9 research outputs found

    A comparative assessment of RNF38 and P53 genes expression in the sperm samples obtained from males with normozoospermia and asthenospermia: A case-control study

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    Background: Infertility is considered as a common problem appears in about 10-12% of couples in their reproductive ages. Ring finger protein 38 (RNF38) gene is a ubiquitinprotein ligase that can regulate Protein 53 (P53) and affect cellular motility. Objective: Considering the role of P53 on cellular motility and RNF38 on the regulation of P53, the present study aimed to assess the difference between RNF38 and P53 genes expression in normozoospermic and asthenospermic samples as a diagnostic biomarker in males. Materials and Methods: The present study was conducted among 21 asthenospermics and 63 healthy individuals. First, the real-time polymerase chain reaction technique was applied to measure the expression level of the P53 and RNF38 genes extracted from sperm samples, and the glyceraldehyde-3phosphate dehydrogenase gene was selected as the reference gene. Results: An increase and a decrease occurred in the level of P53 and RNF38 genes expressions in asthenospermic and normozoospermic samples, respectively. In addition, a significant difference was observed between increasing P53 gene expression (p < 0.001), reducing RNF38 one, and decreasing sperm motility (p < 0.001) in asthenospermic cells compared to that of normozoospermic ones. Conclusion: Based on the results, an increase in the expression of the P53 gene and a decrease in the expression of the RNF38 gene had a significant relationship with asthenospermia in men. Therefore, it is expected that an effective step should be adopted to diagnose the asthenospermia expression pattern by using these results. Key words: RNF38, P53, Asthenozoospermia, Motility

