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2.
Immun Inflamm Dis ; 9(4): 1648-1655, 2021 12.
Article in English | MEDLINE | ID: mdl-34438471

ABSTRACT

INTRODUCTION: This study aims to investigate in-hоsрitаl mоrtаlity in severe асute resрirаtоry syndrоme соrоnаvirus 2 Ñ€Ð°tients strаtified by serum ferritin levels. METHODS: Patients were stratified based on ferritin levels (ferritin levels ≤ 1000 or >1000). RESULTS: Approximately 89% (118) of the patients with ferritin levels > 1000 had pneumonia, and 51% (67) had hypertension. Fever (97, 73.5%) and shortness of breath (80, 61%) were two major symptoms among the patients in this group. Logistic regression analysis indicated that ferritin level (odds ratio [OR] = 0.36, 95% confidence interval [CI] = 0.21-0.62; p < .001), male sex (OR = 2.63, 95% CI = 1.43-5.06; p = .003), hypertension (OR = 4.16, 95% CI = 2.42-7.36; p < .001) and pneumonia (OR = 8.48, 95% CI = 3.02-35.45; p < .001) had significance in predicting in-hospital mortality. Additionally, the Cox proportional hazards analysis and Kaplan-Meier survival probability plot showed a higher mortality rate among patients with ferritin levels > 1000. CONCLUSION: In this study, higher levels of serum ferritin were found to be an independent predictor of in-hоsрitаl mоrtаlity.


Subject(s)
COVID-19 , Pneumonia , Ferritins , Humans , Male , SARS-CoV-2
3.
Materials (Basel) ; 12(23)2019 Nov 27.
Article in English | MEDLINE | ID: mdl-31783544

ABSTRACT

In this research work, graphene nanoplatelets (GNP) were selected as alternative reinforcing nanofillers to enhance the properties of polypropylene (PP) using different compatibilizers called polypropylene grafted maleic anhydride (PP-g-MA) and ethylene-octene elastomer grafted maleic anhydride (POE-g-MA). A twin screw extruder was used to compound PP, GNP, and either the PP-g-MA or POE-g-MA compatibilizer. The effect of GNP loading on mechanical and thermal properties of neat PP was investigated. Furthermore, the influence and performance of different compatibilizers on the final properties, such as mechanical and thermal, were discussed and reported. Tensile, flexural, impact, melting temperature, crystallization temperature, and thermal stability were evaluated by using a universal testing system, differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). For mechanical properties, it was found that increasing GNP content from 1 wt.% to 5 wt.% increased tensile strength of the neat PP up to 4 MPa. The influence of compatibilizers on the mechanical properties had been discussed and reported. For instance, the addition of PP-g-MA compatibilizer improved tensile strength of neat PP with GNP loading. However, the addition of compatibilizer POE-g-MA slightly decreased the tensile strength of neat PP. A similar trend of behavior was observed for flexural strength. For thermal properties, it was found that both GNP loading and compatibilizers have no significant influence on both crystallization and melting temperature of neat PP. For thermal stability, however, it was found that increasing the GNP loading had a significant influence on improving the thermal behavior of neat PP. Furthermore, the addition of compatibilizers into the PP/GNP nanocomposite had slightly improved the thermal stability of neat PP.

4.
Am J Med Genet A ; 167A(4): 805-9, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25692795

ABSTRACT

Microcephaly-capillary malformation syndrome (MIC-CAP syndrome) is a newly recognized autosomal recessive congenital neurocutaneous central nervous system disorder characterized by severe microcephaly, early-onset seizures, profound psychomotor disability, and multiple cutaneous capillary lesions. In addition, affected patients have variable dysmorphic facial features and hypoplastic distal phalanges. It is distinctively caused by mutations in a newly characterized gene, STAMBP, encoding the deubiquitinating (DUB) isopeptidase that has a key role in cell surface receptor-mediated endocytosis and sorting. Herein, we describe an Arab family of two siblings with classic features of MIC-CAP syndrome that harbor a novel predicted splice mutation in STAMBP, which additionally display previously unreported findings of congenital hypothyroidism and alopecia areata.


