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原发性干燥综合征患者初诊的临床特征分析被引量:21
2012年
目的:了解原发性干燥综合征(primary Sjgren’s syndrome,pSS)患者起病形式和临床特点,为临床提供诊断治疗资料。方法:采用流行病学中现况调查的研究方法,对北京大学人民医院风湿免疫科就诊的224例pSS患者进行现况调查,内容包括患者性别、发病年龄、病程、腺体外表现、合并症及家族史,并进一步分析相互间的关系。结果:本组pSS患者平均年龄为(53.5±11.7)岁,男性11例,女性213例,男女之比为1∶19.4,平均发病年龄为(46.1±10.7)岁,中位病程9.4年(0.2~40.0年)。224例患者中确诊pSS前的临床表现中最常见的腺体外表现从高至低依次为白细胞减低74例(33%,74/224),关节炎56例(25%,56/224),雷诺现象37例(16.5%,37/224),肝损伤35例(15.6%,35/224),肺间质病变27例(12.1%,27/224),双下肢特发性血小板减少性紫癜26例(11.6%,26/224),血色素减低18例(8.0%,18/224),血小板减低13例(5.8%,13/224),肾小管酸中毒8例(3.6%,8/224)。分析患者脏器受累的影响因素显示,肺间质病变的独立危险因素为:年龄(OR=1.074,95%CI=1.031~1.118)和病程(OR=1.075,95%CI=1.023~1.128);肝受累的危险因素主要为病程(OR=1.050,95%CI=1.002~1.100)。患者中有自身免疫病家族史者占8.0%(18/224),有肿瘤家族史者占11.2%(25/224)。结论:pSS患者绝大多数为女性,发病隐匿,病程迁延,容易延误诊断,诊断时多有腺体外脏器受累,尤其是白细胞减低,肝损伤及肺间质病变等严重的系统受累常见,并且该病可能有遗传倾向,应引起临床上更多的重视。
何菁丁艳李玉慧冯敏戴逸君张学武栗占国
关键词:干燥综合征
Serum IgA against type 3 muscarinic acetylcholine receptor is a novel marker in diagnosis of Sjoegren's syndrome被引量:1
2011年
Background Antibodies against type 3 muscarinic acetylcholine receptor (M3R) are involved in the pathogenesis of Sj6gren's syndrome (SS), but the clinical value of them in SS patients has been controversial. The aims of this study were to: (1) establish an improved enzyme-linked immunosorbent assay (ELISA) to detect IgA antibodies against M3R; (2) evaluate the value of IgA antibodies against the second extracellular loop of M3R205-220 (c2M3RP) in diagnosis of SS. Methods To increase the ELISA sensitivity, c2M3RP was coupled to bovine serum albumin (BSA) by the glutaraldehyde method and a 96-well microplate was treated by ultraviolet rays before coated. Concentrations of anti-c2M3RP, anti-SSA, and anti-SSB were measured in the sera of 240 individuals: 91 patients with primary SS and 149 controls (16 secondary SS, 27 systemic lupus erythematosus, 40 rheumatoid arthritis and 66 healthy controls). Diagnostic properties of anti-c2M3RP were determined by receiver-operating characteristic curve analysis. Results The prevalence of serum IgA anti-c2M3RP antibodies in patients with pSS (46%, 42/91) was significantly higher than that in patients with systemic lupus erythematosus (19%, 5/27), in rheumatoid arthritis (15%, 6/40) and in healthy controls (5%, 3/66). However, there was no significant difference between the two $S groups (P=-0.727). The diagnostic performance of IgA anti-M3RP antibodies was similar to anti-SSA assay, but had 22% higher sensitivity than anti-SSB. By analyzing of IgA anti-c2M3RP antibodies, combination of anti-SSA and anti-SSB resulted in increased sensitivity, whereas their specificity was not significantly changed. Conclusions The improved anti-c2M3RP ELISA is a novel, sensitive, and specific serological test for the diagnosis of SS. The combined application of anti-c2M3RP, anti-SSA and anti-SSB tests can improve the laboratory diagnosis of SS. The IgA anti-c2M3RP antibodies may serve as a novel diagnostic marker for SS.
LI Ying-niGUO Jian-pingHE JingLIU XiaYIN Fang-ruiDING YanYAO Hai-hongKANG Ai-junLI Zhan-guo
关键词:AUTOANTIBODIES
原发性干燥综合征患者合并周围神经病的临床和实验室特点被引量:11
2013年
目的了解原发性干燥综合征(pSS)合并周围神经病变的临床及实验室特点。方法入选符合2002年美国一欧洲(US.Euro)分类标准的pSS患者86例,由风湿免疫专科医师调查及分析患者的临床症状和实验室指标;由神经内科专科医师完成神经系统查体,并完善肌电图检查。对患者的临床症状、查体、实验室检查及肌电图检查进行分析,判断患者是否合并周围神经病变,并比较2组临床症状及实验室特征。数据分析采用t检验、r检验及Logistic回归分析。结果共人组86例pSS患者,男性4例,女性82例,合并周围神经系统病变者占26%(22/86),pSS患者的周围神经病变症状多样,受累神经主要见于正中神经、胫神经、腓神经、腓肠神经等,受累部位以下肢常见(16/22,73%),神经病变类型以感觉运动纤维受累为主。此外,周围神经病均在Dss发病后出现,其中约有45%的患者在pSS发病早期出现周围神经病变。Dss合并周围神经系统病变组与无周围神经病变组相比,除手足麻木(68%与5%,P〈0.01)外,雷诺现象(32%与5%,P=0.002)较为常见,且该组患者的欧洲抗风湿病联盟干燥综合征疾病活动度评分(ESSDAI)明显升高(5.3+2.5与3.4~1.9,P〈0.01)。雷诺现象(OR=9.489,95%CI2.191.41.093,P=0.003)及ESSDAI(OR=1.528,95%C11.179~1.979,P=O,001)是周围神经病的独立危险因素。pSS合并周围神经系统病变组抗核抗体滴度(雎0.003)和类风湿因子滴度明显升高(辟O。023)。结论pSS患者合并周围神经系统病变的发生率较高,病程早期即可出现周围神经系统病变,雷诺现象、高疾病活动度是合并周围神经病变的独立危险因素。
冯敏何菁李英妮栗占国高辉李永杰霍阳丁艳
关键词:干燥综合征神经病学表现
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