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1.
Cell Transplant ; 21(9): 1899-907, 2012.
Article in English | MEDLINE | ID: mdl-23356668

ABSTRACT

Amyotrophic lateral sclerosis is characterized by the selective death of motor neurons. Stem cells have been proposed as a potential therapeutic strategy. The safety of stem cell transplantation into the frontal motor cortex to improve upper motor neuron function is described. Sixty-seven patients with definite amyotrophic lateral sclerosis were included. After giving their informed consent, the patients underwent magnetic resonance imaging, functional rating, pulmonary function test, and laboratory tests. Their bone marrow was stimulated with daily filgrastim (300 µg) given subcutaneously for 3 days. Peripheral blood mononuclear cells were obtained by leukapheresis. Isolated CD133(+) stem cells were suspended in 300 µl of the patient's cerebrospinal fluid and implanted into the motor cortex. Adverse events were recorded at each step of the procedure and were classified according to the Common Terminology Criteria for Adverse Events v3.0. The survival at 1 year was 90% after transplantation. with a mean long-term survival rate of 40.17 months from diagnosis. The most common adverse events were in grades I-II and involved transient skin pain (19.5% of patients) attributed to the insertion of the Mahurkar catheter into the subclavian vein, minor scalp pain (15.9%), and headache (12.2%) from the surgical procedure. Several patients (1.5 - 4.5%) reported diverse grade I adverse events. There were two deaths, one considered to be associated with the procedure (1.5%) and the other associated with the disease. Autologous stem cell transplantation into the frontal motor cortex is safe and tolerated well by patients. Further controlled studies are required to define the efficacy of this procedure.


Subject(s)
Amyotrophic Lateral Sclerosis/surgery , Mesenchymal Stem Cell Transplantation/methods , Amyotrophic Lateral Sclerosis/blood , Amyotrophic Lateral Sclerosis/cerebrospinal fluid , Feasibility Studies , Female , Filgrastim , Granulocyte Colony-Stimulating Factor/administration & dosage , Humans , Leukapheresis/methods , Male , Middle Aged , Motor Cortex/surgery , Recombinant Proteins/administration & dosage
2.
Stroke ; 42(4): 897-901, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21393588

ABSTRACT

BACKGROUND AND PURPOSE: A delay in recognizing early warning signs (WS) and risk factors (RF) of ischemic stroke causes a delay in treatment. We evaluated knowledge of RF and WS and the impact of an educational program by medical students. METHODS: We first surveyed individuals to determine knowledge of WS and RF. Then, after a 6-month education program, knowledge was reassessed. The questionnaire included sociodemographic and comorbidity data. A χ(2) and Mann-Whitney U test, as well as a multivariate logistic regression analysis to determine variables associated with knowledge, were used. RESULTS: We performed 329 baseline and 355 posteducation surveys. Initially, 57.1% mentioned at least 1 RF; this later increased to 65.9%. Mentions of obesity, dyslipidemias, hypertension, and diabetes mellitus increased significantly. With regard to WS, 37.6% mentioned at least 1, which increased to 48.1% who mentioned weakness in 1 limb, in half the body, severe headache, and altered vision. Educational level (OR, 2.53; 95% CI, 1.42-4.53; P=0.001), employment (OR, 1.72; 95% CI, 1.08-2.74; P=0.021), a family history of brain infarction (OR, 2.35; 95% CI, 1.35-4.11; P=0.02), obesity (OR, 1.63; 95% CI, 1.026-2.6; P=0.038), and having received information in the last 6 months (OR, 2.7; 95% CI, 1.51-4.83; P=0.001) were associated with a better understanding of RF and WS. CONCLUSIONS: The educational program was cost-effective and had a positive impact on knowledge of RF and WS of ischemic stroke. More education programs are required to improve knowledge of ischemic stroke.


