简介：AIM:Tocharacterizetheclinicalfeatures,diagnosis,treatmentandprognosisofuveitisassociatedwithankylosingspondylitis(AS)inChinesepatients.·METHODS:TwohundredandthreepatientswithuveitisassociatedwithASfollowed-upintheThirdMilitaryMedicalUniversityDapingHospitalbetween2005and2010wereretrospectivelyevaluatedinthisstudy.Completeophthalmologicalexaminationswereevaluatedatbaselineandduringthefollow-upperiod.Thegender,age,follow-uptime,meanfrequencyofuveitisonset,andaccompanyingeyeexaminationfindings,history,demographicalparameterswerereviewed.Allthepatientspresentedcompleteclinicalandradiologic(sacroiliac,lumbar,dorsalandcervicalspine,knee,ankle,shoulder,hip,elbow)evaluation.HLA-B27typingwasalsosearched.·RESULTS:Therewere203patientsdiagnosedwithASassociateduveitis.AllshowedsacroiliacX-raychangesindicativeofAS.Therewere184maleand19femalepatients.Theaverageageofpatientswas35±12(range18-50).Meanfollow-upperiodwas2.4years(1-5years).Acuteanterioruveitiswasthemostcommontypeofuveitisinbothgenders.121eyespresentedunilateralinvolvement(55.2%),and92eyespresentedbilateralinvolvement(45.3%)withonsetalternately.22eyesoccurredhypopyon,16eyeswerefoundanteriorvitreouscells,7eyeswerenotedreactivemacularedemaorexudation,29eyespresentedposteriorsynechiaeofiris,and14eyespresentedcataract,9eyespresentedsecondaryglaucoma,2eyespresentedbendcornealdegenerationand1eyespresentedatrophyofeyeball.Atthefinalvisit,uveitiswaswellcontrolledinmostpatients.·CONCLUSION:ASassociatedwithuveitisinChinesepatientsmainlymanifestsasacuteanterioruveitis.AcombinationofcorticosteroidswithothermydriasisagentsiseffectiveformostASassociatedwithuveitispatients.Ingeneral,theprognosisisgoodinthesecases.

简介：目的：研究在高糖诱导人晶状体上皮细胞向间充质转化的过程中JAK-STAT通路的作用及AG490对此过程的影响。方法：低糖（5.5mmol/L）DMEM培养液体外培养人晶状体上皮细胞系SRA01/04。高糖（30.5mmol/L）处理细胞,按照是否加入AG490及其浓度的不同分为实验组和对照组。CCK-8试剂盒检测晶状体上皮细胞的活性,选择实验组AG490浓度为10μmol/L和50μmol/L,处理时间分别为6,12,24和48h；细胞划痕实验检测细胞迁移能力的变化；RT-PCR方法半定量检测TGF-β1,FN和α-SMA的mRNA表达量变化。结果：在不同的处理时间（6,12,24,48h）,高糖组（HG组）与低糖组相比,细胞的迁移能力增加（P〈0.05）,TGF-β1,FN和α-SMA表达量增高（P〈0.05）；AG490组与HG组相比,细胞的迁移能力降低（P〈0.05）,TGF-β1,FN和α-SMA的mRNA表达量下降。结论：JAK-STAT通路通过影响TGF-β1和细胞外基质转录表达参与了高糖诱导的人晶状体上皮细胞向间充质转化的过程。JAK抑制剂AG490对此过程有抑制作用,且随着AG490浓度的增加其抑制作用增强。

简介：AIM:Toassesstheeffectofmyopiaonthethicknessofretinalnervefiberlayer(RNFL)measuredby3Dopticalcoherencetomography(3D-OCT)inagroupofnonglaucomatousChinesesubjects.METHODS:Twohundredandfifty-eighteyesof258healthyChinesemyopicindividualswererecruitedandfourgroupswereclassifiedaccordingtotheirsphericalequivalent(SE):lowmyopia(n=42,-0.50

简介：目的：利用频域三维相干光学断层扫描（threedimensionalfrequencydomaincoherentopticaltomography,3D-OCT）评估准分子激光原位角膜磨镶术（laserinsitukeratomileusis,LASIK）对视网膜神经纤维层厚度（retinalnervefibrelayerthickness,RNFLT）的影响。方法：对83例83右眼接受LASIK治疗的受试者分别于术前及术后1d;1wk;1,3mo行3D-OCT检查,测量视乳头上方、下方、鼻侧、颞侧及12个钟点位RNFLT,利用重复测量方差分析及配对t检验对术前及术后的数据统计学处理。结果：术前及术后各时间点行重复测量方差分析显示,视乳头下方、颞侧、5：00～11：00位RNFLT均值无显著差异（P〉0.05）,而视乳头上方、鼻侧、1：00～4：00位、12：00位RNFLT有显著差异（P〈0.05）;进一步对术前及术后各时间点视乳头上方、鼻侧、1：00～4：00位、12：00位RNFLT分别行配对t检验得出,术后1d时视乳头上方、鼻侧及1：00～4：00位、12：00位RNFLT较术前变薄,差异有统计学意义（P〈0.05）,术后1wk;1,3mo时以上各方位RNFLT较术前比较均无统计学差异（P〉0.05）。同时表明RNFLT变薄与屈光度及激光时间成正相关。结论：LASIK术后早期上方及鼻侧RNFLT变薄,但术后1wk恢复至正常水平,LASIK手术对RNFLT无长远影响。

