18 results on '"Khair SM"'
Search Results
2. Genetic variants of XRCC1and risk of hepatocellular carcinoma in chronic hepatitis C patients
- Author
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Arafa, M, Besheer, T, El-Eraky, AM, Abo El-khair, SM, and Elsamanoudy, AZ
- Abstract
ABSTRACTBackground: Hepatitis C virus (HCV) related liver cirrhosis occurs in about 20% of chronically infected patients over a duration of 10–20 years, and within 5 years approximately 10–20% of these cirrhotic patients will develop hepatocellular carcinoma (HCC). Previous studies report that the X-ray repair cross-complementing group1 gene (XRCC1) is important in the risk of HCC development; however, results obtained from these studies are conflicting rather than conclusive. We hypothesised an association between single nucleotide polymorphisms (SNPs) in XRCC1with the HCC risk on a background of chronic hepatitis C.Materials and methods: We recruited 210 subjects, 70 with HCC, 70 with cirrhosis and 70 healthy controls. Two SNPs [c.1254C>T(rs2293035) and c.1517G>C(rs139599857)] in XRCC1were genotyped using created restriction site-polymerase chain reaction (CRS-PCR) and PCR-restriction fragment length polymorphism (PCR-RFLP) methods.Results: The TT genotype, CT genotype and T-allele in c.1254C>T (rs2293035) were linked to risk of HCC compared to the CC genotype: OR 3.58 [confidence interval (CI) 95%: 1.19–10.7] p= 0.019; OR 2.16 (CI 95%: 1.04–4.47) p= 0.037 and OR 2.10 (CI 95%: 1.2–3.3) p= 0.006, respectively. Regarding c.1517G>C (rs139599857), the CC genotype, GC genotype and C-allele were linked with higher risk of developing HCC compared to GG genotype: OR 4.77 (CI 95%: 1.3–16.9), p= 0.016; OR 3.02 (CI 95%: 1.46–6.2), p= 0.002 and OR 2.4 (CI 95%: 1.4–4.0), p= 0.001, respectively.Conclusion: We conclude that the T-allele of c.1254C>T (rs2293035) and the C allele of c.1517G>C (rs139599857) genetic variants may be associated with increased HCC risk among chronic hepatitis C patients.
- Published
- 2019
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3. The relation between autophagy modulation by intermittent fasting and aquaporin 2 expression in experimentally induced diabetic nephropathy in albino rat.
- Author
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Hassan NH, Saleh D, Abo El-Khair SM, Almasry SM, and Ibrahim A
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- Animals, Rats, Male, Kidney metabolism, Kidney pathology, Polyuria metabolism, Polyuria pathology, Blood Glucose metabolism, Intermittent Fasting, Aquaporin 2 metabolism, Aquaporin 2 genetics, Diabetic Nephropathies metabolism, Diabetic Nephropathies pathology, Autophagy, Fasting blood, Diabetes Mellitus, Experimental metabolism, Diabetes Mellitus, Experimental pathology
- Abstract
Polyuria is an early sign of diabetic nephropathy (DN) that produces dehydration in diabetic patients. This could be caused by alteration of renal aquaporin 2 (AQP2) expression. This study aimed to describe the relation between autophagy modulation via intermittent fasting (IF) and renal AQP2 expression and polyuria in case of DN. We divided the rats into control, DN and IF groups. After 2 and 4 weeks of diabetes induction, blood glucose (BG), serum creatinine (Scr), urine volume, and 24 hours urine protein (UP) were examined. Diabetic nephropathy histopathological index (DNHI) was calculated to evaluate histopathological changes. Immunohistochemistry and real-time PCR were performed to measure the levels of AQP2 and the autophagy marker; LC3 in kidney tissue. DNHI was correlated to the PCR and immunoexpression of AQP2 and LC3. Intermittent fasting significantly decreased the BG, Scr, urine volume, 24 hours UP, and DNHI as compared diabetes. Diabetes significantly elevated the immunoreactivity and mRNA expression levels of AQP2 and LC3 as compared to the control. However, the IF decreased AQP2 and stimulated autophagy in cyclic fashion. Our data revealed significant positive correlations between AQP2 and LC3 at the level of immunoexpression and mRNA at 2nd weeks. Taken together, these data showed that autophagy stimulation didn't regulate AQP2 expression in case of diabetic nephropathy, however IF decreased polyuria through improvement of glycemic state., Competing Interests: Declaration of Competing Interest The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article, (Copyright © 2024 Elsevier Ltd. All rights reserved.)
