7 results match your criteria: "2Laboratório de Clinico[Affiliation]"

Levels of sCD163 in women rheumatoid arthritis: Relationship with cardiovascular risk markers.

Clin Investig Arterioscler

May 2024

Laboratory of Multidisciplinary Research and Biomedical Innovation, Universidad Autónoma de Guerrero, Chilpancingo, Guerrero, Mexico. Electronic address:

Aim: The soluble scavenger receptor differentiation antigen 163 (sCD163), a monocyte/macrophage activation marker, is related to cardiovascular mortality in the general population. This study aimed to evaluate their relationship between serum levels of sCD163 with cardiovascular risk indicators in rheumatoid arthritis (RA).

Methods: A cross-sectional study was performed on 80 women diagnosed with RA.

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Article Synopsis
  • * Using data from 12 European EDs, researchers analyzed presenting symptoms and management of febrile children under 18, identifying those suitable for a fast track system based on simplicity and minimal resource use.
  • * Findings revealed that respiratory symptoms were the most common, while neurological patients utilized more imaging and had higher admission rates, and gastrointestinal patients underwent more lab tests, indicating varying needs among the different symptom groups.
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TLR4 polymorphism and haplotype are associated with obesity and lipid profile in young population: a pilot study.

J Endocrinol Invest

May 2023

Laboratorio de Investigación en Microbiología. Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, México. Av. Lázaro Cárdenas S/N, Ciudad Universitaria Sur Col. Haciendita, C. P. 39090, Chilpancingo, Guerrero, México.

Background: The single nucleotide polymorphisms in the TLR4 gene can decrease or increase the response to lipopolysaccharide, increasing the susceptibility to inflammatory diseases, affecting the expression or receptor function by inducing a low-grade chronic inflammatory response.

Purpose: The objective of this study was to evaluate the association of SNPs - 2570 A > G (rs2737190), - 2081 G > A (rs10983755), 896 A > G (rs 4986790), and 1196 C > T (rs4986791) of the TLR4 gene with obesity and metabolic alterations in the young population.

Results: In this study, it was found that the carriers of the heterozygous genotype of the SNPs - 2081 G > A, 896 A > G, and 1196 C > T confer a higher risk of developing obesity (OR = 3.

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Molecular characterization of and spp. coinfection in mammals of Venezuelan coendemic areas.

J Vector Borne Dis

August 2020

Instituto de Investigaciones Biomédicas "Dr. Francisco J. Triana Alonso" (BIOMED); Departamento de Parasitología, Facultad de Ciencias de la Salud, Universidad de Carabobo Sede Aragua, Maracay, estado Aragua, Venezuela.

Background & Objectives: Trypanosoma cruzi and Leishmania spp. are protozoans that cause American trypanosomiasis and leishmaniasis, respectively. In endemic foci where both diseases coincide, coinfection can occur.

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are mites commonly found within domestic feline hair stems. The infested animal presents an opaque fur with a "salt and pepper" aspect. The contamination may occur by direct contact with other infected animals or by fomites, and the main diagnostic tool is the direct examination of the fur.

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Molecular diagnosis of Trypanosoma cruzi/Leishmania spp. coinfection in domestic, peridomestic and wild mammals of Venezuelan co-endemic areas.

Vet Parasitol Reg Stud Reports

December 2018

Instituto de Investigaciones Biomédicas "Dr. Francisco J. Triana Alonso" (BIOMED), Universidad de Carabobo Sede Aragua, Maracay, estado Aragua, Venezuela; Departamento de Parasitología, Facultad de Ciencias de la Salud, Universidad de Carabobo Sede Aragua, Maracay, estado Aragua, Venezuela. Electronic address:

American trypanosomiasis and leishmaniases are diseases caused by protozoans of the Trypanosomatidae family. In Venezuela, although several endemic foci of both diseases coincide, there are no reports of coinfection in mammals. The molecular diagnosis of the coinfection T.

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Article Synopsis
  • - POEMS syndrome is a rare disease linked to plasma cell issues, and autologous stem cell transplantation has been studied as an effective treatment option for it.
  • - A study of 127 patients revealed that 90% were alive after a median follow-up of 48 months, with significant improvements in symptoms, particularly neurological ones, after undergoing the procedure.
  • - Treatment results showed a 3-year progression-free survival rate of 84% and an overall survival rate of 94%, indicating the potential effectiveness of the transplantation approach for managing POEMS syndrome.
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