Metabolic syndrome: review

The psychosomatic component of the metabolic syndrome, historical aspect of the problem under study, physiological and biochemical mechanisms of pathogenesis are considered in the article. The symptomatic components of the metabolic syndrome and their interrelation are outlined, the ways of diagnosis and therapy and  directions of modern research in this field are outlined

Interlaboratory evaluation of an ELISA performed using a robotic automatic workstation versus manually testing for screening of Salmonella Typhimurium and Salmonella Choleraesuis antibodies in pig serum

An enzyme-linked immunosorbent assay (ELISA) was developed to detect antibodies directed against Salmonella spp. in porcine serum. This assay is based on the Exiqon VetScreen TM Salmonella Covalent Mix-ELISA 96-well microtiter plates (Jauho et al, 2000). These microtiter plates are photochemically coated with Salmonella typhimurium and Salmonella choleraesuis PS- antigens 1,4,5,6,7, and 12 using the ExiqonDs patented photochemical method for covalent coupling of ligands to polymer surfaces (Wiuff et al, 2000). The assay was developed using an automatic robotic workstation. The Exiqon VetScreen TM Salmonella Covalent Mix-ELISA plates do not require any blocking steps. The developed assay showed 30 minutes incubation time for porcine serum samples as optimal, thereby giving a total assay time of two hours. In order to evaluate the assay, a comparison study between the FSD, Canada; Exiqon, Copenhagen Denmark was performed. A panel of positive and negative porcine serum samples was tested. The tests were carried out using a robotic automatic workstation and using a manually performed assay in three different laboratories (Exiqon and Danish Veterinary Lab, Denmark; Svanova, Sweden).The developed assay showed high specificity, sensitivity and excellent reproducibility. The interlaboratory study gave results of substantial agreement. No difference between manual and robotized performance could be identified. The automated ELISA can be used in high throughput screening of swine Salmonella spp. antibodies in seroprevalence studies

SLC11A1 (NRAMP1) Polymorphisms and Tuberculosis Susceptibility: Updated Systematic Review and Meta-Analysis

Background: Natural resistance associated macrophage protein 1 (NRAMP1), encoded by the SLC11A1 gene, has been described to regulate macrophage activation and be associated with infectious and autoimmune diseases. The relation between SLC11A1 polymorphisms and tuberculosis susceptibility has been studied in different populations. Methods: We systematically reviewed published studies on SLC11A1 polymorphisms and tuberculosis susceptibility until September 15, 2010 and quantitatively summarized associations of the most widely studied polymorphisms using metaanalysis. Results: In total, 36 eligible articles were included in this review. In Meta-analysis, significant associations were observed between tuberculosis risk and widely studied SLC11A1 polymorphisms with summarized odds ratio of 1.35 (95%CI, 1.17– 1.54), 1.25 (95 % CI, 1.04–1.50), 1.23 (95 % CI, 1.04–1.44), 1.31 (95%CI, 1.08–1.59) for 39 UTR, D543N, INT4, and 59 (GT)n, respectively. Heterogeneity between studies was not pronounced, and the associations did not remarkably vary in the stratified analysis with respect to study population and study base. Conclusions: The association between SLC11A1 polymorphisms and tuberculosis susceptibility observed in our analyses supports the hypothesis that NRAMP1 might play an important role in the host defense to the development of tuberculosis

The relationship between psychological, cognitive, and contextual factors and rehabilitation outcomes in Achilles tendinopathy: A prospective feasibility cohort study

Objectives This study aimed to investigate the feasibility of conducting a full-scale study investigating the influence of patient-related factors on rehabilitation outcomes in Achilles tendinopathy (AT). A secondary aim was to investigate preliminary relationships between patient-related factors and clinical outcomes at 12- and 26- weeks. Design feasibility cohort. Setting Australian healthcare settings. Methods Participants with AT receiving physiotherapy in Australia were recruited via treating physiotherapists and online. Data were collected online at baseline, 12- and 26-weeks. Progression criteria for a full-scale study were recruitment rate of ≥10 per month, conversion rate ≥20%, and response rate to questionnaires ≥80%. The relationship between patient-related factors and clinical outcomes was investigated using Spearman's rho correlation coefficient. Results The average recruitment rate was 5/month, conversion rate was 97%, and response rate to questionnaires was ≥97% at all timepoints. There was a fair to moderate correlation (rho = 0.225 to 0.683) between patient-related factors and clinical outcomes at the 12-week, but no to weak correlation at the 26-week (rho = 0.002 to 0.284). Conclusions Feasibility outcomes suggest a future full-scale cohort study is feasible with the caveat of utilizing strategies to improve recruitment rate. Preliminary bivariate correlations at 12-weeks warrant further investigations in larger studies

