观看 | 亚洲一区高清亚洲精品| 亚洲欧美精品综合一区二区三区| 黄片小视频在线播放| 亚洲色图 男人天堂 中文字幕| 亚洲精品av麻豆狂野| 久久欧美精品欧美久久欧美| 免费观看人在逋| 国产激情久久老熟女| 亚洲五月色婷婷综合| 长腿黑丝高跟| 91麻豆av在线| 黄色 视频免费看| 国产一区二区三区在线臀色熟女| 久久草成人影院| 国产精品1区2区在线观看.| 亚洲成人国产一区在线观看| 精品熟女少妇八av免费久了| 欧美日本视频| 午夜免费观看网址| 夜夜夜夜夜久久久久| 成人国产综合亚洲| 亚洲精品美女久久久久99蜜臀| 精品一区二区三区四区五区乱码| 亚洲最大成人中文| 免费高清视频大片| 国产亚洲欧美精品永久| 美女午夜性视频免费| 亚洲aⅴ乱码一区二区在线播放 | 亚洲中文字幕日韩| 叶爱在线成人免费视频播放| 国产激情久久老熟女| 日本黄色视频三级网站网址| 欧美日韩中文字幕国产精品一区二区三区| 日本在线视频免费播放| 日本免费一区二区三区高清不卡| 香蕉丝袜av| 国产成人啪精品午夜网站| 岛国在线观看网站| 黄网站色视频无遮挡免费观看| 性欧美人与动物交配| 欧美色欧美亚洲另类二区| 中文字幕久久专区| 色老头精品视频在线观看| 亚洲精品在线美女| 久久婷婷人人爽人人干人人爱| 黄色视频,在线免费观看| 亚洲成a人片在线一区二区| 久久青草综合色| 国产男靠女视频免费网站| 亚洲黑人精品在线| 91在线观看av| 美女高潮喷水抽搐中文字幕| x7x7x7水蜜桃| 久久精品91蜜桃| 91成年电影在线观看| 午夜福利成人在线免费观看| 欧美三级亚洲精品| 日日干狠狠操夜夜爽| 精品第一国产精品| 亚洲国产看品久久| 无人区码免费观看不卡| 一区二区三区激情视频| 日日干狠狠操夜夜爽| 亚洲avbb在线观看| 国产精品1区2区在线观看.| 国产成人系列免费观看| 亚洲av第一区精品v没综合| 18禁黄网站禁片午夜丰满| 国产成人av激情在线播放| 一二三四在线观看免费中文在| 天天躁狠狠躁夜夜躁狠狠躁| 一个人免费在线观看的高清视频| 午夜精品久久久久久毛片777| 伦理电影免费视频| 国产午夜福利久久久久久| 午夜福利一区二区在线看| 最近最新中文字幕大全免费视频| 久久久精品国产亚洲av高清涩受| 国产精品电影一区二区三区| 精品国产超薄肉色丝袜足j| 久久狼人影院| 18禁裸乳无遮挡免费网站照片 | 精品国产乱子伦一区二区三区| 亚洲欧美精品综合一区二区三区| 午夜福利欧美成人| 久久久久九九精品影院| 啦啦啦观看免费观看视频高清| 日韩欧美国产一区二区入口| 又大又爽又粗| 成人永久免费在线观看视频| 亚洲成av片中文字幕在线观看| 亚洲一区高清亚洲精品| 久久精品人妻少妇| 成年人黄色毛片网站| 757午夜福利合集在线观看| 在线观看免费日韩欧美大片| 国产亚洲精品一区二区www| 国产一卡二卡三卡精品| 久久草成人影院| 一进一出抽搐gif免费好疼| 亚洲国产欧美一区二区综合| 亚洲av成人一区二区三| 一二三四社区在线视频社区8| 成年女人毛片免费观看观看9| 999久久久精品免费观看国产| 久久精品国产亚洲av高清一级| 国内精品久久久久精免费| 午夜福利欧美成人| 亚洲成国产人片在线观看| 精品国产超薄肉色丝袜足j| а√天堂www在线а√下载| 可以在线观看毛片的网站| avwww免费| 99热6这里只有精品| 亚洲中文字幕日韩| 午夜福利在线观看吧| 韩国av一区二区三区四区| 免费在线观看完整版高清| 亚洲成国产人片在线观看| 午夜视频精品福利| 