- Published
- 2024
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4. Methylation degree of metalloproteinase inhibitor RECK gene: Links to RECK protein level and hepatocellular carcinoma in chronic HCV infection patients.
- Author
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Abo El-Khair SM, Elalfy H, Diasty M, Ebrahim EE, and Elsamanoudy AZ
- Subjects
- Adult, Aged, Carcinogenesis genetics, Carcinogenesis metabolism, Carcinoma, Hepatocellular blood, Case-Control Studies, Epigenesis, Genetic, Female, GPI-Linked Proteins blood, Genes, Tumor Suppressor, Genotype, Hepacivirus immunology, Hepatitis C, Chronic blood, Hepatitis C, Chronic virology, Humans, Liver Neoplasms blood, Lymphatic Metastasis genetics, Male, Middle Aged, Promoter Regions, Genetic genetics, Carcinoma, Hepatocellular complications, Carcinoma, Hepatocellular genetics, DNA Methylation genetics, GPI-Linked Proteins genetics, Hepacivirus genetics, Hepatitis C, Chronic complications, Hepatitis C, Chronic genetics, Liver Neoplasms complications, Liver Neoplasms genetics, Metalloproteases antagonists & inhibitors
- Abstract
The RECK gene, a tumor suppressor gene, inhibits angiogenesis, invasion, and tumor metastasis. Epigenetic regulation of the RECK gene constitutes a potent approach to the molecular basis of liver malignancy. This study aims to evaluate the promoter methylation status of the RECK gene and its serum level in patients with hepatitis C virus (HCV)-related hepatocellular carcinoma (HCC) and the potential association of RECK gene methylation with clinical criteria of HCC. One hundred and fifty-five subjects were included (healthy control [55], chronic HCV patients [55], HCV-related HCC patients [45]). The methylation status of the RECK gene promoter and serum RECK level were investigated by methylation-specific PCR and enzyme-linked immunosorbent assay techniques, respectively. RECK gene promoter hypermethylation was recorded in 46.7% of HCC patients, and 10.9% of HCV patients, but not in control subjects (0%). It was related to RECK protein level, varices, edema, ascites, lymph node metastasis, vascular invasion, and the largest diameter of focal lesions. Meanwhile, it was not associated with focal lesion number nor distant metastasis of HCC. In conclusion, RECK gene promoter hypermethylation is linked to HCV genotype-4-related HCC. Moreover, different degrees of RECK gene promoter methylation are associated with serum RECK level, lymph node metastasis, and vascular invasion, which could prove its pathogenic role in hepatocarcinogenesis in chronic HCV-infected patients., (© 2021 Wiley Periodicals LLC.)
- Published
- 2021
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5. Cellular Senescence and Vitamin D Deficiency Play a Role in the Pathogenesis of Obesity-Associated Subclinical Atherosclerosis: Study of the Potential Protective Role of Vitamin D Supplementation.
