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1.
Cir Cir ; 79(2): 175-81, 2011.
Article in English | MEDLINE | ID: mdl-21631979

ABSTRACT

BACKGROUND: The World Health Organization reports that waist circumference (WC) independent of weight or body mass index (BMI) predicts cardiovascular risk. We undertook this study to determine the change of prevalence in comorbidities associated with obesity and cardiovascular risk after favorably modifying WC. METHODS: We studied 153 nondiabetic patients with obesity (BMI =30 kg/m²) and WC in women =80 cm and in men =94 cm who entered a weight control program for 2 years. We evaluated the evolution of their anthropometric measurements and metabolic status. Ninety patients (58.8%) completed the study. With the prior acceptance of the patients, they received nutritional advice and psychological and physical activity support during their monthly visits. Also, anthropometric measurements and blood pressure were evaluated. At the beginning and after each 6 months, glucose, total cholesterol, HDL cholesterol and triglycerides were determined. At the beginning and at the end of study the Framingham risks were evaluated. RESULTS: Of the 90 patients, 37 (group 1) decreased their WC: in women <80 cm and in men <94 cm. In 53 patients (group 2) there were no significant changes. Changes were shown in group 1 for blood pressure (from 36.6% to 21.6%), hyperglycemia >100 mg/dl decreased from 18.8% to 8.1%, triglycerides >150 mg/dl decreased from 28.8% to 18.9% and Framingham risk at 10 years decreased. CONCLUSIONS: There is a direct relationship between WC and cardiovascular risk. When WC decreases, cardiovascular risk is favorably modified. Measurement of WC is a good predictor of cardiovascular risk.


Subject(s)
Cardiovascular Diseases/epidemiology , Obesity/epidemiology , Waist Circumference , Adult , Antihypertensive Agents/therapeutic use , Blood Glucose/analysis , Blood Pressure , Body Mass Index , Combined Modality Therapy , Comorbidity , Cyclobutanes/therapeutic use , Diabetes Mellitus/drug therapy , Diabetes Mellitus/epidemiology , Directive Counseling , Female , Humans , Hypertension/drug therapy , Hypertension/epidemiology , Hypoglycemic Agents/therapeutic use , Lactones/therapeutic use , Lipids/blood , Male , Metabolic Syndrome/epidemiology , Middle Aged , Motor Activity , Obesity/diet therapy , Obesity/drug therapy , Obesity/psychology , Obesity/therapy , Orlistat , Risk , Weight Loss
2.
Cir Cir ; 79(2): 168-74, 2011.
Article in English | MEDLINE | ID: mdl-21631978

ABSTRACT

BACKGROUND: In the Mexican population we are unaware if the Framingham model is a better system than the SCORE system for stratifying cardiovascular risk. The present study was conducted to compare risk stratification with the Framingham tables using the same procedure but using the SCORE, with the aim of recommending the use of the most appropriate method. METHODS: We analyzed a database of apparently healthy workers from the Mexico City General Hospital included in the study group "PRIT" (Prevalencia de Factores de Riesgo de Infarto del Miocardio en Trabajadores del Hospital General de México) and we calculated the risk in each simultaneously with the Framingham method and the SCORE method. RESULTS: It was possible to perform risk calculation with both methods in 1990 subjects from a total of 5803 PRITHGM study participants. When using the SCORE method, we stratified 1853 patients into low risk, 133 into medium risk and 4 into high risk. The Framingham method qualified 1586 subjects as low risk, 268 as medium risk and 130 as high risk. Concordance between scales to classify both patients according to the same risk was 98% in those classified as low risk, 19.4% among those classified as intermediate risk and only 3% in those classified as high risk. CONCLUSIONS: According to our results, it seems more appropriate in our country to recommend the Framingham model for calculating cardiovascular risk due to the fact that the SCORE model underestimated risk.