欧美成狂野欧美在线观看| 757午夜福利合集在线观看| 色综合站精品国产| 国产99久久九九免费精品| 一区福利在线观看| 97超级碰碰碰精品色视频在线观看| 亚洲中文字幕一区二区三区有码在线看 | 国产精品亚洲一级av第二区| 精品国产乱码久久久久久男人| 我的亚洲天堂| 亚洲第一青青草原| 成年女人毛片免费观看观看9| 国内少妇人妻偷人精品xxx网站 | 欧美在线一区亚洲| 一本大道久久a久久精品| 哪里可以看免费的av片| 久久久久久久久免费视频了| 午夜福利欧美成人| 亚洲第一欧美日韩一区二区三区| 久久精品人妻少妇| 欧美日韩福利视频一区二区| 亚洲熟女毛片儿| 亚洲aⅴ乱码一区二区在线播放 | 国产在线观看jvid| 亚洲免费av在线视频| 少妇粗大呻吟视频| 91国产中文字幕| 亚洲午夜精品一区,二区,三区| 久久久精品欧美日韩精品| 国内精品久久久久精免费| 久久婷婷人人爽人人干人人爱| 十分钟在线观看高清视频www| 欧美亚洲日本最大视频资源| 最近最新免费中文字幕在线| 亚洲专区字幕在线| 国产精品日韩av在线免费观看| 最新美女视频免费是黄的| 国产一区在线观看成人免费| 99久久精品国产亚洲精品| 亚洲一区二区三区色噜噜| 啪啪无遮挡十八禁网站| 中文字幕精品免费在线观看视频| 欧美性猛交黑人性爽| 级片在线观看| 久久精品国产亚洲av香蕉五月| www国产在线视频色| 亚洲av成人不卡在线观看播放网| 青草久久国产| 日本黄色视频三级网站网址| 色精品久久人妻99蜜桃| 欧美精品亚洲一区二区| 母亲3免费完整高清在线观看| 熟妇人妻久久中文字幕3abv| 一个人免费在线观看的高清视频| 可以在线观看毛片的网站| 亚洲男人天堂网一区| 狂野欧美激情性xxxx| 一二三四在线观看免费中文在| 欧美精品啪啪一区二区三区| 中文资源天堂在线| 91成人精品电影| 亚洲欧美一区二区三区黑人| 亚洲国产中文字幕在线视频| 精品少妇一区二区三区视频日本电影| 哪里可以看免费的av片| 中文字幕精品亚洲无线码一区 | 欧美一区二区精品小视频在线| 久久久久九九精品影院| 一区二区三区激情视频| 亚洲五月婷婷丁香| 久久久久久免费高清国产稀缺| 色精品久久人妻99蜜桃| 国产乱人伦免费视频| 少妇裸体淫交视频免费看高清 | 国产精品免费视频内射| 视频在线观看一区二区三区| 欧美 亚洲 国产 日韩一| 极品教师在线免费播放| 成人永久免费在线观看视频| 嫩草影院精品99| 男男h啪啪无遮挡| 亚洲精品美女久久av网站| 男女那种视频在线观看| 男女床上黄色一级片免费看| 精品第一国产精品| 亚洲久久久国产精品| 两个人看的免费小视频| 岛国视频午夜一区免费看| 国产激情久久老熟女| 精品国产一区二区三区四区第35| 可以免费在线观看a视频的电影网站| 99国产极品粉嫩在线观看| 18禁黄网站禁片午夜丰满| 日韩欧美 国产精品| 欧美乱妇无乱码| 夜夜看夜夜爽夜夜摸| 又大又爽又粗| 久久久久久免费高清国产稀缺| 久久久久九九精品影院| 国产一区二区三区视频了| 十八禁人妻一区二区| 在线观看66精品国产| 亚洲欧美一区二区三区黑人| 欧美性长视频在线观看| 免费搜索国产男女视频| 一二三四在线观看免费中文在| 男女视频在线观看网站免费 | 久久婷婷人人爽人人干人人爱| 国产激情久久老熟女| av欧美777| 欧美中文综合在线视频| 少妇被粗大的猛进出69影院| www.熟女人妻精品国产| 久久天堂一区二区三区四区| 日本三级黄在线观看| 在线观看一区二区三区| 久久久久精品国产欧美久久久| 国内揄拍国产精品人妻在线 | 亚洲欧美日韩无卡精品| 亚洲av电影不卡..