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1.
Eur Rev Med Pharmacol Sci ; 27(16): 7823-7830, 2023 08.
Artigo em Inglês | MEDLINE | ID: mdl-37667959

RESUMO

OBJECTIVE: COVID-19 is a febrile infectious disease caused by severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2). This virus affects several organs, including the skin. Acute telogen effluvium (TE) is a non-scarring hair loss characterized by diffuse hair shedding that begins three months after a stressful event and can last up to six months. COVID-19 infection is one of these potential stressors. Recently, there has been a reported link between increased scalp hair shedding and post-infection patients during the COVID-19 outbreak. The present work aimed to study the possible effects of COVID-19 on hair and the relationship between COVID-19 and TE and to assess the level of awareness about TE in the Asir region of Saudi Arabia. SUBJECTS AND METHODS: A questionnaire-based cross-sectional study was conducted using a pre-validated questionnaire. The study involved 561 participants from the Asir region of Saudi Arabia. Eligible participants were individuals from the Asir region who were 20 years of age or older, had previously contracted COVID-19 and had no history of TE before infection. All statistical methods used were two-tailed with an alpha level of 0.05, considering significance if the p-value was lower than or equal to 0.05. RESULTS: A total of 1,000 eligible participants completed the study questionnaire. The mean age was 32.5 ± 13.9 years, and 494 (88.1%) participants were females. In addition, 558 (99.5%) of the study participants had received the COVID-19 vaccine. A total of 411 (73.3%) participants experienced an increase in hair loss after COVID-19 infection, and 171 (30.5%) began suffering from pain when combing their hair. In addition, 182 participants (32.4%) had a family history of TE. Only 109 (10.9%) participants had a good awareness level about TE, while 452 (80.6%) had an overall poor awareness level. There was a significant relationship between the level of awareness and age, where 23.9% of the participants aged 20-29 years had a good level of awareness vs. 16.1% of others aged 40 years or older (p = 0.041). Moreover, 26.9% of participants with a family history of TE had a good awareness of TE, vs. 15.8% of those with no family history of TE (p = 0.002). In addition, significant correlations were found between increased hair loss post-COVID-19 infection and female gender (77.3% vs. 43.3%; p = 0.001) as well as suffering from pain when combing hair (86.5% vs. 65.5%; p = 0.001). CONCLUSIONS: In our study, the incidence of TE was highly related to COVID-19 infections among both sexes. However, the incidence was greater among the female population. The awareness level toward post-COVID-19 TE was poor among most of the participants in our study.


Assuntos
Alopecia em Áreas , COVID-19 , Masculino , Humanos , Feminino , Adolescente , Adulto Jovem , Adulto , Pessoa de Meia-Idade , COVID-19/epidemiologia , Estudos Transversais , Vacinas contra COVID-19 , SARS-CoV-2 , Dor
2.
Arch Razi Inst ; 77(6): 2145-2149, 2022 12.
Artigo em Inglês | MEDLINE | ID: mdl-37274919

RESUMO

Using microorganisms to make this nanomaterial is a new research technique. In a culture medium, Trichophyton rubrum was permitted to biosynthesis silver nanoparticles. This study used Trichophyton rubrum, a dermatophytes fungus, to make silver nanoparticles. These species' clinical strains were produced in a medium containing mineral salt and cultured for 5-7 days at 25°C. Each culture's cell-free filtrate was taken and used to make AgNps in the presence of 1 mM AgNO3. The reduction of Ag+ ions in metal nanoparticles was virtually studied by observing the colour of the solution, which changed to a reddish-light brown after 72 hours. SEM was used to establish the presence of AgNo3. The presence of AgNPs was confirmed by SEM, which revealed that they are primarily spherical and 100nm in size. Furthermore, the findings showed that silver nanoparticles have antifungal activity against both infections in a concentration-dependent manner. At (150 ppm) of AgNPs, the growth decreased.


Assuntos
Arthrodermataceae , Nanopartículas Metálicas , Animais , Antifúngicos/farmacologia , Prata/farmacologia
3.
Eur J Clin Microbiol Infect Dis ; 34(10): 1923-8, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26231169

RESUMO

Sequela of infectious diseases include not only morbidity and mortality, but are also associated with chronic illnesses that has long constituted public health problems and huge economic burdens. This review gives a brief idea about important infectious diseases (ID) in Egypt, the main lines taken to combat them, the challenges still existing, and the possible barriers keeping IDs still forming threats to the community. Egypt has the highest prevalence rates of HCV infection worldwide. Significant evidence points towards that the HCV epidemic was initiated and propagated by the anti-schistosomal mass campaigns during the last century. Though the rates of HCV infection are declining, still the decline has not yet met the full expectations. Therefore, infection control programs are gaining more ground all over the country, especially with the growing problem of antimicrobial resistance complicating healthcare-associated infections (HAI) worldwide. Also, mass immnunization of childhood, mycobacterial tuberculosis infections, and avian influenza will be discussed.