- Author
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Bima AI, Mahdi AS, Al Fayez FF, Khawaja TM, Abo El-Khair SM, and Elsamanoudy AZ
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- Animals, Atherosclerosis complications, Male, Nitric Oxide Synthase Type III metabolism, Rats, Sprague-Dawley, Tumor Suppressor Protein p53 metabolism, Vitamin D pharmacology, Vitamin D Deficiency complications, Rats, Atherosclerosis drug therapy, Atherosclerosis pathology, Cellular Senescence, Dietary Supplements, Obesity pathology, Vitamin D therapeutic use, Vitamin D Deficiency drug therapy, Vitamin D Deficiency pathology
- Abstract
The exact link between obesity, vitamin D deficiency, and their relation to cellular senescence in the pathogenesis of subclinical atherosclerosis is still under debate. Therefore, the current study aims to verify the possible role of vitamin D deficiency and cellular senescence in the pathogenesis of obesity-related subclinical atherosclerosis. Moreover, it aims to investigate the possible protective role of vitamin D supplementation. Fifty-seven male albino rats were enrolled in the study and classified into four groups: negative (10) and positive control groups (10), an obese model group (24), and a vitamin-D-supplemented obese group (13). Aortic tissue samples and fasting blood samples were collected. The following biochemical investigations were performed: serum cholesterol, triglycerides, HDL-C, LDL-C, ALT, AST, CPK, CK-MB, and hs-cTnt. HOMA-IR was calculated. Moreover, serum SMP-30, 25 (OH)Vitamin D
3 , and eNOS were determined by the ELISA technique. Aortic gene expression of eNOS, SMP-30, and P53 was estimated by real-time qRT-PCR. Serum 25(OH) D3 and SMP-30 were lower in the obese group. In addition, the obese group showed higher serum lipid profile, HOMA-IR, eNOS, ALT, AST, CPK, CK-MB, and hs-cTnt than the control groups, while decreased levels were found in the vitamin-D-treated obese group. Gene expression of eNOS and SMP-30 were in accordance with their serum levels. A positive correlation was found between vitamin D level and SMP-30. In conclusion, obesity is associated with vitamin D deficiency and enhanced cellular senescence. They could play a role in the pathogenesis of obesity-associated subclinical atherosclerosis and endothelial dysfunction. Vitamin D supplements could play a protective role against such obesity-related comorbidity.- Published
- 2021
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6. Association of genetic variants in the 3'-untranslated region of the mesothelin (MSLN) gene with ovarian carcinoma.
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Abou-El-Naga AM, Abo El-Khair SM, Mahmoud AZ, Hamza M, and Elshazli RM
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- Case-Control Studies, Egypt, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Mesothelin, Middle Aged, Multivariate Analysis, Principal Component Analysis, 3' Untranslated Regions, GPI-Linked Proteins genetics, Ovarian Neoplasms genetics, Polymorphism, Genetic
- Abstract
Limited information has been offered regarding the association of mesothelin (MSLN) gene variants at the 3'-untranslated region with the risk of ovarian carcinoma. The primary objective of this work is to assess the impact of the MSLN (rs1057147 and rs57272256) variants on the progression of ovarian carcinoma among Egyptian women. The study was conceived based on 127 women diagnosed with ovarian carcinoma and 106 unrelated cancer-free controls. Genomic DNA of these MSLN variants was genotyped utilizing the PCR technique. The frequencies of the MSLN (rs1057147) variant revealed a significant association with increased risk of ovarian carcinoma under allelic and dominant models (P < .05). Nonetheless, ovarian cancer patients with the MSLN (rs57272256) variant did not attain considerable significance under all genetic models (P > .05). Together, our findings suggested that the MSLN (rs1057147) variant was associated with an increased risk of ovarian carcinoma, but not the MSLN (rs57272256) variant., (© 2020 Wiley Periodicals LLC.)
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- 2021
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7. Development of a novel glycated protein-based fibrosis prediction score for determination of significant liver fibrosis in HCV-infected patients, a preliminary study.
- Author
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Abo El-Khair SM, El-Alfy HA, Elsamanoudy AZ, Elhammady D, Abd-Elfattah N, Eldeek B, and Farid K
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- Humans, Male, Female, Middle Aged, Adult, Sensitivity and Specificity, Glycated Serum Albumin, Aged, Platelet Count, Liver Function Tests methods, Biopsy, Severity of Illness Index, Liver pathology, alpha-Fetoproteins analysis, Liver Cirrhosis diagnosis, Liver Cirrhosis blood, Liver Cirrhosis pathology, Hepatitis C, Chronic complications, Hepatitis C, Chronic pathology, Hepatitis C, Chronic blood, Biomarkers blood, Glycation End Products, Advanced blood, Glycated Hemoglobin analysis, Serum Albumin analysis
- Abstract
The current study aimed to investigate the diagnostic value of glycated albumin (GA), glycated hemoglobin (HbA1c), and a number of routine biomarkers as noninvasive indicators of liver fibrosis in patients with chronic hepatitis C (CHC). One hundred patients with CHC were subjected to full medical history and examination, in addition to ultrasound-guided liver biopsy and histopathological examination for assessment of liver fibrosis stage. GA and HbA1c values, GA/HbA1c ratio, liver function tests, complete blood count, and alpha fetoprotein (AFP) were determined. A novel noninvasive index, dubbed Fibrosis Prediction Score (FPS), was selected for predicting significant liver fibrosis based on total bilirubin, glycated albumin, platelet count, age, and AFP. A validation study for FPS was applied on archival data which include 66 diabetics' patients. The FPS had area under the curve (AUC) of 0.92 for classification of patients with significant fibrosis with 81% sensitivity and 95% specificity. The AUCs of FPS in predicting advanced fibrosis and cirrhosis were 0.86 and 0.82, respectively. Comparison of AST-to-platelet ratio index (APRI) and FIB-4 with FPS indicated increased sensitivity and specificity of FPS over APRI and FIB4 in both significant and advanced fibrosis. FPS has a good sensitivity and specificity for prediction of significant and advanced liver fibrosis in patients with CHC., (© 2020 Wiley Periodicals LLC.)