Subject(s)
Abnormalities, Multiple/diagnosis , Capillaries/abnormalities , Endosomal Sorting Complexes Required for Transport/genetics , Microcephaly/diagnosis , Ubiquitin Thiolesterase/genetics , Vascular Malformations/diagnosis , Abnormalities, Multiple/genetics , Arabs , Child , Child, Preschool , Consanguinity , DNA Mutational Analysis , Genetic Association Studies , Humans , Male , Microcephaly/genetics , Point Mutation , Syndrome
5.
Int J Clin Pharm ; 36(5): 1023-30, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25108411

ABSTRACT

BACKGROUND: Advances in medical technology and research documenting clinical effectiveness have led to the increased use of insulin pumps worldwide. However, their use by children in the UK is relatively limited and there is little evidence regarding their impact on patients' lives. OBJECTIVE: This study aimed to examine the impact of switching from multiple daily injections to insulin pumps on the glycaemic control and daily lives of children/young people and their families. SETTING: University College London Hospital, London. METHOD: Face-to-face semi-structured interviews were conducted with children/young people with type 1 diabetes mellitus (5-17 years; N = 34) and their parents (N = 38), receiving insulin pump therapy and attending paediatric diabetes outpatients clinics at a major university teaching hospital in London. Glycated haemoglobin A1c values from 6 months prior to, and after pump therapy were obtained. Qualitative and quantitative approaches were undertaken for data analysis. MAIN OUTCOME MEASURE: Glycated haemoglobin A1c and the impact of the use of insulin pumps on the children and their families. RESULTS: The majority of parents (N = 32) and the children/young people (N = 30) reported that glycaemic control was easier to maintain within the target range with pumps compared to injections. This was supported by glycated haemoglobin A1c measures. Participants generally found the devices easy to use and more acceptable than injections. However, parents and children/young people reported many challenges in the early stages of pump therapy (e.g. 7 children/young had worse control at 6 months after starting CSII). Parents and children/young people reported an overall increase in lifestyle flexibility and an improved ability to participate in home, school and social activities whilst maintaining glycaemic control. CONCLUSION: Administration of insulin via pumps rather than injections was generally preferred. Participants reported most difficulty at the commencement of use. Pump therapy conferred benefits in terms of glycaemic control, general well-being, enabling young people to be more in control of their condition and live more normal lives, as reported by most participants. These are important goals of health policy for children/young people with long-term conditions in the UK.


Subject(s)
Diabetes Mellitus, Type 1/drug therapy , Diabetes Mellitus, Type 1/psychology , Insulin Infusion Systems/psychology , Parents/psychology , Quality of Life , Adolescent , Adult , Child , Child, Preschool , Diabetes Mellitus, Type 1/metabolism , Female , Glycated Hemoglobin/metabolism , Humans , Male , Middle Aged , Patient Satisfaction
6.
Am J Hum Genet ; 93(3): 471-81, 2013 Sep 05.
Article in English | MEDLINE | ID: mdl-23993193

ABSTRACT

Nuclear genetic disorders causing mitochondrial DNA (mtDNA) depletion are clinically and genetically heterogeneous, and the molecular etiology remains undiagnosed in the majority of cases. Through whole-exome sequencing, we identified recessive nonsense and splicing mutations in FBXL4 segregating in three unrelated consanguineous kindreds in which affected children present with a fatal encephalopathy, lactic acidosis, and severe mtDNA depletion in muscle. We show that FBXL4 is an F-box protein that colocalizes with mitochondria and that loss-of-function and splice mutations in this protein result in a severe respiratory chain deficiency, loss of mitochondrial membrane potential, and a disturbance of the dynamic mitochondrial network and nucleoid distribution in fibroblasts from affected individuals. Expression of the wild-type FBXL4 transcript in cell lines from two subjects fully rescued the levels of mtDNA copy number, leading to a correction of the mitochondrial biochemical deficit. Together our data demonstrate that mutations in FBXL4 are disease causing and establish FBXL4 as a mitochondrial protein with a possible role in maintaining mtDNA integrity and stability.


