中华神经科杂志
中華神經科雜誌
중화신경과잡지
Chinese Journal of Neurology
2010年
11期
770-773
,共4页
范欣%杨丽%杨春生%张大启%翟翬%程焱
範訢%楊麗%楊春生%張大啟%翟翬%程焱
범흔%양려%양춘생%장대계%적휘%정염
重症肌无力%受体蛋白质酪氨酸激酶类%荧光免疫测定
重癥肌無力%受體蛋白質酪氨痠激酶類%熒光免疫測定
중증기무력%수체단백질락안산격매류%형광면역측정
Myasthenia gravis%Receptor protein-tyrosine kinases%Fluoroimmunoassay
目的 探讨不同血清抗体重症肌无力(MG)的临床特征.方法 用荧光免疫沉淀法(FIPA)和荧光免疫细胞染色法(CBA)检测119例MG患者血清乙酰胆碱受体抗体(AChR-Ab)和肌肉特异性受体酪氨酸激酶抗体(MuSK-Ab)水平.比较AChR-Ab阳性、MuSK-Ab阳性、血清抗体阴性MG的临床特征.结果 纳入119例患者中,90例AChR-Ab阳性(75.6%),29例阴性:其中5例MuSK-Ab阳性(17.2%),24例血清抗体阴性(82.8%).AChR-Ab阳性、MuSK-Ab阳性和血清抗体阴性MG 3组比较,男女比例和平均发病年龄差异均无统计学意义.3例MuSK-Ab阳性的患者主要表现为延髓肌受累;79.2%(19/24)的血清抗体阴性MG患者表现为美国MG协会(MGFA)Ⅰ型;2例MuSK-Ab阳性的患者MGFA≥Ⅲ型;MuSK-Ab滴度水平与患者病情严重程度相关(r=0.941,P=0.014);MuSK-Ab阳性的患者均未发现有胸腺的异常.结论 MuSK-Ab仅出现在AChR-Ab阴性患者的血清中.MuSK-Ab阳性的患者主要表现为延髓肌受累,病情较重且不伴有胸腺的病变.MuSK-Ab阳性的MG可能是不同于血清AChR-Ab阳性的MG的又一亚型.
目的 探討不同血清抗體重癥肌無力(MG)的臨床特徵.方法 用熒光免疫沉澱法(FIPA)和熒光免疫細胞染色法(CBA)檢測119例MG患者血清乙酰膽堿受體抗體(AChR-Ab)和肌肉特異性受體酪氨痠激酶抗體(MuSK-Ab)水平.比較AChR-Ab暘性、MuSK-Ab暘性、血清抗體陰性MG的臨床特徵.結果 納入119例患者中,90例AChR-Ab暘性(75.6%),29例陰性:其中5例MuSK-Ab暘性(17.2%),24例血清抗體陰性(82.8%).AChR-Ab暘性、MuSK-Ab暘性和血清抗體陰性MG 3組比較,男女比例和平均髮病年齡差異均無統計學意義.3例MuSK-Ab暘性的患者主要錶現為延髓肌受纍;79.2%(19/24)的血清抗體陰性MG患者錶現為美國MG協會(MGFA)Ⅰ型;2例MuSK-Ab暘性的患者MGFA≥Ⅲ型;MuSK-Ab滴度水平與患者病情嚴重程度相關(r=0.941,P=0.014);MuSK-Ab暘性的患者均未髮現有胸腺的異常.結論 MuSK-Ab僅齣現在AChR-Ab陰性患者的血清中.MuSK-Ab暘性的患者主要錶現為延髓肌受纍,病情較重且不伴有胸腺的病變.MuSK-Ab暘性的MG可能是不同于血清AChR-Ab暘性的MG的又一亞型.
목적 탐토불동혈청항체중증기무력(MG)적림상특정.방법 용형광면역침정법(FIPA)화형광면역세포염색법(CBA)검측119례MG환자혈청을선담감수체항체(AChR-Ab)화기육특이성수체락안산격매항체(MuSK-Ab)수평.비교AChR-Ab양성、MuSK-Ab양성、혈청항체음성MG적림상특정.결과 납입119례환자중,90례AChR-Ab양성(75.6%),29례음성:기중5례MuSK-Ab양성(17.2%),24례혈청항체음성(82.8%).AChR-Ab양성、MuSK-Ab양성화혈청항체음성MG 3조비교,남녀비례화평균발병년령차이균무통계학의의.3례MuSK-Ab양성적환자주요표현위연수기수루;79.2%(19/24)적혈청항체음성MG환자표현위미국MG협회(MGFA)Ⅰ형;2례MuSK-Ab양성적환자MGFA≥Ⅲ형;MuSK-Ab적도수평여환자병정엄중정도상관(r=0.941,P=0.014);MuSK-Ab양성적환자균미발현유흉선적이상.결론 MuSK-Ab부출현재AChR-Ab음성환자적혈청중.MuSK-Ab양성적환자주요표현위연수기수루,병정교중차불반유흉선적병변.MuSK-Ab양성적MG가능시불동우혈청AChR-Ab양성적MG적우일아형.
Objectives To compare the characteristics of myasthenia gravis (MG) with different antibodies.Methods The muscle specific receptor tyrosine kinase (MuSk) and acetylcholine receptor (AChR) antibodies were detected in the sera of 119 MG patients,and fluoroimmunoprecipitation assay and cell based assay were applied. The clinical features of AChR-Ab positive,MuSK-Ab positive and serum negative MG patients were compared.Results There were 90 AChR-Ab positive sera tested out from the 119 MG sera,and 5 sera found with MuSK-Ab in the 29 AChR-Ab negative sera.There was no significant difference among the three groups regarding sex and age at onset.There were 3/5 of MuSK-Ab positive patients with predominantly bulbar paralysis,2/5 of MuSK-Ab positive patients were classified as MGFA Ⅲ to Ⅴ,and 79.2% (19/24) of serum negative patients were classified as MGFA Ⅰ.There was significantly positive relation between the levels of MuSK antibodies and disease severity (r=0.941,P=0.014).Neither thymic hyperplasia nor hymoma were found in MuSK-Ab positive patients.Conclusions MuSK antibodies are only detected out in the sera without AChR-Ab.The MuSK-Ab positive patients are mainly involved bulbar muscles,and without thymus abnormality.MuSK-MG is different with the AChR MG.