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磁共振成像在肌营养不良疾病诊断中的应用价值 被引量:1

Magnetic resonance imaging for the diagnosis of muscular dystrophy
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摘要 目的总结肌营养不良(muscular dystrophy,MD)常见亚型下肢肌肉骨骼肌磁共振成像(magnetic resonance imaging,MRI)特点,积累应用MRI协助诊断MD的经验。方法选取经基因检测确诊的48例MD患儿为研究对象,分析其下肢肌肉MRI特点,统计各亚型肌肉脂肪浸润累计评分,并分析Duchenne型肌营养不良脂肪浸润累计评分与临床指标的相关性。结果Duchenne型肌营养不良以臀大肌、大收肌受累为著,Becker型肌营养不良以股外侧肌受累为著,肢带型肌营养不良以大收肌、股中间肌、股内侧肌、股外侧肌受累为著。Duchenne型肌营养不良下肢肌肉脂肪浸润累计评分与年龄、病程、肌肉力量及运动功能明显相关(P<0.05),与血清肌酸激酶无相关性(P>0.05)。结论不同亚型MD的MRI表现特点不同,MRI有助于MD的诊断与病情评估。 Objective To summarize the skeletal muscle magnetic resonance imaging(MRI)features of the lower limbs in common subtypes of muscular dystrophy(MD)and the experience in the application of MRI in the diagnosis of MD.Methods A total of 48 children with MD who were diagnosed by genetic testing were enrolled as subjects.The muscle MRI features of the lower limbs were analyzed.Cumulative fatty infiltration score was calculated for each subtype,and the correlation of cumulative fatty infiltration score with clinical indices was analyzed for Duchenne muscular dystrophy(DMD).Results DMD was characterized by the involvement of the gluteus maximus and the adductor magnus.Becker muscular dystrophy was characterized by the involvement of the vastus lateralis muscle.Limb-girdle muscular dystrophy was characterized by the involvement of the adductor magnus,the vastus intermedius,the vastus medialis,and the vastus lateralis muscle.For DMD,the cumulative fatty infiltration score of the lower limb muscles was significantly correlated with age,course of the disease,muscle strength,and motor function(P<0.05),while it was not significantly correlated with the serum creatine kinase level(P>0.05).Conclusions Different subtypes of MD have different MRI manifestations,and MRI may help with the diagnosis and assessment of MD.
作者 唐静 张家鹏 杨学军 钟京梓 谢彦舒 孟琦 蓝丹 TANG Jing;ZHANG Jia-Peng;YANG Xue-Jun;ZHONG Jing-Zi;XIE Yan-Shu;MENG Qi;LAN Dan(Department of Pediatrics,First Affiliated Hospital of Guangxi Medical University,Nanning 530021,China)
出处 《中国当代儿科杂志》 CAS CSCD 北大核心 2022年第11期1231-1237,共7页 Chinese Journal of Contemporary Pediatrics
基金 国家自然科学基金(81760215)。
关键词 磁共振成像 肌营养不良 DUCHENNE肌营养不良 诊断 儿童 Magnetic resonance imaging Muscular dystrophy Duchenne muscular dystrophy Diagnosis Child
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  • 1Bushby K, Finkel R, Birnkrant D J, et al. Diagnosis and management of Duchenne muscular dystrophy, part 1 : diagnosis, and pharmacological and psychosocial management [ J ]. Lancet Neurol, 2010, 9 ( 1 ) : 77-93. DO!: 10. 1016/S1474-4422 (09)70271-6.
  • 2Engel AG, Franzini-Armatrong C. Myology [ M ]. 3rd ed. New York : McGraw-Hill Inc, 2004 : 961-1025.
  • 3Zhang H, Zhu Y, Sun Y, et al. Serum creatinine level: a supplemental index to distinguish Duchenne muscular dystrophy from Becker muscular dystrophy [ J ]. Dis Markers, 2015, 2015 : 141856. DOI: 10. 1155/2015/141856.
  • 4Wagner KR, Lechtzin N, Judge DP. Current treatment of adult Duchenne muscular dystrophy[ J]. Bioehim Biophys Aeta, 2007, 1772 (2) : 229-237. DOI : 10. 1016/j. bbadis. 2006.06. 009.
  • 5Li X, Zhao L, Zhou S, et al. A comprehensive database of Duchenne and Becket muscular dystrophy patients (0-18 years old) in East China[J]. Orphanet J Rare Dis, 2015, 10: 5. DOI: 10. 1186/s13023-014-0220-7.
  • 6Yang J, Li SY, Li YQ, et al. MLPA-based genotype-phenotype analysis in 1053 Chinese patients with DMD/BMD[ J]. BMC Med Genet, 2013, 14: 29. DOI: 10. 1186/1471-2350-14-29.
  • 7Chen WJ, Lin QF, Zhang QJ, et al. Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation- dependent probe amplification and Sanger sequencing [ J ]. C/in Chim Acta, 2013, 423 : 35-38. DOI: 10. 1016/j. cca. 2013.04. 006.
  • 8Bushby K, Finkel R, Birnkrant DJ, et al. Diagnosis and management of Duehenne muscular dystrophy, part 2: implementation of muhidiseiplinary care [ J ]. Lancet Neurol, 2010, 9 (2) : 177-189. DOI : 10. 1016/S1474-4422 ( 09 ) 70272- 8.
  • 9Bowles DE, McPhee SW, Li C, et al. Phase 1 gene therapy for Duchenne muscular dystrophy using a translational optimized AAV vector[J]. Mol Ther, 2012, 20(2) : 443-455. DOI: 10. 1038/ mt. 2011. 237.
  • 10Li HL, Fujimoto N, Sasakawa N, et al. Precise correction of the dystrophin gene in duchenne muscular dystrophy patient induced pluripotent stem ceils by TALEN and CRISPR-Cas9 [ J ]. Stem Cell Reports, 2015, 4( 1 ) : 143-154. DOI: 10. 1016/j. stemcr. 2014.10. 013.

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