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Showing 2 results for Zeinalzadeh
N Kalantari, S Ghaffari, M Bayani, R Agapour, M Zeinalzadeh, F Gavipanjeh, Z Abedian, Volume 22, Issue 4 (9-2014)
Abstract
Introduction: Toxoplasmosis is one of the most common infectious diseases in the world and it caused by an intracellular protozoan called Toxoplasma gondii. This parasitic infection is usually asymptomatic in adults, but it become complicated if fetus infection occurred. This study aimed to determine the prevalence and incidence of toxoplasmosis in pregnant women in Babol, northern Iran.
Materials and Methods: In this cross-sectional study during the years 2012-2013, 175 pregnant women in the first trimester of their pregnancy participated. Two ml blood was obtained from each participant and serum was separated. Then, anti-Toxoplasma antibodies were measured using ELISA method. Participants' demographic information and the risk factors were collected by questionnaire. Anti-Toxoplasma antibodies were measured in the second and third trimesters of pregnancy for who attended to the study.
Results: The mean of age was 27.4 ± 9.5 years. 106 cases (60.6 %) had anti- Toxoplasma gondii antibodies (IgG) and 64 women (36.6 % ) had no specific antibody. The prevalence of infection was different in relation with age and location, but the difference is not statistically significant (p >0.05). Also, a statistically significant difference between prevalence of infection and other risk factors, such as abortion was not demonstrated. No case of acute Toxoplasma infection in the mother or congenital toxoplasmosis was reported.
Conclusion: This study showed that over fifty percent of Toxoplasma infection occurs in twenty-five years of age. Furthermore, it showed that 36.6% of the studied population (pregnant women) was seronegative. Therefore, Toxoplasma infection should be screened in pregnant women in the first trimester of pregnancy in order to perform preventative measure of congenital toxoplasmosis.
Fatemeh Mahmoudi, Leila Mehdizadeh Fanid, Narges Zeinalzadeh, Mohammad Ali Hosseinpour Feizy, Volume 29, Issue 4 (10-2021)
Abstract
Introduction: Heroin dependence is a chronic relapsing disorder caused by a combination of genetic, epigenetic, and environmental factors. The genetic contribution in the vulnerability to heroin dependence is 40%-60%. Alterations in dopamine transport in the CNS are implicated in drug and alcohol dependence, and according to linkage studies, the HTR2A rs6313 single nucleotide polymorphism plays an important role in drug dependence and abuse. This case-control study aimed to investigate the association between HTR2A rs6313 and heroin dependence among a population from Northwest Iran.
Material & Methods: The study included a sample of 100 heroin-dependent patients and 102 control subjects. After DNA extraction from blood samples, the genotype of HTR2A rs6313 polymorphism was investigated among patients and controls using the PCR-RFLP method. The obtained data were analyzed in SPSS software to explore a significant association.
(Ethic code: 5/4/12152)
Findings: Frequencies of CC, CT, and TT genotypes were 23%, 50%, and 27% in the patient group and 32.35%, 44.12%, and 23.53% in the control group. According to statistical analysis, there were no significant differences between case and control groups in this regard (P>0.05).
Discussion & Conclusion: The results of the study could not support a significant association between HTR2A rs6313 polymorphism and heroin dependence in the Azeri population of Northwest Iran. This indicates the need to investigate other candidate genetic polymorphisms in the study population.
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