{"title":"Expression of resistin in serum of TAO patients","authors":"L. Hongxia, W. Zhongyao","doi":"10.3969/J.ISSN.1003-0808.2010.06.018","DOIUrl":"https://doi.org/10.3969/J.ISSN.1003-0808.2010.06.018","url":null,"abstract":"BackgroundResistin is the member of human cytokines,but its function is below understood.Research revealed that the expression of resistin in serum is regulated by sexual gland,thyroid hormone.ObjectiveThe goal of this study was to investigate the expression of resistin in the serum of TAO patients.MethodsThe serum samples were obtained from 35 patients with thyroid-associated ophthalmopathy(TAO).These patients rejected the administration of glucocorticoid and immunity inhibitor within 3 months and were assigned to inactive TAO group(CAS4,18 cases)and active TAO group(CAS≥4,17 cases).Fifteen normal subjects were as control group.The level of resistin in serum was detected using ELISA kit.Written informed consent was obtained from each individual at initial of the medical process.Results No significant difference was found in serum resistin level between inactive TAO group and active TAO group(12.103±5.042 versus 13.470±3.749)mg/L(t=0.906,P=0.371).However,serum resistin level was significant declined in inactive TAO group or active TAO group in comparison with normal group(12.103±5.042 versus 21.894±10.589;13.470±3.749 versus 21.894±10.589)mg/L(t=3.074,P=0.004;t=3.485,P=0.001).No obvious difference was seen between male patients and female patients(13.175±4.483 versus 12.335±4.511)mg/L(t=0.552,P=0.585).Serum resistin level was gradually elevated with the increase of age in TAO patients(F=24.978,P=0.000).ConclusionThe serum resistin level of TAO patients is lower than the control subjects,suggesting that the level of serum resistin is regulated by thyroid hormones.The serum resistin level increases with age in TAO patient.","PeriodicalId":186994,"journal":{"name":"Chinese Ophthalmic Research","volume":"47 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2010-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125028195","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Current research incomplications after intravitreal injection of bevacizumab","authors":"刘晓娟","doi":"10.3969/J.ISSN.1003-0808.2010.06.025","DOIUrl":"https://doi.org/10.3969/J.ISSN.1003-0808.2010.06.025","url":null,"abstract":"玻璃体腔注射bevacizumab治疗多种新生血管性眼病的短期疗效较好,但随着对其研究的不断深入,由玻璃体腔注射的操作过程以及bevacizumab毒性作用等原因引起的一些眼部及全身并发症已逐渐成为临床中不可忽视的问题.就玻璃体腔注射bevacizumab临床应用中出现的并发症,如眼内炎、非感染性眼内炎症反应、一过性眼压升高、结膜下出血、球结膜水肿、视网膜色素上皮(RPE)撕裂、视网膜色素上皮脱离(RPED)、血栓性疾病及子宫不规则出血等进行综述。","PeriodicalId":186994,"journal":{"name":"Chinese Ophthalmic Research","volume":"19 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2010-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114221522","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Exclusive mapping for all known locus linked with congenital iris and retinochoroidal coloboma in a Chinese family","authors":"布娟, 董佳梅, 杜伟, 李静, 卓彦玲, 王乐今","doi":"10.3969/CMA.J.ISSN.1003-0808.2010.06.017","DOIUrl":"https://doi.org/10.3969/CMA.J.ISSN.1003-0808.2010.06.017","url":null,"abstract":"目的 对1个3代常染色体显性遗传性先天性眼组织缺损家系进行致病基因的定位.方法 对家系所有成员进行详细的临床检查,排除其他系统疾患.提取家系成员外周血DNA,选取20个位于4、7、10、11号染色体上已知与先天性眼组织缺损相关的4个致病基因及已知基因位点20q13.1附近的微卫星标记物进行多重PCR扩增,经ABI3130型遗传分析仪,Genscan 2.1收集数据,Genotyper 2.1进行基因分型,Linkage软件计算两点LOD值.研究过程遵循赫尔辛基宣言.结果 未发现所选微卫星位点与该家系疾病表型共分离,LOD值均为负值.致病基因与已知的先天性眼组织缺损候选基因不存在连锁关系.结论 该家系的遗传与目前已知的致病基因无关,是否存在新的致病基因有待进一步研究。","PeriodicalId":186994,"journal":{"name":"Chinese Ophthalmic Research","volume":"144 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2010-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130204306","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}