Subject(s)
Cardiovascular Diseases/epidemiology , Personnel, Hospital , Risk Assessment/methods , Adult , Aged , Blood Glucose/analysis , Blood Pressure , Cardiovascular Diseases/ethnology , Cohort Studies , Female , Humans , Lipids/blood , Male , Mexico , Middle Aged , Myocardial Infarction/epidemiology , Myocardial Infarction/ethnology , Risk , Smoking/epidemiology
3.
Arch Med Res ; 39(2): 215-21, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18164967

ABSTRACT

BACKGROUND: We undertook this study to establish the prevalence of overweight, obesity, abdominal obesity, high blood pressure, and high glucose and triglyceride levels in school-age children from Mexico City, as well as to determine how overweight and obesity are related to the other risk factors. METHODS: The study was a cross-sectional survey comprised of 1819 children (6-13 years of age) attending six elementary schools. Gender, age, weight, height, waist circumference, blood pressure, and levels of triglycerides and glucose were registered. Percentiles were calculated according to American standards for BMI, height, waist circumference, and blood pressure. RESULTS: Compared to American references, mean percentiles for waist circumference and BMI were >50, and mean height percentiles were <50. Prevalence of overweight was 22.3 and 23.6% for boys and girls, respectively; obesity, 28 and 21.2%; abdominal obesity, 22.1 and 11.7%; high triglyceride levels, 11.3 and 15.4%; high blood pressure, 4.8 and 5.8%, respectively. Overweight, obesity, and abdominal obesity are associated with higher blood pressure and triglyceride levels (odds ratio>1.0, p<0.05). Percentiles for BMI, waist circumference, systolic blood pressure, and diastolic blood pressure also had significant correlations (r>0.2, p<0.001). CONCLUSIONS: This population of Mexican school-age children was shorter and heavier than their American standards. The prevalence of metabolic risks was similar to those reported in American adolescents in NHANES surveys.


Subject(s)
Metabolic Diseases/epidemiology , Obesity/epidemiology , Adolescent , Blood Glucose/analysis , Blood Pressure , Body Mass Index , Child , Female , Humans , Male , Metabolic Diseases/blood , Metabolic Diseases/physiopathology , Mexico , Obesity/blood , Obesity/physiopathology , Prevalence , Triglycerides/blood
4.
Epilepsia ; 47(7): 1203-12, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16886984

ABSTRACT

PURPOSE: Our aim was to evaluate the efficacy of ESCM (electrical stimulation of the centromedian thalamic nucleus) in treatment of generalized seizures of the Lennox-Gastaut syndrome (LGS) and improvement of patient disability. METHODS: Thirteen patients with LGS were studied. They had severe generalized tonic-clonic seizures (GTC) and atypical absences (AA). All patients had at least a 6-month baseline before bilateral electrode implantation to the centromedian (CM) nuclei of the thalamus to undergo therapeutic ESCM. Once implanted, electrodes were temporally externalized through a retromastoid point for electrophysiologic confirmation of their placement. After target confirmation, stimulation parameters were set. Patients came for follow-up assessment of seizures and neurophysiologic tests every 3 months during an 18-month period of time; AED therapy was not modified. RESULTS: The surgical procedure as well as electrical stimulation was well tolerated by all patients. No side effects occurred with the therapeutic stimulation parameters used, and patients were not aware of device activation. Two patients were explanted because of repeated and multiple skin erosions that could not be controlled by plastic surgery procedures. Overall seizure reduction was 80%. The three patients with poorest outcomes for seizure control did not improve their ability scale score. In contrast, the two patients rendered seizure free are living a normal life at present. The remaining eight patients experienced progressive improvement, from being totally disabled to becoming independent in five cases and partially dependent in two. Patients with adequate electrode placement had a seizure reduction >87%. To consider that an electrode is correctly placed, both stereotactic placement and neurophysiologic responses are taken into account. CONCLUSIONS: ESCM provides a nonlesional, neuromodulatory method with improvement in seizure outcome and in the abilities of patients with severe LGS.


Subject(s)
Electric Stimulation Therapy/methods , Epilepsy, Generalized/therapy , Epilepsy/therapy , Intralaminar Thalamic Nuclei/physiology , Quality of Life , Adolescent , Adult , Brain Mapping , Child , Child, Preschool , Disease-Free Survival , Electrodes, Implanted , Electroencephalography/statistics & numerical data , Epilepsy, Generalized/diagnosis , Follow-Up Studies , Functional Laterality/physiology , Humans , Neuropsychological Tests , Stereotaxic Techniques , Syndrome , Treatment Outcome
5.
Salud ment ; 29(1): 28-34, ene.-feb. 2006.
Article in Spanish | LILACS | ID: biblio-985933

