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Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy

Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy
Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy
Haematopoietic stem cell transplantation has been proposed as treatment for mitochondrial neurogastrointestinal encephalomyopathy, a rare fatal autosomal recessive disease due to TYMP mutations that result in thymidine phosphorylase deficiency. We conducted a retrospective analysis of all known patients suffering from mitochondrial neurogastrointestinal encephalomyopathy who underwent allogeneic haematopoietic stem cell transplantation between 2005 and 2011. Twenty-four patients, 11 males and 13 females, median age 25 years (range 10-41 years) treated with haematopoietic stem cell transplantation from related (n = 9) or unrelated donors (n = 15) in 15 institutions worldwide were analysed for outcome and its associated factors. Overall, 9 of 24 patients (37.5%) were alive at last follow-up with a median follow-up of these surviving patients of 1430 days. Deaths were attributed to transplant in nine (including two after a second transplant due to graft failure), and to mitochondrial neurogastrointestinal encephalomyopathy in six patients. Thymidine phosphorylase activity rose from undetectable to normal levels (median 697 nmol/h/mg protein, range 262-1285) in all survivors. Seven patients (29%) who were engrafted and living more than 2 years after transplantation, showed improvement of body mass index, gastrointestinal manifestations, and peripheral neuropathy. Univariate statistical analysis demonstrated that survival was associated with two defined pre-transplant characteristics: human leukocyte antigen match (10/10 versus <10/10) and disease characteristics (liver disease, history of gastrointestinal pseudo-obstruction or both). Allogeneic haematopoietic stem cell transplantation can restore thymidine phosphorylase enzyme function in patients with mitochondrial neurogastrointestinal encephalomyopathy and improve clinical manifestations of mitochondrial neurogastrointestinal encephalomyopathy in the long term. Allogeneic haematopoietic stem cell transplantation should be considered for selected patients with an optimal donor.
mitochondrial neurogastroinstesinal encephalomyopathy (MNGIE), allogeneic haematopietic stem cell transplantation, outcome, risk factors, thymidine phosphorylase
0006-8950
2847-2858
Halter, Joerg P.
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Michael, W.
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Schüpbach, M.
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Mandel, Hanna
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Casali, Carlo
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Orchard, Kim
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Collin, Matthew
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Valcarcel, David
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Rovelli, Attilio
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Filosto, Massimiliano
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Dotti, Maria T.
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Marotta, Giuseppe
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Pintos, Guillem
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Barba, Pere
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Accarino, Anna
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Ferra, Christelle
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Illa, Isabel
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Beguin, Yves
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Bakker, Jaap A.
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Boelens, Jaap J.
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de Coo, Irenaeus F. M.
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Fay, Keith
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Sue, Carolyn M.
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Nachbaur, David
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Zoller, Heinz
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Sobreira, Claudia
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Pinto Simoes, Belinda
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Hammans, Simon R.
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Savage, David
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Martí, Ramon
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Chinnery, Patrick F.
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Elhasid, Ronit
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Gratwohl, Alois
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Hirano, Michio
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Halter, Joerg P.
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Michael, W.
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Schüpbach, M.
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Mandel, Hanna
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Casali, Carlo
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Orchard, Kim
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Collin, Matthew
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Valcarcel, David
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Rovelli, Attilio
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Filosto, Massimiliano
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Dotti, Maria T.
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Marotta, Giuseppe
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Pintos, Guillem
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Barba, Pere
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Accarino, Anna
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Ferra, Christelle
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Illa, Isabel
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Beguin, Yves
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Bakker, Jaap A.
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Boelens, Jaap J.
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de Coo, Irenaeus F. M.
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Fay, Keith
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Sue, Carolyn M.
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Nachbaur, David
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Zoller, Heinz
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Sobreira, Claudia
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Pinto Simoes, Belinda
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Hammans, Simon R.
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Savage, David
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Martí, Ramon
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Chinnery, Patrick F.
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Elhasid, Ronit
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Gratwohl, Alois
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Hirano, Michio
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Halter, Joerg P., Michael, W. and Schüpbach, M. et al. (2015) Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy. Brain, 138 (Part 10), 2847-2858. (doi:10.1093/brain/awv226). (PMID:26264513)

