上肢(PUL)模块在肢带性肌萎缩症中的作用。

Q3 Medicine Acta Myologica Pub Date : 2022-01-01 DOI:10.36185/2532-1900-084
Eleonora Diella, Antonella LoMauro, Morena Delle Fave, Rossella Cima, Maria Grazie D'Angelo
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引用次数: 0

摘要

四肢带状肌营养不良症(LGMD)是一种遗传性肌肉疾病,导致肢体近端肌肉组织无力和萎缩。当不能行走时,必须将注意力转移到上肢肌肉的功能上。我们通过上肢表现量表和上肢MRC评分对15例LGMDR1/LGMD2A和13例LGMDR2/LGMD2B的上肢肌力及相应功能进行了研究。LGMD2B/R2组近端K项和远端N、R项较低。在LGMD2B/ r2中,K项各肌肉的平均MRC评分呈线性相关(r2 = 0.922)。LGMD2B/R2的功能恶化与肌肉无力平行。相比之下,在近端水平,尽管存在肌肉无力,LGMD2A/R1的功能仍被保留,可能是由于代偿策略。有时,参数的组合可能比单独考虑它们更能提供信息。PUL量表和MRC可能是非流动患者的有趣结果测量。
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The Performance of Upper Limb (PUL) module in limb-girdle muscular dystrophy.

Limb-girdle muscular dystrophy (LGMD) is a genetic muscle disorder causing weakness and wasting of the proximal limb musculature. When ambulation is lost, the attention must be shifted to the upper limb muscles' function. We studied the upper limb muscle strength and the corresponding function in 15 LGMDR1/LGMD2A and 13 LGMDR2/LGMD2B, through the Performance of Upper Limb scale and the MRC score of upper limbs. The proximal item K and the distal items N and R were lower in LGMD2B/R2. The mean MRC score of all the muscles involved linearly correlated (r2 = 0.922) for item K in LGMD2B/R2. The functional worsening paralleled the muscles weakness in LGMD2B/R2. By contrast, at proximal level the function of LGMD2A/R1 was preserved despite muscle weakness was present, presumably due to compensatory strategies. Sometimes the combination of parameters might be more informative than considering them separately. PUL scale and MRC might be interesting outcome measures in non-ambulant patients.

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来源期刊
Acta Myologica
Acta Myologica Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.70
自引率
0.00%
发文量
0
期刊最新文献
PROCEEDINGS OF THE XXIII CONGRESS OF THE ITALIAN ASSOCIATION OF MYOLOGY: PadovaJune 8-10, 2023. Year 2023: a new look for Acta Myologica. Experience with telemedicine in neuromuscular clinic during COVID-19 pandemic. VCP-related myopathy: a case series and a review of literature. Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.
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