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  1. Article ; Online: Novel biomarkers for subtle myocardial involvement in type I diabetes mellitus.

    El-Saiedi, Sonia A / Hafez, Mona H / Sedky, Yasser M / Sharaf, Sahar A / Kamel, Mona S / AbdelMassih, Antoine F

    Cardiovascular endocrinology & metabolism

    2020  Volume 10, Issue 3, Page(s) 175–181

    Abstract: Background: Evaluation of certain biomarkers could be used to predict left ventricular (LV) and right ventricular (RV) function impairment in children with type 1 diabetes mellitus. The aim of this study was to determine the best cardiac biomarker for ... ...

    Abstract Background: Evaluation of certain biomarkers could be used to predict left ventricular (LV) and right ventricular (RV) function impairment in children with type 1 diabetes mellitus. The aim of this study was to determine the best cardiac biomarker for prediction of diabetic cardiomyopathy.
    Methodology: This study was designed as case-control study. A total of 55 children with type 1 diabetes mellitus (group/G1) and 55 healthy controls (G2) were subjected to echocardiography including 3D-Speckle Tracking Echocardiography and tissue Doppler imaging for assessment of RV and LV systolic and diastolic functions. As well as HbA1c, troponin I, brain natriuretic peptide (BNP), plasma cardiotrophin (CT-1), activin-A, transforming growth factor-β, and human insulin-like growth factor binding protein-7 (IGFBP-7) measurements.
    Results: Diabetic patients showed RV and LV systo-diastolic dysfunction compared to controls, the best predictor of LV systolic dysfunction was CT-1 (sensitivity: 69%, while IGFBP-7 was found to be the best predictor of RV systolic dysfunction (sensitivity: 63%). BNP was found to the best predictor of diastolic RV and LV dysfunction (sensitivity: 82% for both).
    Conclusion: CT-1 has proven to be a diagnostic superiority in LV systolic dysfunction whilst BNP continues to prove every day through our study and through many others that it is the chief marker of diastolic dysfunction and HFpEF. This potential accuracy and the increasing availability of BNP in the outpatient setting make it clear that it should be used as a screening test for diabetic patients.
    Language English
    Publishing date 2020-11-19
    Publishing country United States
    Document type Journal Article
    ISSN 2574-0954
    ISSN (online) 2574-0954
    DOI 10.1097/XCE.0000000000000240
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: ASD device closure in pediatrics: 3-Dimensional transthoracic echocardiography perspective.

    El-Saiedi, Sonia A / Agha, Hala M / Shaltoot, Mohamed F / Nassar, Hayat H / El Sisi, Amal M / Attia, Wael A / Sedky, Yasser M

    Journal of the Saudi Heart Association

    2017  Volume 30, Issue 3, Page(s) 188–197

    Abstract: Objective: Real-time three-dimensional echocardiography, using both reconstruction methods and RT3D, has been used as an extra helping tool in several forms of congenital heart diseases. Our aim was to understand the relation of the ASD device to all ... ...

    Abstract Objective: Real-time three-dimensional echocardiography, using both reconstruction methods and RT3D, has been used as an extra helping tool in several forms of congenital heart diseases. Our aim was to understand the relation of the ASD device to all surrounding structures by 3-dimensional echocardiography (3D).
    Methods: This prospective study included 37 patients diagnosed as ASD secundum by transthoracic (TTE) and transesophageal echocardiography (TEE) referred for transcatheter closure from October 2013 to July 2016. Follow-up for 1 year using 2D and 3D-echocardiography was performed to assess the relations of the device to the surrounding structures.
    Results: Transcatheter ASD closure and echocardiographic examinations were successfully performed for all patients. By 3D echocardiography, 16 patients (43.24%) had their ASD device close to the aortico-mitral continuity plane without apparent regurgitation, while the rest of our patients (56.75%) the devices were away from this plane. The following variables were significantly different between the two groups; body surface area, atrioventricular rim (AV), device size, left disc size and ratio of left disc to interatrial septum. A cut-off AV rim length not less than 8 mm was found optimal to avoid device encroachment on the sensitive surrounding structures. New Formula was constructed to aid in device choice.
    Conclusion: Use of 3D before and after ASD closure is of value to determine the device relation to the surrounding structures. AV rim by TEE is an important rim to avoid eventual encroachment on the mitral valve and aorta.
    Language English
    Publishing date 2017-11-26
    Publishing country Saudi Arabia
    Document type Journal Article
    ZDB-ID 2515647-0
    ISSN 1016-7315
    ISSN 1016-7315
    DOI 10.1016/j.jsha.2017.11.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Ficolin-1 gene (FCN1) -144 C/A polymorphism is associated with adverse outcome of severe pneumonia in the under-five Egyptian children: A multicenter study.

