Karageorgiou Ioannis, Bhatia Unnati, Alakhras Hazem, Celik Berk, Halalau Alexandra
Corewell Health William Beaumont University Hospital, Royal Oak, Michigan.
Corewell Health William Beaumont University Hospital, Royal Oak, and Oakland University William Beaumont School of Medicine, Rochester, Michigan.
ACR Open Rheumatol. 2025 Apr;7(4):e70026. doi: 10.1002/acr2.70026.
Our objective was to review the available literature on cardiac magnetic resonance imaging (cMRI) findings in patients with antineutrophil cytoplasmic antibody-associated vasculitides (AAV), evaluate its diagnostic utility, and assess its potential as a screening tool.
We systematically searched PubMed, Embase, Scopus, and Web of Science from inception to March 29, 2023, following Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) 2020 guidelines. English-language studies involving adult patients diagnosed with AAV-eosinophilic granulomatosis with polyangiitis (EGPA), granulomatosis with polyangiitis (GPA), or microscopic polyangiitis (MPA)-using recognized classification criteria were included. Studies had to report specific cMRI parameters in at least three patients. Three independent reviewers conducted study selection, data extraction, and quality assessment.
Of 2,251 studies, 30 met the inclusion criteria, encompassing 1,149 patients with AAV (87% with EGPA, 13% with GPA, and 0.3% with MPA). The mean patient age was 52 ± 5 years, with 50.4% being female. The mean left ventricular ejection fraction (LVEF) was 55.6% ± 11.3%, and 29% of patients had an LVEF less than 50%. Myocardial fibrosis, indicated by late gadolinium enhancement (LGE), was present in 49% of patients, with predominantly subendocardial or endocardial (23%), intramyocardial (14%), and subepicardial (10%) patterns. Patients in remission (26%), when compared to those not in remission (74%), exhibited higher proportions of LGE (55% vs 47%) and glucocorticoid use (77% vs 68%), despite similar rates of abnormal electrocardiograms (44% vs 42%).
This systematic review reveals a high prevalence of myocardial fibrosis detected by cMRI in patients with AAV, even during remission. Significant subclinical cardiac involvement may be missed by conventional diagnostic methods, underscoring the utility of cMRI during routine evaluation.
我们的目的是回顾关于抗中性粒细胞胞浆抗体相关性血管炎(AAV)患者心脏磁共振成像(cMRI)结果的现有文献,评估其诊断效用,并评估其作为筛查工具的潜力。
我们按照系统评价和Meta分析的首选报告项目(PRISMA)2020指南,从数据库建立至2023年3月29日,系统检索了PubMed、Embase、Scopus和Web of Science。纳入了涉及使用公认分类标准诊断为AAV-嗜酸性肉芽肿性多血管炎(EGPA)、肉芽肿性多血管炎(GPA)或显微镜下多血管炎(MPA)的成年患者的英文研究。研究必须报告至少三名患者的特定cMRI参数。三名独立的审阅者进行了研究筛选、数据提取和质量评估。
在2251项研究中,30项符合纳入标准,涵盖1149例AAV患者(87%为EGPA,13%为GPA,0.3%为MPA)。患者的平均年龄为52±5岁,50.4%为女性。平均左心室射血分数(LVEF)为55.6%±11.3%,29%的患者LVEF低于50%。钆延迟增强(LGE)显示的心肌纤维化在49%的患者中存在,主要为心内膜下或内膜(23%)、心肌内(14%)和心外膜下(10%)模式。缓解期患者(26%)与未缓解期患者(74%)相比,LGE比例(55%对47%)和使用糖皮质激素的比例(77%对68%)更高,尽管心电图异常率相似(44%对42%)。
这项系统评价显示,AAV患者即使在缓解期,通过cMRI检测到的心肌纤维化患病率也很高。传统诊断方法可能会遗漏显著的亚临床心脏受累情况,这突出了cMRI在常规评估中的效用。