- Published
- 2020
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8. Prognostic value of vascular endothelial growth factor in both conventional and drug eluting beads transarterial chemoembolization for treatment of unresectable hepatocellular carcinoma in HCV patients.
- Author
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Farid K, Elalfy H, Abo El-Khair SM, Elgamal H, Besheer T, Elmokadem A, Shabana W, Abed S, Elegezy M, El-Khalek AA, El-Morsy A, Negm A, Elsamanoudy AZ, El Deek B, Amer T, and El-Bendary M
- Subjects
- Aged, Biomarkers, Tumor blood, Carcinoma, Hepatocellular blood, Carcinoma, Hepatocellular diagnostic imaging, Carcinoma, Hepatocellular etiology, Female, Hepatitis C, Chronic complications, Humans, Liver Cirrhosis etiology, Liver Neoplasms blood, Liver Neoplasms diagnostic imaging, Liver Neoplasms etiology, Male, Microspheres, Middle Aged, Prognosis, Prospective Studies, Treatment Outcome, Antibiotics, Antineoplastic administration & dosage, Carcinoma, Hepatocellular therapy, Chemoembolization, Therapeutic methods, Doxorubicin administration & dosage, Liver Neoplasms therapy, Vascular Endothelial Growth Factor A blood
- Abstract
Objectives: This work aimed to measure serum vascular endothelial growth factor (VEGF) levels before and after Conventional transarterial chemoembolization (cTACE) versus drug-eluting beads (DEB)-TACE and evaluate its efficacy in predicting response to therapy and tumor recurrence., Methods: 114 patients with unresectable hepatocellular carcinoma complicating hepatitis C virus-related cirrhosis were included. They underwent cTACE (58) or DEB-TACE (56). VEGF serum levels were measured before and on days 1 and 30 after TACE. Patients with complete response (CR) after TACE were followed-up for one year. Statistical analysis was done., Results: VEGF level was higher than baseline after cTACE ( P < 0.001), and DEB-TACE ( P = 0.004). It was also significantly higher in patients with progressive disease ( P < 0.001). VEGF level at cut off values of 97.3, 149.8, and 104.1 pg/ml could discriminate disease progression from treatment success with area under ROC curves of 0.806, 0.775, and 0.771, respectively. The sensitivity was 88.9%, 88.9%, and 77.8% and specificity was 62.5%, 64.6 and 66.7%, respectively. However, no relation to tumor recurrence in CR group could be detected after one year., Conclusion: VEGF serum levels may predict response to therapy in patients treated by DEB-TACE or cTACE but it has no relation to tumor recurrence.
- Published
- 2020
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9. The Protective Role of Prenatal Alpha Lipoic Acid Supplementation against Pancreatic Oxidative Damage in Offspring of Valproic Acid-Treated Rats: Histological and Molecular Study.
