Levels of Salivary IFN-gamma, TNF-Alfa, and TNF Receptor-2 As Prognostic Markers in (Erosive) Oral Lichen Planus

To explore the feasibility of detecting salivary levels of IFN-γ, TNF-α, and sTNFR-2 from erosive oral lichen planus (ELP) patients for clinical application, 20 ELP patients were enrolled in the study as were 20 age-sex-matched controls. From all subjects, saliva level of the tested biomarkers was determined by ELISA. Salivary profiles were assessed in ELP patients by ELISA after being treated with prednisone. A significantly higher level of IFN-γ (P ≤ .01), TNF-α (P ≤ .0001), and sTNFR-2 (P ≤ .01) was detected in ELP patients before treatment than in controls. Following treatment, the salivary levels of IFN-γ (P ≤ .01), TNF-α (P ≤ .05), and sTNFR-2 (P ≤ .01) decreased significantly when compared to their pretreatment levels. This study demonstrated that salivary IFN-γ, TNF-α, and sTNFR-2 can be detectable in ELP patients and decreased significantly after treatment with prednisone, which may reveal the possibility of using these disease-related biomarkers in diagnosis and monitoring

FOXO3a gene polymorphism and bronchial asthma in Egyptian children INTRODUCTION Bronchial asthma is the most prevalent chronic immunological disorder in childhood period. It is characterized by airways inflammation and bronchial hyper-responsiveness where

Background: FOXO3a proteins play multiple crucial roles in immune response. FOXO3 inhibits T cell proliferation, induces T cell apoptosis via upregulation of proapoptotic proteins and it suppresses T cell activation preventing autoimmunity. The role of FOXO3a gene in the pathogenesis of bronchial asthma has been studied in few ethnic groups and revealed its implication in asthma pathogenesis.Objectives: The aim of the current study is to detect the association between single nucleotide polymorphism of the FOXO3a gene (rs13217795) and bronchial asthma, atopy and asthma severity in Egyptian children.Methods: The current cross-sectional case-control study was performed on 75 asthmatic children aged 2 to 12 years following up in the pulmonology outpatient clinic in Children's hospital, Cairo University and 75 age and sex matched healthy controls. Candidates were subjected to clinical evaluation in addition to genotyping for the FOXO3a gene polymorphism using PCR-RFLP technique.Results: The highest frequency was for the heterozygous type CT in both cases and controls groups. The genotype frequencies of mutant type TT for cases and controls were 12 % and 16% respectively, and the T allele frequencies were 37.2% in cases and 46.7% in the control group while CC genotype was present in 37.3% of asthmatic patients and 22.6% in the controls and the C allele was detected in 62.8% and 53.3% for cases and controls respectively. No statistically significant differences were observed between asthmatic patients and controls regarding the different genotypes of the FOXO3a gene polymorphism (p=0.161). No significant association was detected between the different genotypes of the FOXO3a gene polymorphism and the atopic status (p=0.536) or the different grades of asthma severity (p= 0.545).Conclusions: The study of FOXO3a gene polymorphism (rs13217795) in asthmatic Egyptian children revealed low frequency of the mutant TT genotype among cases and controls. In the current study, FOXO3a polymorphism has no role in the pathogenesis of asthma or atopy. Moreover, it has no relation to degree of disease severity.Keywords: Asthma, FOXO3a, gene, children, Egyptian, polymorphis

Study of the effect of HFE gene mutations on iron overload in Egyptian thalassemia patients

