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1.
Neurol Sci ; 42(8): 3357-3366, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33411195

ABSTRACT

BACKGROUND: In the last years, there has been an intense technological development of robotic devices for gait rehabilitation in spinal cord injury (SCI) patients. The aim of the present study was to evaluate energy cost and psychological impact during a rehabilitation program with two different types of robotic rehabilitation systems (stationary system on a treadmill, Lokomat, and overground walking system, Ekso GT). METHODS: Fifteen SCI patients with different injury levels underwent robot-assisted gait training sessions, divided into 2 phases: in the first phase, all subjects completed 3 sessions both Lokomat and Ekso GT. Afterwards, participants were randomly assigned to Lokomat or the Ekso for 17 sessions. A questionnaire, investigating the subjective psychological impact (SPI) during gait training, was administered. The functional outcome measures were oxygen consumption (VO2), carbon dioxide production (VCO2), metabolic equivalent of task (MET), walking economy, and heart rate (HR). RESULTS: The metabolic responses (7.73 ± 1.02 mL/kg/min) and MET values (3.20 ± 1.01) during robotic overground walking resulted to be higher than those during robotic treadmill walking (3.91 ± 0.93 mL/kg/min and 1.58 ± 0.44; p < 0.01). Both devices showed high scores in emotion and satisfaction. Overground walking resulted in higher scores of fatigue, mental effort, and discomfort while walking with Lokomat showed a higher score in muscle relaxation. All patients showed improvements in walking economy due to a decrease in energy cost with increased speed and workload. CONCLUSIONS: Overground robotic-assisted gait training in rehabilitation program needs higher cognitive and cardiovascular efforts than robot-assisted gait training on a treadmill.


Subject(s)
Robotic Surgical Procedures , Spinal Cord Injuries , Exercise Therapy , Gait , Humans , Walking
2.
Spinal Cord ; 58(9): 988-997, 2020 09.
Article in English | MEDLINE | ID: mdl-32251368

ABSTRACT

STUDY DESIGN: Prospective, quasi-experimental study, pre- and post-design, single arm study. OBJECTIVES: Investigate whether persons affected by SCI can safely experience walking function using Robotic Exoskeletons and Functional Electrical Stimulation (FES). SETTING: Inpatient METHODS: 52 persons with SCI were recruited (36 completed the protocol) and assigned to one of two groups based on their Lower Limb Motor Scores (LEMS): Group A: LEMS ≥ 10 and Group B: LEMS < 10. Participants in Group A (n = 19) underwent 20 sessions of Robot-Assisted Gait Training (RAGT) on a treadmill followed by 20 sessions of FES during Overground Gait (FES-OG). Participants in Group B (n = 17) received 20 sessions of FES-cycling followed by 20 sessions of overground RAGT. The main outcome measures were: WISCI-II, 10MWT, 6MWT, TUG and SCIM-II. RESULTS: 36 persons completed the study with no complications; only 4 of the 16 dropped out because of mild complications during the RAGT. Participants in Group A exhibited significant improvements in WISCI-II, 10MWT, 6MWT and TUG (p < 0.05), while those in Group B did not significantly improve their gait function but their walking velocity and resistance with the assistance of the robotic exoskeleton increased. SCIM-II scores increased followed therapy only in Group A. CONCLUSIONS: Persons affected by SCI can safely experience their walking function with RAGT and FES therapy; only few mild complications were observed. Our data provides initial evidence of the potential value of these technologies, especially in persons with SCI having LEMS > 10.


Subject(s)
Electric Stimulation Therapy , Exercise Therapy , Exoskeleton Device , Gait Disorders, Neurologic/rehabilitation , Neurological Rehabilitation , Outcome and Process Assessment, Health Care , Spinal Cord Injuries/rehabilitation , Adult , Combined Modality Therapy , Female , Gait Disorders, Neurologic/etiology , Humans , Male , Middle Aged , Neurological Rehabilitation/methods , Prospective Studies , Spinal Cord Injuries/complications
3.
Ann Neurol ; 56(6): 886-90, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15562428

ABSTRACT

We studied 14 patients with neurological manifestations of subacute combined degeneration (SCD) and 40 control patients not cobalamin (Cbl)-deficient. The cerebrospinal fluid (CSF) markers of Cbl deficiency (Cbl and total homocysteine [tHCYS] levels) and the CSF levels of tumor necrosis factor (TNF)-alpha and epidermal growth factor (EGF) were measured. Significantly higher levels of tHCYS and TNF-alpha, and significantly lower levels of Cbl and EGF were found in the SCD patients. In human CSF, as in human serum and the rat central nervous system, decreased Cbl concentrations are concomitant with an increase in TNF-alpha and a decrease in EGF-levels. Ann Neurol 2004;56:886-890.


