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：目的观察球后注射山莨菪碱联合高压氧治疗非动脉炎性前部缺血性视神经病变的疗效。方法选取2015年6月-2016年6月我院收治的60例非动脉炎性前部缺血性视神经病变患者,随机分为2组：治疗组和对照组,2组均给予皮质激素、血管扩张剂、营养神经类药物等治疗。治疗组在此基础上给予山莨菪碱球后注射联合高压氧,15天后除了停止球后注射山莨菪碱,其余治疗不变,30天后比较2组治疗前后视力、视野的改变。结果视力治疗组治愈13眼,显效4眼,有效10眼,无效3眼。对照组治愈6眼,显效12眼,有效8眼,无效4眼。两组对比经ridit分析Z=-3.074,P=0.002。视野治疗组治愈15眼,显效9眼,有效3眼,无效3眼。对照组治愈3眼,显效8眼,有效14眼,无效5眼,两组经ridit分析Z=-3.504,P=0.000。结论球后注射山莨菪碱联合高压氧治疗缺血性视神经病变疗效较好。

简介：目的：对比分析伴虹膜异色的青光眼睫状体炎综合征与Fuchs综合征患者的临床表现及特点,对两种疾病的鉴别要点作出分析及总结,利于临床医生对这两种疾病进行鉴别诊断。方法：对本院自2000年至今收治住院的3例伴虹膜异色的青光眼睫状体炎综合征（Posner-Schlossman’ssyndrome,PSS）患者进行详细的临床检查及研究,根据其临床资料总结出该病的临床特点,并对伴虹膜异色的PSS与Fuchs综合征的鉴别要点作出分析及总结。结果：共收集了3例伴虹膜异色的PSS患者,均为单眼反复发病,病程均在10a以上,发作时眼压明显升高,可达30.00～60.00mmHg,持续时间一般为3～7d,可自行缓解或用药后缓解,间歇期眼压正常,该3例患者除了具有典型的PSS表现外,虹膜均轻度异色。总结了该病在发作期及间歇期的临床表现,从发病情况、眼压波动情况、KP形态、晶状体情况、眼底及视功能情况详细论述了伴虹膜异色的青光眼睫状体炎综合征与Fuchs综合征的区别,并针对两种疾病的治疗提出了不同建议。结论：结合我们所提出的鉴别要点,对患者进行详细的临床检查,可以对这两种疾病进行鉴别诊断。

简介：·AIM:Toexploretheeffectofimmunizationwithcopolymer-1(COP-1)andretinalstemcells(RSCs)transplantationoninterferon-gamma(IFN-γ)levelsinaratexperimentalglaucomamodel.·METHODS:Anexperimentalglaucomawasinducedbyargonlaserphotocoagulationoftheepiscleralveinsandlimbalplexusintherighteyeofrats.Immediatelyfollowingglaucomainduction,ratswereimmunizedwithCOP-1.RSCswereculturedandtransplantedintravitreallyintotheeyesofglaucomamodelanimals1weekpost-lasertreatment.Sixexperimentalgroupswereused:COP-1/RSC,PBS/RSC,COP-1/PBS,PBS/PBS,glaucomamodelgroup,andanormalcontrolgroup.TheconcentrationofIFN-γinaqueoushumor(AH)andserumwasmeasuredbyenzyme-linkedimmunosorbentassay(ELISA)ineachofthesixgroups.Retinalganglioncell(RGC)survivalwasassessedbyquantifyingapoptosisusingHoechststaining.·RESULTS:ConcentrationsofIFN-γinAHandserumofratsthathadundergoneglaucomainductionwerehigherthanthoseofnon-inducedcontrolrats.TheconcentrationsofIFN-γinAHandserumoftheCOP-1/RSCstreatedgroupweredeterminedtobe2371.9ng/Land710.9ng/L,respectively,whichweresignificantlylowerthanthoseintheothertreatedgroups(P<0.05).Infact,IFN-γlevelsinthedualtreatedgroupwerereducedtobackgroundlevels.TheCOP-1/RSCgrouphadlowernumberofapoptoticRGCsthantheotherthreeexperimentalgroups(P<0.05).·CONCLUSION:ThereducedlevelsofIFN-γinAHandserumoftheCOP-1/RSCgroupmayberelatedtosynergisticeffectsbetweenRSCstransplantationandCOP-1immunemodulation.ItislikelythatthelowerlevelsofIFN-γpreventedRGCsglaucomatousapoptosis.·

简介：目的比较急性中心性浆液性脉络膜视网膜病变（CSC）的患侧与对侧眼视网膜频域相干光断层扫描（OCT）的图像特征。方法应用频域OCT对30例（60眼）单眼发病急性CSC患者患侧和对侧眼的黄斑部视网膜显微结构进行检测，比较患侧组与对侧组黄斑中心凹外核层厚度、光感受器层（IS／OS层）、视网膜色素上皮（RPE）形态差异。结果所有30例患者患侧眼均有不同程度黄斑部视网膜浆液性脱离，对侧眼中有4眼（13．3％）存在轻度视网膜浆液性脱离；患侧组黄斑中心凹外核层厚度均值为（95．32±24．87）μm，对侧组为（98．80±14．36）μm，两组差异无统计学意义（t=1．627，P=0．110）。患侧组中IS／OS层厚度均匀一致者12眼（40．0％），对侧组20眼（66．7％）；患侧组IS／OS层厚度均匀一致伴内外节缺损、不均、凸起增厚者共18眼（60．O％），对侧组共10眼（33．3％），差异有统计学意义（X2=4．28，P=0．038）。患侧组中出现RPE异常者有24眼（80．0％），对侧组中有8眼（26．7％），差异有统计学意义（x。=17．143，P=0．000）。结论频域OCT能清晰显示急性CSC患者的细微病理结构改变，单眼发病CSC患者中一部分对侧眼存在IS／OS层和RPE异常，但是其发生率较患侧眼低。（中国眼耳鼻喉科杂志，2013，13：165—167）