ABSTRACT

resumen está disponible en el texto completo


Abstract: Composition and quantity of food in-taken varies considerably between one meal and another, or between one day and the following. Non biological factors -such as emotional, social, day time, feasibility in the type of food, and cost- are, among others, factors that in some way affect the degree of energy in-take by food, which generally is not related with daily energy expenditure. These phenomena represent an active process of regulation that is characterized by the balance between signs that stimulate hunger, called orexigenics and those that produce satiation to stop in-take, called anorexigenics, that promotes the stability in the quantity of corporal energy manifested as fat. In this feeding regulatory process there are many molecular signs that participate and regulate the in-take of behaviour food for homeostasis. There are two hypothalamic centers related with the food in-take control: the hunger centre in the lateral hypothalamus and the satiation centre in the ventromedial nucleus. In this control many impulses participate, regulated by substances called neurotransmitters, such as: neuropeptide Y, galanine, orexines for the hunger centre and nor epinephrine, serotonin, and dopamine for the satiation centre. Insulin reaches the brain through circulation and acts reducing the contribution of energy, it was the first hormonal sign that was implicated in weight control by CNS. The second identified hormone, secreted by the adiposity, was leptin. Both hormones circulate in levels proportional to the corporal fat and get to the CNS in proportion to its plasmatic concentrations. Receptors as leptin and insulin are expressed by brain neurons involved in the contribution of energy, and the administration of any of both peptides directly to the brain, reduce the in-take of food. The lack of any of these hormones produces the opposite. Leptin has a more important role than insulin in the control of the energetic homeostasis in the CNS. For example, the lack of leptin causes severe obesity with hyperfagia that persists regardless the levels of elevated insulin. In contrast, obesity isn't induced by the lack of insulin. Insulin has a critic role to promote the storage of fat and the synthesis of leptin through the fat cellule. The neuropeptide Y, produced in the arcuate nucleus of the hypothalamus has an anabolic effect. The gene of expression and secretion of this peptide in the hypothalamus increases during depletion, in the storage of corporal fat and/or when the signs of leptin/insulin are decreased in the brain. Leptin inhibits the gene of expression of the neuropeptide Y in the arcuate nucleus and the genetic "knockout" of the NPY reduces hyperfagia and obesity in mice ob/ob, indicating that the total response to the lack of leptin requires the signs of the NPY. Other substances like the Agouti protein (AGRP), the orexines (hypocretines A and B) and the concentrations of the melancortin hormone have been added to the molecule candidate list with anabolic effects. Also in the adjoining neurons of the arcuate nucleus, are originated anorexigenic peptides like alfa-MSH (a derivated of the pro-opiomelancortin, POMC) and CART (transcript protein related with cocaine and amphetamine). Both types of neurons (NPY/AGRP and POMC/CART) coexpress the leptin receptors. In those situations in which the levels of leptin or insulin are low, the NPY/AGRP neurons activate and the POMC/CART are inhibited. This suggests that the main site of adiposity signs transformation is a neuronal response in the arched nucleus. The link between the lateral hypothalamus and the elevated centers of the brain that regulate hunger and satiation is a very important aspect of the regulation system. There have been typified two types of neuropeptides linked to neurons, that appear to be exclusively of the lateral hypothalamus area: the concentrated melanin hormone (MCH) and the orexines. At the lateral zone, there have been specified two types of hypothalamic neuropeptides, the orexines A and B, also known as hypocretines 1 and 2, which are cellular bodies of the hypothalamus, especially at the lateral hypothalamus and the perifornical area, which stimulate the appetite in an independent way to other neuropeptides known. On the other hand, the orexines A and B derive (by proteolysis) of a common precursor, and are capable of activating their two respective receptors that work in conjunction with proteins G. The central administration of orexines stimulates the in-take and production of orexines' increase with fasting. These neuropeptides match with the hypocretines described by other authors, with expression in late ral hypothalamus, arched nucleus, septal nucleus and forebrain. Monoaminergic neurotransmitters. Noradrenalin Noradrenalin is synthesized in different areas of the brain such as the dorsal nucleus of the vague and the locus coeruleus.Noradrenalin shares the same place with NPY and the injection of both inside the preventricular nucleus increase the in-take of food. The repeated injection can result in weight increase; leptin can inhibit noradrenalin secretion. Dopamine Critic dependence of the in-take of food in the CNS is given by the dopamine sign, which is implicated in the voluntary lack of the food in-take. Motor alterations associated with the lack of dopamine affect also the alimentary behavior. The dopamine effect over the alimentary behavior varies depending of the studyied area. For example the routes of dopamine in the mesolimbic area contribute to the reward of the in-take of savory food. SerotoninThe 5HT2c receptor of serotonin is implicated in the decrease of the in-take of food and the weight increase, due to its effect in the impulse of the satiation centre. To maintain the homeostasis of normal energy it is necessary that the serotonin sign be intact. New alternative hypothesis. On one hand, the knowledge of regulation of the appetite-satiety neuroendocrine cycle, and on the other, the new techniques of neuromodulation through stereotaxic surgery, allow to offer an extraordinarily interesting field of research in certain patients with feeding disorders of difficult control and with an increase in the mortality risk. The alternative of controlling specific centers of hunger/satiation regulation, is still a hypothesis, though there are some data that allow us to assume that it could be feasible and we will mention them after. Current experience. Stereotaxic (Latin: stereo, three-dimensional; taxis, positioning) is a modern technique of neurosurgery that allows the localization and precise access to intra-cerebral structures, through a small orifice in the skull. If we have identified the places that regulate the intake of food or satiety, it is feasible that through this technique we can stimulate or inhibit this function and offer the patient an alternative that in theory could be feasible. Some of its possible advantages will be that we are talking about a minimum invasive surgery, generally performed using local anesthesia; patients need a minimum hospitalization stay and surgical risks are minimized. This allows us to predict in the majority of the patients a satisfactory evolution of weight decrease. The current experience of stereotaxic used in eating disorders is null; everything about it is hypothetic. However, the use of this proceeding for other accepted indications where there is previous experience, has allowed us to obtain interesting data of the evolution of these patients that shows indirectly, that the procedure has influenced in the corporal weight. We present these indirect results, which motivate us to continue considering its possible use in patients that show the approved profile according to an ethic committee properly authorized. In depression or bipolar disorder cases, the use of the stereotaxic surgery applying electrodes in the bottom pedunculo thalamic region (ITP), independently that they show an improve in their basal alteration, the patients show a weight increase, inferring a relationship of this area and the one of the hypothalamus for the appetite/satiation control, situation that hypothetically could benefit patients with anorexia nervosa or bulimia. In the cases with Parkinson Disease, the stereotaxic procedure has been made in the pre-lemniscal (RAPRL) or the subtalamic region (STN) in a unilateral or bilateral way, and although the response hasn't been uniform, the weight changes showed a decrease, making this a possible alternative to be used in some patients with morbid obesity according to the inclusion criteria. Final comments. The expectative of stereotaxic surgery in handling patients with difficult to control feeding disorders or with high risk of morbid-mortality, is shown as an hypothesis, that should consider the specific rules of good clinical practices and adjust to the rules of an approved ethics committee, for these procedures.