简介：目的:研究巩膜扣带术(scleralbuckling,SB)联合玻璃体注气术治疗孔源性视网膜脱离(rhegmatogenousretinaldetachment,RRD)的临床疗效及对患者血清中氨基酸、血管内皮生长因子(vascularendothelialgrowthfactor,VEGF)的影响。方法:回顾性分析我院收治的RRD患者150例150眼临床资料,将仅接受SB的患者81例81眼纳入未注气组,接受SB+玻璃体注气术的患者69例69眼纳入注气组,比较两组患者手术疗效和术前、术后血清中氨基酸、VEGF水平等情况。结果:两组患者术后各时间点视网膜复位率比较,差异均无统计学意义(P>0.05);注气组术后1d眼压明显高于未注气组,差异有统计学意义(P<0.05),两组患者术后5d眼压比较差异无统计学意义(P>0.05);两组患者术后术眼裸眼视力较术前均明显改善,差异有统计学意义(P<0.05);术后5d,两组患者血清中组氨酸、谷氨酸、苯丙氨酸、VEGF水平较术前均显著降低,差异有统计学意义(P<0.05),但组间比较差异无统计学意义(P>0.05);两组患者血清中精氨酸、亮氨酸、异亮氨酸、甘氨酸水平与术前比较,差异无统计学意义(P>0.05);术后1mo,两组患者视功能相关生活质量总分和各维目评分均较术前明显升高,差异有统计学意义(P<0.05),但两组间各评分比较差异无统计学意义(P>0.05);注气组术后并发症总发生率为7.2%(5/69)与未注气组的9.9%(8/81)比较,差异无统计学意义(P>0.05)。结论:SB联合玻璃体注气术有助于RRD患者视功能和眼压的早期恢复,降低血清中组氨酸、谷氨酸、苯丙氨酸、VEGF水平,且安全性较高。

简介：AIM:Toinvestigatethelevelsofserumsolubleintercellularadhesionmolecules-1(sICAM-1)andneutrophilicexpressionofCD18inpatientswithvariousstagesofdiabeticretinopathyandtodeterminetheirdifferentexpressionpatterninthedevelopmentofdiabeticretinopathy(DR).·METHODS:LevelsofserumsICAM-1andCD18onthesurfaceofneutrophileweremeasuredin41DRpatients,theywereclassifiedinthreesubgroupsaccordingtothestageofretinopathyasdeterminedbyfund’sophthalmoscopy;10controlsubjectswerealsostudied.sICAM-1weremeasuredbyenzyme-linkedimmunosorbentassayandCD18byflowcytometry.·RESULTS:TheneutrophilicCD18expressionandserumsICAM-1levelwereallsignificantlyelevatedinalldiabeticsubgroupscomparedtocontrolsubjects(P<0.01).ThedifferencesofCD18andsICAM-1amongthediabeticsubgroupsweresignificantinCD18butnotinsICAM-1.TheprogressionofretinopathywasassociatedwithanincreasebothinCD18andinsICAM-1levelsbysimplecorrelationanalysis(β=0.74,P<0.001;β=0.38,P<0.01,respectively).ButstepwisemultipleregressionanalysisrevealedthatonlyCD18wasindependentdeterminantofretinopathy(β=1.04,P<0.01).·CONCLUSION:OurresultsconfirmthecontributionofendothelialandneutrophilicactivationinthedevelopmentofDRasindicatedbyincreasedlevelsofCD18andsICAM-1.However,adirectimplicationofCD18andICAM-1intheprogressionofDRcanbesupportedonlyintheCD18butnotICAM-1.CD18andICAM-1mayplaydifferentroleinthedevelopmentofdiabeticretinopathy.

简介：AIM:ToInvestigatetheeffectsoftransforminggrowthfactorβ2(TGF-β2)andconnectivetissuegrowthfactor(CTGF)ontransdifferentiationofhumanlensepithelialcells(HLECs)culturedinvitroandsynthesisofextracellularmatrix(ECM).METHODS:HLECsweretreatedwithTGF-β2(0,0.5,1.0,5,10μg/L)andCTGF(0,15,30,60,100μg/L)fordifferenttimes(0,24,48,72h)invitroandtheexpressionofα-smoothmuscleactin(α-SMA),themaincomponentoftheextracellularmatrixtypeⅠcollagen(Col-1)andfibronectin(Fn)weremeasuredbyusingreal-timepolymerasechainreaction(PCR)andwestern-blot.RESULTS:TGF-β2andCTGFsignificantlyincreasedexpressionofα-SMAmRNAandprotein(P<0.05,P<0.001),FnmRNAandprotein(P<0.001),Col-1mRNAandprotein(P<0.001).TGF-β2couldinduceHLECsexpressionofCTGFmRNAandproteinindosedependentmanner(P<0.05,P<0.001).TGF-β2andCTGFcouldinduceHLECstoexpressα-SMA,FnandCol-1intime-dependentmanner.EachtimeofTGF-β2andCTGFinducedHELCsexpressionofα-SMA,Fn,Col-1mRNAandproteinwassignificantincreasecomparedwithcontrol(P<0.05,P<0.001).CONCLUSION:TGF-β2andCTGFcouldinduceHLECsepithelialmesenchymaltransitionandECMsynthesis.