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BACKGROUND: Endometriosis is an estrogen-dependent and chronic inflammatory disease affecting up to 10% of women. It is the result of a combined interaction of genetic, epigenetic, environmental, lifestyle, reproductive and local inflammatory factors. In this study, we investigated whether single nucleotide polymorphisms (SNPs) mapping to TNF-alpha (TNF, rs1800629) and IL-1beta (IL1B, rs1143634) and variable number tandem repeat polymorphism mapping to IL1-Ra (IL1RN intron 2, rs2234663) genetic loci are associated with risk for endometriosis in a Mexican mestizo population. METHODS: This study included 183 women with confirmed endometriosis (ENDO) diagnosed after surgical laparoscopy and 186 women with satisfied parity and without endometriosis as controls (CTR). PCR/RFLP technique was used for genotyping SNPs (rs1800629 and rs1143634); PCR for genotyping rs2234663. RESULTS: We found no statistical differences in age between groups nor among stages of endometriosis and the CTR group. We observed no difference in genotype and allele frequencies, nor carriage rate between groups in none of the three studied polymorphisms. The prevalence of TNF*2-allele heterozygotes (p = 0.025; OR 3.8), TNF*2-allele (p = 0.029; OR 3.4), IL1B*2-allele heterozygotes (p = 0.044; OR 2.69) and its carriage rate (p = 0.041; OR 2.64) in endometriosis stage IV was higher than the CTR group. Surprisingly, the carriage rate of IL1RN*2-allele (ENDO: p = 0.0004; OR 0.4; stage I: p = 0.002, OR 0.38; stage II: p = 0.002, OR 0.35; stage III: p = 0.003, OR 0.33), as well as the IL1RN*2-allele frequencies (ENDO: p = 0.0008, OR 0.55; I: p = 0.037, OR 0.60; II: p = 0.002, OR 0.41; III: p = 0.003, OR 0.38) were lower than the CTR group. Women with endometriosis stage IV (severe) had frequencies more alike to the CTR group in the IL1RN*2 allele frequency (31.2% vs. 27.2%) and carriage rate (37.5% vs. 41.9%). CONCLUSION: Although these polymorphisms are not associated with the risk of endometriosis, Mexican mestizo women with severe stage of endometriosis have higher frequencies of TNF*2-, IL1B*2- and IL1RN*2-alleles, which may explain a possible correlation with disease severity rather than predisposition or risk.

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Abstract Stress is conceptualized as a systemic response triggered by a stimulus potentially harmful to an organism. Instead of an adaptive outcome, life-threatening experiences may contribute to the development of anxiety disorders and depression. Predator scent stress (PSS) is one of the most utilized rodent models of stress-induced psychopathology, in which rodents are exposed to a volatile predator cue that signifies imminent danger. It is unclear if the duration of a life-threatening experience could have differential consequences on the expression of anxiety-like and depression-like behaviors. For this reason, the goal of this present study was to evaluate the effect of different exposure durations (3 min., 10 min., or 20 min.) to the scent of bobcat urine. Wistar rats housed under 12/12 dark cycle in standard laboratory conditions were exposed to the PSS model and 24 hrs. after the stressor, behavioral consequences were evaluated in the open field test, saccharin preference test, and forced swim test. The results obtained show that a 10-minute exposure is sufficient to induce an anxiety-like and a depression-like behavioral profile. We conclude that the time exposure could be a major variable to obtain clear and trustable results and to avoid overexposure to stressor.