6.
Adv Ther ; 22(6): 642-9, 2005.
Article in English | MEDLINE | ID: mdl-16510381

ABSTRACT

A study on the treatment of obese adolescents with the use of sibutramine in private practice is presented. Patients consisted of 24 boys and 43 girls with obesity (body mass index [BMI]>85th percentile sex-specific BMI for age and sex) ranging from 12 to 18 years of age. Patients were given sibutramine 10 mg per day for 6 months. With the last observation carried forward adjustment, after 6 months of treatment, patients' average weight changed from 91.6+/-19.7 kg to 81.9+/-19.0 kg (P<.001), that is, 89.5+/-7.3% of initial weight. The most frequently reported adverse events included increased blood pressure and pulse rate (n=7), constipation (n=8), dry mouth (n=4), and constipation and dry mouth (n=3). Sibutramine may be considered effective for the treatment of obese adolescents, with a level of safety similar to that observed in adult patients.


Subject(s)
Appetite Depressants/therapeutic use , Cyclobutanes/therapeutic use , Obesity/drug therapy , Adolescent , Appetite Depressants/adverse effects , Blood Pressure/drug effects , Body Mass Index , Body Weight/drug effects , Child , Cyclobutanes/adverse effects , Female , Heart Rate/drug effects , Humans , Male , Mexico
7.
Clin Ther ; 26(9): 1427-35, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15531005

