Rasha Elzehery
Mansoura University
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Publication
Featured researches published by Rasha Elzehery.
European Journal of Gastroenterology & Hepatology | 2016
Ahmed Abdel-Razik; Nasser Mousa; Walaa Shabana; Mohamed Refaey; Youssif ElMahdy; Rania Elhelaly; Rasha Elzehery; Khaled Zalata; Mohammad Arafa; Sherif Elbaz; Mohamed Hafez; Mahmoud Awad
Background and aim Nonalcoholic fatty liver disease (NAFLD) is a leading cause of progressive and chronic liver injury. Mean platelet volume (MPV) and the neutrophil–lymphocyte ratio (N/L ratio) may be considered cheap and simple markers of inflammation in many disorders. We aimed to investigate the clinical utility of MPV and the N/L ratio to predict fibrosis in NAFLD patients and the presence of nonalcoholic steatohepatitis (NASH). Materials and methods A total of 873 patients with biopsy-proven NAFLD and 150 healthy controls were included. Patients were divided into two groups: non-NASH group (n=753) and NASH group (n=120). Liver biopsy, MPV, lymphocyte, and neutrophil counts were registered; the N/L ratio was calculated. Proinflammatory cytokines (tumor necrosis factor-&agr; and interleukin-6) were measured by an ELISA. Results NASH patients had higher MPV compared with non-NASH patients (10.9±1.8 and 9.5±1.6 fl, respectively, P<0.001). MPV correlated positively with the NAFLD activity score, proinflammatory cytokines, and C-reactive protein (CRP) (P<0.001). Patients with advanced fibrosis (F3–4) had increased MPV (11.3±0.9 fl) compared with patients with early fibrosis (F1–2) (10.2±0.8 fl, P<0.001). NASH patients had an increased N/L ratio compared with non-NASH cases (2.6±1.1 and 1.9±0.7 fl, respectively, P<0.001). The N/L ratio correlated positively with NAFLD activity score, proinflammatory cytokines, and CRP (P<0.001). In addition, patients with advanced fibrosis (F3–4) had an N/L ratio (2.5±1.1) comparable with that of patients with early fibrosis (F1–2) (1.8±0.9) (P<0.001). Conclusion MPV and the N/L ratio were elevated in NASH patients versus non-NASH cases, and in patients with advanced fibrosis (F3–4) versus early fibrosis (F1–2). They can be used as noninvasive novel markers to predict advanced disease.
Gut and Liver | 2016
Ahmed Abdel-Razik; Nasser Mousa; Dina Elhammady; Rania Elhelaly; Rasha Elzehery; Sherif Elbaz; Mohamed Eissa; Niveen El-Wakeel; Waleed Eldars
Background/Aims The diagnosis of spontaneous bacterial peritonitis (SBP) is based on a polymorphonuclear leukocytes (PMNs) exceeding 250/μL in ascitic fluid. The aim of the study was to evaluate serum procalcitonin and ascitic fluid calprotectin as accurate diagnostic markers for detecting SBP. Methods Seventy-nine patients with cirrhotic ascites were included. They were divided into a SBP group, including 52 patients, and a non-SBP group of 27 patients. Serum procalcitonin, ascitic calprotectin, and serum and ascitic levels of tumor necrosis factor α (TNF-α) and interleukin 6 (IL-6) were measured using an enzyme-linked immunosorbent assay. Results Serum procalcitonin and ascitic calprotectin were significantly higher in SBP patients than in non-SBP patients. Significant increases in both serum and ascitic levels of TNF-α and IL-6 were observed in SBP patients versus non-SBP patients. At a cutoff value of 0.94 ng/mL, serum procalcitonin had 94.3% sensitivity and 91.8% specificity for detecting SBP. In addition, at a cutoff value of 445 ng/mL, ascitic calprotectin had 95.4% sensitivity and 85.2% specificity for detecting SBP. Both were positively correlated with ascitic fluid proteins, PMN count, TNF-α, and IL-6. Conclusions According to our findings, determination of serum procalcitonin levels and ascitic calprotectin appears to provide satisfactory diagnostic markers for the diagnosis of SBP.
