Evidence map›Paper›PMID 24711886›Full record

ArticleThe American journal of case reports2014

Autologous bone marrow mononuclear cell transplantation in Duchenne muscular dystrophy - a case report.

Alok Sharma, Hemangi Sane, Amruta Paranjape, Khushboo Bhagawanani, Nandini Gokulchandran, Prerna Badhe

Open access · hybridAbstract read
In one paragraph

Article in The American journal of case reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Autologous cord blood in children with cerebral palsy: a review.International journal of molecular sciences · 2019
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Duchenne muscular dystrophy: current cell therapies.Therapeutic advances in neurological disorders · 2015
    Review
  11. Aquapuncture Using Stem Cell Therapy to Treat Mdx Mice.Evidence-based complementary and alternative medicine : eCAM · 2015
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Alok SharmaDepartment of Medical Services and Clinical Research, NeuroGen Brain and Spine Institute, Mumbai, India.
Hemangi SaneDepartment of Research and Development, NeuroGen Brain and Spine Institute, Mumbai, India.
Amruta ParanjapeDepartment of Research and Development, NeuroGen Brain and Spine Institute, Mumbai, India.
Khushboo BhagawananiDepartment of Neuro-Rehabilitation, NeuroGen Brain and Spine Institute, Mumbai, India.
Nandini GokulchandranDepartment of Medical Services and Clinical Research, NeuroGen Brain and Spine Institute, Mumbai, India.
Prerna BadheDepartment of Medical Services and Clinical Research, NeuroGen Brain and Spine Institute, Mumbai, India.
Neurogen Brain & Spine Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

patientMale, 9 FINAL DIAGNOSIS: Duchenne muscular dystrophy Symptoms: Hyporeflexia • hypotonia • weaknes of lower limbs MEDICATION: - Clinical Procedure: - Specialty: Neurology.

objectiveCongenital defects/diseases.

backgroundDuchenne muscular dystrophy (DMD) is a fatal, genetic, progressive, degenerating muscle disorder. Current treatment options are palliative. Newer options of cellular therapy promise to alter the disease process. Preclinical studies have successfully tested myogenic, neurogenic potential and dystrophin expression of bone marrow mononuclear cells. CASE REPORT: We treated a 9-year-old boy suffering from DMD with serial autologous bone marrow mononuclear cell transplantations followed by multidisciplinary rehabilitation. Brooke-Vignos score was 10 and he was wheelchair-bound. Over 36 months, gradual progressive improvement was noticed in muscle strength, ambulation with assistive devices, fine motor movements, Brooke-Vignos score, and functional independence measure score. Nine months after the transplantation, electromyography findings showed development of new normal motor unit potentials of the vastus medialis muscle.

conclusionsMagnetic resonance imaging scan of musculoskeletal systems showed no increase in fatty infiltration. This case report provides early investigative findings or the restorative effects of cellular therapy in DMD.

Indexed as

Autologous Bone Marrow Mono Nuclear CellsDuchenne – congenitalElectromyographyMuscular DystrophyStem Cell Transplantation

Identifiers

PMID24711886
PMCPMC3976215
OpenAlexW2413102942

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.