Resumen El estrés es una respuesta sistémica desencadenada por un estímulo potencialmente peligroso para el organismo. Esta respuesta permite al organismo adaptarse a la condición estresante, sin embargo, experiencias que amenazan a la vida pueden incrementar el riesgo de desarrollar trastornos de ansiedad y depresión. La exposición al olor de depredador (EOD) es el modelo animal de patología inducida por estrés más utilizado. Consta de la exposición a una pista olfativa que significa peligro inminente. Aún no está claro si la duración a una experiencia que amenaza la vida puede generar diferencias en la expresión conductas tipo-ansiedad o tipo-depresión. Por esta razón, el objetivo de este estudio fue evaluar el efecto de diferentes duraciones de exposición (3 min., 10 min. o 20 min.) al aroma de lince. Se utilizaron ratas hembra de la cepa Wistar en un ciclo luz oscuridad 12/12 en condiciones estándar de laboratorio, los sujetos fueron evaluados en la prueba de campo abierto, preferencia de sacarina y nado forzado 24 hrs. después de terminado el estresor. Los resultados indican que la exposición a 10 min. es suficiente para inducir el perfil conductual tipo-depresión y tipo-ansiedad. Concluimos que el tiempo de exposición puede ser una variable de mayor importancia para obtener resultados confiables y prevenir exposiciones innecesarias al estrés.

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BACKGROUND: Genetic polymorphisms of antioxidant enzymes CAT, GPX, and SOD are involved in the etiology of obesity and its principal comorbidities. The aim of the present study was to analyze the effect of aforementioned SNPs over the output of several variables in people with obesity after a nutritional intervention. The study included 92 Mexican women, which received a dietary intervention by 3 months. Participants were genotyped and stratified into two groups: (1) carriers; mutated homozygous plus heterozygous (CR) and (2) homozygous wild type (WT). A comparison between CR and WT was done in clinical (CV), biochemical (BV), and anthropometric variables (AV), at the beginning and at the end of the intervention. RESULTS: Participants (n = 92) showed statistically significant differences (p < 0.05) at the end of the nutritional intervention in several CV, BV, and AV. However, two kinds of responses were observed after genotyping participants: (A) CR and WT showed statistically significant differences (p < 0.05) in several CV, BV, and AV for the SNPs 599C>T GPX1 (rs1050450), - 251A>G SOD1 (rs2070424), and - 262C>T CAT (rs1001179). (B) Only CR showed statistically changes (p < 0.05) in several CV, BV, and AV for the SNPs - 21A>T CAT (rs7943316) and 47C>T SOD2 (rs4880). The dietary intervention effect was statistically significantly between the polymorphisms of 47C>T SOD2 and BMI, SBP, TBARS, total cholesterol, and C-LCL (p < 0.05) and between the polymorphisms of - 21A>T CAT (rs7943316) and SBP, DBP, total cholesterol, and atherogenic index (p < 0.05). CONCLUSION: People with obesity display different response in several CV, BV, and AV after a nutritional intervention, depending on the antioxidant genetic background of SOD and CAT enzymes.

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STUDY OBJECTIVE: Describe the impact of teen pregnancy on later ovarian activity and metabolic hormones considering the concentration of current levels of ovarian steroids and leptin in a sample of Mexican females. DESIGN: Cross-sectional study in the maternity of the General Hospital of Atlacomulco and campus of the Autonomous University of the State of Mexico. PARTICIPANTS: 71 women between the ages of 18 and 24, and 160 neonates seen between March 2010 and June 2012. MAIN OUTCOME MEASURES: The measurements obtained included anthropometric body composition (bioelectrical impedance), serum hormone quantification of ovarian steroids and leptin (immunoassays), and the Apgar scores, height, and weight in neonates. Statistical analysis included ANOVA, Student, and chi-square for P < .05. RESULTS: Adolescent mothers showed significantly lower concentrations of estradiol (P = .001) and progesterone (P = .001). However, higher levels of leptin in adolescent mothers were not statistically different compared with older mothers (P = .84). Also, leptin was correlated with all measures of adiposity. The mean birth weights (P = .001) and Apgar scores (P = .001) were lower in neonates of adolescent mothers than in neonates of adult mothers. There was no association between maternal age with the anthropometric variables studied. CONCLUSIONS: Early reproduction represents a metabolic stress condition that modifies the long term ovarian activity and metabolic hormones, and impacts the morbidity-mortality of the mother and offspring in a later vital life cycle stage.

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