- Author
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Ghoneim FM, Alrefai H, Elsamanoudy AZ, Abo El-Khair SM, and Khalaf HA
- Abstract
Background: Sodium valproate (VPA) is an antiepileptic drug (AED) licensed for epilepsy and used during pregnancy in various indications. Alpha-lipoic acid (ALA) is a natural compound inducing endogenous antioxidant production. Our study aimed to investigate the effect of prenatal administration of VPA on the pancreas of rat offspring and assess the potential protective role of ALA co-administration during pregnancy., Methods: Twenty-eight pregnant female albino rats were divided into four groups: group I (negative control), group II (positive control, ALA treated), group III (VPA-treated), and group IV (VPA-ALA-treated). The pancreases of the rat offspring were removed at the fourth week postpartum and prepared for histological, immune-histochemical, morphometric, molecular, and oxidative stress marker studies., Results: In group III, there were pyknotic nuclei, vacuolated cytoplasm with ballooning of acinar, α, and β cells of the pancreas. Ultrastructural degeneration of cytoplasmic organelles was detected. Additionally, there was a significant increase in oxidative stress, a decrease in insulin-positive cell percentage, and an increase in glucagon positive cells in comparison to control groups. Moreover, VPA increased the gene expression of an apoptotic marker, caspase-3, with a decrease in anti-apoptotic Bcl2 and nuclear factor erythroid 2-related factor 2 (Nrf2) transcriptional factor. Conversely, ALA improved oxidative stress and apoptosis in group VI, and a consequent improvement of the histological and ultrastructure picture was detected., Conclusion: ALA co-administration with VPA significantly improved the oxidative stress condition, histological and morphometric picture of the pancreas, and restored normal expression of related genes, including Nrf2, caspase-3, and Bcl-2. Administration of α-lipoic acid has a protective effect against VPA-induced pancreatic oxidative damage via its cytoprotective antioxidant effect.
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- 2020
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10. Molecular and ultrastructure study of endoplasmic reticulum stress in hepatic steatosis: role of hepatocyte nuclear factor 4α and inflammatory mediators.
- Author
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Abo El-Khair SM, Ghoneim FM, Shabaan DA, and Elsamanoudy AZ
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- Animals, Diet, High-Fat adverse effects, Disease Models, Animal, Inflammation metabolism, Inflammation physiopathology, Male, Rats, Rats, Sprague-Dawley, Endoplasmic Reticulum Stress, Fatty Liver metabolism, Hepatocyte Nuclear Factor 4 metabolism, Inflammation Mediators metabolism
- Abstract
Endoplasmic reticulum (ER) stress could participate in high-fat diet (HFD)-induced hepatic steatosis. The current study aims to investigate the role of ER stress as well as inflammation as possible pathophysiologic mechanisms of HFD-induced hepatic steatosis at ultrastructure and molecular levels. Fifteen control rats on ordinary diet and 30 HFD-fed rats were enrolled in the study. Histological and EM examinations of rats' liver were carried out. Molecular study of TNF-α, CRP, and HNF4α by RT qPCR as well as biochemical investigation of liver function and lipids profile were done. Hepatic steatosis was induced with lipid droplets accumulation at histological level and mega-mitochondria with reduced ER-mitochondrial distance at EM level. Increased gene expression of TNF-α and CRP was significantly correlated with the reduced HNF4α expression and with other ER stress markers. In conclusion, endoplasmic reticulum stress, confirmed at ultrastructure level, plays an important role in pathogenesis of HFD-induced hepatic steatosis. HNF4α downregulation as well as increased expression of hs-CRP and TNF-α enforce the concept of interplay between ER stress, hepatic subclinical inflammation, and disturbed gene expression regulation in the pathogenesis of HFD-induced hepatic steatosis.
- Published
- 2020
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11. Programmed cell death 1 gene polymorphism as a possible risk for systemic lupus erythematosus in Egyptian females.
- Author
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Abo El-Khair SM, Sameer W, Awadallah N, and Shaalan D
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- Adult, Alleles, Case-Control Studies, Egypt epidemiology, Female, Genotype, Haplotypes, Humans, Lupus Erythematosus, Systemic blood, Lupus Erythematosus, Systemic diagnosis, Retrospective Studies, Risk Factors, Lupus Erythematosus, Systemic genetics, Polymorphism, Single Nucleotide genetics, Programmed Cell Death 1 Receptor genetics
- Abstract
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease with a suggested genetic basis. The newly identified human programmed cell death 1 gene could be associated with SLE susceptibility. We aimed to investigate the association between programmed cell death 1 polymorphism (PD1.3G/A (rs11568821) and PD1.5C/T (rs2227981)) with the risk of SLE in the Egyptian female population. This retrospective case-control study included 150 Egyptian females; 70 patients diagnosed to have SLE and 80 age-matched healthy controls. The two single nucleotide polymorphisms of the pdcd1 gene were genotyped by allelic discrimination through TaqMan real-time polymerase chain reaction. The PD1.3GG genotype and G allele as well as the PD1.5CC genotype were significantly more frequent in SLE patients (67.1%; p = 0.023, 82.1%; p = 0.0021, 62.9%; p = 0.0287 respectively). The GC haplotype was the most common haplotype among SLE patients (70.77%) with a reported significant linkage disequilibrium between the two studied polymorphisms ( p = 0.0041). Although most of the studies showed significant association of SLE with the minor alleles, we reported a significant association between the dominant genotypes (PD1.3GG and PD1.5CC) as well as the major G allele with the risk of SLE among Egyptian females.
