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1.
Ann. afr. méd. (En ligne) ; 16(1): 4931-4938, 2022. tales, figures
Artigo em Francês | AIM | ID: biblio-1410559

RESUMO

Contexte et objectif. La maladie athéromateuse dont la coronaropathie étant une pathologie diffuse peut être prévenue par le contrôle des facteurs de risqué cardiovasculaire. Le but de cette étude était de décrire les caractéristiques pharmaco doppler pénien des patients coronariens souffrant de dysfonction érectile. Méthodes. Il s'agissait d'une série analytique des cas suivie entre juin 2020 et février 2021. Elle concernait des patients ayant des lésions athéromateuses significatives à la coronographie et souffrant de dysfonction érectile. Nous avons évalué les caractéristiques pharmaco doppler pénien. La qualité d'érection était appréciée par le score de rigidité Erectile Hardness Score (EHS). Résultats. Trente-six patients étaient inclus. L'âge moyen était de 56 ± 8,4 ans. le pic de Vitesse systolique au repos (PSVr) moyen des patients était de 13,7 cm/s ± 5,9. Le pic de vitesse systolique post injection (PSV pi) moyen des patients était de 23,9 cm/s ± 5,4. Les causes étaient principalement artérielles de 75%. La qualité d'érection était appréciée selon le score EHS : E1 (83%), E2 (22%), E3 (5%) et E4 (3%). Conclusion. La dysfunction érectile est associée aux facteurs de risque cardiovasculaire selon plusieurs études. L'echodoppler pénien avait occupé une place importante dans le diagnostic étiologique. Les causes retrouvées étaient principalement artérielles avec une baisse de PSVpi<25 cm/s.


Assuntos
Humanos , Doença da Artéria Coronariana , Fatores de Risco de Doenças Cardíacas , Pressão Sanguínea , Vasos Coronários , Disfunção Erétil
2.
Artigo | IMSEAR | ID: sea-209721

RESUMO

Background:Women commonly harbour filarial infections during their childbearing years, raising the possibility that the developing foetus may be exposed to filarial antigens in the uterus and thereby have altered immunity and susceptibility to infection during early childhood. However, there are no concrete proofs to justify the risk of infections in infants born from mothers having filarial infections during pregnancy. Aim:The purpose of this study was to assess the prevalence of microfilariae in umbilical cord blood and respective mothers and to evaluate the relationship between the cord blood filarial infection and the oxidative stress status and concentration of IL-2, IL-10, IL-13, INF-γ and IgG in umbilical cord blood.Methods:This was a nested case–control study of cords and mothers of normal gestational age (>250 days of gestation). A total of 316 pairs of umbilical cords and mothers were examined. The presence of microfilariae was assessed by microscopy in mothers and cords. Oxidative stress status (total oxidative stress and total oxidative defence) and nitric oxide of umbilical cord and mother’s blood were investigated by the colorimetric method. ELISA was carried out for IL-2, IL-10, IL-13, INF-γ in umbilical cord and mother’s blood. Equally, umbilical cords were subjected to ELISA for total IgG.Results:Results obtained showed that microfilariae had a prevalence of 32.9% and 29.7% in umbilical cord blood and womenat time of delivery respectively. High levels of total oxidative stress (TOS) with low total oxidative defence (TAD) was found in filarial infected (Mf +ve) umbilical cord and mother’s blood compared to controls or uninfected (Mf -ve) cords and mothers blood. IL-2 was lower in the blood of microfilariae infected cords and mothers, while INF-γ, IL-13 and IL-10 were higher as compared to microfilariae negative cords and mothers. Equally, plasma total IgG concentration was higher in microfilariae positive cords compared to the negative cords and positively correlated with IL-10.Conclusions: There is high frequency of transplacental transmission of microfilariae. Cord blood filarial infections were associated with a high TOS, a protective immune response with low IL-2 and high INF-γ, and a typical Th2 immune response that was associated with higher concentration of immune total IgG regulatory cytokine IL-10 and IL-13 in neonate

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