European Journal of Gastroenterology & Hepatology | 2016
Ahmed Abdel-Razik; Rania Elhelaly; Rasha Elzehery; Amany El-Diasty; Sally Abed; Dina Elhammady; Ahmed M. Tawfik
Background Hepatocellular carcinoma (HCC) is the third most common cause of cancer mortality among men worldwide. Serotonin is a biogenic amine, which may be involved in the tumorigenesis of HCC. Aim We aimed to determine whether serotonin is a dependable marker for the diagnosis of HCC in cirrhotic patients in comparison with &agr;-fetoprotein protein (AFP) and prothrombin induced by vitamin K absence-II (PIVKA-II). Patients and methods Serum serotonin, AFP, and PIVKA-II were measured in 262 patients with chronic hepatitis C (CHC): 82 cirrhotic patients with HCC (group I), 80 cirrhotic patients without HCC (group II), and 100 CHC-infected patients without cirrhosis (group III); in addition, 60 healthy controls were studied (group IV). Results AFP showed significant statistical differences among the groups studied (P<0.001). PIVKA-II and serotonin levels showed no statistically significant differences between the patients with CHC group and the healthy controls (P1=0.614 and P1=0.13, respectively), whereas their levels were statistically higher in cirrhotic patients than patients with CHC (all P values <0.001) and in the cirrhotic patients with HCC group than the cirrhotic patients without HCC (P<0.001). A significant positive correlation was found between serum serotonin and AFP (rho=0.794; P<0.001) and serum serotonin and PIVKA-II (rho=0.889; P<0.001) among the patient groups. The receiver operator characteristic curve showed a higher area under the curve for serotonin than AFP and PIVKA-II (0.942, 0.824, and 0.921, respectively). Conclusion Serotonin may be used together with PIVKA-II to screen for HCC in cirrhotic patients with CHC.
Endocrine Research | 2016
Amany Mousa; Mohamed Ghonem; El hadidy M. Elhadidy; Emad Azmy; Magda Elbackry; Azza A. El-Baiomy; Rasha Elzehery; Gehan A. Shaker; Omyma Saleh
ABSTRACT Objective: to assess the growth and pubertal development among a group of patients with β-Thalassemia Major (β-TM) and to evaluate the role of the pituitary gland and liver MRI signal intensity (SI) reduction in assessing and predicting the clinical severity of growth and pubertal dysfunctions. Methods: Thirty-eight patients with β-TM were examined and divided into two groups: Group I patients were of normal height and puberty and Group II patients had short statures and hypogonadism. Laboratory investigations included serum ferritin, LH, FSH, prolactin, TSH, and basal and dynamic growth hormones. Pituitary and liver MRIs were performed to assess the pituitary to fat (P/F) and liver to muscle (L/M) signal intensities (SI), respectively. Fifteen healthy and sex- and age-matched subjects were included as controls. Results: Both patient groups had significantly elevated serum ferritin and significantly decreased prolactin and IGF1 compared to control subjects. Group II showed a significant reduction in LH, FSH, and IGF1 and a significant increase in ferritin in comparison with Group I and the control group, and it had a highly significant reduction in both P/F and L/M SI in comparison with Group I (p<0.001 and 0.008, respectively). The reduced P/F ratio was significantly correlated with FSH and LH, and a cutoff for a P/F ratio ≥0.94 was obtained to differentiate between Group I and II. Conclusion: MRI in conjunction with the P/F signal intensity ratio is a useful and noninvasive tool for the early diagnosis of pituitary iron overload.
