细胞移植在改善肢带肌营养不良病程中的作用:一项为期5年的纵向研究。

Degenerative Neurological and Neuromuscular Disease Pub Date : 2015-09-14 eCollection Date: 2015-01-01 DOI:10.2147/DNND.S71775
Alok Sharma, Hemangi Sane, Nandini Gokulchandran, Sushant Gandhi, Pradnya Bhovad, Dipti Khopkar, Amruta Paranjape, Khushboo Bhagwanani, Prerna Badhe
{"title":"细胞移植在改善肢带肌营养不良病程中的作用:一项为期5年的纵向研究。","authors":"Alok Sharma,&nbsp;Hemangi Sane,&nbsp;Nandini Gokulchandran,&nbsp;Sushant Gandhi,&nbsp;Pradnya Bhovad,&nbsp;Dipti Khopkar,&nbsp;Amruta Paranjape,&nbsp;Khushboo Bhagwanani,&nbsp;Prerna Badhe","doi":"10.2147/DNND.S71775","DOIUrl":null,"url":null,"abstract":"<p><p>Limb girdle muscular dystrophy (LGMD), a group of progressive degenerative disorders, causes functional limitation affecting the quality of life. Cell therapy is being widely explored and preliminary studies have shown beneficial effects. Cell therapy induces trophic-factors release, angiogenesis, anti-inflammation, and protein synthesis, which helps in the reparative process at the microcellular level. In this 5-year longitudinal study, the effect of autologous bone marrow mononuclear cells is studied on the natural course of 65 patients with LGMD. Functional Independence Measure and manual muscle testing showed statistically significant improvement, post-cell transplantation. The key finding of this study was demonstration of a plateau phase in the disease progression of the patients. No adverse events were noted. Autologous bone marrow mononuclear cells may be a novel, safe, and effective treatment approach to control the rate of progression of LGMD, thus improving the functional outcomes. Further randomized controlled trials are required.</p>","PeriodicalId":11147,"journal":{"name":"Degenerative Neurological and Neuromuscular Disease","volume":"5 ","pages":"93-102"},"PeriodicalIF":0.0000,"publicationDate":"2015-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2147/DNND.S71775","citationCount":"5","resultStr":"{\"title\":\"The role of cell transplantation in modifying the course of limb girdle muscular dystrophy: a longitudinal 5-year study.\",\"authors\":\"Alok Sharma,&nbsp;Hemangi Sane,&nbsp;Nandini Gokulchandran,&nbsp;Sushant Gandhi,&nbsp;Pradnya Bhovad,&nbsp;Dipti Khopkar,&nbsp;Amruta Paranjape,&nbsp;Khushboo Bhagwanani,&nbsp;Prerna Badhe\",\"doi\":\"10.2147/DNND.S71775\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Limb girdle muscular dystrophy (LGMD), a group of progressive degenerative disorders, causes functional limitation affecting the quality of life. Cell therapy is being widely explored and preliminary studies have shown beneficial effects. Cell therapy induces trophic-factors release, angiogenesis, anti-inflammation, and protein synthesis, which helps in the reparative process at the microcellular level. In this 5-year longitudinal study, the effect of autologous bone marrow mononuclear cells is studied on the natural course of 65 patients with LGMD. Functional Independence Measure and manual muscle testing showed statistically significant improvement, post-cell transplantation. The key finding of this study was demonstration of a plateau phase in the disease progression of the patients. No adverse events were noted. Autologous bone marrow mononuclear cells may be a novel, safe, and effective treatment approach to control the rate of progression of LGMD, thus improving the functional outcomes. Further randomized controlled trials are required.</p>\",\"PeriodicalId\":11147,\"journal\":{\"name\":\"Degenerative Neurological and Neuromuscular Disease\",\"volume\":\"5 \",\"pages\":\"93-102\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-09-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.2147/DNND.S71775\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Degenerative Neurological and Neuromuscular Disease\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2147/DNND.S71775\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2015/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Degenerative Neurological and Neuromuscular Disease","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2147/DNND.S71775","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2015/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

摘要

肢带性肌营养不良症(LGMD)是一组进行性退行性疾病,其导致的功能限制影响生活质量。细胞疗法正在被广泛探索,初步研究显示出有益的效果。细胞治疗诱导营养因子释放、血管生成、抗炎和蛋白质合成,这有助于在微细胞水平的修复过程。在这项为期5年的纵向研究中,研究了自体骨髓单个核细胞对65例LGMD患者自然病程的影响。细胞移植后,功能独立性测量和手工肌肉测试显示有统计学意义的改善。这项研究的关键发现是患者疾病进展的平台期。未发现不良事件。自体骨髓单个核细胞可能是一种新的、安全、有效的治疗方法,可以控制LGMD的进展速度,从而改善功能预后。需要进一步的随机对照试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The role of cell transplantation in modifying the course of limb girdle muscular dystrophy: a longitudinal 5-year study.

The role of cell transplantation in modifying the course of limb girdle muscular dystrophy: a longitudinal 5-year study.

Limb girdle muscular dystrophy (LGMD), a group of progressive degenerative disorders, causes functional limitation affecting the quality of life. Cell therapy is being widely explored and preliminary studies have shown beneficial effects. Cell therapy induces trophic-factors release, angiogenesis, anti-inflammation, and protein synthesis, which helps in the reparative process at the microcellular level. In this 5-year longitudinal study, the effect of autologous bone marrow mononuclear cells is studied on the natural course of 65 patients with LGMD. Functional Independence Measure and manual muscle testing showed statistically significant improvement, post-cell transplantation. The key finding of this study was demonstration of a plateau phase in the disease progression of the patients. No adverse events were noted. Autologous bone marrow mononuclear cells may be a novel, safe, and effective treatment approach to control the rate of progression of LGMD, thus improving the functional outcomes. Further randomized controlled trials are required.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信