期刊文献+

dysferlinopathy 患者大腿骨骼肌 MRI 改变及其与临床表现的相关性 被引量:8

Muscle magnetic resonance imaging changes and relationship with clinical symptoms in patients with dysferlinopathy
原文传递
导出
摘要 目的:探讨dysferlinopathy患者大腿肌肉水肿及脂肪化规律及其与临床表现之间的关系。方法收集2005-2013年就诊于北京大学第一医院的32例dysferlinopathy患者,包括13例肢带型肌营养不良2B型(limb girdle muscular dystrophy type 2B,LGMD2B)、13例Miyoshi肌病、4例近远端肌病及2例高肌酸激酶血症患者。对患者进行改良Gardner-Medwin and Walton ( GM-W)评分和大腿肌肉MRI检查,对MRI的脂肪化和水肿改变进行评分。计算LGMD2B和Miyoshi肌病患者在发病年龄、病程、GM-W评分、肌肉脂肪化和水肿评分以及分布模式之间的差异,并分析所有患者大腿肌肉脂肪化和水肿总评分与其病程、GM-W评分之间的相关性。结果所有患者的GM-W中位数评分为4.00(2.00,5.00)分,其中LGMD2B为4.00(3.00,4.50)分,Miyoshi肌病为4.00(2.00,5.00)分。30例患者(93.75%)出现肌肉脂肪化,在LGMD2B和Miyoshi肌病患者中分布模式相同,骨骼肌脂肪化平均总评分为(28.20±12.86)分,其中 LGMD2B 为(28.50±13.03)分,Miyoshi 肌病为(29.00±12.63)分。26例患者(81.25%)存在肌肉水肿,在LGMD2B和Miyoshi肌病患者中分布模式相同,骨骼肌水肿平均总评分为(18.36±13.60)分。其中LGMD2B为(22.88±11.59)分,Miyoshi 肌病为(16.77±13.80)分。两组患者在发病年龄、病程、GM-W评分、肌水肿和脂肪化评分之间差异无统计学意义。所有患者的肌肉脂肪化总评分与其GM-W评分( rs =0.737,P=0.000)和病程( rs =0.637, P=0.000)均呈正相关。结论大腿肌肉脂肪化和水肿均是dysferlinopathy 患者常见的MRI改变,主要临床亚型具有类似的影像学改变。肌肉脂肪化可用于该病的进展评估。 Objective To investigate the characteristics of muscle edema and fatty infiltration in thighs and relationship with clinical symptoms in Chinese patients with different phenotypes of dysferlinopathy.Methods A total of 32 patients were enrolled , including 13 limb-girdle muscular dystrophy 2B (LGMD2B), 13 Miyoshi myopathy (MM), 4 proximodistal myopathy and 2 hyper-creatine-kinase-emia.Clinical symptoms were evaluated using modified Gardner-Medwin and Walton ( GM-W) score.Muscle MRI was performed in thighs to observe fatty infiltration and edema.We then compared the age of onset , disease duration, GM-W score, muscle edema and muscle fatty infiltration between LGMD 2B and MM groups,and the relationship of muscle edema score and fatty infiltration score with disease duration and GM-W score in all patients.Results The median GM-W score was 4.00 (2.00,5.00) in all patients, 4.00 (3.00,4.50)in LGMD2B and 4.00(2.00,5.00)in MM, respectively.Muscle fatty infiltration appeared in 30 cases (93.75%), with the same pattern in LGMD2B and MM.The mean fatty infiltration score was 28.20 ±12.86 in all patients, 28.50 ±13.03 in LGMD2B and 29.00 ±12.63 in MM, respectively.Muscle edema appeared in 26 cases (81.25%) with same pattern in LGMB2B and MM.The mean edema score was 18.36 ±13.60 in all patients, 22.88 ±11.59 in LGMD2B and 16.77 ±13.80 in MM.The age of onset , disease duration, GM-W score, muscle fatty infiltration and edema score were not significantly different between LGMD2B and MM patients.Muscle fatty infiltration score significantly correlated with GM-W score (rs=0.737,P=0.000) and disease duration (rs=0.637,P=0.000).Conclusions Fatty infiltration and edema in thigh muscles are very common in patients with dysferlinopathy , with similar radiological changes in main subtypes.The muscle fatty infiltration can be used as a predictor of disease progression.
出处 《中华神经科杂志》 CAS CSCD 北大核心 2014年第6期412-417,共6页 Chinese Journal of Neurology
基金 科技部一二五重大专项课题资助项目(2011ZX09307-001-07)
关键词 肌营养不良 肢带型 骨骼 水肿 磁共振成像 Muscular dystrophies,limb-girdle Leg Muscle,skeletal Edema Magnetic resonance imaging
  • 相关文献

