Neuro-Ophthalmology Service, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston2Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor.
Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor.
JAMA Neurol. 2015 Oct;72(10):1170-4. doi: 10.1001/jamaneurol.2015.1444.
The sensitivity of acetylcholine receptor (AChR) antibody testing is thought to be lower in ocular myasthenia gravis (OMG) compared with generalized disease, although estimates in small-scale studies vary. There is little information in the literature about the implications of AChR antibody levels and progression from OMG to generalized myasthenia gravis.
To test the hypothesis that serum AChR antibody testing is more sensitive in OMG than previously reported and to examine the association between AChR antibody levels and progression from OMG to generalized myasthenia gravis.
DESIGN, SETTING, AND PARTICIPANTS: A retrospective, observational cohort study was conducted of 223 patients (mean [SD] age, 59.2 [16.4] years; 139 [62.3%] male) diagnosed with OMG between July 1, 1986, and May 31, 2013, at 2 large, academic medical centers.
Baseline characteristics, OMG symptoms, results of AChR antibody testing, and progression time to generalized myasthenia gravis (if this occurred) were recorded for each patient. Multiple logistic regression was used to measure the association between all clinical variables and antibody result. Kaplan-Meier survival analysis was performed to examine time to generalization.
Among the 223 participants, AChR antibody testing results were positive in 158 participants (70.9%). In an adjusted model, increased age at diagnosis (odds ratio [OR], 1.03; 95% CI, 1.01-1.04; P = .007) and progression to generalized myasthenia gravis (OR, 2.92; 95% CI, 1.18-7.26; P = .02) were significantly associated with positive antibody test results. Women were less likely to have a positive antibody test result (OR, 0.36; 95% CI, 0.19-0.68; P = .002). Patients who developed symptoms of generalized myasthenia gravis had a significantly higher mean (SD) antibody level than those who did not develop symptoms of generalized myasthenia gravis (12.7 [16.5] nmol/L vs 4.2 [7.9] nmol/L; P = .002).
We demonstrate a higher sensitivity of AChR antibody testing than previously reported in the largest cohort of patients with OMG available to date. Older age, male sex, and progression to generalized myasthenia gravis were significantly associated with a positive antibody test result. In addition, to our knowledge, this is the first report of an association between high AChR antibody levels and progression from OMG to generalized disease.
与全身性重症肌无力 (gMG) 相比,乙酰胆碱受体 (AChR) 抗体检测的敏感性被认为较低,尽管小规模研究中的估计值有所不同。文献中关于 AChR 抗体水平与眼肌型重症肌无力 (OMG) 向全身性重症肌无力进展之间关系的信息很少。
检验血清 AChR 抗体检测在 OMG 中比以前报告的更敏感的假设,并检查 AChR 抗体水平与 OMG 向全身性重症肌无力进展之间的关系。
设计、设置和参与者:这是一项回顾性、观察性队列研究,纳入了 1986 年 7 月 1 日至 2013 年 5 月 31 日期间在 2 家大型学术医疗中心确诊为 OMG 的 223 名患者(平均[标准差]年龄 59.2[16.4]岁;139 名[62.3%]为男性)。
记录每位患者的基线特征、OMG 症状、AChR 抗体检测结果以及进展为 gMG 的时间(如果发生)。采用多变量逻辑回归分析评估所有临床变量与抗体结果之间的关系。Kaplan-Meier 生存分析用于检查泛化时间。
在 223 名参与者中,158 名(70.9%)的 AChR 抗体检测结果为阳性。在调整模型中,诊断时年龄较大(比值比[OR],1.03;95%CI,1.01-1.04;P = .007)和进展为 gMG(OR,2.92;95%CI,1.18-7.26;P = .02)与阳性抗体检测结果显著相关。女性更不可能有阳性抗体检测结果(OR,0.36;95%CI,0.19-0.68;P = .002)。发展为 gMG 症状的患者的平均(标准差)抗体水平明显高于未发展为 gMG 症状的患者(12.7[16.5]nmol/L 比 4.2[7.9]nmol/L;P = .002)。
我们在迄今为止最大的 OMG 患者队列中证明了 AChR 抗体检测的敏感性高于以前的报告。年龄较大、男性和进展为 gMG 与阳性抗体检测结果显著相关。此外,据我们所知,这是首次报告 AChR 抗体水平与 OMG 向全身性疾病进展之间存在关联。