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1.
J Paediatr Child Health ; 58(9): 1561-1565, 2022 09.
Artículo en Inglés | MEDLINE | ID: covidwho-1868676

RESUMEN

AIM: SARS-CoV-2 infection in children is generally asymptomatic or mild; however, it can lead to a life-threatening clinical condition, multisystem inflammatory syndrome in children (MIS-C), days or weeks after the infection. Increased intestinal permeability isa possible triggering factor at the onset of the hyperinflammation associated with MIS-C. Zonulin and claudin-5 are involved in intestinal permeability. In this study, we aimed to investigate serum zonulin and claudin-5 levels in SARS-CoV-2 infection and MIS-C disease. METHODS: The study group consisted of children diagnosed with MIS-C or SARS-CoV-2 infection who presented to a university hospital paediatric emergency or infectious diseases departments. The control group included well patients seen at the General Pediatrics units for routine follow-up. Serum zonulin and claudin-5 levels were measured at the time of diagnosis. RESULTS: Fifteen patients were included in the MIS-C group, 19 in the SARS-CoV-2 infection group and 21 in the control group. The mean zonulin level in the MIS-C group was significantly higher than in the control group (P < 0.001). Mean Claudin-5 levels were Psignificantly lower in the SARS-CoV-2 infection group than in the control group (P < 0.001). CONCLUSION: These results indicate that increased intestinal permeability may be involved in the pathogenesis of SARS-CoV-2 infection and MIS-C disease. Larger clinical trials are needed to clarify the role of serum zonulin and claudin-5 on intestinal permeability in MIS-C and SARS-CoV-2 infection in children.


Asunto(s)
COVID-19 , Claudina-5/metabolismo , Haptoglobinas/metabolismo , COVID-19/complicaciones , Niño , Claudina-5/sangre , Haptoglobinas/análisis , Humanos , Precursores de Proteínas , SARS-CoV-2 , Síndrome de Respuesta Inflamatoria Sistémica
2.
Int J Lab Hematol ; 43 Suppl 1: 142-151, 2021 Jul.
Artículo en Inglés | MEDLINE | ID: covidwho-1069396

RESUMEN

INTRODUCTION: Studies have shown that iron metabolism is affected by coronavirus disease 19 (COVID-19), which has spread worldwide and has become a global health problem. Our study aimed to evaluate the relationship between COVID-19 and serum erythropoietin (EPO), hepcidin, and haptoglobin (Hpt) levels with disease severity, and other biochemical values. METHODS: Fifty nine COVID-19 patients hospitalized in the intensive care unit (ICU) and wards in our hospital between March and June 2020 and 19 healthy volunteers were included in the study. Participants were divided into mild, severe, and critical disease severity groups. Group mean values were analyzed with SPSS according to disease severity, mortality, and intubation status. RESULTS: Hemoglobin (Hb) levels were significantly lower in the critical patient group (P < .0001) and deceased group (P < .0001). The red blood cell distribution width-coefficient of variation (RDW-CV) and ferritin values were significantly higher in the intubated (P = .001, P = .005) and deceased (P = .014, P = .003) groups. Ferritin values were positively correlated with disease severity (P < .0001). Serum iron levels were lower in the patient group compared with the reference range. (P < .0001). It was found that the transferrin saturation (TfSat) was lower in the patient group compared with the control group (P < .0001). It was found that the mean EPO of the deceased was lower than the control group and the survived patient group (P = .035). Hepcidin levels were found to be significantly lower in the patient group (P < .0001). Hpt values were found to be significantly lower in the intubated group (P = .004) and the deceased group (P = .042). CONCLUSION: In our study, while serum iron and hepcidin levels decreased in patients diagnosed with COVID-19, we found that EPO and Hpt levels were significantly lower in critical and deceased patient groups. Our study is the first study examining EPO and Hpt levels in patients diagnosed with COVID-19.


Asunto(s)
COVID-19/sangre , Eritropoyetina/sangre , Haptoglobinas/análisis , Hepcidinas/sangre , SARS-CoV-2 , Anciano , Biomarcadores , Estudios Transversales , Femenino , Ferritinas/sangre , Hemoglobinas/análisis , Homeostasis , Humanos , Intubación Intratraqueal/estadística & datos numéricos , Hierro/sangre , Masculino , Persona de Mediana Edad , Índice de Severidad de la Enfermedad , Transferrina/análisis
3.
Infect Dis (Lond) ; 52(9): 659-661, 2020 09.
Artículo en Inglés | MEDLINE | ID: covidwho-526880

RESUMEN

While the COVID-19 epidemic occurred since December 2019, as of end April 2020, no treatment has been validated or invalidated by accurate clinical trials. Use of hydroxychloroquine has been popularised on mass media and put forward as a valid treatment option without strong evidence of efficacy. Hydroxychloroquine (HCQ) has its own side effects, some of which are very serious like acute haemolysis in glucose-6-phosphate dehydrogenase (G6PD) deficient patients. Side effects may be worse than the disease itself. Belgian national treatment guidelines recommend the use of HCQ in mild to severe COVID-19 disease. As opinions, politics, media and beliefs are governing COVID-19 therapy, performance of randomised controlled blinded clinical trials became difficult. Results of sound clinical trials are eagerly awaited. We report a case of acute haemolysis leading to admission in intensive care unit and renal failure in a patient with uncovered G6PD deficiency.


Asunto(s)
Infecciones por Coronavirus/complicaciones , Infecciones por Coronavirus/tratamiento farmacológico , Inhibidores Enzimáticos/efectos adversos , Deficiencia de Glucosafosfato Deshidrogenasa/complicaciones , Hemólisis , Hidroxicloroquina/efectos adversos , Neumonía Viral/complicaciones , Neumonía Viral/tratamiento farmacológico , Anciano , Azitromicina/uso terapéutico , Betacoronavirus/genética , Betacoronavirus/aislamiento & purificación , Transfusión Sanguínea , COVID-19 , Terapia de Reemplazo Renal Continuo , Quimioterapia Combinada , Inhibidores Enzimáticos/uso terapéutico , Haptoglobinas/análisis , Humanos , Hidroxicloroquina/uso terapéutico , Hipoxia/inducido químicamente , Hipoxia/complicaciones , Masculino , Nasofaringe/virología , Pandemias , Síndrome de Dificultad Respiratoria/complicaciones , Coronavirus Relacionado al Síndrome Respiratorio Agudo Severo/genética , Coronavirus Relacionado al Síndrome Respiratorio Agudo Severo/aislamiento & purificación , SARS-CoV-2
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