Background: HFE gene mutations have been shown to be responsible for hereditaryhemochromatosis. Their effect on iron load in β-thalassemia patients and carriers remains controversial.Objectives: We aimed to determine the prevalence of HFE gene mutations (C282Y and H63D) in β-thalassemia patients and carriers and to investigate its effect on their serum ferritin levels.Patients and methods: A total of 100 β-thalassemia subjects; 75 patients and 25 carriers were screened for HFE gene mutations by PCR-RFLP. Serum ferritin measured by ELISA was evaluated in relation to HFE mutations.Results: Twenty-eight β-thalassemia patients (37.3%) were heterozygotes for H63D mutation (H/D), 8 (10.7%) were D/D and 39 (52%) were negative (H/H). Among carriers, 4 (16%) were D/D and 21 (84%) were H/H homozygotes. C282Y mutant allele was not detected in any of the subjects. Serum ferritin levels were significantly higher in β-thalassemia patients heterozygotes or homozygotes for H63D mutation compared to those without mutation (p= 0.000). Carriers homozygotes for H63D mutation showed significantly higher serum ferritin levels compared to those without mutation (p< 0.001).Conclusion: Homozygosity for H63D mutation tends to be associated with higher ferritin levels in beta-thalassemia patients and carriers suggesting its modulating effect on iron load in these cases

Prediction of Modulus of Rupture from Modulus of Elasticity for Some Egyptian Hardwoods

The MOE and MOR of 112 air-dry small, clear specimens (2 x 2 x 30 cm) of six species of hardwoods grown in Egypt were determined. Simple linear regression analysis revealed that MOR is highly correlated with MOE of Eucalyptus camaldulensis, Khaya senegalensis, Tamarix articulata and Casuarina spp. However, the "r" values for Jacaranda ovalifolia and Melia azedarach were not significant. In addition, covariance analysis showed that the six regressions equations have different slopes and Y-intercepts and therefore cannot be grouped. The only grouping was that between the regression lines of the first three species mentiones above.Introducing specific gravity in the regression equation did not result in improving the correlation coefficients, except in the case of Casuarina spp. Using specific gravity alone for predicting the MOR was found to be unreliable due to the relatively low "r" values obtained for the species except in the case of Casuarina spp

Constrained Probabilistic Continuous Review Inventory System with Mixture Shortage and Stochastic Lead Time Demand

This paper derives the probabilistic continuous review backorders and lost sales inventory system when the order cost is a function of the order quantity. Our objective is to minimize the expected annual total cost under a restriction on the expected annual holding cost when the lead time demand follows some continuous distributions by using the Lagrangian method. Some published special cases are deduced and an illustrative numerical example with some graphs is added

Study of Urinary Alpha Glutathione-S-Transferase in Children with Idiopathic Nephrotic Syndrome

Glomerulopathy associated with recurrent or persistent proteinuria may lead to progressive tubulointerstitial fibrosis. Early detection of tubulointerstitial fibrosis may result in a more favorable outcome of chronic kidney disease (CKD) because nephroprotective treatment may be instituted in due course. One of the early markers of tubulointerstitial fibrosis is glutathione S-transferase (GST). The aim of this study was to determine urinary alpha-GST in children with idiopathic nephrotic syndrome (INS), either in remission or relapse. This case–control study included 40 children with primary nephrotic syndrome (NS), either in remission or relapse. Also, 40 healthy children, age- and sex-matched as controls, were selected from the outpatients and the pediatric nephrology unit of Al-Zahraa Hospital, Al-Azhar University. Urinary alpha-GST was investigated in the study groups on the same lines as that of routine investigations of INS. Children with INS have significantly higher urinary GST either in remission or relapse, it was (5.23 ± 1.90) ng/mL, (5.32 ± 1.52) ng/mL respectively compared with healthy controls, it was (2.59 ± 1.12) ng/mL with (P = 0.001). A positive correlation between urinary alpha-GST and body weight BW, height, body mass index (BMI), white blood cells (WBCs) count, erythrocyte sedimentation rate, serum (cholesterol, triglyceride [TG]) level, blood urea nitrogen (BUN), and duration of the disease. Urinary alpha-GST was increased in children with NS even after remission, and it consequently led to oxidative stress and tubulointerstitial fibrosis. Nephroprotective treatment is recommended even in cases with INS, either in remission or relapse

An Intelligent Information System for Groundwater Resources Categorization and Assessment