Assuntos
Controle de Doenças Transmissíveis/história , Doenças Transmissíveis/epidemiologia , Doenças Transmissíveis/história , Egito/epidemiologia , História do Século XX , História do Século XXI , Humanos , Prevalência
4.
J Perinatol ; 34(6): 453-7, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24674983

RESUMO

OBJECTIVE: Retinopathy of prematurity (ROP) constitutes a significant morbidity in premature infants that can lead to blindness. Multiple retrospective studies have identified neonatal hyperglycemia as a risk for developing ROP. However, in the absence of any reported prospective study, it is not clear whether hyperglycemia is associated with ROP independent of the commonly associated comorbidities. The objective of this study was to investigate whether hyperglycemia in premature infants is independently associated with ROP. STUDY DESIGN: Premature infants (<1500 g or⩽32 weeks gestational age) were enrolled in a prospective longitudinal cohort study. All demographic, clinical and laboratory data were collected. Bedside whole-blood glucose concentration was measured every 8 h daily for 7 days. For any glucose reading<50 or>150 mg dl(-1), serum sample was sent to the laboratory for confirmation. Hyperglycemia was defined as any blood glucose level⩾150 mg dl(-1). ROP patients were compared with non-ROP patients in a bivariate analysis. Variables significantly associated with ROP were studied in a logistic regression model. RESULT: A total of 65 patients were enrolled with gestational age 31.1±1.2 weeks and birth weight 1385±226 g. Thirty-one patients (48%) were identified with hyperglycemia. On eye examination, 19 cases (29.2%) had ROP (13 with stage 1, 4 with stage 2 and 2 with stage 3). There were more cases of ROP in the hyperglycemia group compared with the euglycemia group (45% vs 15%, P=0.007). Patients who developed ROP had significantly higher maximum and average glucose concentrations when compared with non-ROP patients. Multiple factors have been associated with ROP on bivariate analysis, including gestational age, exposure to oxygen, respiratory support and poor weight gain. However, in a logistic regression model including all significant variables, average blood glucose in the first week of life was the factor independently associated with ROP with an odds ratio of: 1.77 (95% confidence interval: 1.08 to 2.86), P=0.024. CONCLUSION: In a cohort of premature infants, elevated average blood glucose concentrations in the first week of life is independently associated with the development of ROP.


Assuntos
Glicemia/metabolismo , Hiperglicemia/complicações , Retinopatia da Prematuridade/complicações , Estudos de Coortes , Feminino , Idade Gestacional , Humanos , Hiperglicemia/sangue , Recém-Nascido , Recém-Nascido Prematuro , Estudos Longitudinais , Masculino , Estudos Prospectivos , Retinopatia da Prematuridade/sangue , Fatores de Risco
5.
Br J Neurosurg ; 27(4): 436-41, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23445331

RESUMO

INTRODUCTION: Glioblastomas multiformes (GBM) remain incurable in most cases. Their invasion into normal brain makes current therapies ineffective. Post-mortem studies suggest about a 25% of GBMs invade less than 1 cm from the tumour bulk and 20% invade more than 3 cm. AIM OF STUDY: The study aims to use DTI to assess tumour extension and determine how previously reported patterns relate to the progression-free survival (PFS). MATERIALS AND METHODS: Twenty-five patients with GBM treated according to the EORTC/NCIC protocol were retrospectively analysed. Patients were imaged post-operatively at 1.5 T. The sequences were composed of standard anatomical and a standard DTI sequence. As described earlier p and q maps were constructed. For each of the p and q maps, regions of interest were drawn around the visible abnormality. Patients were assigned a diffuse, localised or minimally invasive pattern. Progression was defined according to the RANO criteria (4) and PFS determined in days. Kaplan-Meier plots of survival for the three groups were plotted as were the proportion of patients who had not progressed at 24 months. RESULTS: The median PFS for the diffuse group was 278 days, for the localised group 605 days and 820 days for the minimally invasive group. Three-fourth of the minimally invasive group were progression-free at 24 months (LOG RANK 9.25; p = 0.010). CONCLUSION: It is possible to identify three invasive phenotypes in GBMs using Diffusion tensor imaging , and these three phenotypes have different progression free survival. A minimal phenotype (20% of patients) predicts a greater delay to progression.


