心肌炎的发病率及其对原发性心肌肥厚病程的影响

Y. Lutokhina, O. V. Blagova, E. A. Kogan, A. A. Nartov, V. R. Nartova, E. V. Zaklyazminskaya, S. Dzemeshkevich
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All patients underwent electrocardiography, 24-hour electrocardiographic monitoring, echocardiography, as well as DNA analysis (n=96), myocardium pathological study (n=29), cardiac magnetic resonance imaging (n=31), cardiac multislice computed tomography (n=26), assessment of anti-cardiac antibodies (n=43), free light chain level in serum and urine by immunofixation method (n=10); 99mTc-pyrophosphate myocardial scintigraphy (n=5); biopsy of the rectal mucosa and/or subcutaneous fat for amyloid (n=9).Results. In 68%, true (sarcomeric) hypertrophic cardiomyopathy (HCM) was diagnosed, in 16% — amyloidosis with cardiac involvement, in 10% — storage diseases, in 3% — neuromuscular diseases, in 2% — myocardial hypertrophy was combined with severe restriction (mixed phenotype), and in 1% — LEOPARD syndrome. Concomitant myocarditis was diagnosed in 30% of patients. In HCM, myocarditis was detected in 31% of cases. 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引用次数: 0

摘要

目的评估原发性心肌肥厚患者心肌炎的发病率,并研究其对病程的影响。研究对象包括 100 名原发性左心室心肌肥厚患者,其中男性 52 人,女性 48 人(平均年龄为 51.5±15.7 岁;随访时间为 10.4 [2.1; 36.1] 个月)。所有患者均接受了心电图、24 小时心电监测、超声心动图以及 DNA 分析(96 人)、心肌病理研究(29 人)、心脏磁共振成像(31 人)、心脏多层计算机断层扫描(26 人)、抗心肌抗体评估(43 人)、免疫固定法检测血清和尿液中游离轻链水平(10 人);99m锝-焦磷酸心肌闪烁扫描(5人);直肠粘膜和/或皮下脂肪淀粉样蛋白活检(9人)。结果。68%的患者被确诊为真正的(肉瘤型)肥厚型心肌病(HCM),16%的患者被确诊为累及心脏的淀粉样变性,10%的患者被确诊为贮积性疾病,3%的患者被确诊为神经肌肉疾病,2%的患者被确诊为心肌肥厚合并严重受限(混合表型),1%的患者被确诊为LEOPARD综合征。30%的患者被诊断出合并心肌炎。在 HCM 患者中,31% 的病例检测出心肌炎。这些患者的心衰分级(心衰分级 3 [2; 3] vs 2 [1; 3],P=0,026)和死亡率(33.3% vs 6.4%,P=0,01)明显较高。在淀粉样变性患者中,心肌炎的发病率为 31.3%。在这些患者中,室性心动过速的发生率明显更高:80.0% 对 18.2% (P=0.036)。在贮积性疾病亚组中,合并心肌炎的发病率为 30%:2名患者患有法布里病,1名患者患有达农病。在患有限制性表型和 LEOPARD 综合征的亚组中,没有心肌炎病例的记录。心肌炎的治疗使患者的病情得以稳定。合并心肌炎会导致心力衰竭恶化、室性心律失常加重,从而增加心脏性猝死的风险。因此,有必要积极诊断和治疗原发性心肌肥厚患者的心肌炎。
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Prevalence of myocarditis and its contribution to the course of primary myocardial hypertrophy
Aim. To assess the incidence of myocarditis in patients with primary myocardial hypertrophy and to study its contribution to the disease course.Material and methods. The study included 100 patients with primary left ventricular myocardial hypertrophy, 52 men and 48 women (mean age, 51,5±15,7 years; followup period 10,4 [2,1; 36,1] months). All patients underwent electrocardiography, 24-hour electrocardiographic monitoring, echocardiography, as well as DNA analysis (n=96), myocardium pathological study (n=29), cardiac magnetic resonance imaging (n=31), cardiac multislice computed tomography (n=26), assessment of anti-cardiac antibodies (n=43), free light chain level in serum and urine by immunofixation method (n=10); 99mTc-pyrophosphate myocardial scintigraphy (n=5); biopsy of the rectal mucosa and/or subcutaneous fat for amyloid (n=9).Results. In 68%, true (sarcomeric) hypertrophic cardiomyopathy (HCM) was diagnosed, in 16% — amyloidosis with cardiac involvement, in 10% — storage diseases, in 3% — neuromuscular diseases, in 2% — myocardial hypertrophy was combined with severe restriction (mixed phenotype), and in 1% — LEOPARD syndrome. Concomitant myocarditis was diagnosed in 30% of patients. In HCM, myocarditis was detected in 31% of cases. These patients had a significantly higher heart failure class (heart failure class 3 [2; 3] vs 2 [1; 3], p=0,026) and mortality (33,3% vs 6,4%, p=0,01). In amyloidosis, the incidence of myocarditis was 31,3%. In these patients, ventricular tachycardia was observed significantly more often: 80,0% vs 18,2% (p=0,036). The prevalence of concomitant myocarditis in the subgroup of storage diseases was 30%: 2 patients with Fabry disease and 1 patient with Danon disease. Of the three patients with neuromuscular diseases, myocarditis was diagnosed in 1. In the subgroups with the restrictive phenotype and LEOPARD syndrome, no cases of myocarditis were recorded. Treatment of myocarditis made it possible to stabilize the patients' condition.Conclusion. Concomitant myocarditis led to heart failure progression, worsening ventricular arrhythmias and, as a consequence, an increased risk of sudden cardiac death. It is necessary to actively diagnose and treat myocarditis in patients with primary myocardial hypertrophy.
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来源期刊
Russian Journal of Cardiology
Russian Journal of Cardiology Medicine-Cardiology and Cardiovascular Medicine
CiteScore
2.20
自引率
0.00%
发文量
185
审稿时长
1 months
期刊介绍: Russian Journal of Cardiology has been issued since 1996. The language of this publication is Russian, with tables of contents and abstracts of all articles presented in English as well. Editor-in-Chief: Prof. Eugene V.Shlyakhto, President of the Russian Society of Cardiology. The aim of the journal is both scientific and practical, also with referring to organizing matters of the Society. The best of all cardiologic research in Russia is submitted to the Journal. Moreover, it contains useful tips and clinical examples for practicing cardiologists. Journal is peer-reviewed, with multi-stage editing. The editorial board is presented by the leading cardiologists from different cities of Russia.
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