Improved Bowel Function in Patients with Spina Bifida After Bone Marrow-Derived Mononuclear Cell Transplantation: A Report of 2 Cases

Nguyen Thanh Liem, Vu Duy Chinh, Nguyen Thi Thinh, Ngo Duy Minh, Hoang Minh Duc, Nguyen Thanh Liem, Vu Duy Chinh, Nguyen Thi Thinh, Ngo Duy Minh, Hoang Minh Duc

Abstract

BACKGROUND Bowel dysfunction is observed in 42.2-71.2% of patients with spina bifida. Traditional treatments yield limited results. The objective of this paper is to report on improvement in bowel function in 2 children with spina bifida following bone marrow-derived mononuclear cells transplantation. CASE REPORT Two patients - 14 years old and 11 years old - with bowel dysfunction after myelomeningocele repair underwent 2 BMMNC transplantations without complications. Those patients had normal defecation, assessed through follow-ups of 21 months and 16 months, respectively. CONCLUSIONS BMMNC transplantation can improve bowel function, as demonstrated in 2 patients with spina bifida.

Conflict of interest statement

Conflict of interest: None declared

Conflict of Interests

The authors have declared that no competing interests exist.

Figures

Figure 1.
Figure 1.
MRI shows a low termination of the spinal cord.
Figure 2.
Figure 2.
(A) Pretransplantation cystography of the first patient demonstrates many diverticula. (B) Post-transplantation cystography of the first patient still shows many diverticula.
Figure 3.
Figure 3.
(A) Pre-transplantation urodynamic investigation of the first patient reveals a very underactive detrusor function. (B) Post-transplantation urodynamic investigation of the first patient shows increased detrusor function.
Figure 4.
Figure 4.
Flow cytometry of CD34+ analysis of the first patient. Calculation of CD34+ population from the BMMNCs at the 1st transplantation (A) and 2nd transplantation (B).
Figure 5.
Figure 5.
Spinal MRI of the second patient demonstrates a low termination of the spinal cord.
Figure 6.
Figure 6.
(A) Pre-transplantation cystography of the second patient shows multiple diverticula. (B) Post-transplantation cystography of the second patients still shows multiple diverticula.
Figure 7.
Figure 7.
(A) Pre-transplantation urodynamic investigation of the second patient shows hyperactive detrusor functions. (B) Post-transplantation urodynamic investigation of the second patient reveals reduced hyperactive detrusor function.
Figure 8.
Figure 8.
Flow cytometry of CD34+ analysis of the second patient. Calculation of the CD34+ population from the BMMNCs at the 1st transplantation (A) and 2nd transplantation (B).