    Childhood Epilepsy; Prognostic Factors in Predicting the Treatment Failure

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    How to Cite This Article: Taghdiri MM, Omidbeigi M, Asaadi S, Mohebbi M, Azarghashb E, Ghofrani M. Childhood Epilepsy; Prognostic Factors in Predicting the Treatment Failure. Iran J Child Neurol. Winter 2017; 11(1):21-28.AbstractObjectiveWe aimed to find the prognostic factors to detect the patients who fail the treatment of epilepsy, in the early stages of the disease.Materials & MethodsThis study was done on the epileptic patients attending the Neurology Clinic of Mofid Children’s Hospital, Tehran, Iran from September 2013 to October 2014. After defining the criteria for exclusion and inclusion, the patients were divided to two groups based on responding to the medical treatment for their epilepsy and indices were recorded for all the patients to be used in the statistical analyses.ResultsThe patients’ age ranged from 1 to 15 yr. There was 188 patients with refractory seizure in group 1 (experimental group) and 178 patient with well controlled seizure in group 2(control group).There was a significant different between serum drug level in both groups and patients with refractory seizure group had a lower serum drug level than control group. In both groups tonic-clonic was the most common type of seizure. Also the prevalence of brain imaging Abnormalityand other neurologic disorders was significantly higher in patients with refractory seizure in compare with control group.ConclusionChildren with seizure who suffer from refractory epilepsy need more attention and exact observation by the medical staff. References 1. Kozyrskyj AL, Prasad AN. The burden of seizures in Manitoba children: a population-based study. Can J Neurol Sci 2004;31:48-52. 2. Camfield PR, Camfield CS, Gordon Kandet al. If a first antiepileptic drug fails to control a child’s epilepsy, what are the chances of success with the next drug? J Pediatr 1997; 131:821-4.3. Arts WF, Brouwer OF, Peters ACet al. Course and prognosis of childhood epilepsy: 5-year follow-up of the Dutch study of epilepsy in childhood. Brain 2004;127:1774–84.4. Berg AT, Shinnar S, Levy SR, et al. Early Development of intractable epilepsy in children: a prospective study. Neurology 2001;56:1445–52.5. Berg AT, Vickrey BG, Testa FM, et al. How long does it take for epilepsy to become intractable? A prospective investigation. Ann Neurol 2006;60:73–9. 6. Kwan P, Brodie M. Early identification of refractory epilepsy. N Eng J Med2000;342:314–9.7. Mohanraj R, Brodie MJ. Diagnosing refractory epilepsy: response to sequential treatment schedules. Eur J Neurol 2006;13:277–82.8. Berg A. Identification of Pharmacoresistant Epilepsy. Neurol Clin 2009;27(4):1003-1013.9. Luciano AL, Shorvon SD. Results of treatment changes in patients with apparently drug-resistant chronic epilepsy. Ann Neurol 2007;62:375–381. 10. Carpay HA, Arts WF, GeertsAT, et al. Epilepsy in childhood: An audit of clinical practice. Arch Neurol 1998;55:668–73.11. Dudley RW, Penney SJ, Buckley DJ. First-drug treatment failures in children newly diagnosed with epilepsy. Pediatr Neurol 2009;40:71–7.12. Berg AT, Vickrey BG, Testa FM, et al. How long does it take epilepsy to become intractable? A prospective investigation. Ann Neurol 2006;60:73–79.13. Spooner CG, Berkovic SF, Mitchell LA, et al. New onset temporal lobe epilepsy in children: lesion on MRI predicts poor seizure outcome. Neurology 2006;67:2147–2153. 14. Robinson RO, Baird G, Robinson Get al. Landau– Kleffner syndrome: course and correlates with outcome. Dev Med Child Neurol2001;43:243-7.15. Berg AT, Shinnar S, Levy SR, et al. Defining early seizure outcomesin pediatric epilepsy: the good, the bad and the in-between. Epilepsy Res 2001;43:75-84.16. Shinnar S, Berg AT. Does antiepileptic drug therapy prevent the development of ‘‘chronic’’ epilepsy? Epilepsia 1996;37:701-8.Neurol Clin 2009;27(4):1003-1013.17. Engel J. The goal of epilepsy therapy: no seizures, no side effects,as soon as possible. CNS Spectrums 2004;9:95–97.18. Mathern GW, Pretorius JK, Babb TL. Influence of the type ofinitial precipitating injury and at what age it occurs on courseand outcome in patients with temporal lobe seizures. J Neurosurg1995;82:220 –227.19. Cross JH, Jaykar P, Nordli D and et al. Propose criteria for referraland evaluation of children for epilepsy surgery: recommendations of the Subcomission for Pediatric Epilepsy Surgery. Epilepsia2006;47:953–959.20. Weiner HL, Carlson C, Ridgway EBet al. Epilepsy surgery inyoung children with tuberous sclerosis: results of a novel approach. Pediatrics 2006;117:1494 –1502.21. Del Felice A, Beghi E, Boero G, La Neve A, Bogliun G, De Palo A, et al. Early versus late remission in a cohort of patients with newly diagnosed epilepsy. Epilepsia 2010;51(1):37-42.22. Levy SR, Novotny EJ, Shinnar S. Predictors of intractable epilepsy in childhood: a case–control study. Epilepsia 1996;37:24–30.23. Berg AT, Shinnar S, Levy SR and et al. Smith- Rappaport S, Beckerman B. Early development of intractable epilepsy in children: a prospective study. Neurology2001;56:1445–52.24. Casetta I, Granieri E, Monetti VC et al. Early predictors of intractability in childhood epilepsy: a community-basedcase–control study in Copparo, Italy. Acta Neurologica Scandinavica 1999;99:329–33.25. Chawla S, Aneja S, Kashyap Ret al. Etiology and clinical predictors ofintractable epilepsy. Pediatric Neurology 2002;27:186–91.26. Ko TS, Holmes GL. EEG and clinical predictors of medically intractable childhood epilepsy. Clin Neurophysiol 1999;110:1245–51. 27. Kwong KL, Sung WY, Wong SN, et al. Early predictors of medical intractability in childhood epilepsy. Pediatr Neurol2003;29:46–52.28. Oskoui M, Webster RI, Zhang X and et al. Factors predictive of outcome inchildhood epilepsy. 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    Expression of Recombinant Human Coagulation Factor VII by the Lizard Leishmania Expression System

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    The variety of recombinant protein expression systems have been developed as a resource of FVII gene expression. In the current study, the authors used a novel protein expression system based on the Iranian Lizard Leishmania, a trypanosomatid protozoan as a host for expression of FVII. Plasmid containing cDNA encoding full-length human FVII was introduced into Lizard Leishmania and positive transfectants were analyzed by SDS-PAGE and Western blot analysis. Furthermore, biological activity of purified protein was detected by PT assay. The recombinant strain harboring a construct was analyzed for expression of FVII at the mRNA and protein level. Purified rFVII was obtained and in order to confirm the purified compound was in fact rFVII. Western blot analysis was carried out. Clotting time in PT assay was reduced about 30 seconds with the purified rFVII. In Conclusion, this study has demonstrated, for the first time, that Leishmania cells can be used as an expression system for producing recombinant FVII

