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1.
Rev Med Inst Mex Seguro Soc ; 60(Suppl 2): 127-133, 2022 Dec 19.
Article in Spanish | MEDLINE | ID: mdl-36796053

ABSTRACT

Pediatric obesity is a pathological process explained by genetic susceptibility, inappropriate diet, sedentary life patterns, and other environmental factors. It is related with psychological disturbances and chronic diseases in childhood or later in adulthood. Obesity prevention must start early in life and requires lifestyle multicomponent intervention (diet, physical activity and behavior), include children, family, and community, and offered in the primary health care service by the healthcare staff (physicians, nurses, dietists, and psychologists). Obesity treatment may include in addition other treatment alternatives. It must be provided by physicians, to simultaneously treat obesity and the associated morbidity. Pediatric obesity is a global problem, and its management has not been effective. Therefore, scientific research must be involved to identify new management options.


La obesidad pediátrica es un proceso patológico que se puede explicar por la predisposición genética, la dieta inadecuada, el sedentarismo y otros factores ambientales. Se asocia a trastornos psicológicos y enfermedades crónicas en la niñez o más tarde, en la edad adulta. La prevención de la obesidad debe iniciar desde etapas tempranas de la vida y requiere cambios integrales en el estilo de vida (dieta, ejercicio y conductual) involucrando al niño, la familia y la comunidad; se debe realizar por todo el equipo de salud en el primer nivel de atención (médicos, enfermeras, nutriólogos y psicólogos). El tratamiento de la obesidad puede incluir otras alternativas de tratamiento y debe ser otorgado por el médico (apoyado por el equipo de salud) para atender simultáneamente la obesidad y la morbilidad asociada. El problema de la obesidad pediátrica es mundial y su manejo ha sido poco eficiente hasta ahora, por lo que se requiere la participación de la investigación científica para identificar nuevas estrategias de manejo.


Subject(s)
Pediatric Obesity , Child , Humans , Adolescent , Pediatric Obesity/prevention & control , Diet , Life Style , Exercise
2.
J Pediatr Endocrinol Metab ; 33(3): 347-354, 2020 Mar 26.
Article in English | MEDLINE | ID: mdl-32069236

ABSTRACT

Introduction Hyperandrogenism (HA), either clinical or biochemical, is associated with obesity in adolescent girls. Long chain polyunsaturated fatty acids ω3 (LCPUFA-ω3) play protective roles in some obesity-associated morbidities, but their contribution to preventing HA is unclear. Our aim was to examine the potential positive relationships between erythrocyte LCPUFA-ω3, with or without supplementation, and hyperandrogenemia. Methods Secondary analysis of a clinical trial that was conducted previously to analyze the effect of LCPUFA-ω3 on insulin resistance and body weight. Here, we present a cross-sectional analysis of 180 girls with obesity, and a longitudinal analysis of 117 girls who completed a 3-month supplementation period (57 LCPUFA-ω3 [DO3] and 60 placebo [DP)]). Dehydroepiandrosterone sulfate (DHEAS), total testosterone (TT) and steroid hormone binding globulin (SHBG) were measured with chemiluminescence; free testosterone (FT) was calculated. Erythrocyte fatty acids were determined by gas chromatography. Non-parametric statistics was used for analysis. Results In cross-sectional analysis, age (odds ratio [OR] = 1.35; 95% confidence interval [CI] = 1.03, 1.78; p = 0.027), insulin (OR = 1.05; 95% CI: 1.00, 1.10; p = 0.018), and erythrocytes eicosapentaenoic acid (EPA) (OR = 0.04; 95% CI: 0.01, 0.65; p = 0.012) were predictors of hyperandrogenemia (FT >0.63 ng/mL). In longitudinal analysis, EPA, adiponectin and SHBG increased, while FT decreased, in the DO3 group (p < 0.05). The risk of hyperandrogenemia at the end of follow-up was predicted by basal hyperandrogenemia (OR = 18.16, 95% CI: 5.37, 61.4; p < 0.001) and by increases in EPA (OR = 0.40; 95% CI: 0.01, 0.65; p = 0.06 marginal significance). Conclusions Our results suggest a preventive role of EPA on the risk for hyperandrogenemia in girls with obesity, but further studies are needed to demonstrate a benefit.


Subject(s)
Fatty Acids, Omega-3/blood , Fatty Acids, Omega-3/therapeutic use , Hyperandrogenism/blood , Obesity/blood , Puberty , Adolescent , Body Mass Index , Body Weight , Cross-Sectional Studies , Dehydroepiandrosterone Sulfate/blood , Dietary Supplements , Female , Humans , Insulin Resistance , Longitudinal Studies , Sex Hormone-Binding Globulin/analysis , Testosterone/blood , Waist Circumference
3.
Nutr. hosp ; 37(1): 211-222, ene.-feb. 2020. tab
Article in Spanish | IBECS | ID: ibc-187591