Journal of the Egyptian Womenʼs Dermatologic Society | 2017
Youssef M. Mosaad; Manar Sallam; Moustafa A. Elsaied; Hanan Fathy; Zakaria Fawzy; Rasha Elzehery; Rana M. Shaat; Abdel-Hady El-Gilany
Background Vitiligo is a common, chronic skin disease characterized by selective destruction of melanocytes. The worldwide disease prevalence ranges from 0.1 to 8.8% with no sex preference. The catalase (CAT) gene expression and polymorphism affect the CAT level and activity. Association between some CAT gene polymorphisms and vitiligo has been reported; however, the results were inconsistent. Objective To analyze whether CAT 389 T/C and −89 T/A gene polymorphisms are associated with vitiligo and to investigate their effect on the serum level of CAT and malondialdehyde (MDA) in those patients. Patients and methods Typing of CAT 389 T/C and CAT −89 T/A using PCR-restriction fragment length polymorphism and evaluation of serum levels of CAT and MDA were carried out for 106 vitiligo patients and 95 healthy controls. Results Nonsignificant differences were found between patients and healthy controls for the allele and genotype frequencies of CAT 389 and CAT −89 except for the increased frequency of T allele of CAT 389 in patients with vitilgo (P=0.02 and Pc=0.04). The frequency of combined CCAT genotype was increased in healthy controls versus that in the patients (P=0.007 and Pc=0.014). In vitiligo patients, the serum level of CAT was lower and the level of MDA was higher compared with healthy controls (P⩽0.001). No significant associations were found between the genotypes and haplotypes of the studied single-nucleotide polymorphisms and disease activity, disease extent, serum levels of CAT, and MDA. Conclusion The T allele of CAT 389 may be a susceptibility risk factor for vitiligo and the combined CCAT genotype may be protective in the studied sample of patients. Decreased levels of CAT with increased levels of MDA may indicate increased oxidative stress in nonsegmental vitiligo patients.
The American Journal of the Medical Sciences | 2016
Ahmed Abdel-Razik; Youssif ElMahdy; Ehab El hanafy; Rania Elhelaly; Rasha Elzehery; Ahmed M. Tawfik; Waleed Eldars
Background: Despite the presence of various diagnostic tools, the differential diagnosis between malignant and benign biliary obstructions is so difficult. This study aimed to evaluate the role of serum and biliary insulin‐like growth factor‐1 (IGF‐1) and vascular endothelial growth factor (VEGF) in this differential diagnosis. Materials and Methods: Patients (n = 109, 61 men and 48 women) with diagnosis of benign (n = 62) or malignant (n = 47) biliary obstruction were included. Serum and biliary IGF‐1 and VEGF markers were analyzed by the chemiluminescent immunometric method. Results: Mean age was 62.7 ± 8.1 years for the malignant group and 58.5 ± 15.4 years for the benign group (P = 0.092). Choledocholithiasis (79%), cancer head of the pancreas (53.2%) and cholangiocarcinoma (38.3%) were the most common etiologies. No statistical difference was detected regarding serum IGF‐1 and VEGF levels between 2 groups. At a cutoff value of 308.55 and 0.5 ng/mL, biliary IGF‐1 and VEGF had (91.4% and 90.3%) sensitivity and (89.5% and 84.9%) specificity differential diagnosis between malignant and benign biliary obstructions (area under the curve: 0.943, 0.915), respectively. Conclusions: Biliary levels of IGF‐1 and VEGF significantly increase in malignant than benign obstructive lesions. Measurement of these markers in the bile of these patients may aid in the detection of biliary tumors.
Journal of Gastroenterology and Hepatology | 2016
Ahmed Abdel-Razik; Waleed Eldars; Rania Elhelaly; Rasha Elzehery
Insulin‐like growth factor‐1 (IGF‐1) and C‐reactive protein (CRP) are produced mainly by the liver; the output of these markers in response to inflammatory processes may be affected in patients with hepatic dysfunction. This may explain the differences in IGF‐1 and CRP values in patients with non‐portal and portal hypertension ascites. We aimed to evaluate serum and ascitic fluid IGF‐1 and CRP as diagnostic markers in the differential diagnosis of benign and malignant ascites.