Subject(s)
Brain Ischemia/prevention & control , Education, Medical, Undergraduate/methods , Health Education/methods , Stroke/prevention & control , Surveys and Questionnaires/standards , Adolescent , Adult , Aged , Aged, 80 and over , Brain Ischemia/diagnosis , Brain Ischemia/epidemiology , Education, Medical, Undergraduate/statistics & numerical data , Education, Medical, Undergraduate/trends , Female , Health Education/statistics & numerical data , Health Education/trends , Humans , Male , Mexico/epidemiology , Middle Aged , Risk Factors , Stroke/diagnosis , Stroke/epidemiology , Young Adult
3.
J Stroke Cerebrovasc Dis ; 18(3): 208-13, 2009.
Article in English | MEDLINE | ID: mdl-19426892

ABSTRACT

INTRODUCTION: Knowledge of risk factors (RF) and warning signs of stroke by the general population is fundamental to implement efficient preventive measures and provide timely treatment. The objective of this study was to assess this knowledge in a sample population of Mexico City. METHODS: Personal interview was conducted in a multifamily building complex in Mexico City. The questionnaire included sociodemographic and comorbidity factors. Knowledge was determinated according to the number of correct answers. Chi-square and Wilcoxon rank tests were performed and significant variables were included in a multivariate logistic regression model using level of knowledge as the dependent variable. RESULTS: A total of 330 subjects were interviewed. Of the respondents, 66.7% named one RF associated with ischemic stroke, whereas only 12.1% identified 3 or more; one warning sign was identified by 36.7% and only 2.1% identified 3 or more. The factors associated with knowledge of RF were history of hypertension, educational level, and family history of ischemic stroke. Educational level and a family history of stroke were also associated with knowledge of warning signs. DISCUSSION: A Family history of ischemic stroke was the most important way to receive information about RF and warning signs of ischemic stroke. The study shows the need for informing the public about prevention and early detection of ischemic stroke.


Subject(s)
Brain Ischemia/complications , Stroke/diagnosis , Adolescent , Adult , Age Factors , Aged , Aged, 80 and over , Analysis of Variance , Data Collection , Education , Female , Health Education , Health Knowledge, Attitudes, Practice , Humans , Logistic Models , Male , Mexico/epidemiology , Middle Aged , Risk Factors , Socioeconomic Factors , Stroke/etiology , Stroke/prevention & control , Surveys and Questionnaires , Young Adult
4.
Cytotherapy ; 11(1): 26-34, 2009.
Article in English | MEDLINE | ID: mdl-19191058

ABSTRACT

BACKGROUND AIMS: Amyotrophic lateral sclerosis (ALS) is characterized by the selective death of motor neurons. CD133(+) stem cells are known to have the capacity to differentiate into neural lineages. Stem cells may provide an alternative treatment for ALS and other neurodegenerative diseases. METHODS: Five men and five women (aged 38-62 years) with confirmed ALS were included in this study. Our institutional ethics and research committees approved the protocol. After informed consent was obtained, patients underwent Hidrogen-Magnetic Resonance Imaging (H-MRI) spectroscopy and were given scores according to an ALS functional rating scale, Medical Research Council power muscle scale and daily living activities. Bone marrow was stimulated with 300 microg filgrastim subcutaneously daily for 3 days. Peripheral blood mononuclear cells were obtained after admission by leukapheresis. The cell suspension was conjugated with anti-human CD133 superparamagnetic microbeads, and linked cells were isolated in a magnetic field. The isolated cells (2.5-7.5x10(5)) were resuspended in 300 microL of the patient's cerebrospinal fluid, and implanted in motor cortexes using a Hamilton syringe. Ten patients with confirmed ALS without transplantation were used as a control group. Patients were followed up for a period of 1 year. RESULTS: The autologous transplantation of CD133(+) stem cells into the frontal motor cortex is a safe and well-tolerated procedure in ALS patients. The survival of treated patients was statistically higher (P=0.01) than untreated control patients. CONCLUSIONS: Stem-cell transplantation in the motor cortex delays ALS progression and improves quality of life.


Subject(s)
Amyotrophic Lateral Sclerosis/surgery , Hematopoietic Stem Cell Transplantation/methods , Motor Cortex/surgery , AC133 Antigen , Adult , Amyotrophic Lateral Sclerosis/mortality , Antigens, CD/metabolism , Female , Filgrastim , Glycoproteins/metabolism , Granulocyte Colony-Stimulating Factor/administration & dosage , Hematopoietic Stem Cells/drug effects , Hematopoietic Stem Cells/physiology , Humans , Male , Middle Aged , Peptides/metabolism , Recombinant Proteins , Transplantation, Autologous/methods
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