ABSTRACT

BACKGROUND: The management of type 2 diabetes mellitus is complicated by the presence of risk factors related to overweight and obesity, particularly visceral adiposity. However, weight loss and weight maintenance are difficult for patients with diabetes, and the benefits of dietary modifications are typically modest. Sibutramine is a serotonin- and norepinephrine-reuptake inhibitor that reduces food intake by inducing early satiety and attenuates the decrease in basal energy expenditure associated with weight loss. Previous trials of sibutramine in overweight and obese patients with type 2 diabetes have shown significant weight loss accompanied by better glycemic control. OBJECTIVE: The goal of this study was to assess the effect on body weight and glycemic control of sibutramine in combination with glibenclamide in obese Hispanic patients with type 2 diabetes. METHODS: This was a 12-month, randomized, double-blind, placebo-controlled clinical trial conducted at the Endocrinology Service, General Hospital of Mexico, Mexico City. Included were overweight or obese (body mass index [BMI] >27 kg/M2) patients with type 2 diabetes between the ages of 24 and 65 years who had been receiving glibenclamide monotherapy for at least 2 weeks and whose glucose concentrations were stable. Patients were randomized to receive sibutramine 10 mg or placebo once daily. The primary efficacy measures were change in body weight, waist circumference, and glycosylated hemoglobin (HbA1c). Anthropometrics and fasting glucose concentrations were measured monthly. HbA1c was determined at baseline and at 6 and 12 months. Laboratory parameters were measured at baseline and at the end of the study. RESULTS: Forty-four patients were randomized to receive sibutramine (28 women, 16 men; mean [SD] age, 47.6 [9.0] years), and 42 were randomized to receive placebo (31 women, 11 men; mean age, 45.8 [8.1] years). Twenty-four patients in the sibutramine group and 23 in the placebo group completed the trial. In the sibutramine group, body weight was reduced from a mean (SD) of 73.9 (10.3) kg at baseline to 69.8 (10.6) kg at month 12; BMI decreased from 29.9 (2.6) to 28.2 (2.9) kg/M2; waist circumference was reduced from 94.9 (8.4) to 90.8 (8.4) cm; the plasma fasting glucose concentration decreased from 140.4 (29.4) to 114.2 (32.0) mg/dL; and the HbA1c value was reduced from 8.9% (1.2) to 8.3% (1.2) (all, P < 0.001). In the placebo group, the corresponding changes were from 74.5 (10.3) kg at baseline to 73.1 (11.2) kg at month 12; from 30.1 (2.5) to 29.5 (2.9) kg/M2; from 94.4 (7.3) to 93.1 (8.3) cm (P < 0.05); from 140.7 (25.2) to 123.9 (38.3) mg/dL (P < 0.05); and from 9.0% (1.2) to 9.1% (1.3). In the sibutramine group, weight loss continued for up to 12 months. CONCLUSION: In this population of obese Hispanic patients with type 2 diabetes, sibutramine combined with glibenclamide therapy achieved weight loss for up to 12 months and was associated with better glycemic control than placebo.


Subject(s)
Appetite Depressants/therapeutic use , Cyclobutanes/therapeutic use , Diabetes Mellitus, Type 2/drug therapy , Obesity/drug therapy , Weight Loss/drug effects , Adult , Aged , Blood Glucose/drug effects , Diabetes Mellitus, Type 2/complications , Double-Blind Method , Female , Glyburide/therapeutic use , Humans , Hypoglycemic Agents/therapeutic use , Male , Obesity/complications , Time Factors
8.
Obes Res ; 12(2): 215-23, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14981213

ABSTRACT

OBJECTIVE: To establish the prevalence of overweight and obesity in Mexican children 10 to 17 years of age according to the percentiles from both the Centers of Disease Control and Prevention (CDC) and the International Obesity Task Force (IOTF). RESEARCH METHODS AND PROCEDURES: Heights and weights were measured in children from nationally representative, randomly chosen households in the Mexican National Health Survey 2000. The study population consisted of 7862 boys and 8947 girls, 10 to 17 years of age. Measurements used were the percentage of children in the corresponding BMI categories for overweight and obesity specified by the CDC and the IOTF BMI percentiles. RESULTS: The children were short, with mean Z scores for height by age varying from - 0.62 +/- 1.26 to -1.12 +/- 1.06 in boys and from -0.45 +/- 1.25 to -1.19 +/- 1.12 in girls. CDC-based overweight prevalences varied by age from 10.8% to 16.1% in boys and 14.3% to 19.1% in girls, with obesity prevalences from 9.2% to 14.7% in boys and 6.8% to 10.6% in girls; these prevalences did not relate to stunting. IOTF-based excess weight prevalences were similar, with higher overweight rates (boys, 15.4% to 18.8%; girls, 18.4% to 22.3%) but lower obesity rates (boys, 6.1% to 9%; girls, 5.9% to 8.2%). DISCUSSION: Mexican children have one-half the overweight/obesity prevalences of U.S. Mexican-American children; however, there are higher rates in Northern Mexico, which is closer to the U.S. These escalating rates of excess weight demand new prevention, as well as management, policies.