Interlaboratory evaluation of an ELISA performed using a robotic automatic workstation versus manually testing for screening of Salmonella Typhimurium and Salmonella Choleraesuis antibodies in pig serum

An enzyme-linked immunosorbent assay (ELISA) was developed to detect antibodies directed against Salmonella spp. in porcine serum. This assay is based on the Exiqon VetScreen TM Salmonella Covalent Mix-ELISA 96-well microtiter plates (Jauho et al, 2000). These microtiter plates are photochemically coated with Salmonella typhimurium and Salmonella choleraesuis PS- antigens 1,4,5,6,7, and 12 using the ExiqonDs patented photochemical method for covalent coupling of ligands to polymer surfaces (Wiuff et al, 2000). The assay was developed using an automatic robotic workstation. The Exiqon VetScreen TM Salmonella Covalent Mix-ELISA plates do not require any blocking steps. The developed assay showed 30 minutes incubation time for porcine serum samples as optimal, thereby giving a total assay time of two hours. In order to evaluate the assay, a comparison study between the FSD, Canada; Exiqon, Copenhagen Denmark was performed. A panel of positive and negative porcine serum samples was tested. The tests were carried out using a robotic automatic workstation and using a manually performed assay in three different laboratories (Exiqon and Danish Veterinary Lab, Denmark; Svanova, Sweden).The developed assay showed high specificity, sensitivity and excellent reproducibility. The interlaboratory study gave results of substantial agreement. No difference between manual and robotized performance could be identified. The automated ELISA can be used in high throughput screening of swine Salmonella spp. antibodies in seroprevalence studies.</p

Phenotype prediction by DNA-based typing of clinically significant blood group systems in Jordanian blood donors.

BACKGROUND AND OBJECTIVES: During the past 10 years several DNA-typing methods have been developed to complement routine serological typing for determination of polymorphisms in the ABO, RH, KEL, JK and FY blood group genes. However, the molecular basis of blood groups can differ widely between ethnic groups. The purpose of this study was to evaluate selected DNA-based methods for phenotype prediction in a population not previously investigated. MATERIALS AND METHODS: Blood samples from a random sample of Jordanian blood donors were collected and red cells isolated from these blood samples were phenotyped for common ABO (n = 150) and KEL/FY/JK (n = 90) antigens. RHD-negative and -positive donors were selected for RH typing (n = 120 and 30, respectively). DNA was prepared and blood group genotyping performed according to selected methods in current use. Discordant samples required further investigation by extended serology and DNA sequencing. RESULTS: The degree of concordance between phenotype and genotype was high, but some exceptions were noted. Two of 14 A2/A2B samples lacked all mutations associated with known A2 alleles of the ABO system. RH typing revealed four samples with the c(cyt48) marker, causing false-positive RHC typing. A single D-negative sample was positive for D-specific exon 10 markers. The RHD pseudogene was not found in the 150 donors tested. Nine samples revealed discrepancies that were associated with unknown silent or weakly expressing Fyb-like alleles. CONCLUSIONS: With the exception of the FY system, we conclude that the molecular background of the clinically important blood group antigens studied here is similar to that reported for Caucasoids

Oxidative stress and lipid peroxidation in experimental peritonitis

Peritonitis is one of the most serious complications of pathology of the abdominal organs, which is characterized by a high mortality rate. Violation of the natural mechanisms of detoxification (immune, detoxification functions of the liver and kidneys), which occur in acute peritonitis, due to primary damage to their structure and the development of maladaptation mechanisms, accompanied by endogenous intoxication syndrome. One of the characteristic and aggravating manifestations of the syndrome of endogenous intoxication is the activation of lipid peroxidation (LPO). The aim: study of the dynamics of primary and secondary products of lipid peroxidation in experimental peritonitis. In the first hour simulated fecal peritonitis development in the rats blood revealed an increase in the level of diene conjugates and malondialdehyde (p <0.001 compared with the results of intact animals. In the second stage was detected more pronounced increase in the level of primary and secondary products of lipid peroxidation (p <0.001) as compared with the data of the same hole in the first stage, and compared with the results of group No. 1. On the 3rd day of simulated peritonitis development in rats there is a marked deterioration of the animal condition, which was manifested in lipid peroxidation progression: the diene conjugates level increased at the significance level p <0.001, and the level of malondialdehyde compared to p <0.05 data from the previous stage of the same group