    Elkoumi, Mohamed A / Abdellatif, Sawsan H / Mohamed, Faisal Y / Sherif, Ahmed H / Elashkar, Shaimaa S A / Saleh, Rabab M / Boraey, Naglaa F / Abdelaal, NourEldin M / Akeel, Nagwa E / Elhewala, Ahmed A / Mosbah, Amira A / Zakaria, Mervat T / Soliman, Mohammed M / Salah, Ahmed / Sedky, Yasser M / Sobieh, Alaa A / Mashali, Mohamed H / Waked, Nevin M / Elshreif, Anas M /
    Hafez, Sahbaa F / Hashem, Mustafa I A / Shehab, Mohamed M / Soliman, Attia A / Emam, Ahmed A / Ahmed, Abdelrahman A A / Fahim, Mohamed S / Elshehawy, Naglaa A / Abdel-Aziz, Marwa M / Abdou, Adel M / El-Shehawy, Ahmed A / Youssef, Manal A A / Fahmy, Dalia S / Malek, Mai M / Osman, Sherif F / Ibrahim, Mohamed A M / Alanwar, Mohamed I / Zeidan, Nancy M S

    Pediatric pulmonology

    2020  Volume 55, Issue 5, Page(s) 1175–1183

    Abstract: Background: Pneumonia is the foremost cause of child death worldwide. M-ficolin is encoded by the FCN1 gene and represents a novel link between innate and adaptive immunity.: Objectives: To investigate the FCN1 -144 C/A (rs10117466) polymorphism as a ...

    Abstract Background: Pneumonia is the foremost cause of child death worldwide. M-ficolin is encoded by the FCN1 gene and represents a novel link between innate and adaptive immunity.
    Objectives: To investigate the FCN1 -144 C/A (rs10117466) polymorphism as a potential marker for pneumonia severity and adverse outcome namely complications or mortality in the under-five Egyptian children.
    Methods: This was a prospective multicenter study that included 620 children hospitalized with World Health Organization-defined severe pneumonia and 620 matched healthy control children. Polymorphism rs10117466 of the FCN1 gene promoter was analyzed by PCR-SSP, while serum M-ficolin levels were assessed by ELISA.
    Results: The FCN1 A/A genotype and A allele at the -144 position were more frequently observed in patients compared to the control children (43.4% vs 27.6%; odds ratio [OR]: 1.62; [95% confidence interval {CI}: 1.18-2.2]; for the A/A genotype) and (60.8% vs 52.5%; OR: 1.4; [95% CI: 1.19-1.65]; for the A allele); P < .01. The FCN1 -144 A/A homozygous patients had significantly higher serum M-ficolin concentrations (mean: 1844 ± 396 ng/mL) compared with those carrying the C/C or C/A genotype (mean: 857 ± 278 and 1073 ± 323 ng/mL, respectively; P = .002). FCN1 -144 A/A genotype was an independent risk factor for adverse outcomes in children with severe pneumonia (adjusted OR = 4.85, [95% CI: 2.96-10.25]; P = .01).
    Conclusion: The FCN1 A/A genotype at the -144 position was associated with high M-ficolin serum levels and possibly contributes to enhanced inflammatory response resulting in the adverse outcome of pneumonia in the under-five Egyptian children.
    MeSH term(s) Child, Preschool ; Egypt/epidemiology ; Female ; Genetic Predisposition to Disease ; Genotype ; Humans ; Infant ; Lectins/blood ; Lectins/genetics ; Male ; Odds Ratio ; Pneumonia/blood ; Pneumonia/epidemiology ; Pneumonia/genetics ; Polymorphism, Single Nucleotide ; Promoter Regions, Genetic ; Prospective Studies ; Risk Factors ; Ficolins
    Chemical Substances Lectins
    Language English
    Publishing date 2020-03-06
    Publishing country United States
    Document type Journal Article ; Multicenter Study
    ZDB-ID 632784-9
    ISSN 1099-0496 ; 8755-6863
    ISSN (online) 1099-0496
    ISSN 8755-6863
    DOI 10.1002/ppul.24719
    Database MEDical Literature Analysis and Retrieval System OnLINE

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