ABSTRACT

Los edulcorantes no calóricos (ENC) son aditivos de alimentos que se utilizan para sustituir azúcares y potencialmente para reducir la ingesta energética. Existe un debate científico en torno a los beneficios reales de su uso. Los ENC son sustancias ampliamente evaluadas en la literatura científica. Su seguridad es revisada por las agencias regulatorias internacionales del campo de la salud. Los profesionales de la salud y los consumidores con frecuencia carecen de educación e información rigurosa, objetiva y sustentada en la evidencia científica y el juicio clínico sobre el uso de aditivos en los alimentos. Los ENC se han empleado como sustitutos de la sacarosa, en especial por las personas con diabetes mellitus y obesidad. Sin embargo, se han planteado inquietudes relacionadas con su posible asociación con el parto pretérmino y con su uso durante el embarazo y la lactancia, ante la posibilidad de consecuencias metabólicas o de otra índole en la madre o en el neonato. Este análisis de la evidencia en ginecología y obstetricia presenta una revisión que intenta responder a preguntas que habitualmente se hacen al respecto los profesionales de la salud y sus pacientes. En este documento se evalúan diversas publicaciones científicas bajo el tamiz de la medicina basada en la evidencia y del marco regulatorio para aditivos de alimentos con el fin dilucidar si el uso de ENC en las mujeres durante las etapas críticas del embarazo y la lactancia supone o no un posible riesgo


Non-nutritive sweeteners (NNS) are food additives that have been used as a possible tool to reduce energy and sugar intake. There is a scientific debate around the real benefits of their use. NNS are substances widely evaluated in the scientific literature. Their safety is reviewed by international regulatory health agencies. Health professionals and consumers often lack education and objective information about food additives based on the best scientific evidence. NNS have been used as a substitute for sucrose, especially by people with diabetes mellitus and obesity. However, concerns related to their possible association with preterm birth have been raised, and also with their use during pregnancy and lactation because of the possibility of metabolic or other consequences in both the mother and offspring. This analysis of the evidence in gynecology and obstetrics presents a review of the most commonly asked questions regarding this matter by health professionals and their patients. This document evaluates a diversity of scientific publications under the sieve of evidence-based medicine and the regulatory framework for food additives to elucidate whether the use of NNS in women in these critical stages of pregnancy and breastfeeding represents a potential risk


Subject(s)
Humans , Female , Pregnancy , Non-Nutritive Sweeteners/administration & dosage , Consensus , Pregnancy Complications/diet therapy , Lactation , Non-Nutritive Sweeteners/metabolism , Reproductive Health , Food Additives/administration & dosage , Obstetric Labor, Premature/diet therapy , Risk Factors
4.
Nutr Hosp ; 37(1): 211-222, 2020 Feb 17.
Article in Spanish | MEDLINE | ID: mdl-31960692

ABSTRACT

INTRODUCTION: Non-nutritive sweeteners (NNS) are food additives that have been used as a possible tool to reduce energy and sugar intake. There is a scientific debate around the real benefits of their use. NNS are substances widely evaluated in the scientific literature. Their safety is reviewed by international regulatory health agencies. Health professionals and consumers often lack education and objective information about food additives based on the best scientific evidence. NNS have been used as a substitute for sucrose, especially by people with diabetes mellitus and obesity. However, concerns related to their possible association with preterm birth have been raised, and also with their use during pregnancy and lactation because of the possibility of metabolic or other consequences in both the mother and offspring. This analysis of the evidence in gynecology and obstetrics presents a review of the most commonly asked questions regarding this matter by health professionals and their patients. This document evaluates a diversity of scientific publications under the sieve of evidence-based medicine and the regulatory framework for food additives to elucidate whether the use of NNS in women in these critical stages of pregnancy and breastfeeding represents a potential risk.


INTRODUCCIÓN: Los edulcorantes no calóricos (ENC) son aditivos de alimentos que se utilizan para sustituir azúcares y potencialmente para reducir la ingesta energética. Existe un debate científico en torno a los beneficios reales de su uso. Los ENC son sustancias ampliamente evaluadas en la literatura científica. Su seguridad es revisada por las agencias regulatorias internacionales del campo de la salud. Los profesionales de la salud y los consumidores con frecuencia carecen de educación e información rigurosa, objetiva y sustentada en la evidencia científica y el juicio clínico sobre el uso de aditivos en los alimentos. Los ENC se han empleado como sustitutos de la sacarosa, en especial por las personas con diabetes mellitus y obesidad. Sin embargo, se han planteado inquietudes relacionadas con su posible asociación con el parto pretérmino y con su uso durante el embarazo y la lactancia, ante la posibilidad de consecuencias metabólicas o de otra índole en la madre o en el neonato. Este análisis de la evidencia en ginecología y obstetricia presenta una revisión que intenta responder a preguntas que habitualmente se hacen al respecto los profesionales de la salud y sus pacientes. En este documento se evalúan diversas publicaciones científicas bajo el tamiz de la medicina basada en la evidencia y del marco regulatorio para aditivos de alimentos con el fin dilucidar si el uso de ENC en las mujeres durante las etapas críticas del embarazo y la lactancia supone o no un posible riesgo.


