Previous Page  5 / 13 Next Page
Information
Show Menu
Previous Page 5 / 13 Next Page
Page Background

Notes:

Page 29

Regenerative & Precision Medicine 2016

December 1-2, 2016

Volume 7, Issue 3(Suppl)

J Tissue Sci Eng

ISSN: 2157-7552 JTSE, an open access journal

conferenceseries

.com

December 1-2, 2016 | San Antonio, USA

Global Congress on

Tissue Engineering, Regenerative &

Precision Medicine

Wael Abo Elkheir, J Tissue Sci Eng 2016, 7:3(Suppl)

http://dx.doi.org/10.4172/2157-7552.C1.030

Allogenic bone marrow-derived mesenchymal stem therapy in Duchenne muscular dystrophy

Wael Abo Elkheir

Military Medical Academy, Egypt

Background:

Duchenne muscular dystrophy (DMD) is the commonest hereditary muscular dystrophy. It is characterized by

progressive muscle leading loss of walking ability and complete wheelchair dependence. Further, disability leads to respiratory

failure, which is the common cause of death.

Aim:

The aimof the present work is to evaluate the safety and therapeutic efficacy of allogenic bonemarrowderivedmesenhymal

stem cell therapy in Duchenne muscular dystrophy

Subjects &Methods:

This study was conducted on 40 myopathic patients, ages ranging from 6-18 years. DMDwas documented

by family history, history of disease progression, laboratory investigations, muscle biopsy and genetic study. Patients with

fixed deformities were excluded. The study group was randomly divided into patient and control groups. Both groups were

given traditional treatment (physiotherapy & medical treatment drugs); while the patient group received additionally stem

cell treatment. Stem cells were administered in 6 doses 4 weeks apart in a dose of 3×106 cells/kg suspended in 50 ml PBS. Cell

suspension was injected locally in 0.5 ml doses intramuscularly. A single systemic injection in a dose of 3 X10 6 cells/kg was

given with the sixth intramuscular dose. Follow-up was done using North Star Ambulatory Assessment CHAQ (Child Health

Assessment Questionnaire), manual muscle strength testing using Medical Research Council strength scores and functional

outcome measures. Scoring was done before and after every month for 12 months. Any complications or adverse effect were

recorded.

Results & Conclusions:

During the one year follow-up, no serious complications were recorded. Self-limited pain and mild

fever were reported for 48 hours after injection. Significant improvement in assessment scores and quality of life questionnaire

was seen in the treatment group. This was translated into substantial improvement in ambulation.

Biography

Wael Abo Elkheir has completed his PhD from Cairo University, Egypt. He is the Co-Founder and Board Member of the Egyptian Society for Progenitor Stem Cell

Research, a society initiated with the mission of enhancing scientific research and cooperation in the field of stem cell research and regenerative medicine. He is the

Director of a number of registered clinical trials in the field of stem cell therapy, especially for neuro-regeneration and musculoskeletal disorders. He has published

more than 20 papers in reputed journals.

dr.wael2008@yahoo.com