在线观看| 男女下面进入的视频免费午夜 | 无遮挡黄片免费观看| 十分钟在线观看高清视频www| 欧美日本亚洲视频在线播放| 欧美黄色淫秽网站| 日韩 欧美 亚洲 中文字幕| 欧美日韩亚洲国产一区二区在线观看| 国产免费av片在线观看野外av| 国产精品永久免费网站| 美女高潮喷水抽搐中文字幕| 精品国产乱子伦一区二区三区| 免费高清视频大片| 男男h啪啪无遮挡| 淫秽高清视频在线观看| 国产伦在线观看视频一区| 黄色视频,在线免费观看| 香蕉久久夜色| 狠狠狠狠99中文字幕| 曰老女人黄片| 18美女黄网站色大片免费观看| 日韩国内少妇激情av| 国产成人精品久久二区二区91| 国产免费男女视频| 视频区欧美日本亚洲| 国产区一区二久久| 亚洲国产精品合色在线| 男女床上黄色一级片免费看| 国产区一区二久久| 少妇熟女aⅴ在线视频| 国产黄a三级三级三级人| 老司机福利观看| 欧美日韩黄片免| 黄频高清免费视频| 国产aⅴ精品一区二区三区波| 不卡一级毛片| or卡值多少钱| 欧美大码av| 999精品在线视频| 18禁美女被吸乳视频| 国产精品一区二区免费欧美| 久久久国产欧美日韩av| 日本 欧美在线| 国内精品久久久久精免费| 日韩成人在线观看一区二区三区| 国产色视频综合| 亚洲va日本ⅴa欧美va伊人久久| 国产精品二区激情视频| 久久九九热精品免费| 一区二区三区国产精品乱码| 欧美+亚洲+日韩+国产| 叶爱在线成人免费视频播放| e午夜精品久久久久久久| 中文字幕精品亚洲无线码一区 | 中文字幕av电影在线播放| 亚洲国产精品999在线| 免费人成视频x8x8入口观看| 午夜日韩欧美国产| 久热这里只有精品99| 日本撒尿小便嘘嘘汇集6| 精品国产超薄肉色丝袜足j| 51午夜福利影视在线观看| 成人精品一区二区免费| 亚洲精品久久成人aⅴ小说| 非洲黑人性xxxx精品又粗又长| 黑人巨大精品欧美一区二区mp4| 国内毛片毛片毛片毛片毛片| 久久伊人香网站| 午夜影院日韩av| 亚洲色图 男人天堂 中文字幕| 久久久久国产精品人妻aⅴ院| 亚洲av美国av| 国产av一区在线观看免费| 国产三级在线视频| 亚洲色图 男人天堂 中文字幕| 黑人操中国人逼视频| 一进一出好大好爽视频| 真人一进一出gif抽搐免费| 欧美激情久久久久久爽电影| 19禁男女啪啪无遮挡网站| 国产精品 欧美亚洲| 成人av一区二区三区在线看| 最近最新免费中文字幕在线| av电影中文网址| 亚洲精品美女久久久久99蜜臀| www.精华液| 91成人精品电影| 欧美成狂野欧美在线观看| 国产精品一区二区精品视频观看| 国产黄色小视频在线观看| 9191精品国产免费久久| 变态另类丝袜制服| 黄色a级毛片大全视频| 国产私拍福利视频在线观看| 老司机午夜福利在线观看视频| 老汉色∧v一级毛片| 啪啪无遮挡十八禁网站| 国产伦在线观看视频一区| 黄片小视频在线播放| 精品欧美一区二区三区在线| 国产一级毛片七仙女欲春2 | 久久久久精品国产欧美久久久| 美女大奶头视频| 午夜精品久久久久久毛片777| 一级黄色大片毛片| 日本免费a在线| 一级毛片高清免费大全| 亚洲熟妇中文字幕五十中出| 观看免费一级毛片| 色综合亚洲欧美另类图片| 国产成人啪精品午夜网站| 亚洲国产看品久久| 91麻豆av在线| 久久狼人影院| 精品久久久久久成人av| 搡老岳熟女国产| 在线av久久热| 亚洲专区中文字幕在线| 午夜精品在线福利| 