Subject(s)
Non-Nutritive Sweeteners , Abnormalities, Drug-Induced/etiology , Abnormalities, Drug-Induced/prevention & control , Diabetes, Gestational/etiology , Diabetes, Gestational/prevention & control , Evidence-Based Medicine , Female , Fetus/drug effects , Humans , Hypersensitivity/etiology , Lactation , Milk, Human/chemistry , Non-Nutritive Sweeteners/adverse effects , Non-Nutritive Sweeteners/pharmacokinetics , Non-Nutritive Sweeteners/therapeutic use , Obstetric Labor, Premature/chemically induced , Overweight/prevention & control , Preconception Injuries/chemically induced , Preconception Injuries/prevention & control , Pregnancy , Pregnancy Complications , Prenatal Exposure Delayed Effects , Weight Gain
5.
Nutrients ; 11(3)2019 03 23.
Article in English | MEDLINE | ID: mdl-30909605

ABSTRACT

The influence of obesity on maternal iron homeostasis and nutrition status during pregnancy remains only partially clarified. Our study objectives were (1) to describe how obesity influences broad iron nutrition spectrum biomarkers such as available or circulating iron (serum transferrin receptor (sTfr) and serum iron), iron reserves (ferritin), and functional iron (hemoglobin); and (2) to depict the regulating role of hepcidin. The above was carried out while considering influential factors such as initial iron nutrition status, iron intake, and the presence of inflammation. Ninety three non-anemic pregnant adult women were included, 40 with obesity (Ob) and 53 with adequate weight (AW); all took ≈30 mg/day of supplementary iron. Information on iron intake and blood samples were obtained at gestational weeks 13, 20, 27, and 35. A series of repeated measure analyses were performed using General Linear Models to discern the effect of obesity on each iron indicator; iron intake, hepcidin, and C-reactive protein were successively introduced as covariates. Available and circulating iron was lower in obese women: sTfr was higher (p = 0.07) and serum iron was lower (p = 0.01); and ferritin and hemoglobin were not different between groups. Hepcidin was higher in the Ob group (p = 0.01) and was a significant predictor variable for all biomarkers. Obesity during pregnancy dysregulates iron homeostasis, resembling "obesity hypoferremia".


Subject(s)
Homeostasis , Iron/blood , Maternal Nutritional Physiological Phenomena/physiology , Obesity/blood , Pregnancy Complications/blood , Adult , Biomarkers/blood , C-Reactive Protein/metabolism , Dietary Supplements , Female , Ferritins/blood , Hemoglobins/metabolism , Hepcidins/blood , Humans , Inflammation/blood , Iron/administration & dosage , Linear Models , Nutritional Status , Obesity/complications , Obesity/physiopathology , Pregnancy , Pregnancy Complications/etiology , Pregnancy Complications/physiopathology , Receptors, Transferrin/blood , Young Adult
6.
Gac Med Mex ; 153(Supl. 2): S34-S41, 2017.
Article in Spanish | MEDLINE | ID: mdl-29099111

ABSTRACT

Objective: To evaluate the frequency of some subtle metabolic alterations in a group of adolescents with obesity and polycystic ovary syndrome (PCOS). Materials and Methods: A cross-sectional, comparative study was conducted in a group of adolescents with obesity, and characterized as with or without PCOS according with the Rotterdam Consensus. Medical history, anthropometry, gynecologic pelvic ultrasound (to evaluate ovarian volumes, number of antral follicles and endometrial width), as well as serum glucose, insulin, lipoproteins, interleukin-6, tumor necrosis factor alpha, total testosterone, dehydroepiandrosterone, sexual hormones binding globulin, leptin, adiponectin and insulin-like growth factor 1, the free-androgen index, free and available testosterone, and homeostatic model assessment index were calculated. For statistics, mean and standard deviation, or median and ranges were used for description as appropriate. Likewise, Student t-test or Mann-Whitney test were used for comparisons. Results: From a sample of 180 adolescents, 47 attached to selection criteria. Mean age was 13.5 year and Z-score 2.5. Eighty percent of adolescents presented central distribution of body fat and 95% hyperinsulinemia. The more frequent dyslipidemias were hypertriglyceridemia in 57% and hypercholesterolemia in 12.8%; 25.5% of adolescents presented two out of three criteria for polycystic ovary syndrome (PCOS). Body mass index and insulin were correlated with free testosterone, but the multivariate analysis demonstrated that the magnitude of the association was significantly higher in SOP patients. Conclusions: The metabolic alterations detected in obese adolescents with SOP suggest that the clinical manifestations that accompany the syndrome characterize the PCOS as a metabolic disease, which carry important health risks at short, medium and long term. Therefore, they merit intervening actions to prevent, diagnose and provide timing treatment in order to limit the damage in the course of the natural history of PCOS.


Subject(s)
Dyslipidemias/etiology , Pediatric Obesity/complications , Polycystic Ovary Syndrome/complications , Adolescent , Body Mass Index , Cross-Sectional Studies , Female , Humans , Hypercholesterolemia/etiology , Hyperinsulinism/etiology , Hypertriglyceridemia/etiology , Insulin/blood , Pediatric Obesity/blood , Polycystic Ovary Syndrome/blood , Testosterone/blood
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