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[经形态学证实的淋巴细胞性心肌炎病毒阴性和病毒阳性患者免疫抑制治疗的疗效]

[Efficiency of immunosuppressive therapy in virus-negative and virus-positive patients with morphologically verified lymphocytic myocarditis].

作者信息

Blagova O V, Nedostup A V, Kogan E A, Sulimov V A

机构信息

I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia, Moscow, Russia.

出版信息

Ter Arkh. 2017;89(8):57-67. doi: 10.17116/terarkh201789857-67.

Abstract

AIM

To evaluate the efficiency of immunosuppressive therapy (IST) in virus-negative (V-) and virus-positive (V+) patients with lymphocytic myocarditis (LM).

SUBJECTS AND METHODS

60 patients (45 males) (mean age 46.7±11.8 years) with dilated cardiomyopathy (mean left ventricular (LV) end diastolic size (EDS) 6.7±0.7 cm; ejection fraction (EF) 26.2±9.1%) were examined. The diagnosis of active/borderline LM was verified by right ventricular endomyocardial biopsy in 38 patients, by intraoperative LV biopsy in 10, in the study of explanted hearts from 3 patients and at autopsy in 9. The investigators determined the genomes of parvovirus B19, herpes viruses types 1, 2 and 6, Epstein-Barr (EBV), zoster, and cytomegalovirus in the blood and myocardium and, if antibodies were present in the blood, hepatitis B and C viruses, as well as antibodies against antigens in the endothelium, cardiomyocytes and their nuclei, smooth muscles, fibers of the conducting system. IST was used in terms of histological, immune, and viral activities. IST was performed in 22 V+ patients (Group 1) and in 24 V- patients (Group 2); this was not done in 10 V+ patients (Group 3) and V- patients (Group 4). IST comprised methylprednisolone at a mean dose of 24 mg/day (n=40), hydroxychloroquine 200 mg/day (n=20), azathioprine at a mean dose of 150 mg/day (n=21); antiviral therapy included acyclovir, ganciclovir, intravenous immunoglobulin (n=24). The follow-up period was 19 (7.3-40.3) months.

RESULTS

The viral genome was detected in the myocardium of 32 patients who made up a V+ group. The degree of histological activity did not differ in relation to the presence of viral genome in the myocardium. The degree of immune activity (anticardiolipin antibody titers) in the V+ patients was as high as that in V- ones. At baseline, the V+ patients had a significantly higher LV EDS and a lower EF than the V- patients. Overall, IST only could lead to a significant increase in EF (from 26.5±0.9 to 36.0±10.8%; p<0.001) and reductions in NYHA functional class from III to II (p<0.001), LV EDS (from 6.7±0.7 to 6.4±0.8 cm; p<0.01), pulmonary artery systolic pressure (from 48.9±15.5 to 39.4±11.5 mm Hg (p<0.01); the IST group had significantly lower mortality rates than the non-IST group (23.9 and 64.3%; p<0.01). At the same time, a significant trend was seen in both V- and V+ patients. The mortality rate in the V+ patients, as a whole, was higher (46.9 and 17.9%; p<0.05).

CONCLUSION

IST leads to a significant improvement of functional indices and it is associated with lower mortality rates in both myocardial V- and V+ patients with LM. A more than 10% EF increase in the first 2 months is associated with a good prognosis. The presence of viral genome in the myocardium (primarily herpesviruses rather than parvovirus-19) is accompanied by more severe initial dysfunction, a less pronounced effect of IST, and higher mortality rates. However, the positive effect of IST also persists in V+ patients. No positive changes (a decrease in EF was observed) were absent only in IST-naïve V+ patients.

摘要

目的

评估免疫抑制治疗(IST)对淋巴细胞性心肌炎(LM)病毒阴性(V-)和病毒阳性(V+)患者的疗效。

对象与方法

研究了60例扩张型心肌病患者(45例男性)(平均年龄46.7±11.8岁)(平均左心室(LV)舒张末期内径(EDS)6.7±0.7 cm;射血分数(EF)26.2±9.1%)。38例患者通过右心室心内膜活检、10例通过术中LV活检、3例通过对移植心脏的研究以及9例通过尸检确诊为活动性/临界性LM。研究人员测定了血液和心肌中细小病毒B19、1、2和6型疱疹病毒、爱泼斯坦-巴尔(EBV)、带状疱疹病毒和巨细胞病毒的基因组,以及如果血液中存在抗体,则测定乙型和丙型肝炎病毒,以及针对内皮、心肌细胞及其细胞核、平滑肌、传导系统纤维中抗原的抗体。根据组织学、免疫和病毒活性使用IST。22例V+患者(第1组)和24例V-患者(第2组)接受了IST治疗;10例V+患者(第3组)和V-患者(第4组)未接受治疗。IST包括平均剂量为24 mg/天的甲泼尼龙(n = 40)、200 mg/天的羟氯喹(n = 20)、平均剂量为150 mg/天的硫唑嘌呤(n = 21);抗病毒治疗包括阿昔洛韦、更昔洛韦、静脉注射免疫球蛋白(n = 24)。随访期为19(7.3 - 40.3)个月。

结果

32例患者的心肌中检测到病毒基因组,构成V+组。组织学活性程度与心肌中病毒基因组的存在无关。V+患者的免疫活性程度(抗心磷脂抗体滴度)与V-患者一样高。基线时,V+患者的LV EDS显著高于V-患者,EF显著低于V-患者。总体而言,仅IST可导致EF显著增加(从26.5±0.9%增至36.0±10.8%;p<0.001),纽约心脏协会(NYHA)功能分级从III级降至II级(p<0.001),LV EDS降低(从6.7±0.7 cm降至6.4±0.8 cm;p<0.01),肺动脉收缩压降低(从48.9±15.5降至39.4±11.5 mmHg(p<0.01);IST组的死亡率显著低于未接受IST组(23.9%和64.3%;p<0.01)。同时,V-和V+患者均出现显著趋势。总体而言,V+患者的死亡率更高(46.9%和17.9%;p<0.05)。

结论

IST可显著改善功能指标,且与心肌V-和V+的LM患者死亡率降低相关。最初2个月内EF增加超过10%与良好预后相关。心肌中病毒基因组的存在(主要是疱疹病毒而非细小病毒-19)伴随着更严重的初始功能障碍、IST效果不明显以及更高的死亡率。然而,IST在V+患者中也持续产生积极效果。仅未接受过IST的V+患者未出现阳性变化(观察到EF降低)。

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