Subject(s)
Tumor Necrosis Factor-alpha/cerebrospinal fluid , Vitamin B 12 Deficiency/cerebrospinal fluid , Vitamin B 12/cerebrospinal fluid , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Statistics, Nonparametric , Vitamin B 12/metabolism
4.
Article in English | MEDLINE | ID: mdl-12215226

ABSTRACT

BACKGROUND: Although the pathogenic mechanisms of selective loss of motor neurons in amyotrophic lateral sclerosis (ALS) are unknown, there is increasing evidence for the hypothesis of an oxidative stress-related mitochondrial involvement as key determinant of motor neuron degeneration OBJECTIVE: The aim of our study has been to assess blood levels of peroxidation markers and to relate them to in-vivo oxidative metabolism in exercising muscle in patients affected by ALS. METHOD: For this purpose 10 patients (seven men and three women, mean age 58.5 +/- 8.2 SD), performed an incremental bicycling test for the assessment of lipoperoxides and lactate during exercise. RESULTS: At rest, the ALS patients had higher than normal levels of both lactate (2.82 +/- 0.76 mmol/L; normal range: 0.67-2.47 mmol/L) and lipoperoxides (361.7 +/- 40.2 AU; normal range: 250-320 AU), the latter corresponding to a level of moderate oxidative stress. A further increment during exercise was observed both at lactate threshold and maximal power output levels. Values of blood lipoperoxides were significantly higher (P < 0.05) than those in control patients affected by chronic motor denervating processes of different origins and related (P < 0.01) to lactate production on exercising. CONCLUSIONS: These findings indicate the occurrence of an abnormally increased size of blood free radical pool in resting conditions and during exercise in ALS patients. The relationship between the levels of reactive oxygen species and lactate production is indicative of a tight link between mitochondrial function and oxidative stress in ALS.


Subject(s)
Amyotrophic Lateral Sclerosis/physiopathology , Lactic Acid/blood , Lipid Peroxides/blood , Muscle, Skeletal/physiopathology , Aged , Amyotrophic Lateral Sclerosis/blood , Amyotrophic Lateral Sclerosis/pathology , Biopsy , Exercise Test , Female , Humans , Male , Middle Aged , Muscle, Skeletal/pathology , Statistics, Nonparametric
5.
J Neurol Sci ; 196(1-2): 41-4, 2002 Apr 15.
Article in English | MEDLINE | ID: mdl-11959155

ABSTRACT

Sera from 40 patients with Guillain-Barré syndrome (GBS), including the subtypes acute inflammatory demyelinating polyneuropathy (AIDP), acute motor axonal neuropathy (AMAN), acute motor and sensory axonal neuropathy (AMSAN), and Miller Fisher syndrome (MFS) were examined for the presence of anti-ganglioside antibodies using the ganglioside agglutination assay, and the enzyme-linked immunosorbent assay (ELISA). In the ELISA system, sera were tested for IgM and IgG antibodies to GM1, GM2, GD1a, GD1b, GT1b, and GQ1b gangliosides. Antibodies to gangliosides were detected in 21 (53%) of the GBS patients by agglutination assay and in 17 (43%) of the patients by ELISA. Some of the sera reacted with more than one ganglioside. Antibodies were not found in the control sera that were studied. The agglutination assay may be useful for rapid screening of GBS sera for antibodies to multiple gangliosides.


Subject(s)
Agglutination Tests/methods , Antibodies/blood , Axons/immunology , Gangliosides/immunology , Guillain-Barre Syndrome/blood , Guillain-Barre Syndrome/immunology , Peripheral Nerves/immunology , Axons/pathology , Enzyme-Linked Immunosorbent Assay , G(M1) Ganglioside/immunology , G(M2) Ganglioside/immunology , Humans , Immunoglobulin G/blood , Immunoglobulin M/blood , Peripheral Nerves/pathology , Peripheral Nerves/physiopathology , Reproducibility of Results
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