- Published
- 2019
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12. Diverse drivers of unsustainable groundwater extraction behaviour operate in an unregulated water scarce region.
- Author
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Khair SM, Mushtaq S, Reardon-Smith K, and Ostini J
- Subjects
- Conservation of Natural Resources, Humans, Pakistan, Water Resources, Groundwater, Water
- Abstract
Depletion of groundwater resources is of increasing concern in many parts of the world; however, farmers' perceptions of resource status and the role these have in influencing decisions about groundwater use are rarely considered and even more rarely analysed. This paper investigates the links between farmers' perceptions of resource condition and drivers of groundwater decline and patterns of groundwater use in the semi-arid highland region of Balochistan, Pakistan. Key factors associated with groundwater over-exploitation in this region, identified by farmers, include: high returns from irrigated fruit and vegetable cultivation; drought; mass installation of tubewells; inefficient irrigation practices; government policies and subsidies that promote groundwater development; and lack of effective groundwater governance. Critically, while a majority of farmers in this study believe that groundwater is a limited resource, there is little evidence to indicate that this then leads to sustainable groundwater use decision making within these communities. Without effective intervention, groundwater resources in this region will potentially suffer the consequences of human behaviour associated with the use of common pool resources identified in Hardin's (1968) seminal 'Tragedy of the Commons' paper. This study exemplifies the importance to the future of rural communities in water scarce regions of effective governance, regulations and economic incentives for sustainable water management., (Copyright © 2018. Published by Elsevier Ltd.)
- Published
- 2019
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13. Clinicopathological impact of anti-smooth muscle antibodies in patients with non-alcoholic fatty liver disease.
- Author
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Elalfy H, El-Maksoud MA, Abed S, El Aziz MA, Elsamanoudy AZ, Abo El-Khair SM, Mohamed MA, Elkashef W, Zalata K, Farag R, and Arafa M
- Subjects
- Adult, Antibodies, Anti-Idiotypic immunology, Bilirubin blood, Bilirubin immunology, Female, Humans, Liver immunology, Liver metabolism, Liver pathology, Liver Cirrhosis immunology, Liver Cirrhosis pathology, Male, Myocytes, Smooth Muscle metabolism, Non-alcoholic Fatty Liver Disease blood, Non-alcoholic Fatty Liver Disease pathology, Prothrombin Time, Serum Albumin, Triglycerides blood, Triglycerides immunology, Antibodies, Anti-Idiotypic blood, Liver Cirrhosis blood, Myocytes, Smooth Muscle immunology, Non-alcoholic Fatty Liver Disease immunology
- Published
- 2019
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14. The Association of XRCC1 Gene Polymorphisms and Chronic Hepatitis C Induced Insulin Resistance in Egyptian Patients.
- Author
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Abo El-Khair SM, Arafa M, Besheer T, El-Eraky AM, and Elsamanoudy AZ
- Abstract
Chronic hepatitis C is implicated in insulin resistance (IR) susceptibility. An X-ray repair cross-complementing group 1 gene ( XRCC1 ) is proposed to be a candidate gene for a study of IR susceptibility. So, this study aims to investigate the possible association of the XRCC1 gene polymorphisms with the risk of IR related to chronic hepatitis C virus (HCV) infection in Egyptian patients. In a case-control study, a total of 210 subjects, including 140 chronic HCV patients (87 patients with IR and 53 without IR) and 70 healthy controls, were included. Two genetic polymorphisms (c.1254C > T and c.1517G > C) of the XRCC1 gene were genotyped via the PCR-restriction fragment length polymorphism (PCR-RFLP) technique. The result of the current study revealed that these two single nucleotide polymorphisms (SNPs) have statistically significant influences on susceptibility to IR in chronic HCV infected Egyptian patients. It could be concluded that c.1254C > T, the TT genotype, CT/CC carriers as well as c.1517G > C, the CC genotype and GC/GG carriers might be associated with increased IR susceptibility. Moreover, T-allele of c.1254C > T and the C-allele of c.1517G > C genetic variants might influence the susceptibility.