Subject(s)
Body Mass Index , Obesity/epidemiology , Adolescent , Body Height , Body Weight , Centers for Disease Control and Prevention, U.S. , Child , Cross-Sectional Studies , Female , Humans , Male , Mexico/epidemiology , Mexico/ethnology , Nutrition Surveys , Obesity/diagnosis , Obesity/prevention & control , Prevalence , United States/epidemiology
9.
Adv Ther ; 20(2): 101-13, 2003.
Article in English | MEDLINE | ID: mdl-12836810

ABSTRACT

This 6-month randomized study evaluated the safety and efficacy of sibutramine in 57 overweight Hispanic patients with hypertension. Following a 2-week washout to confirm the diagnosis of hypertension, antihypertensive medication was adjusted to achieve a blood pressure less than 140/90 mm Hg before institution of either sibutramine 10 mg or placebo once a day. A body mass index in excess of 27 kg/m2 was required for entry. At study end, weight had changed from 75.4+/-9.6 to 70.0+/-9.5 kg in the sibutramine group and from 77.9+/-9.0 to 74.5+/-9.4 kg in the placebo group. In the sibutramine group, systolic blood pressure was 127.8+/-5.8 mm Hg after stabilization and 125.2+/-8.5 mm Hg after completion of the trial; respective values for diastolic blood pressure were 82.4+/-3.7 and 81.5+/-4.6 mm Hg. With placebo, blood pressure dropped from 129.0+/-7.1/80.9+/-4.9 mm Hg to 122.8+/-9.7/80.3+/-5.4 mm Hg at the same timepoints. In the sibutramine group, 14 patients reported 21 adverse events, most frequently headache (n=5), constipation (n=4), and dry mouth (n=4). In the placebo group, 13 patients had 20 adverse events. Sibutramine is safe and effective in overweight Hispanic patients with hypertension, but monitoring of blood pressure and titration of antihypertensive medication are necessary.


Subject(s)
Antihypertensive Agents/therapeutic use , Appetite Depressants/therapeutic use , Cyclobutanes/therapeutic use , Hypertension/prevention & control , Obesity/drug therapy , Adult , Antihypertensive Agents/adverse effects , Appetite Depressants/adverse effects , Blood Pressure/physiology , Body Mass Index , Body Weight , Cyclobutanes/adverse effects , Female , Humans , Hypertension/complications , Hypertension/physiopathology , Male , Mexico , Middle Aged , Obesity/complications , Obesity/physiopathology , Placebos , Treatment Outcome , Weight Loss/drug effects
11.
Gac. méd. Méx ; 136(1): 83-86, ene.-feb. 2000. ilus, CD-ROM
Article in Spanish | LILACS | ID: lil-304308

ABSTRACT

Durante muchos años la osteoporosis se ha considerado una enfermedad que afecta al sexo femenino, sin embargo en el hombre, el envejecimiento y la disminución de las concentraciones de testosterona se encuentran asociados a la disminución de la masa ósea. Al igual que en la mujer, la osteoporosis en el hombre debe tratarse con suplementos de calcio y vitamina D. Recientemente se ha demostrado que el alendronato, un bisfosfonato ha tenido éxito para mejorar la densidad ósea y disminuir la incidencia de fracturas en el hombre. La terapia de reemplazo con andrógenos se espera tenga efecto benéfico sobre el hueso, pero se requieren estudios clínicos controlados que lo comprueben.


Subject(s)
Humans , Male , Alendronate , Osteoporosis , Testosterone , Fractures, Bone/physiopathology
12.
Arch. med. res ; 29(4): 325-9, oct.-dic. 1998. tab, ilus
Article in English | LILACS | ID: lil-232653