参考文献16

  • 1张丽冉,胡静,赵哲,李娜,沈宏锐,邴琪.dysferlinopathy患者40例临床和病理分析[J].中华神经科杂志,2013,46(7):438-442. 被引量:3
  • 2Amato AA, Brown RH Jr. Dysferlinopathies [ J ]. Handb Clin Neurol, 2011, 101 : 111-118. 被引量:1
  • 3刘琳琳,杜婧,肖江喜,袁云.磁共振成像在骨骼肌疾病的临床应用研究进展[J].中华神经科杂志,2014,47(1):49-51. 被引量:12
  • 4Kesper K, Kornblum C, Reimann J, et al. Pattern of skeletal muscle involvement in primary dysferlinopathies: a whole-body 3.0-T magnetic resonance imaging study [ J ]. Acta Neurol Scand, 2009, 120: 111-118. 被引量:1
  • 5Brummer D, Walter MC, Palmbaeh M, et al. Long-term MRI and clinical follow-up of symptomatic and presymptomatie carriers of dysferlin gene mutations [ J ]. Aeta Myol, 2005, 24: 6-16. 被引量:1
  • 6Okahashi S, Ogawa G, Suzuki M, et al. Asymptomatic sporadic dysferlinopathy presenting with elevation of serum ereatine kinase. Typical distribution of muscle involvement shown by MRI but not by CT [J]. Intern Med, 2008, 47: 305-307. 被引量:1
  • 7Paradas C, Llauger J, Diaz-Manera J, et al. Redefining dysferlinopathy phenotypes based on clinical findings and muscle imaging studies [J]. Neurology, 2010, 75: 316-323. 被引量:1
  • 8Angelini C, Peterle E, Gaiani A, et al. Dysferlinopathy course and sportive activity:clues for possible treatment [J]. Acta Myol, 2011, 30: 127-132. 被引量:1
  • 9Mereuri E, Piehieeehio A, Allsop J, et al. Muscle MRI in inherited neuromuscular disorders:past, present, and future [ J]. J Magn Reson Imaging, 2007, 25: 433-440. 被引量:1
  • 10Stramare R, Beltrame V, Dal Borgo R, et al. MRI in the assessment of muscular pathology: a comparison between limb- girdle muscular dystrophies, hyaline body myopathies and myotonic dystrophies [ J]. Radiol Med, 2010, 115 : 585-599. 被引量:1

二级参考文献40

  • 1袁云.骨骼肌疾病的临床病理诊断[J].中华神经科杂志,2006,39(8):505-507. 被引量:12
  • 2Glover L, Brown RH Jr. Dysferlin in membrane trafficking and patch repair. Traffic, 2007, 8 : 785-794. 被引量:1
  • 3Therrien C, Dodig D, Karpati G, et al. Mutation impact on dysferlin inferred from database analysis and computer-based structural predictions. J Neurol Sci, 2006, 250 : 71-78. 被引量:1
  • 4Bansal D, Miyake K, Vogel SS, et al. Defective membrane repair in dysferlin-deficient muscular dystrophy. Nature, 2003, 423 : 168-172. 被引量:1
  • 5Ho M, Gallardo E, McKenna-Yasek D, et al. A novel, blood- based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathy. Ann Neural, 2002,51: 129-133. 被引量:1
  • 6Mahjneh I, Marconi G, Bushby K, et al. Dysferlinopathy (LGMD2B) : a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations. Neuromuscul Disord, 2011, 11 : 20-26. 被引量:1
  • 7Illa I, Serrano-Munuera C, Gallardo E, et al. Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype. Ann Neurol, 2001,49:130-134. 被引量:1
  • 8Han R, Campbell KP. Dysferlin and muscle membrane repair. Curt Opin Cell Biol, 2007,19 : 409-416. 被引量:1
  • 9McNeil PL. Repairing a torn cell surface : make way, lysosomes to the rescue. J Cell Sci, 2002, 115: 873-879. 被引量:1
  • 10Lennon NJ , Kho A, Bacskai B J, et al. Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing. J Biol Chem, 2003, 278: 50466-50473. 被引量:1

共引文献15

同被引文献74

  • 1赵重波,卢家红,吕传真.肢带型肌营养不良症[J].中国临床神经科学,2005,13(2):198-201. 被引量:6
  • 2任守臣,焉传祝,李茂绪,刘淑萍,吴金玲,赵玉英,李伟,李大年.肢带型肌营养不良和Miyoshi肌病dysferlin表达分析[J].中华医学杂志,2007,87(21):1486-1490. 被引量:6
  • 3Amato AA, Brown RH Jr. Dysferlinopathies[J]. Handb Clin Neurol, 2011, 101:111-118. 被引量:1
  • 4Blandin G, Beroud C, Labelle V, et al. UMD-DYSF, a novel locus specific database for the compilation and interactive analysis of mu- tations in the dysferlin gene[J]. Hum Murat, 2012, 33: E2317-2331. 被引量:1
  • 5Ro LS, Lee-Chen GJ, Lin TC, et al. Phenotypic features and genetic findings in 2 chinese families with Miyoshi distal myopathy[J]. Arch Neurol, 2004, 61:1594-1599. 被引量:1
  • 6Shunchang S, Fan Q, Huacheng W, et al. Dysferlin mutation in a Chinese pedigree with Miyoshi myopathy[J]. Clin Neurol Neurosurg, 2006, 108:369-373. 被引量:1
  • 7Zhao Z, Hu J, Sakiyama Y, et al. DYSF mutation analysis in a group of Chinese patients with dysferlinopathy[J]. Clin Neurol Neurosurg, 2013, 115:1234-1237. 被引量:1
  • 8Xi J, Btandin G, Lu J, et al. Clinical heterogeneity and a high pro- portion of novel mutations in a Chinese cohort of patients with dys- ferlinopathy[J]. Neurol India, 2014, 62:635-639. 被引量:1
  • 9Bashir R, Britton S, Strachan T, et al. A gene related to Caenorhab- ditis elegans spermatogenesis factor fer- 1 is mutated in limb-girdle muscular dystrophy type 2B[J]. Nat Genet, 1998, 20:37-42. 被引量:1
  • 10Ho M, Gallardo E, Mckenna-Yasek D, et al. A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathy[J]. Ann Neurol, 2002, 51 : 129-133. 被引量:1

引证文献8

二级引证文献21

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部