利用心脏磁共振成像评估马凡综合征的心肌纤维化。

IF 1.5 4区 医学 Q4 GENETICS & HEREDITY Molecular Genetics & Genomic Medicine Pub Date : 2024-11-01 DOI:10.1002/mgg3.70024
Anthony Demolder, Dan Devos, Julie De Backer, Laura Muiño-Mosquera
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引用次数: 0

摘要

背景:心肌功能受损和心律失常是马凡氏综合征(MFS)的重要表现。评估心肌纤维化与这些表现相关性的研究很少:这项横断面单中心研究通过心脏磁共振成像(CMR)评估了携带(可能)致病性 FBN1 变异的马凡氏综合征患者的心室容积、心室功能和心肌纤维化。通过晚期钆增强(LGE)和细胞外容积测量(ECV)评估纤维化的存在和程度。从电子病历中提取了24小时Holter监测数据和临床数据:研究纳入了 32 名未经筛选的 MFS 患者(中位年龄 38 岁 [范围 10-69],41% 为女性)。未发现局灶性心肌纤维化。6名患者(21%)有弥漫性纤维化(ECV > 29%)。弥漫性纤维化的存在与临床相关的心肌功能障碍之间没有关联。五名患者(16%)的左心室射血分数降低(LVEF 29%)。MAD患者的左心室指数容积增大(舒张末期容积中位数为92 mL/m2 [IQR, 78-100] vs. 78 mL/m2 [IQR, 71-87];收缩末期容积中位数为31 mL/m2 [IQR, 23-46] vs. 22 mL/m2 [IQR, 21-28]),在调整二尖瓣和主动脉瓣反流的存在后也是如此。有二尖瓣反流和没有二尖瓣反流的患者之间的心血管容量没有差异:在这组 MFS 患者中,CMR 未检测到局灶性心肌纤维化。虽然在 21% 的患者中观察到了弥漫性纤维化,但并未发现与临床相关的心肌功能障碍有明显联系。进一步的研究应评估弥漫性纤维化对临床结果预测的影响。
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Assessment of Myocardial Fibrosis in Marfan Syndrome Using Cardiac Magnetic Resonance Imaging.

Background: Impaired myocardial function and arrhythmia are important manifestations of Marfan syndrome (MFS). Studies assessing myocardial fibrosis in relation to these manifestations are scarce.

Methods: This cross-sectional, single-center study assessed ventricular volumes, ventricular function, and myocardial fibrosis by cardiac magnetic resonance imaging (CMR) in patients with MFS harboring a (likely) pathogenic FBN1 variant. The presence and extent of fibrosis were assessed by late gadolinium enhancement (LGE) and extracellular volume measurement (ECV). Data on 24-h Holter monitoring and clinical data were extracted from electronic patient records.

Results: The study included 32 unselected patients with MFS (median age 38 years [range 10-69], 41% women). No focal myocardial fibrosis was detected. Six patients (21%) had diffuse fibrosis (ECV > 29%). No association was found between the presence of diffuse fibrosis and clinically relevant myocardial dysfunction. Five patients (16%) had reduced left ventricular ejection fraction (LVEF < 55%). While all of these exhibited mitral annular disjunction (MAD), only two had ECV > 29%. Patients with MAD had increased indexed LV volumes (median end-diastolic volume, 92 mL/m2 [IQR, 78-100] vs. 78 mL/m2 [IQR, 71-87]; median end-systolic volume, 31 mL/m2 [IQR, 23-46] vs. 22 mL/m2 [IQR, 21-28]), also after adjusting for the presence of mitral and aortic valve regurgitation. No differences in ECV were seen between patients with and without MAD.

Conclusions: In this cohort of patients with MFS, focal myocardial fibrosis was not detected using CMR. Although diffuse fibrosis was observed in 21% of patients, no evident connection to clinically relevant myocardial dysfunction was found. Further studies should evaluate the impact of diffuse fibrosis on clinical outcome prediction.

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来源期刊
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
4.20
自引率
0.00%
发文量
241
审稿时长
14 weeks
期刊介绍: Molecular Genetics & Genomic Medicine is a peer-reviewed journal for rapid dissemination of quality research related to the dynamically developing areas of human, molecular and medical genetics. The journal publishes original research articles covering findings in phenotypic, molecular, biological, and genomic aspects of genomic variation, inherited disorders and birth defects. The broad publishing spectrum of Molecular Genetics & Genomic Medicine includes rare and common disorders from diagnosis to treatment. Examples of appropriate articles include reports of novel disease genes, functional studies of genetic variants, in-depth genotype-phenotype studies, genomic analysis of inherited disorders, molecular diagnostic methods, medical bioinformatics, ethical, legal, and social implications (ELSI), and approaches to clinical diagnosis. Molecular Genetics & Genomic Medicine provides a scientific home for next generation sequencing studies of rare and common disorders, which will make research in this fascinating area easily and rapidly accessible to the scientific community. This will serve as the basis for translating next generation sequencing studies into individualized diagnostics and therapeutics, for day-to-day medical care. Molecular Genetics & Genomic Medicine publishes original research articles, reviews, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented.
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