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1.
Cell Mol Biol (Noisy-le-grand) ; 62(7): 102-9, 2016 Jun 30.
Artigo em Inglês | MEDLINE | ID: mdl-27453281

RESUMO

Inflammatory bowel disease(IBD) is progressing rapidly in developing countries such as Iran. This research is intended to compile the frequency distribution of the drug metabolizing enzyme, thiopurine methyl transferase(TPMT) and the drug transporter, Multi drug resistance(MDR1) which are involved in metabolism of many therapeutics such as thiopurines in inflammatory bowel disease(IBD). Ethnicity is an important variable influencing drug response. The aims of this research were to investigate the association of TPMT phenotypes with MDR1 genotypes. TPMT activity was measured by using a non-extraction HPLC method and genotype for the C3435T polymorphism of MDR1 gene was determined in 215 unrelated IBD patients including of 85 males and 130 females and 212 unrelated healthy individuals consisted of 96 males and 116 females as control group by PCR-RFLP in Iran's western population. TPMT phenotypes demonstrated no frequency for deficient, 2.2% for low and 97.8% for normal activity that is different with results of other studies. Interestingly there were a significant negative correlation between TPMT activities as calculated based on nmol/grHb/h and positive correlation calculated in mU/L with Hb levels in IBD patients and control subjects. Dominant and codominant MDR1 C3435T gene polymorphism increased the risk of IBD by 1.45 and 1.46 times, respectively. IBD patients with MDR1 mutant genotypes C3435T, had lower TPMT activites and Hb concentrations. Using of mU/L is more appropriate than nmol6MTG/grHb/h for expressing TPMT activity. TPMT frequency of deficient and low activity in western Iran is low. The carriers of mutant C3435T MDR1 are not good TPMT methylators.


Assuntos
Doenças Inflamatórias Intestinais/enzimologia , Doenças Inflamatórias Intestinais/genética , Metiltransferases/metabolismo , Polimorfismo Genético , Subfamília B de Transportador de Cassetes de Ligação de ATP/genética , Adulto , Índice de Massa Corporal , Estudos de Casos e Controles , Cromatografia Líquida de Alta Pressão , Demografia , Feminino , Humanos , Masculino , Razão de Chances , Farmacogenética , Fenótipo , Fatores de Risco , Tioguanina/análogos & derivados , Tioguanina/metabolismo
2.
Iran J Parasitol ; 7(4): 49-56, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23323091

RESUMO

BACKGROUND: Visceral leishmaniasis (VL) or kala-azar is a parasitic disease caused by the species of Leishmania donovani complex. It is endemic in some parts of provinces of Iran. According to the reported cases of VL in Kermanshah Province in recent years, this study was conducted to determine the seroprevalence of VL in high risk villages of the province. METHODS: Totally, 1622 serum samples obtained from children under 15 years old and 178 from adults in 22 villages of studied areas. Serum samples were examined by direct agglutination test (DAT) for the detection of anti-Leishmania antibodies. Data were analyzed using SPSS software ver.11.5. RESULTS: Only 6 serum samples (0.33%) showed anti-Leishmania antibodies against L.infantum at titers ≥ 1/3200. Four of the seropositive cases had a history of kala-azar and Leishman bodies were seen in their bone marrows. The highest (0.5%) and lowest (0.29%) seroprevalence was seen in the age groups of 5-9 and 10-14 years old, respectively. None of the adults were seropositive. There were not any significant differences between the rate of seropositivity in males (0.36%) and females (0.31%). 66.7% of seropositive individuals showed clinical manifestations. The most important symptoms in Kala-azar patients were fever, hepato-spleenomegally and anemia. CONCLUSION: Kala-azar is occurred sporadically in Kermanshah Province. But presence of significant number of positive sera confirms the necessity for attention of people and clinicians to kala-azar.

4.
J Prosthet Dent ; 54(2): 263-71, 1985 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-3863934

RESUMO

This study was designed to evaluate the effectiveness of four radiographic techniques in demonstrating the TMJ. Mandibular condyles of a variety of sizes, as well as horizontal and vertical angulation, were selected. The location and size of the defects also varied. The mandibular condyles, in which 12 defects were created, were divided into two groups of six large and six small each. On examination of the condyles with the different defects, using each of the four radiographic techniques, the defects were localized with silver amalgam and reexamined with the radiographic techniques. The visualization of the defects was compared using the radiographs.


Assuntos
Côndilo Mandibular/diagnóstico por imagem , Transtornos da Articulação Temporomandibular/diagnóstico por imagem , Humanos , Côndilo Mandibular/anatomia & histologia , Transtornos da Articulação Temporomandibular/patologia , Tomografia por Raios X/métodos
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