无限看片的www在线观看| 国产黄a三级三级三级人| 最近最新中文字幕大全电影3 | 亚洲av美国av| 欧美久久黑人一区二区| av欧美777| 国产区一区二久久| 999久久久精品免费观看国产| 国产精品久久视频播放| 午夜激情av网站| 69av精品久久久久久| 国产精品国产高清国产av| 两个人视频免费观看高清| 久久久久国产精品人妻aⅴ院| 免费女性裸体啪啪无遮挡网站| 韩国av一区二区三区四区| 亚洲成人国产一区在线观看| 午夜福利成人在线免费观看| 欧美+亚洲+日韩+国产| 后天国语完整版免费观看| 搞女人的毛片| 午夜福利免费观看在线| xxx96com| 亚洲第一青青草原| 日韩欧美国产在线观看| 亚洲欧美日韩无卡精品| 久久香蕉激情| 成年版毛片免费区| 两个人视频免费观看高清| www日本在线高清视频| 日日干狠狠操夜夜爽| 女性被躁到高潮视频| 欧美在线一区亚洲| 亚洲精品一卡2卡三卡4卡5卡| 又大又爽又粗| 国产一级毛片七仙女欲春2 | 国产视频一区二区在线看| 十八禁人妻一区二区| 国产99白浆流出| 午夜福利在线观看吧| av电影中文网址| 亚洲性夜色夜夜综合| 国产99久久九九免费精品| 国产av一区二区精品久久| 成熟少妇高潮喷水视频| 在线视频色国产色| 在线观看日韩欧美| 黄色成人免费大全| 夜夜爽天天搞| 成年版毛片免费区| 国产精品久久视频播放| 国产亚洲av高清不卡| 一本久久中文字幕| 国产精品亚洲一级av第二区| 亚洲五月婷婷丁香| 亚洲成a人片在线一区二区| 丁香欧美五月| 久久伊人香网站| 亚洲成av片中文字幕在线观看| 真人做人爱边吃奶动态| 黄色视频,在线免费观看| 女性被躁到高潮视频| 1024视频免费在线观看| 国产一级毛片七仙女欲春2 | 午夜激情av网站| 亚洲精品色激情综合| 一边摸一边抽搐一进一小说| √禁漫天堂资源中文www| av在线播放免费不卡| 91大片在线观看| 国产精品免费一区二区三区在线| 我的亚洲天堂| videosex国产| 欧美日韩瑟瑟在线播放| 18禁裸乳无遮挡免费网站照片 | 99re在线观看精品视频| 伦理电影免费视频| 黄色女人牲交| 国产aⅴ精品一区二区三区波| 18禁国产床啪视频网站| 两个人看的免费小视频| 十八禁网站免费在线| 国产1区2区3区精品| 日本黄色视频三级网站网址| 久久中文字幕人妻熟女| 国产亚洲精品av在线| 免费观看人在逋| 国产黄片美女视频| 国产成人影院久久av| 国产视频一区二区在线看| 黄片大片在线免费观看| 亚洲中文字幕日韩| 欧美人与性动交α欧美精品济南到| 国产视频一区二区在线看| 老鸭窝网址在线观看| 欧美精品亚洲一区二区| a在线观看视频网站| 亚洲中文字幕日韩| tocl精华| 99久久久亚洲精品蜜臀av| 国产真实乱freesex| 国产一级毛片七仙女欲春2 | netflix在线观看网站| 搡老妇女老女人老熟妇| 欧美不卡视频在线免费观看 | av福利片在线| 亚洲成人精品中文字幕电影| 精品久久久久久成人av| 欧美激情 高清一区二区三区| 麻豆一二三区av精品| 亚洲精品久久国产高清桃花| 无遮挡黄片免费观看| 精品国产乱子伦一区二区三区| 69av精品久久久久久| 精品人妻1区二区| 人人澡人人妻人| 欧美性猛交黑人性爽| 两性午夜刺激爽爽歪歪视频在线观看 | 久久精品人妻少妇| av片东京热男人的天堂| 久久人人精品亚洲av| 精品欧美一区二区三区在线| av在线播放免费不卡| 在线播放国产精品三级| 免费在线观看完整版高清| 久久人妻av系列|