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口腔呼吸链酶功能障碍的非侵入性评估在线粒体疾病中的应用:与肌肉活检研究的比较

Non-invasive evaluation of buccal respiratory chain enzyme dysfunction in mitochondrial disease: comparison with studies in muscle biopsy.

机构信息

Section of Neurology, Department of Pediatrics, St. Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA 19134, USA.

出版信息

Mol Genet Metab. 2012 Mar;105(3):457-62. doi: 10.1016/j.ymgme.2011.11.193. Epub 2011 Nov 30.

DOI:10.1016/j.ymgme.2011.11.193
PMID:22189081
Abstract

Making a diagnosis of mitochondrial disease (MD) is extremely challenging and often employs the analysis of respiratory complex (RC) activities in biopsied skeletal muscle. Given both the invasive nature and expense of biopsied-muscle based testing for mitochondrial defects, buccal swab enzyme analysis has been explored as an alternative approach to the more invasive muscle biopsy. Case studies have recently suggested that buccal swabs from patients can be used to accurately assess mitochondrial enzyme activities including RC I and RC IV using a dipstick methodology combined with spectrophotometric analysis. In this study, forty patients with suspected MD who have previously been found to have significant defects in either RC I or RC IV in skeletal muscle were assessed by buccal swab analysis and compared to enzyme values obtained with unaffected controls (n=106) in the same age range. Buccal citrate synthase was used as an indicator of overall mitochondrial content, correlating well with overall buccal mitochondrial frataxin levels and was found to be elevated above control levels in 28% of the patients in this cohort. Of 26 cases with significant muscle RC I deficiency, 20 displayed significantly reduced levels of buccal RC I activity. All 7 of the patients with muscle RC IV deficiency showed significant buccal RC IV defect and 6 of the 7 patients with combined defects in muscle RC I and IV activity levels also exhibited analogous deficiencies in both buccal RC I and RC IV activities. In conclusion, the relatively high correlation (over 82%) of buccal and muscle RC deficiencies further supports the validity of this non-invasive approach as a potentially useful tool in the diagnosis of MD.

摘要

诊断线粒体疾病 (MD) 极具挑战性,通常需要分析活检骨骼肌中的呼吸复合物 (RC) 活性。鉴于基于肌肉活检的线粒体缺陷检测具有侵入性和昂贵的特点,人们探索了使用口腔拭子酶分析作为替代方法。最近的病例研究表明,使用比色法联合分光光度分析,通过一种试纸方法可以从患者的口腔拭子中准确评估线粒体酶活性,包括 RC I 和 RC IV。在这项研究中,对 40 名患有疑似 MD 的患者进行了口腔拭子分析,并与同一年龄范围内的 106 名无异常对照者(n=106)的酶值进行了比较。口腔柠檬酸合酶被用作整体线粒体含量的指标,与整体口腔线粒体 frataxin 水平密切相关,并且在该队列中的 28%的患者中发现其水平高于对照水平。在 26 例 RC I 肌肉严重缺乏的病例中,有 20 例显示口腔 RC I 活性明显降低。所有 7 例 RC IV 肌肉缺乏的患者均表现出明显的口腔 RC IV 缺陷,并且在 7 例 RC I 和 IV 肌肉活性水平均有缺陷的患者中,有 6 例也表现出口腔 RC I 和 RC IV 活性的类似缺陷。总之,口腔和肌肉 RC 缺陷的相对高相关性(超过 82%)进一步支持了这种非侵入性方法作为 MD 诊断的潜在有用工具的有效性。

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