Literature DB >> 11176364

Correlation between progression of spinal deformity and pulmonary function in Duchenne muscular dystrophy.

T Yamashita1, K Kanaya, K Yokogushi, Y Ishikawa, R Minami.   

Abstract

The purpose of this study was to investigate how age at and value of the plateau of vital capacity (VC plateau) correlate with the severity of the progression of spinal deformity in patients with Duchenne muscular dystrophy (DMD). Changes in spinal deformity and pulmonary function in 36 DMD patients were examined in a retrospective longitudinal study. Patterns of progression of spinal deformity were classified into three types according to Oda's classification. Of the 32 patients who showed spinal deformity, six were classified as type 1, 19 as type 2, and seven as type 3. The correlation between the patterns of progression of spinal deformity and the VC plateau was examined using a discriminant analysis. Rapid and severe progression of spinal deformity could be expected in patients whose VC plateau was less than 1,900 mL and in those in which it occurred before age 14 years. Thus VC plateau may be an indicator of the severity of the progression of spinal deformity in DMD patients.

Entities:  

Mesh:

Year:  2001        PMID: 11176364     DOI: 10.1097/00004694-200101000-00022

Source DB:  PubMed          Journal:  J Pediatr Orthop        ISSN: 0271-6798            Impact factor:   2.324


  3 in total

1.  Successful surgery for scoliosis supported by pulmonary rehabilitation in a duchenne muscular dystrophy patient with forced vital capacity below 10%.

Authors:  Jang Woo Lee; Yu Hui Won; Won Ah Choi; Soon Kyu Lee; Seong Woong Kang
Journal:  Ann Rehabil Med       Date:  2013-12-23

2.  Arginine metabolism by macrophages promotes cardiac and muscle fibrosis in mdx muscular dystrophy.

Authors:  Michelle Wehling-Henricks; Maria C Jordan; Tomomi Gotoh; Wayne W Grody; Kenneth P Roos; James G Tidball
Journal:  PLoS One       Date:  2010-05-21       Impact factor: 3.240

3.  Surgical management of severe scoliosis with high-risk pulmonary dysfunction in Duchenne muscular dystrophy.

Authors:  Masashi Takaso; Toshiyuki Nakazawa; Takayuki Imura; Naonobu Takahira; Moritoshi Itoman; Kazuhisa Takahashi; Masashi Yamazaki; Seiji Otori; Tsutomu Akazawa; Shohei Minami; Toshiaki Kotani
Journal:  Int Orthop       Date:  2009-04-02       Impact factor: 3.075

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.