C-C chemokine receptor type 5 (CCR5) is known for its role as a co-receptor for HIV-1 infection. Some individuals possess a 32 bp deletion, known as Delta-32 allele which has been reported to confer resistance to HIV-1 infection. In order to estimate the distribution of Delta-32 allele of CCR5 gene, 1034 mestizo individuals from the Northwest of Mexico, including 385 HIV-1-infected individuals, 472 healthy controls and 177 uninfected female sex workers; were examined by allele-specific PCR. There was no statistically significant difference in the frequency of Delta-32 allele between HIV-1 positive and healthy individuals (OR= 1.1, p= 0.6). However, we found a significantly reduced prevalence of CCR5 Delta-32 heterozygous genotype in female patients (OR= 0.084, 95% CI= 0.011 - 0.630, p= 0.002), as well as in allele frequency, compared to male patients. Furthermore, we observed an inverse relationship between allele frequency and the risk of HIV-1 transmission and AIDS progression among female healthy controls, sex workers and HIV-1 infected groups. Our findings support previous data showing Delta-32 as a genetic protective factor against HIV-1 infection in Mexican women, as well as in women from other populations.

Myeloproliferative neoplasms (MPN) are considered a risk factor for Budd-Chiari syndrome (BCS reaction (AS-PCR). The association of these mutations is rare, with only a few cases reported in the literature. The patient was treated with oral anticoagulation and antiplatelets with good results and proper follow-up. In conclusion, due to the possible coexistence of multiple prothrombotic factors in patients with Budd-Chiari syndrome, the approach to these patients must be focussed on searching for multiple factors and should include the JAK-2 V617F mutationKeywords: Budd-Chiari syndrome, Factor V G1691A mutation, JAK-2 V617F mutation The patient was found to be a heterozygous carrier of Factor V and homozygous wild type G20210A prothrombin mutations. The JAK-2 V617F mutation was detected by allele-specific polymerase chain reaction [AS-PCR] (9). All family members were also tested for possible mutations and her father, one sister, one daughter and one son were also carriers of Factor V Leiden, and the rest of the family members were negative for G20210A prothrombin and JAK-2 RESUMEN Neoplasias mieloproliferativas (MPN) se consideran un factor de riesgo para el síndrome de BuddChiari (BCS). La clasificación actual de MPN por la Organización Mundial de la Salud se basa en la presencia de la mutación somática JAK-2 V617F, que está presente en 40 a 60% de los pacientes con BCS. La mutación del factor V Leiden se encuentra en alrededor del 53% de los pacientes con BCS

OBJECTIVE: To evaluate the influence of the polymorphisms of the vitamin D receptor gene (FokI: rs2228570, BsmI: rs1544410, ApaI: rs7975232, and TaqI: rs731236) on the clinical parameters of patients with urinary tract infections.MATERIALS AND METHODS: A comparative, prospective, and cross-sectional study was conducted at the Hospital General de Culiacán Dr. Bernardo J. Gastélum within the time frame of August 2016 to July 2017. The polymorphisms were detected through the polymerase chain reaction-restriction fragment length method in 119 patients diagnosed with urinary tract infection and in 206 individuals with no urinary tract infection. The data analysis was carried out using the c2 and odds ratio (OR) with a 95% confidence interval (95%CI). The logistic regression method, adjusted by age and sex, was employed to evaluate the relation between clinical characteristics and genotypes, utilizing the STATA version 13.0 program. Statistical significance was set at a p<0.05.RESULTS: We found differences in the prevalence of the CA-ApaI genotype between the study groups. The FokI and BsmI polymorphisms and the TGAT and CGCT haplotypes were associated with certain clinical characteristics.CONCLUSIONS: A possible link between the vitamin D receptor gene and bacterial urinary tract infection in a Mexican population was suggested.KEYWORDS: Vitamin D receptor; Urinary tract infection; Polymorphisms; Haplotypes.

Background Vitiligo is an autoimmune disease that courses with skin depigmentation because of the destruction of melanocytes. Vitiliginous melanocyte is prone to damage because of oxidative stress which activates cellular stress response and the release of heat shock proteins such as HSP70 promoting immune activation against the melanocyte. Variants in HSP70 genes (HSPA) might alter their expression and thus modulate vitiligo susceptibility. Therefore, we sought to evaluate the role of the 5′ untranslated region HSPA1A G/C (rs1043618) and the exonic HSPA1B A/G (rs1061581) and HSPA1L T/C (rs2227956) gene variants in nonsegmental vitiligo. Methods A total of 200 nonsegmental vitiligo patients and 208 age/gender‐matched healthy subjects were genotyped for rs1043618, rs1061581, and rs2227956 variants by PCR‐RFLP. Results Variants rs1043618 and rs1061581 were not associated with vitiligo susceptibility. On the other hand, the rs2227956 C allele and TC genotype were associated with protection against vitiligo. A similar effect was observed for the GAC haplotype. Any of the aforementioned HSP70 gene variants were associated with the clinical characteristics of vitiligo. Conclusion Our findings suggest that the HSPA1L rs2227956 gene variant might influence the susceptibility to vitiligo. Being the first study of HSP70 gene variants in vitiligo, further research is encouraged to corroborate these results.

Through the monthly data of 71 meteorological stations of the North Pacific Watershed in northwest Mexico, the annual trends of nine temperature variables were estimated using the non-parametric Mann-Kendall test and the Q Sen's slope estimator. Annual Q Sen's slopes were analyzed in spatial terms using geographic variables as independent factors and likewise with Moran's I index. Three major physiographic zones were used to perform a regional analysis using pooled data. The monthly trends were also analyzed. Divergent annual trends were found for the nine proposed variables and warming trends were predominant in almost all of them. Latitude is the most relevant factor in the spatial distribution of the Q Sen's slopes. Four temperature variables were found statistically clustered, as depicted by the Moran's I index. The largest regional Q Sen's slopes values were found in the Coastal Plains. In this area a larger increase in minimum temperatures was observed, in contrast with the Sierra Madre regions, where the largest rate of increasing change was found in maximum temperatures. The monthly analysis indicates warming trends in the first six months of the year with a sudden decrease in July and also a noticeable decrease in the slope values in December.