Clinical observation of immunosuppressive therapy for myasthenia gravis with thymus abnormalities
-
摘要: 目的 观察应用免疫抑制剂治疗重症肌无力(MG)伴胸腺异常患者的临床效果。 方法 纳入2015年1月—2018年12月浙江省人民医院神经内科接诊的106例使用免疫抑制剂治疗的重症肌无力(MG)患者的临床资料做回顾性分析。根据患者是否伴胸腺异常,将其分为2组,分别是A组(MG伴胸腺异常,81例)与B组(MG不伴胸腺异常,25例)。比较2组患者临床资料、实验室生化检查结果、激素使用剂量、合用其他免疫抑制剂情况、重症肌无力复合量表(myasthenia gravis composite,MGC)评分、重症肌无力绝对评分(myasthenia gravis absolute score,MGAS)。 结果 2组患者一般临床资料包括性别、年龄、病程、MGC、MGAS、治疗前血糖及血脂水平比较,差异均无统计学意义(均P>0.05)。治疗后,A组免疫治疗敏感的患者占82.72%(67/81),B组为100.00%(25/25),2组差异有统计学意义(χ2=5.330,P=0.013);A组患者合并使用其他免疫抑制剂的比例为93.83%(76/81),B组合并使用其他免疫抑制剂的为40.00%(10/25),差异具有统计学意义(χ2=36.160,P<0.001)。随访1.5年时A组患者血糖水平指标(餐后2 h血糖、糖化血红蛋白),血脂水平指标(总胆固醇、甘油三酯)均高于B组(t=2.139、2.625、2.010、2.086,均P<0.05)。治疗6个月后A组患者泼尼松日平均剂量大于B组(P<0.05)。治疗6个月后A组MGC评分及MGAS评分高于B组(均P<0.05)。 结论 MG伴胸腺异常患者对免疫抑制剂治疗的反应性相对较差,需使用的糖皮质激素量较大,需联合使用其他免疫抑制剂,提示在治疗前需对患者的胸腺进行详细评估,以利于临床治疗方案的制定及预后的判断。Abstract: Objective To investigate the clinical effect of immunosuppressant in the treatment of myasthenia gravis(MG) with thymus abnormalities. Methods The clinical data of 106 patients with MG admitted to the Department of Neurology of Zhejiang Provincial People's Hospital from January 2017 to December2018 were included for retrospective analysis. All patients received immunosuppressant treatment. The patients were divided into two groups: group A(MG with abnormal thymus, 81 cases) and group B(MG without abnormal thymus, 25 cases). The clinical data, laboratory biochemical examination results, glucocorticoid dosage and combination with other immunosuppressive agents, the myasthenia gravis composite(MGC) score and myasthenia gravis absolute score(MGAs) were compared between the two groups. Results There was no significant difference in general clinical data, including sex ratio, average age, course of disease, MGC, MGAs, blood glucose and blood lipid levels before treatment between the two groups(all P>0.05). After treatment, 82.72%(67/81) of patients in the group A were sensitive to immunotherapy, and 100%(25/25) in the group B, there was statistical difference between the two groups(χ2=5.330, P=0.013). The proportion of patients treated with other immunosuppressants in the group A was 93.83%(76/81), and that in the group B was 40.0%(10/25), the difference was statistically significant(χ2=36.160, P<0.001). After 1.5 years of follow-up, 2-h postprandial blood glucose, glycosylated hemoglobin, total cholesterol and triglyceride in the group A were higher than those in the group B(t=2.139, 2.625, 2.010, 2.086, all P<0.05). After 3 months of treatment, the average daily dose of prednisone in the group A was higher than that in group B(P<0.05). After 6 months of treatment, the MGC score and MGAs score of the group A were higher than those of group B(all P<0.05). Conclusion The response of MG patients with thymus abnormalities to immunosuppressive therapy is relatively poor, and the amount of glucocorticoid needed to be used is large, and other immunosuppressants should be used in combination. It is suggested that the thymus of MG patients should be evaluated in detail before treatment, as it can facilitate the formulation of clinical treatment plan and the judgment of prognosis.
-
Key words:
- Myasthenia gravis /
- Thymus hyperplasia /
- Thymoma /
- Glucocorticoid /
- Immunosuppressant /
- Curative effect
点击查看大图
计量
- 文章访问数: 305
- HTML全文浏览量: 39
- PDF下载量: 1
- 被引次数: 0