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Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy.
Gouveia, Débora; Correia, Jéssica; Cardoso, Ana; Carvalho, Carla; Oliveira, Ana Catarina; Almeida, António; Gamboa, Óscar; Ribeiro, Lénio; Branquinho, Mariana; Sousa, Ana; Lopes, Bruna; Sousa, Patrícia; Moreira, Alícia; Coelho, André; Rêma, Alexandra; Alvites, Rui; Ferreira, António; Maurício, Ana Colette; Martins, Ângela.
Afiliação
  • Gouveia D; Arrábida Veterinary Hospital, Arrábida Animal Rehabilitation Center, Setubal, Portugal.
  • Correia J; Superior School of Health, Protection and Animal Welfare, Polytechnic Institute of Lusophony, Lisboa, Portugal.
  • Cardoso A; Faculty of Veterinary Medicine, Lusófona University, Lisboa, Portugal.
  • Carvalho C; Arrábida Veterinary Hospital, Arrábida Animal Rehabilitation Center, Setubal, Portugal.
  • Oliveira AC; Faculty of Veterinary Medicine, Lusófona University, Lisboa, Portugal.
  • Almeida A; Arrábida Veterinary Hospital, Arrábida Animal Rehabilitation Center, Setubal, Portugal.
  • Gamboa Ó; Superior School of Health, Protection and Animal Welfare, Polytechnic Institute of Lusophony, Lisboa, Portugal.
  • Ribeiro L; Arrábida Veterinary Hospital, Arrábida Animal Rehabilitation Center, Setubal, Portugal.
  • Branquinho M; Arrábida Veterinary Hospital, Arrábida Animal Rehabilitation Center, Setubal, Portugal.
  • Sousa A; Superior School of Health, Protection and Animal Welfare, Polytechnic Institute of Lusophony, Lisboa, Portugal.
  • Lopes B; Faculty of Veterinary Medicine, University of Lisbon, Lisboa, Portugal.
  • Sousa P; Faculty of Veterinary Medicine, University of Lisbon, Lisboa, Portugal.
  • Moreira A; Faculty of Veterinary Medicine, Lusófona University, Lisboa, Portugal.
  • Coelho A; Departamento de Clínicas Veterinárias, Instituto de Ciências Biomédicas de Abel Salaza, Universidade do Porto, Porto, Portugal.
  • Rêma A; Centro de Estudos de Ciência Animal, Instituto de Ciências, Tecnologias e Agroambiente da Universidade do Porto, Porto, Portugal.
  • Alvites R; Associate Laboratory for Animal and Veterinary Science (AL4AnimalS), Lisboa, Portugal.
  • Ferreira A; Departamento de Clínicas Veterinárias, Instituto de Ciências Biomédicas de Abel Salaza, Universidade do Porto, Porto, Portugal.
  • Maurício AC; Centro de Estudos de Ciência Animal, Instituto de Ciências, Tecnologias e Agroambiente da Universidade do Porto, Porto, Portugal.
  • Martins Â; Associate Laboratory for Animal and Veterinary Science (AL4AnimalS), Lisboa, Portugal.
Front Vet Sci ; 10: 1192744, 2023.
Article em En | MEDLINE | ID: mdl-37520009
Introduction: Degenerative myelopathy (DM) is a neurodegenerative spinal cord disease with upper motor neurons, with progressive and chronic clinical signs, similar to amyotrophic lateral sclerosis (ALS). DM has a complex etiology mainly associated with SOD1 gene mutation and its toxic role, with no specific treatment. Daily intensive rehabilitation showed survival time near 8 months but most animals are euthanized 6-12 months after clinical signs onset. Methods: This prospective controlled blinded cohort clinical study aims to evaluate the neural regeneration response ability of DM dogs subjected to an intensive neurorehabilitation protocol with mesenchymal stem cells (MSCs) transplantation. In total, 13 non-ambulatory (OFS 6 or 8) dogs with homozygous genotype DM/DM and diagnosed by exclusion were included. All were allocated to the intensive neurorehabilitation with MSCs protocol (INSCP) group (n = 8) or to the ambulatory rehabilitation protocol (ARP) group (n = 5), which differ in regard to training intensity, modalities frequency, and MSCs transplantation. The INSCP group was hospitalized for 1 month (T0 to T1), followed by MSCs transplantation (T1) and a second month (T2), whereas the ARP group was under ambulatory treatment for the same 2 months. Results: Survival mean time of total population was 375 days, with 438 days for the INSCP group and 274 for the ARP group, with a marked difference on the Kaplan-Meier survival analysis. When comparing the literature's results, there was also a clear difference in the one-sample t-test (p = 0.013) with an increase in time of approximately 70%. OFS classifications between groups at each time point were significantly different (p = 0.008) by the one-way ANOVA and the independent sample t-test. Discussion: This INSCP showed to be safe, feasible, and a possibility for a long progression of DM dogs with quality of life and functional improvement. This study should be continued.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article