Subject(s)
DNA, Mitochondrial/genetics , F-Box Proteins/genetics , Genetic Predisposition to Disease , Mitochondrial Encephalomyopathies/genetics , Mutation/genetics , Ubiquitin-Protein Ligases/genetics , Acidosis, Lactic/complications , Acidosis, Lactic/genetics , Acidosis, Lactic/pathology , Base Sequence , Child , Child, Preschool , Chromosome Segregation/genetics , Electron Transport/genetics , F-Box Proteins/chemistry , Female , Fibroblasts/metabolism , Fibroblasts/pathology , Gene Dosage/genetics , Genes, Recessive/genetics , Humans , Infant , Infant, Newborn , Male , Mitochondrial Encephalomyopathies/complications , Mitochondrial Encephalomyopathies/pathology , Molecular Sequence Data , Muscle, Skeletal/pathology , Oxidative Phosphorylation , Pedigree , Protein Transport , Ubiquitin-Protein Ligases/chemistry
7.
J Med Microbiol ; 61(Pt 4): 514-519, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22174374

ABSTRACT

Peritoneal tuberculosis (TB) is a considerable problem in certain developing nations. Current diagnostic tests for peritoneal TB are difficult and time-consuming. This study aimed to determine the effectiveness of an adenosine deaminase (ADA) assay and the QuantiFERON-Gold (QFT-G) assay in the rapid diagnosis of TB peritonitis. Forty-one patients with a presumptive diagnosis of TB peritonitis with ascites were admitted to Mansoura University Hospital and included in the study. Ascitic fluid and blood samples were collected from each patient. Fluid samples were examined biochemically (protein concentration), cytologically (white blood cell count) and microbiologically (Ziehl-Neelsen stain and TB culture in Löwenstein-Jensen media), and ADA levels were determined using colorimetry. Interferon-γ levels in whole-blood samples were measured using the QFT-G assay. Fourteen (34 %) patients received a final clinical diagnosis of TB peritonitis; these patients were subclassified as definite (positive culture for Mycobacterium tuberculosis; eight patients), highly probable (four patients) and probable (two patients) for TB peritonitis. Of the 14 patients with a final clinical diagnosis of TB peritonitis, 3 (21 %) tested positive using an acid-fast bacilli smear, which showed a sensitivity of 21 % and a specificity of 100 %. A receiver operating characteristic curve showed that a cut-off value of 35 IU l(-1) for the ADA level produced the best results as a diagnostic test for TB peritonitis, yielding the following parameter values: sensitivity 100 %, specificity 92.6 %, positive predictive value (PPV) 87.5 % and negative predictive value (NPV) 100 %. The QFT-G assay yielded the following values: sensitivity 92.9 %, specificity 100 %, PPV 100 % and NPV 96.4 %. The ADA and QFT-G assays might be used to rapidly diagnose TB peritonitis and initiate prompt treatment while waiting for a final diagnosis using the standard culture approach.


Subject(s)
Adenosine Deaminase/metabolism , Mycobacterium tuberculosis/isolation & purification , Peritonitis, Tuberculous/diagnosis , Peritonitis, Tuberculous/enzymology , Adenosine Deaminase/genetics , Adult , Ascitic Fluid/enzymology , Ascitic Fluid/microbiology , Bacteriological Techniques , Egypt/epidemiology , Female , Humans , Male , Middle Aged , Mycobacterium tuberculosis/enzymology , Peritonitis, Tuberculous/epidemiology , Predictive Value of Tests , ROC Curve , Sensitivity and Specificity
8.
Opt Lett ; 31(7): 993-5, 2006 Apr 01.
Article in English | MEDLINE | ID: mdl-16599235

ABSTRACT

We show that photovoltaic fields are capable of efficiently reorienting liquid crystals, leading to new concepts of optically addressable light modulators. Using an arrangement consisting of a liquid-crystal layer between LiNbO3:Fe photovoltaic substrates, we observed spatial filtering due to self-phase modulation in a planar-oriented cell and nonlinear transmission between crossed polarizers in a twist-oriented cell. These processes do not require an external electric field. The substrates are arranged such that light propagates along the +c axis in each substrate, allowing a secondary process of power transfer to occur through contradirectional photorefractive two-beam coupling.

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