ABSTRACT

Background. Self-monitoring of blood glucose levels has become an important instrument for the management of patients with diabetes mellitus. Both patients and physicians expect that monitors will provide reliable results. Numerous environmental, physiologic, and operational factors can affects system performance, yielding results that are inaccurate or unpredictable. Methods. This study examined the effect of one factor -high altitude- on the performance of seven blood glucose monitoring systems. The following monitors were compared. two One Touch II; two One Touch Basic; two Reflolux II (Accu-Chec in the USA); two Glucometer 3; one Glucometer 2, and one Accutrend Alpha. Double blood glucose level values were compared with a cotrolled reference laboratory test values, which was unknown to the investigator until the end of the study because the study was double blind. Blood glucose values were obtained using each of the monitors in 200 patients; 150 with diabetes mellitus, and 50 healthy subjects. Results. The One Touch monitors were the only monitors that reported adjusted straight lines (Y0a+bX) that were very similar for all three techniques. In addition, these adjusted straight lines are those closest to the ideal line, Y=X. These same monitors were the only ones that did not reject the null hypothesis Ho: a=0. The relative deviation index at the 20 percent level was less than 3.5 percent for the One Touch II and One Touch Basic monitors; for the rest of the monitors the index was over 14 percent. The clinically accepted EGA region was similar for all study monitors. Conclusions. In conclusion, the One Touch II and One touch Basic Monitors showed greater accuracy in comparison to the other devices. The evaluation of the clinically acceptable region shows practical reliability for all of the monitor used


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Blood Glucose Self-Monitoring/instrumentation , Diabetes Mellitus/blood , Equipment and Supplies/statistics & numerical data , Reproducibility of Results
13.
Rev. invest. clín ; 50(5): 389-94, sept.-oct. 1998. tab
Article in English | LILACS | ID: lil-234151

ABSTRACT

Objetivo. Determinar los niveles de fibrinógeno en obesos con diabetes tipo 2 y valorar las potenciales modificaciones que induce la metformina. Métodos. Fue un estudio abierto, prospectivo, randomizado y comparativo que incluyó a 60 pacientes con diabetes tipo 2 obesos (IMC > 27) durante dos fases. La fase de pretratamiento fue de 4 semanas con un control con dieta. En la fase de tratamiento se les dividió en dos subgrupos de 30. Uno recibió una tableta de metformina de 850 mg, incrementándose la dosis a dos o tres tabletas de acuerdo al control metabólico; el otro subgrupo recibió insulina DNA-recombinante 24 U, subcutánea (dos tercios antes del desayuno y un tercio antes de la cena), ajustando la dosis de acuerdo a la respuesta. Como grupo control se incluyeron a 60 sujetos obesos no diabéticos, que durante las dos fases sólo recibieron dieta. Resultados. Los valores promedio de glucosa, fibriógeno y del índice de masa corporal (IMC) no cambiaron en la fase de pretratamiento de controles y diabéticos ni en la fase de tratamiento de los controles. En cambio los tres parámetros disminuyeron significativamente en el subgrupo de metformina (p < 0.001) y soló el de glucosa (p< 0.001) en el subgrupo de insulina. Conclusiones. La metformina, además de mejorar el control metabólico, demostró ser una buena alternativa para modificar favorablemente los niveles de fibrinógeno en pacientes con diabetes tipo 2


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus/blood , Fibrinogen/metabolism , Hypoglycemic Agents/therapeutic use , Metformin/therapeutic use
14.
Rev. invest. clín ; 45(1): 37-42, ene.-feb. 1993. tab, ilus
Article in English | LILACS | ID: lil-121170

ABSTRACT

Objetivo. Valorar la utilidad del Gd-DTPA y evidenciar aquellos microadenomas de la glándula hipófisis que no han sido demostrados por IRM sin su empleo en pacientes con enfermedad de Cushing. Método: se practicó a seis pacientes RM con y sin gadolinio para hacer evidente la tumoración, y los hallazgos fueron correlacionados con cirugía y confirmados por estudios inmunohistoquímico e histológico de la pieza quirúrgica. Resultados. En todos los casos postadministración del medio, en la RM se demostró una imagen hipodensa circunscrita que correspondía en forma precisa con la localización y extensión del tejido adenimatoso encontrado duarante la cirugía. La extirpación selectiva del microadenoma no tuvo éxito en la mejoría clínica y bioquímica en dos de los seis pacientes. Dichos casos no presentaron imagen residual hipodensa en la RM con Gd-DTPA en el postoperatorio. Conclusiones. Los resultados suguieren que la IRM con Gd-DTPA es un método útil para detectar microadenomas hipofisiarios no demostrables por IRM sin el medio de contraste; sin embargo, las alteraciones del tejido hipofisiario pueden extenderse más allá de la imagen anormal.


