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1.
Egyptian Journal of Medical Human Genetics [The]. 2017; 18 (1): 29-34
em Inglês | IMEMR | ID: emr-189213

RESUMO

Background: Migraine is a chronic neurological disease characterized by recurrent moderate to severe headaches commonly in association with neuro-inflammation. Interleukin-4 [IL-4], an anti-inflammatory cytokine, plays an important role in modulating pain threshold and has an essential role in stimulation of pain receptors in the trigeminal nerve fibers


Aim of the study: The current study aimed to investigate the possible associations between IL-4 single nucleotide polymorphisms [SNPs] and susceptibility to migraine in Iranian patients


Patients and methods: In a prospective case-control study, we studied blood samples of 190 patients with migraine [migraineurs] and 200 healthy controls [HCs] for analysis of gene variants. Genotyping for the IL-4 SNPs: C-589T [rs2243250], T+2979G [rs2227284], and C-33T [rs2070874] were performed using PCR-RFLP. Statistical analysis was performed using the SPSS version 21.0 [SPSS, Chicago] and SNPStats version 1.14.0


Results and Conclusion: Among IL-4 SNPs, rs2243250 [TC genotype, OR= 0.25, 95% CI= 0.13-0.50, P = 0.001] and rs2227284 [TG and TT genotypes, OR= 0.44, 95% CI= 0.23-0.92, P = 0.029 and OR = 0.38, 95% CI= 0.18-0.79, P = 0.009 respectively] were significantly associated with migraine. No significant associations between IL-4 SNP rs2070874 [TC, TT and CC genotypes] and migraine were found. The most frequent genotypes in the migraineurs were CC in both SNPs rs2243250 [79%], and rs2070874 [71.5%], as well as GG for SNP rs2227284 [64%]. There was no statistically significant relationship between these SNPs and different subclasses [common, classic and complicated] of migraine. Our findings revealed that in IL-4 rs2243250 and rs2227284 genotypes and allele frequencies have a role in susceptibility to migraine in our population. Therefore, it is suggested that in addition to other factors, IL-4 genetic variations also play a pivotal role in the progress of migraine


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Pessoa de Meia-Idade , Idoso , Interleucina-4/genética , Polimorfismo Genético , Estudos Prospectivos , Estudos de Casos e Controles , Polimorfismo de Nucleotídeo Único , Genótipo , Polimorfismo de Fragmento de Restrição , Reação em Cadeia da Polimerase
2.
IJPM-International Journal of Preventive Medicine. 2014; 5 (10): 1231-1238
em Inglês | IMEMR | ID: emr-148954

RESUMO

The aim of this study was to determine the prevalence and viral load of Epstein-Barr virus [EBV] and Human herpesvirus-6 [HHV-6] in different histopathologic grades of oral squamous cell carcinoma [OSCC]. Forty-five formalin-fixed paraffin-embedded tissue section of OSCC patients were analyzed by quantitative real-time polymerase chain reaction for detection of EBV and HHV-6. The mean age of the patients was 58.6 years, 69% of whom were female, and 31% were male. Overall, the positive rate for EBV and HHV-6 were 16.7% and 27.1%, respectively; and the mean viral load EBV was 27.9 x 10[3] and 38.5 x 10[3] for HHV-6. No correlation was demonstrated between the viral load of EBV DNA [P = 0.35] and HHV-6 [P = 0.38] at the different OSCC histopathologic grades. These findings neither lend support to the hypothesis that EBV and HHV-6 are directly involved in OSCC nor rule out the possibility that these viruses play an indirect role in carcinogenesis in this area


Assuntos
Humanos , Masculino , Feminino , Carcinoma de Células Escamosas , Herpesvirus Humano 6 , Infecções por Roseolovirus , Herpesvirus Humano 4 , Infecções por Vírus Epstein-Barr
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