- Published
- 2018
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15. Spermatozoal Fractalkine Signaling Pathway Is Upregulated in Subclinical Varicocele Patients with Normal Seminogram and Low-Level Leucospermia.
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Abo El-Khair SM, Gaballah MA, Abdel-Gawad MM, Ismail SRM, and Elsamanoudy AZ
- Abstract
Background: Fractalkine is produced in seminal plasma in small amounts and correlates with sperm motility., Purpose: To investigate the possible effect of low-level leucospermia on spermatozoa oxidative stress and sDNA fragmentation in patients with subclinical varicocele and apparently normal seminogram, and also to study the role of spermatozoal fractalkine and its receptor (CX3CR1) gene expression as a marker of spermatozoa inflammatory response., Methods: This study included 80 patients with subclinical varicocele (45 fertile and 35 infertile) and 45 age-matched fertile volunteers. In semen samples, fractalkine and CX3CR1 gene expression were investigated by qRT-PCR. Moreover, seminal plasma malondialdehyde (MDA) and total antioxidant capacity (TAC) were measured., Results: There are significant decrease in semen quality and significant increase in seminal leucocytes count in subclinical varicocele. Our results show a significant increase in MDA and TAC levels, DNA fragmentation, and expression levels of fractalkine and its receptor (CX3CR1) in subclinical varicocele groups., Conclusion: Subclinical varicocele induces seminal and spermatozoal subclinical inflammatory response in the form of low-level leucospermia and increased mRNA expression of the fractalkine signaling pathway, leading to increased spermatozoal ROS production, oxidative stress, and DNA fragmentation. These could cooperate in the pathogenesis of delayed fertility in males with subclinical varicocele.
- Published
- 2017
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16. The genetic diversity of metronidazole susceptibility in Trichomonas vaginalis clinical isolates in an Egyptian population.
- Author
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Abdel-Magied AA, El-Kholya EI, Abou El-Khair SM, Abdelmegeed ES, Hamoudaa MM, Mohamed SA, and El-Tantawy NL
- Subjects
- Adolescent, Adult, Egypt, Female, Genetic Variation genetics, Humans, Middle Aged, Parasitic Sensitivity Tests, Polymerase Chain Reaction, Polymorphism, Restriction Fragment Length genetics, Trichomonas Vaginitis parasitology, Trichomonas vaginalis isolation & purification, Vaginal Smears, Young Adult, Antiprotozoal Agents therapeutic use, Drug Resistance genetics, Metronidazole therapeutic use, Trichomonas Vaginitis drug therapy, Trichomonas vaginalis drug effects, Trichomonas vaginalis genetics
- Abstract
Trichomoniasis is the most common curable sexually transmitted disease worldwide. Resistance to metronidazole in treating trichomoniasis is a problematic health issue. We aimed to determine the minimum lethal concentration (MLC) of metronidazole for Trichomonas vaginalis isolates detected in Mansoura, Egypt and studied the genotypic profile of these isolates. Vaginal swab specimens were obtained from 320 symptomatic and 100 asymptomatic females, for whom clinical examination, vaginal discharge wet mount, Giemsa stain, and culture in modified Diamond's media were performed. Metronidazole susceptibility testing by an aerobic tube assay was performed. Both sensitive and resistant isolates were examined by PCR amplification followed by restriction fragment length polymorphism (RFLP). Trichomonas vaginalis was identified in 49/420 (11.7%) using either culture or PCR, while wet mount and Giemsa stain detected the parasite in 8.1 and 7.6% of participants, respectively. After 48 h incubation, most isolates were sensitive to metronidazole with a minimal lethal concentration (MLC) of 1 μg/ml. Mild resistance was observed in two isolates with MLCs of 64 μg\ml and mild to moderate resistance was observed in an additional two isolates with MLCs of 128 μg/ml. The four isolates that demonstrated low to moderate metronidazole resistance displayed a unique genotype band pattern by RFLP compared to the other 45 samples that were metronidazole sensitive. Our results highlight the presence of in vitro metronidazole tolerance in a few T. vaginalis isolates in Mansoura, Egypt that may lead to the development of drug resistance as well as the possibility of an identifying RFLP pattern in the isolates.