Assuntos
Neoplasias Encefálicas/patologia , Imagem de Tensor de Difusão/métodos , Glioblastoma/patologia , Adulto , Idoso , Protocolos Antineoplásicos , Neoplasias Encefálicas/classificação , Neoplasias Encefálicas/terapia , Imagem de Tensor de Difusão/instrumentação , Intervalo Livre de Doença , Feminino , Seguimentos , Glioblastoma/classificação , Glioblastoma/terapia , Humanos , Estimativa de Kaplan-Meier , Masculino , Pessoa de Meia-Idade , Fenótipo , Prognóstico , Estudos Retrospectivos , Resultado do Tratamento
6.
J Perinatol ; 32(9): 671-6, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22134676

RESUMO

OBJECTIVE: Hypoxia-ischemia is the leading cause of neurological handicaps in newborns worldwide. Mesenchymal stem cells (MSCs) collected from fresh cord blood of asphyxiated newborns have the potential to regenerate damaged neural tissues. The aim of this study was to examine the capacity for MSCs to differentiate into neural tissue that could subsequently be used for autologous transplantation. STUDY DESIGN: We collected cord blood samples from full-term newborns with perinatal hypoxemia (n=27), healthy newborns (n=14) and non-hypoxic premature neonates (n=14). Mononuclear cells were separated, counted, and then analyzed by flow cytometry to assess various stem cell populations. MSCs were isolated by plastic adherence and characterized by morphology. Cells underwent immunophenotyping and trilineage differentiation potential. They were then cultured in conditions favoring neural differentiation. Neural lineage commitment was detected using immunohistochemical staining for glial fibrillary acidic protein, tubulin III and oligodendrocyte marker O4 antibodies. RESULT: Mononuclear cell count and viability did not differ among the three groups of infants. Neural differentiation was best demonstrated in the cells derived from hypoxia-ischemia term neonates, of which 69% had complete and 31% had partial neural differentiation. Cells derived from preterm neonates had the least amount of neural differentiation, whereas partial differentiation was observed in only 12%. CONCLUSION: These findings support the potential utilization of umbilical cord stem cells as a source for autologous transplant in asphyxiated neonates.


Assuntos
Asfixia Neonatal/sangue , Diferenciação Celular , Sobrevivência Celular , Sangue Fetal/citologia , Células-Tronco Mesenquimais/citologia , Neuroglia/citologia , Antígenos de Superfície/análise , Proliferação de Células , Separação Celular , Células Cultivadas , Citometria de Fluxo , Proteína Glial Fibrilar Ácida/análise , Humanos , Imuno-Histoquímica , Recém-Nascido , Recém-Nascido Prematuro , Células-Tronco Mesenquimais/metabolismo , Oligodendroglia/imunologia , Tubulina (Proteína)/análise
7.
J Perinatol ; 31(4): 263-8, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21151010

RESUMO

OBJECTIVE: Serum amyloid A (SAA) is an acute phase inflammatory marker that is closely associated with ischemic injuries. Its expression in neonatal hypoxic ischemic encephalopathy (HIE) has not been studied. To test the hypothesis that SAA is increased in neonatal HIE and its concentration correlates with the severity of encephalopathy. STUDY DESIGN: We conducted a prospective case-control study on 54 full-term neonates; 27 cases with evidence of perinatal compromise and 27 healthy controls. Blood samples were collected from cases and controls at postnatal day 1 and day 7, and SAA was measured by ELISA. RESULTS: SAA concentrations (µg ml(-1)) were significantly increased in cases when compared with controls at day 1 and at day 7 (P<0.001). SAA concentrations at day 1 were greater in cases who died when compared with those who survived, and correlated significantly with the severity of HIE (146.9 ± 56.4 vs 79.8 ± 24.7 vs 58.1 ± 21.5) in severe, moderate and mild HIE, respectively (P=0.001). CONCLUSIONS: The expression of SAA is increased in response to hypoxia ischemia of the neonate. The increased concentration correlates with the severity of encephalopathy and is associated with mortality. This is the first study of SAA in neonatal HIE.


Assuntos
Reação de Fase Aguda/sangue , Asfixia Neonatal/complicações , Encéfalo/irrigação sanguínea , Hipóxia-Isquemia Encefálica , Proteína Amiloide A Sérica/análise , Reação de Fase Aguda/etiologia , Biomarcadores , Encéfalo/patologia , Estudos de Casos e Controles , Interpretação Estatística de Dados , Ensaio de Imunoadsorção Enzimática , Humanos , Hipóxia-Isquemia Encefálica/sangue , Hipóxia-Isquemia Encefálica/mortalidade , Hipóxia-Isquemia Encefálica/patologia , Hipóxia-Isquemia Encefálica/fisiopatologia , Recém-Nascido , Monitorização Fisiológica , Estudos Prospectivos , Índice de Gravidade de Doença , Nascimento a Termo
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