Record type: Article

Abstract

Haematopoietic stem cell transplantation has been proposed as treatment for mitochondrial neurogastrointestinal encephalomyopathy, a rare fatal autosomal recessive disease due to TYMP mutations that result in thymidine phosphorylase deficiency. We conducted a retrospective analysis of all known patients suffering from mitochondrial neurogastrointestinal encephalomyopathy who underwent allogeneic haematopoietic stem cell transplantation between 2005 and 2011. Twenty-four patients, 11 males and 13 females, median age 25 years (range 10-41 years) treated with haematopoietic stem cell transplantation from related (n = 9) or unrelated donors (n = 15) in 15 institutions worldwide were analysed for outcome and its associated factors. Overall, 9 of 24 patients (37.5%) were alive at last follow-up with a median follow-up of these surviving patients of 1430 days. Deaths were attributed to transplant in nine (including two after a second transplant due to graft failure), and to mitochondrial neurogastrointestinal encephalomyopathy in six patients. Thymidine phosphorylase activity rose from undetectable to normal levels (median 697 nmol/h/mg protein, range 262-1285) in all survivors. Seven patients (29%) who were engrafted and living more than 2 years after transplantation, showed improvement of body mass index, gastrointestinal manifestations, and peripheral neuropathy. Univariate statistical analysis demonstrated that survival was associated with two defined pre-transplant characteristics: human leukocyte antigen match (10/10 versus <10/10) and disease characteristics (liver disease, history of gastrointestinal pseudo-obstruction or both). Allogeneic haematopoietic stem cell transplantation can restore thymidine phosphorylase enzyme function in patients with mitochondrial neurogastrointestinal encephalomyopathy and improve clinical manifestations of mitochondrial neurogastrointestinal encephalomyopathy in the long term. Allogeneic haematopoietic stem cell transplantation should be considered for selected patients with an optimal donor.

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More information

Accepted/In Press date: 19 June 2015
e-pub ahead of print date: 10 August 2015
Published date: October 2015
Keywords: mitochondrial neurogastroinstesinal encephalomyopathy (MNGIE), allogeneic haematopietic stem cell transplantation, outcome, risk factors, thymidine phosphorylase
Organisations: Human Development & Health

Identifiers

Local EPrints ID: 380389
URI: http://eprints.soton.ac.uk/id/eprint/380389
ISSN: 0006-8950
PURE UUID: cf2684d8-c151-48dd-a353-20289968c7a9
ORCID for Kim Orchard: ORCID iD orcid.org/0000-0003-2276-3925

Catalogue record

Date deposited: 14 Sep 2015 12:26
Last modified: 15 Mar 2024 03:13

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Contributors

Author: Joerg P. Halter
Author: W. Michael
Author: M. Schüpbach
Author: Hanna Mandel
Author: Carlo Casali
Author: Kim Orchard ORCID iD
Author: Matthew Collin
Author: David Valcarcel
Author: Attilio Rovelli
Author: Massimiliano Filosto
Author: Maria T. Dotti
Author: Giuseppe Marotta
Author: Guillem Pintos
Author: Pere Barba
Author: Anna Accarino
Author: Christelle Ferra
Author: Isabel Illa
Author: Yves Beguin
Author: Jaap A. Bakker
Author: Jaap J. Boelens
Author: Irenaeus F. M. de Coo
Author: Keith Fay
Author: Carolyn M. Sue
Author: David Nachbaur
Author: Heinz Zoller
Author: Claudia Sobreira
Author: Belinda Pinto Simoes
Author: Simon R. Hammans
Author: David Savage
Author: Ramon Martí
Author: Patrick F. Chinnery
Author: Ronit Elhasid
Author: Alois Gratwohl
Author: Michio Hirano

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