Department of Biomedical Sciences and of Morphologic and Functional Images, University of Messina, AOU "Policlinico G. Martino", Via Consolare Valeria 1, 98125 Messina, Italy.
Mol Genet Metab. 2013 Nov;110(3):290-6. doi: 10.1016/j.ymgme.2013.06.023. Epub 2013 Jul 9.
Late onset Pompe disease (LOPD) is a rare muscle disorder often characterized, along the disease course, by severe respiratory failure. We describe herein respiratory muscles and lung abnormalities in LOPD patients using MR imaging and CT examinations correlated to pulmonary function tests. Ten LOPD patients were studied: 6 with a limb-girdle muscle weakness, 1 with myalgias, 2 with exertional dyspnoea and 1 with isolated hyperckemia. Respiratory function was measured using forced vital capacity (FVC) in both upright and supine positions, maximal inspiratory pressure (MIP), maximal expiratory pressure (MEP) and peak cough flow (PCF) tests. The involvement (atrophy) of diaphragms, abdominal respiratory muscles and intercostal muscles was ranked by CT and MRI examinations using appropriate scales. Height of lungs and band-like atelectasis presence were also recorded. Seven out of 10 patients showed a functional diaphragmatic weakness (FVC drop percentage >25%). In 8 out of 10 patients, involvement of both diaphragms and of other respiratory muscles was seen. The mean height of lungs in patients was significantly reduced when compared to a control group. Marked elevation of the diaphragms (lung height < 15 cm) was also seen in 6 patients. Multiple unilateral or bilateral band-like atelectasis were found in 4 patients. Statistically significant correlations were found between diaphragm atrophy grading, evaluated by MRI and CT, and FVC in supine position, FVC drop percentage passing from upright to supine position, PCF and MIP. Our data showed that diaphragm atrophy, often associated to reduced lung height and band-like atelectasis, can be considered the CT-MRI hallmark of respiratory insufficiency in LOPD patients. Early recognition of respiratory muscles involvement, using imaging data, could allow an early start of enzyme replacement therapy (ERT) in LOPD.
迟发性庞贝病(LOPD)是一种罕见的肌肉疾病,通常在疾病过程中表现为严重的呼吸衰竭。我们通过磁共振成像(MRI)和计算机断层扫描(CT)检查,并与肺功能测试相关联,来描述 LOPD 患者的呼吸肌和肺部异常。研究了 10 名 LOPD 患者:6 名肢体无力,1 名肌肉疼痛,2 名运动性呼吸困难,1 名孤立性高肌酸血症。使用直立和仰卧位的用力肺活量(FVC)、最大吸气压力(MIP)、最大呼气压力(MEP)和峰值咳嗽流量(PCF)测试来测量呼吸功能。使用适当的量表通过 CT 和 MRI 检查对膈肌、腹部呼吸肌和肋间肌的受累(萎缩)程度进行分级。还记录了肺部的高度和带型肺不张的存在。10 名患者中有 7 名出现功能性膈肌无力(FVC 下降百分比>25%)。10 名患者中有 8 名出现了膈肌和其他呼吸肌的受累。与对照组相比,患者的肺部平均高度明显降低。在 6 名患者中也观察到膈肌明显升高(肺高度<15cm)。4 名患者发现了多个单侧或双侧带型肺不张。通过 MRI 和 CT 评估的膈肌萎缩分级与仰卧位 FVC、从直立位到仰卧位 FVC 下降百分比、PCF 和 MIP 之间存在统计学显著相关性。我们的数据表明,膈肌萎缩,常伴有肺高度降低和带型肺不张,可被视为 LOPD 患者呼吸功能不全的 CT-MRI 标志。使用影像学数据早期识别呼吸肌受累,可以在 LOPD 中早期开始酶替代治疗(ERT)。