Shaimaa M. Mohammed, O. Botrous, Mahmoud Abd Elkhalek, mostAFA ABDEL-MOTaleb
{"title":"Evaluation of Soluble CD25 as a Marker in Chronic Liver Diseases in Children","authors":"Shaimaa M. Mohammed, O. Botrous, Mahmoud Abd Elkhalek, mostAFA ABDEL-MOTaleb","doi":"10.21608/ejmm.2022.265442","DOIUrl":null,"url":null,"abstract":"Background : Based on the crucial pathogenic role of inflammation for the progress of hepatic disorders, we hypothesized that the soluble interleukin-2 receptor (sIL-2R, also known as s CD25) would be a sign of inflammatory cell activation and disease severity in people with chronic liver diseases (CLD). Objectives : Our study aimed to evaluate soluble CD25 as a possible indicator of immune cell activation in CLD and acute liver diseases in a group of pediatric Egyptian patients. Methodology : This study was a case control study that included 120 children presented with liver disease aged 2 month-15 years and 60 unrelated healthy controls. The patients were recruited from Pediatric Hepatology Clinic, Beni- Suef University. All children were subjected to history taking, full clinical examination, laboratory tests (CBC, GGT, ALP, AST, ALT, serum albumin, PT, PC, PTT, INR and Soluble CD25 level). Results : Children with chronic liver disease with fibrosis had serum sIL-2R levels that were considerably lower (19.16±12.33 ng/ml) than children with acute liver disease (27.65±14.19 ng/ml) (p=0.036) and controls (29.23±13.20 ng/ml) (p=0.008). Children with chronic liver disease without fibrosis had a mean CD25 level of (23.33±16.31 ng/ml), which was not statistically different from other groups (p=0.655). Conclusions : further research is needed to clarify the role of sCD25 as an immunological marker to predict the occurrence of liver fibrosis in pediatric hepatic disorders and to differentiate between acute & chronic hepatic disorders.","PeriodicalId":22549,"journal":{"name":"The Egyptian Journal of Medical Microbiology","volume":"112 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Egyptian Journal of Medical Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/ejmm.2022.265442","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background : Based on the crucial pathogenic role of inflammation for the progress of hepatic disorders, we hypothesized that the soluble interleukin-2 receptor (sIL-2R, also known as s CD25) would be a sign of inflammatory cell activation and disease severity in people with chronic liver diseases (CLD). Objectives : Our study aimed to evaluate soluble CD25 as a possible indicator of immune cell activation in CLD and acute liver diseases in a group of pediatric Egyptian patients. Methodology : This study was a case control study that included 120 children presented with liver disease aged 2 month-15 years and 60 unrelated healthy controls. The patients were recruited from Pediatric Hepatology Clinic, Beni- Suef University. All children were subjected to history taking, full clinical examination, laboratory tests (CBC, GGT, ALP, AST, ALT, serum albumin, PT, PC, PTT, INR and Soluble CD25 level). Results : Children with chronic liver disease with fibrosis had serum sIL-2R levels that were considerably lower (19.16±12.33 ng/ml) than children with acute liver disease (27.65±14.19 ng/ml) (p=0.036) and controls (29.23±13.20 ng/ml) (p=0.008). Children with chronic liver disease without fibrosis had a mean CD25 level of (23.33±16.31 ng/ml), which was not statistically different from other groups (p=0.655). Conclusions : further research is needed to clarify the role of sCD25 as an immunological marker to predict the occurrence of liver fibrosis in pediatric hepatic disorders and to differentiate between acute & chronic hepatic disorders.
IF 0.6 4区 农林科学BOSQUEPub Date : 2019-01-01DOI: 10.4067/s0717-92002019000300335
Mariane de Oliveira Pereira, A. Ângelo, M. Navroski, Marcos Filipe Nicoletti, Bruno Nascimento, Alexandra Cristina Schatz Sá, Luciana Magda de Oliveira, Queli Cristina Lovatel