- Published
- 2017
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17. Protective effect of chronic caffeine intake on gene expression of brain derived neurotrophic factor signaling and the immunoreactivity of glial fibrillary acidic protein and Ki-67 in Alzheimer's disease.
- Author
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Ghoneim FM, Khalaf HA, Elsamanoudy AZ, Abo El-Khair SM, Helaly AM, Mahmoud el-HM, and Elshafey SH
- Subjects
- Aluminum Chloride, Aluminum Compounds adverse effects, Alzheimer Disease chemically induced, Alzheimer Disease metabolism, Animals, Brain-Derived Neurotrophic Factor genetics, Chlorides adverse effects, Disease Models, Animal, Glial Fibrillary Acidic Protein genetics, Glial Fibrillary Acidic Protein metabolism, Hippocampus drug effects, Hippocampus pathology, Humans, Ki-67 Antigen genetics, Ki-67 Antigen metabolism, Male, Neurons drug effects, Neurons pathology, Rats, Rats, Sprague-Dawley, Receptor Protein-Tyrosine Kinases genetics, Receptor Protein-Tyrosine Kinases metabolism, Alzheimer Disease drug therapy, Brain-Derived Neurotrophic Factor metabolism, Caffeine pharmacology, Gene Expression Regulation drug effects, Signal Transduction drug effects
- Abstract
Alzheimer's disease (AD) is a neurodegenerative disorder with progressive degeneration of the hippocampal and cortical neurons. This study was designed to demonstrate the protective effect of caffeine on gene expression of brain derived neurotrophic factor (BDNF) and its receptor neural receptor protein-tyrosine kinase-β (TrkB) as well as glial fibrillary acidic protein (GFAP) and Ki-67 immunoreactivity in Aluminum chloride (AlCl3) induced animal model of AD. Fifty adult rats included in this study were classified into 5 group (10 rats each); negative and positive control groups (I&II), AD model group (III), group treated with caffeine from the start of AD induction (IV) and group treated with caffeine two weeks before AD induction (V). Hippocampal tissue BDNF and its receptor (TrkB) gene expression by real time RT-PCR in addition to immunohistochemical study of GFAP and Ki67 immunoreactivity were performed for all rats in the study. The results of this study revealed that caffeine has protective effect through improving the histological and immunohistochemical findings induced by AlCl3 as well as BDNF and its receptor gene expression. It could be concluded from the current study, that chronic caffeine consumption in a dose of 1.5 mg/kg body weight daily has a potentially good protective effect against AD.
- Published
- 2015
18. Groundwater Governance in a Water-Starved Country: Public Policy, Farmers' Perceptions, and Drivers of Tubewell Adoption in Balochistan, Pakistan.
- Author
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Khair SM, Mushtaq S, and Reardon-Smith K
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- Farmers, Pakistan, Water Wells, Conservation of Natural Resources legislation & jurisprudence, Groundwater, Public Policy, Water Supply economics
- Abstract
Pakistan faces the challenge of developing sustainable groundwater policies with the main focus on groundwater management rather than groundwater development and with appropriate governance arrangement to ensure benefits continue into the future. This article investigates groundwater policy, farmers' perceptions, and drivers of tubewell (groundwater bore) adoption and proposes possible pathways for improved groundwater management for Balochistan, Pakistan. Historical groundwater policies were mainly aimed at increasing agricultural production and reducing poverty, without consideration of adverse impact on groundwater availability. These groundwater policies and governance arrangements have resulted in a massive decline in groundwater tables. Tubewell owners' rankings of the drivers of groundwater decline suggest that rapid and widespread installation of tubewells, together with uncontrolled extraction due to lack of property rights, electricity subsidy policies, and ineffective governance, are key causes of groundwater decline in Balochistan. An empirical "tubewell adoption" model confirmed that the electricity subsidy significantly influenced tubewell adoption decisions. The article proposes a more rational electricity subsidy policy for sustaining groundwater levels in the short-run. However, in the long run a more comprehensive sustainable groundwater management policy, with strong institutional support and involvement of all stakeholders, is needed., (© 2014, National Ground Water Association.)
- Published
- 2015
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