Abstract: This paper aims to present an intelligent information system developed for groundwater categorization and classification. The developed system integrates more than one research field and tools, including Decision Support Systems (DSS), Geographic Information Systems (GIS), knowledge base and modeling and visualization enhancement. Visual Basic (VB) environment is used as an inference engine for this system and the code is written using VBA. The system aims to categorize water resources according to the international water quality criteria (FAO, USSL, Gupta and Roades) and to reclassify water resources according to a developed decision matrix from the application of the expert system. A user friendly interface (GUI) is developed to help the user to manage the system and to link different system environments. The system is linked through the GUI with a GIS to display the water resources layers and to provide functions to query and display the spatial locations and associated attributes. The system is used to make a decision about the suitability of water resources to a specific crop and vice versa. The developed system is tested on groundwater recourses in Siwa Oasis, Egypt

EFFECT OF FOLIAR APPLICATION OF ANTIOXIDANTS ON VEGETATIVE GROWTH AND LEAF MINERAL CONTENT OF CHINESE TANGERINE YOUNG TREES BUDDED ON SOME CITRUS ROOTSTOCKS GROWN UNDER SALINE CONDITIONS

Wady El Natroun high way (Beer Hooker Area) in a private orchard in a sandy soil under drip irrigation system with saline water.  in 2015 and 2016 seasons. Chinese tangerine (Citrus tangerine) transplant were budded on three rootstocks namely sour orange (Citrus aurantum, mion), volkamer lemon (Citrus volkameriana, Tem) and X639 hybrid between (Cleopatra mandarin × Ponicurus trifoliata) grown under saline conditions to study the effect of foliar  application of antioxidants namely ascorbic and salicylic acid on vegetative growth and leaf mineral contents. Results showed that, Volkamer lemon rootstock surpassed sour orange and x639 rootstocks under saline conditions, the highest incremental percentage young tree height, stem diameter, number of leaves per shoot and leaf area were registered by Chinese tangarine scion budded on Volkamer lemon rootstock. Among selected antioxidants ascorbic acid at the concentrations of 800 ppm recorded the highest significant values for vegetative growth parameters and surpassed salicylic acid. Also Chinese mandarin scion budded on volkamer lemon accumulated the highest concentrations of nitrogen (N), phosphorus(P), magnesium(Mg), and chloride (Cl-) and the lowest concentration of sodium (Na+). Chinese mandarin scion budded on sour orange rootstock accumulated the highest concentrations of potassium (K) while Chinese tangerine scion budded on x639 accumulated the highest concentrations of sodium (Na)

URINARY MARKERS OF OXIDATIVE DNA DAMAGE IN TYPE 1 DIABETIC CHILDREN: RELATION TO MICROVASCULAR COMPLICATIONS

  Objective: Type 1 diabetes mellitus (T1DM) is a widespread metabolic disease, which frequently carries with it a significant impact on human health. Oxidative damage and tissue inflammation have been claimed to be a typical pathogenic component for the progression of diabetic complications. We aim in this study to explore the relation of urinary 8-oxo-7,8-dihydro-2′-deoxyguanosine (8-oxodG) (as a marker of nucleic acid oxidation) to microvascular complications in T1DM.Methods: A case–control study, enrolling 45 T1DM children and an equivalent number of healthy subjects, was performed. Full clinical examination and anthropometric measurement were performed to all subjects. Urinary assessment for 8-oxodG and albumin was done in addition to blood sampling for lipid profile and glycated Hb (HbA1c) assay. Complete ocular examination for assessment of diabetic retinopathy (DR) was also done.Results: Levels of urinary 8-oxodG, serum cholesterol, triglycerides, and low-density lipoprotein in cases were significantly higher than non-diabetics; these levels were likewise higher in uncontrolled T1DM patients in comparison with well-controlled T1DM subjects. Urinary 8-oxodG and HbA1c were significantly higher in diabetic patients with albuminuria and DR compared to patients without complications. Significant positive correlation was found between 8-oxodG with HbA1c (r=0.8, p<0.01), diastolic blood pressure (DBP) (r=0.4, p=0.02), and cholesterol (r=0.4, p=0.05).Conclusion: Urinary 8-oxodG was found to be a reliable marker for assessing oxidative DNA damage in T1DM and can be used in the determination of microvascular complications related to diabetes