References

    1. Zaganjor I, Sekkarie A, Tsang BL, et al. Describing the prevalence of neural tube defects worldwide: A systematic literature review. PLoS One. 2016;11:e151586.
    1. Parker SE, Mai CT, Canfield MA, et al. Updated National Birth Prevalence estimates for selected birth defects in the United States, 2004–2006. Birth Defects Res A Clin Mol Teratol. 2010;88:1008–16.
    1. Meuli M, Meuli-Simmen C, Yingling CD, et al. Creation of myelomeningocele in utero: A model of functional damage from spinal cord exposure in fetal sheep. J Pediatr Surg. 1995;30:1028–33.
    1. Müslüman AM, Karşıdağ S, DÖ Sucu, et al. Clinical outcomes of myelomeningocele defect closure over 10 years. J Clin Neurosci. 2012;9(7):984–90.
    1. Perry VL, Albright AL, Adelson PD. Operative nuances of myelomeningocele closure. Neurosurgery. 2002;51(3):719–23.
    1. Mattogno PP, Massimi L, Tamburrini G, et al. Myelomeningocele repair: Surgical management based on a 30-year experience. Acta Neurochir Suppl. 2017;124:143–48.
    1. Choi EK, Im YJ, Han SW. Bowel management and quality of life in children with spina bifida in South Korea. Gastroenterol Nurs. 2017;40(3):208–15.
    1. Ponticelli A, Lacobelli BD, Silveri M, et al. Colorectal dysfunction and faecal incontinence in children with spina bifida. Br J Urol. 1988;81(Suppl. 3):117–19.
    1. Lemelle JL, Guillemin F, Aubert D, et al. Quality of life and continence in patients with spina bifida. Qual Life Res. 2006;15(9):1481–92.
    1. Choi EK, Im YJ, Han SW, et al. Long-term outcome of transanal irrigation for children with spina bifida. Spinal Cord. 2015;53:216–20.
    1. Vande Velde S, Van Biervliet S, Van Renterghem K, et al. Achieving fecal continence in patients with spina bifida: A descriptive cohort study. J Urol. 2007;178:2640–44.
    1. Lansen-Koch SM, Govaert B, Oerlemans D, et al. Sacral nerve modulation for defaecation and micturition disorders in patients with spina bifida. Colorectal Dis. 2012;14(4):508–14.
    1. Liem NT, Anh TN, Chinh VD, et al. Outcomes of autologous bone marrow mononuclear cells for cerebral palsy: An open-label uncontrolled clinical trial. BMC Pediatr. 2017;17:104.
    1. Abi Chahine NH, Wehbe TW, Hilal RA, et al. Treatment of cerebral palsy with stem cells: A report of 17 cases. Int J Stem Cells. 2016;9(1):90–95.
    1. Savitz SI, Misra V, Kasam M, et al. Intravenous autologous bone marrow mononuclear cells for ischemic stroke. Ann Neurol. 2011;70(1):59–69.
    1. Park HS, Park HC, Shim YS, et al. Treatment of complete spinal cord injury patients by autologous bone marrow cell transplantation and administration of granulocyte-macrophage colony stimulating factor. Tissue Eng. 2005;11:913–22.
    1. Callera F, do Nascimento RX. Delivery of autologous bone marrow precursor cells into the spinal cord via lumbar puncture technique in patients with spinal cord injury: A preliminary safety study. Exp Hematol. 2006;34:130–31.
    1. Sykova’ E, Homola A, Mazanec R, et al. Autologous bone marrow transplantation in patients with subacute and chronic spinal cord injury. Cell Transplant. 2006;15:675–87.
    1. Yoon SH, Shim YS, Park YH, et al. Complete spinal cord injury treatment using autologous bone marrow cell transplantation and bone marrow stimulation with granulocyte macrophage-colony stimulating factor: Phase I/II clinical train. Stem Cells. 2007;25:2066–73.
    1. Jiang PC, Xiong WP, Wang G, et al. A clinical report of autologous bone marrow-derived mesenchymal stem cell transplantation in patients with spinal cord injury. Exp Ther Med. 2013;6:140–46.
    1. Li H, Gao F, Ma L, et al. Therapeutic potential of in utero mesenchymal stem cell (MSCs) transplantation in rat foetuses with spina bifida aperta. J Cell Mol Med. 2012;16(7):1606–17.
    1. Dionigi B, Ahmed A, Brazzo J, 3rd, et al. Partial or complete coverage of experimental spina bifida by simple intra-amniotic injection of concentrated amniotic mesenchymal stem cells. J Pediatr Surg. 2015;50(1):69–73.
    1. Li X, Yuan Z, Wei X, et al. Application potential of bone marrow mesenchymal stem cell (BMSCs) based tissue-engineering for spinal cord defect repair in rat fetuses with spina bifida aperta. J Mater Sci Mater Med. 2016;27(4):77.
    1. Feng C, Graham CD, Connors JP, et al. A comparison between placental and amniotic mesenchymal stem cells for transamniotic stem cell therapy (TRASCET) in experimental spina bifida. J Pediatr Surg. 2016;51(6):1010–13.
    1. Gupta DK, Sharma S, Venugopal P, et al. Stem cells as a therapeutic modality in pediatric malformations. Transplant Proc. 2007;39(3):700–2.
    1. Banasiuk M, Banaszkiewicz A, Dziekiewicz M, et al. Values from three-dimensional high-resolution anorectal manometry analysis of children without lower gastrointestinal symptoms. Clin Gastroenterol Hepatol. 2016;14(7):993–1000.
    1. Wahl EF, Churchill BM. Detrusor pressure rise in a normal bladder. BJU Int. 2004;94:901–2.
    1. Mahfouz W, Al Afraa T, Campeau L, et al. Normal urodynamic parameters in women: Part II – invasive urodynamics. Int Urogynecol J. 2012;23:267–77.
    1. Gu W, Zhang F, Xue Q, et al. Transplantation of bone marrow mesenchymal stem cells reduces lesion volume and induces axonal regrowth of injured spinal cord. Neuropathology. 2010;30:205–17.
    1. Park WB, Kim SY, Lee SH, et al. The effect of mesenchymal stem cell transplantation on the recovery of bladder and hindlimb function after spinal cord contusion in rats. BMC Neurosci. 2010;11:119–30.
    1. Mitsui T, Kakizaki H, Tanaka H, et al. Immortalized neural stem cells transplanted into the injured spinal cord promote recovery of voiding function in the rat. J Urol. 2013;170:1421–25.

Source: PubMed

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