Subject(s)
Humans , Female , Adolescent , Adult , Pituitary Gland/pathology , Magnetic Resonance Imaging , Pentetic Acid , Prolactinoma/diagnosis , Pituitary Neoplasms/diagnosis , Pituitary Neoplasms/surgery , Prolactinoma , Cushing Syndrome/pathology
15.
Rev. méd. Hosp. Gen. Méx ; 51(3): 129-33, jul.-sept. 1988. ilus
Article in Spanish | LILACS | ID: lil-102214

ABSTRACT

Conocida la utilidad de la tolbutamida para cuantificar la reserva pancreática (RP), se decidió correlacionar el descenso de la glucemia con el incremento de la insulinemia durante la prueba de reserva pancreática (PRP) y, adem , averiguar si el resultado de ésta permite inferir el tipo de terapéutica y la dosis necesarias para un buen control. En la primera fase, 15 diabéticos (grupo I: dependientes de la insulina; grupo II; tratados con hipoglucemiantes orales; grupo III controlados sólo con dieta se sometieron por el método doble ciego y cruzado a la PRP con tolbutamida y luego con placebo; simultáneamente se midió la concentración de insulina. En el grupo I no fue significativa la diferencia entre fármaco y placebo pero si alcanzó validez estadística en los otros dos grupos y al comparar a éstos con el grupo I (p<0.05). En la segunda fase, 17 diabéticos (tipo I y II) se sometieron a la PRP y según el resultado de ésta, fueron tratados con dieta, hipoglucemiantes orales o insulina. Los nueve con valor <35 por 100 requirieron insulina y los ocho con valor mayor pudieron controlarse con dieta o hipoglucemiantes. Además se observó una relación entre el de la PRP y la dosis de medicamentos. Se concluye que la PRP permite diagnosticar el tipo de diabetes y determinar las pautas de esquema terapéutico; además es un recurso con alcance del médico general y del especialista .


Subject(s)
Humans , Tolbutamide/administration & dosage , Blood Glucose/metabolism , Diabetes Mellitus/diagnosis , Diabetes Mellitus/therapy , Insulin/metabolism , Mexico
17.
Arch. invest. méd ; 16(supl 3): 59-73, 1985. ilus, tab
Article in Spanish, English | LILACS | ID: lil-37025

ABSTRACT

Se analizaron los aspectos clínicos, radiológicos y de laboratorio que tuvieron relación con una evolución satisfactoria o desfavorable de 217 casos de adenomas hipofisarios después de operarlos. No mejoraron con la operación las afecciones visuales secundarias a atrofia óptica, el panhipopituitarismo y la diabetes insípida, y la mortalidad más alta ocurrió en los pacientes ciegos antes de operarse. En los acromegálicos, la deformidad faringeotraqueal y torácica con insuficiencia respiratoria aumentó el riesgo quirúrgico (anestésico) en forma considerable. En la enfermedad de Cushing se observaron hiperpigmentación de piel y mucosas y psicosis maniacodepresiva en los pacientes que tuvieron una evolución desfavorable, lo que contrastó con la evolución de los otros sin estos síntomas. El seguimiento con tomografia computarizada de cráneo puso de manifesto que los tumores con extensión parasillar y retrosillar rara vez pudieron extirparse en su totalidad, en tanto que así fue posible hacerlo totalmente con los adenomas situados en la línea media, independientemente de su tamaño. Los niveles basales de prolactina fueron proporcionales al tamaño del tumor, en tanto que los de las hormonas de crecimiento no lo fueron. La evolución fue mejor en pacientes con pruebas de TRH y bromocriptina positivas, y rara vez se lograron volver negativas después de la operación


Subject(s)
Humans , Adenoma/surgery , Pituitary Neoplasms/surgery , Sella Turcica , Adenoma/diagnosis , Follow-Up Studies , Pituitary Neoplasms/diagnosis , Tomography , Tomography, X-Ray Computed
18.
Rev. invest. clín ; 34(4): 321-6, 1982.
Article in Spanish | LILACS | ID: lil-13078

ABSTRACT

Con base en el analisis de los niveles basales de GH, PRL y TSH asi como en sus respuestas a la administracion de TRH, se evaluo la eficacia "terapeutica" de cirugia o radioterapia en 27 pacientes acromegalicos. Los resultados muestran que a largo plazo (48 meses), la eficacia de ambos procedimientos es semejante. Ademas, la persistencia de respuestas paradojicas en el subgrupo de pacientes TRH positivos: asi como los cambios de TSH y PRL en este y el subgrupo TRH negativos, permite cuestionar y evaluar los criterios de curacion e inactividad del sindrome


Subject(s)
Humans , Male , Female , Acromegaly , Radiotherapy , Surgical Procedures, Operative , Growth Hormone , Prolactin , Thyrotropin
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