Early cardiac mechanics abnormalities in patients with mitochondrial diseases

IF 3.9 3区 生物学 Q2 CELL BIOLOGY
Rosa Lillo , Maria Chiara Meucci , Silvia Malara , Guido Primiano , Serenella Servidei , Antonella Lombardo , Maria Grandinetti , Massimo Massetti , Gaetano Antonio Lanza , Giuseppe Limongelli , Francesca Graziani
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Abstract

Background

Evidence about early cardiac mechanics abnormalities in patients with mitochondrial diseases (MDs) before overt cardiomyopathy is limited.

Methods

In this prospective study, we performed a comparative analysis of conventional and speckle tracking echocardiographic parameters between patients with genetically identified MDs and no overt cardiomyopathy vs controls matched for age, sex and cardiovascular risk factors. The Newcastle mitochondrial disease adult scale (NMDAS) was calculated, using a threshold of > 21 as indicator of high disease severity.

Results

We enrolled 24 MDs patients (50 % males, mean age 47.2 ± 14.3 years), the most prevalent mutation was the MT-TL1 m.3243A>G (37.5 %). In MDs patients all dimensional echocardiographic parameters were similar to controls. Conversely, albeit normal, Tissue Doppler septal systolic (p = 0.002) and early diastolic velocities (p = 0.016) were significantly lower and E/e’ ratio was higher (p = 0.032) in MDs. Moreover, LV-GLS was significantly reduced in MDs as compared to their counterparties (20.2 ± 1.6 vs 22.6 ± 1.5, p < 0.001). Similarly, LA reservoir and conduit strain were significantly lower in MDs (31.7 ± 7.0 vs 35.9 ± 6.6, p = 0.038; 19.7 ± 5.6 vs 23.1 ± 6.0, p = 0.049 respectively), while LA contractile strain was similar between the two groups. Lower values of LV-GLS were observed in patients with NMDAS > 21 vs patients with NMDAS ≤ 21 (19.0 ± 1.2 vs 21.0 ± 1.3, p = 0.001).

Conclusions

In patients with MDs and no overt cardiomyopathy Tissue Doppler and speckle tracking analysis unveil worse LV systolic and diastolic function indices as compared to controls. Reduced LV-GLS values were found especially in those with worse disease burden.

线粒体疾病患者的早期心脏力学异常。
背景:方法:在这项前瞻性研究中,我们对比分析了经基因鉴定的线粒体疾病患者和无明显心肌病患者与年龄、性别和心血管风险因素匹配的对照组之间的常规和斑点追踪超声心动图参数。我们计算了纽卡斯尔线粒体疾病成人量表(NMDAS),以大于 21 为疾病严重程度的临界值:我们招募了 24 名 MDs 患者(50% 为男性,平均年龄为 47.2 ± 14.3 岁),最常见的突变是 MT-TL1 m.3243A.G(37.5%)。MDs 患者的所有超声心动图参数均与对照组相似。相反,MDs 患者的组织多普勒室间隔收缩速度(p = 0.002)和舒张早期速度(p = 0.016)显著降低,E/e'比值较高(p = 0.032),尽管正常。此外,与NMDAS≤21的患者相比,MD患者的LV-GLS明显降低(20.2 ± 1.6 vs 22.6 ± 1.5,p 21 vs 19.0 ± 1.2 vs 21.0 ± 1.3,p = 0.001):组织多普勒和斑点追踪分析显示,与对照组相比,MDs 患者的左心室收缩和舒张功能指数较差。特别是在疾病负担较重的患者中,发现 LV-GLS 值降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Mitochondrion
Mitochondrion 生物-细胞生物学
CiteScore
9.40
自引率
4.50%
发文量
86
审稿时长
13.6 weeks
期刊介绍: Mitochondrion is a definitive, high profile, peer-reviewed international research journal. The scope of Mitochondrion is broad, reporting on basic science of mitochondria from all organisms and from basic research to pathology and clinical aspects of mitochondrial diseases. The journal welcomes original contributions from investigators working in diverse sub-disciplines such as evolution, biophysics, biochemistry, molecular and cell biology, genetics, pharmacology, toxicology, forensic science, programmed cell death, aging, cancer and clinical features of mitochondrial diseases.
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