Helicobacter | 2018
Ahmed Abdel-Razik; Nasser Mousa; Walaa Shabana; Mohamed Refaey; Rania Elhelaly; Rasha Elzehery; Mostafa Abdelsalam; Ayman Elgamal; Mervat Ragab Abd El-Rahman Nassar; Atef Abu El-Soud; Ahmed S. Seif; Ahmed M. Tawfik; Niveen El-Wakeel; Waleed Eldars
The relationship between Helicobacter pylori (H. pylori) and nonalcoholic fatty liver disease (NAFLD) is a matter of debate. We achieved this prospective work to study whether H. pylori infection is a risk factor for NAFLD.
European Journal of Gastroenterology & Hepatology | 2017
Nasser Mousa; Ahmed Abdel-Razik; Raghda E. Farag; Walaa Shabana; Ayman Elgamal; Niveen El-Wakeel; Rasha Elzehery; Wagdi Elkashef; Waleed Eldars
Background and aim There are millions of chronic hepatitis C (CHC) virus-infected patients who have been treated with a combination therapy (interferon and ribavirin) and have achieved a virological response (SVR) worldwide. The aim of this study is to evaluate the risk factors for de-novo diabetes mellitus in CHC patients treated with combination therapy (interferon and ribavirin) and have achieved an SVR. Patients and methods A total of 214 nondiabetic CHC patients with SVR and baseline homeostasis model assessment (HOMA) less than or equal to 2 were divided into group A, which included 108 patients with a BMI less than 25, and group B, which included 106 patients with a BMI of at least 25 and less than 30. HOMA insulin resistance (IR) and BMI were measured at the baseline, at achievement of an SVR, and 1 year after achievement of an SVR. Leptin levels were assessed at baseline and 1 year after achievement of an SVR in patients with increased BMI. Results One year after SVR, 36 (33.33%) patients from group A developed increasing BMI with no significant changes in HOMA versus that at SVR (P=0.53), but showed a significant reduction versus baseline HOMA (P=0.02). In group B, 68 (64.1%) patients showed increased BMI of at least 25, with a significant increase in HOMA versus that at SVR (P=0.02), and with no significant reduction versus baseline HOMA (P=0.44). In group B, serum leptin showed a significant reduction 12 months after achievement of an SVR versus baseline in patients with increased BMI. Six patients from group B with increased BMI after 1 year developed de-novo IR and type two diabetes mellitus. Conclusion In nondiabetic CHC patients with SVR and baseline BMI of at least 25, the post-SVR increase in BMI predisposed to an increase in HOMA-IR and could be considered a predisposing factor for diabetes mellitus.
Diabetes & Metabolism Journal | 2017
Ibrahim Elsehely; Hala Abdel Hafez; Mohammed Ghonem; Ali Fathi; Rasha Elzehery
Previous studies showed that early age at menarche is associated with increased risk of metabolic syndrome. However, the definition of early menarche at these studies was based on background data in the communities at which these studies was carried on. The aim of this work is to determine a cutoff for age at menarche discriminating presence or absence of metabolic syndrome in overweight/obese premenopausal women. This study included 204 overweight/obese women. Metabolic syndrome was defined according to NCEP-ATP III (National Cholesterol Education Program Adult Treatment Panel III) criteria. Of a total 204 participants, 82 (40.2%) had metabolic syndrome. By using receiver operating characteristic analysis, age at menarche ≤12.25 year discriminated individuals with from those without metabolic syndrome. The area under the curve was 0.76 (95% confidence interval, 0.70 to 0.83). Sensitivity, specificity, negative predictive value, and positive predictive value were 82%, 70%, 85%, and 64%, respectively. Age at menarche ≤12.25 years predicts the presence of metabolic syndrome in overweight/obese women.