    The Therapeutic Effect of Endoscopic Tumor Resection on Acromegalic Cardiomegaly in Patients With Pituitary Adenoma

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    Background: Acromegaly defines as chronic elevations of insulin-like growth factor-1 (IGF-1) and growth hormone (GH), which results in enlargement of organs and soft tissues. Cardiovascular complications of acromegaly such as cardiomegaly, hypertension contributing to a high risk of cardiovascular events. This study aimed to identify the determinants of the prevalence of cardiomegaly as cardiovascular comorbidity of acromegaly and the potential effect of the curative intervention.Methods: A total of 160 patients with acromegaly due to pituitary adenoma participated in this study. Acromegaly diagnosed was based on clinical manifestations, age-adjusted plasma IGF-I, and elevated plasma GH levels, not suppressible during an oral glucose tolerance test (75 g). Electrocardiogram and chest X-ray obtained in all patients. Treatment approaches included transsphenoidal surgery and hormonal evaluation performed before and six months after surgery.Results: The GH serum level was elevated in all patients before surgery, with a mean of 33.7 ng/mL that reached 5.7 ng/mL after surgery. Mean IGF-1 was 794.1 ng/mL that reached 395.6 ng/mL postoperatively. The prevalence of cardiomegaly was 15% that improved in 5% of patients after trans sphenoidal surgery.Conclusion: Appropriate surgical intervention in acromegaly that complicated by cardiomegaly may result in significant improvement of the cardiac structure

    Evaluation of Anti-CCP Positive in Patients with Systemic Lupus Erythematosus Referred to Loghman Hakim Hospital between 2007-2017; A Descriptive Study

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    Background: It has been found that some patients with Systemic lupus erythematosus (SLE) may have anti-cyclic citrullinated peptide antibodies (anti-CCP), although the clinical significance of such finding is not well established. SLE patients may have joint complaints that are very similar to those observed in rheumatoid arthritis (RA). In early stages of disease, this form of arthritis can be difficult to differentiate from RA, so it is not rare that some SLE patients are initially misdiagnosed to have this disease. This study aims to investigate the prevalence of anti-CCP in SLE patients in Loghman Hakim hospital, Tehran, Iran.Method and Materials: One hundred fourteen SLE patients were studied for anti-CCP. Demographic features and prevalence serum positive Anti-CCP were measured in studied patient.Results: In this study we evaluate 11 men and 103 women. The mean age of patients was 40.26±14.54 y/o. Anti-CCP was positive in 20 of 114 SLE patients. In Anti-CCP positive group also there was 3 men and 17 women with mean age of 45.7±13.Conclusion: We found that 17.5 % of Iranian patients with SLE have positive anti-CCP. Only a careful and prolonged follow-up will reveal the real clinical value of these markers in each patient individually. Key Words: Anti-CCP, Rheumatoid arthritis, Systemic lupus erythematosu

    Frontal assessment battery in a Persian population with Parkinson's disease

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    Background: Several studies have indicated that executive dysfunction is the main neuropsychological feature of Parkinson’s disease (PD). The Frontal Assessment Battery (FAB) is a short tool for the assessment of executive functions. Purpose: The aim of this study was to determine the relationship between Persian version of FAB scores and age, education, Mini-Mental State Examination (MMSE), and severity of the disease in Iranian patients with PD. Methods: The study involved 60 healthy participants and 60 patients with idiopathic PD. Age, sex, disease duration, and Unified Parkinson’s Disease Rating Scale (UPDRS) scores were noted. FAB and MMSE were administered to all participants. Both groups were compared according to FAB scores, MMSE, age, and education. Results: FAB scores were significantly lower in patients with PD than in healthy controls (P<0.05). In patients with PD, FAB scores were correlated with MMSE (P<0.05) but not with UPDRS (P=0.93). Conclusion: FAB scores were significantly lower in Iranian patients with PD in comparison to controls and it can indicate that this battery has good discriminate validity and can be a useful tool to identify executive dysfunction in  Iranian patients with Parkinson’s disease. Also it seems that FAB is not useful test to show disease severity in Iranian patients
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