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47774

Soluble Intracellular Adhesion Molecule 1 (sICAM-1) in post-Streptococcal Acute Glomerulonephritis.

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Last updated: 22 Jan 2023

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Abstract

Background: Glomerulonephritis associated with infiltration of inflammatory cells such as poly-morphonuclear leukocytes, macrophages and T or B-lymophcytes. This is closely related to the expression of cellular adhesion molecules, such as intercellular adhesion molecule 1 (ICAM-1). In human diseases in which unchecked inflammation contributes to the pathogenesis of the diseases process, soluble forms of adhesion molecules including ICAM-1 are elevated. Objectives: To study the changes in sICAM-1 that occur in post-Streptococcal acute glomerulonephritis (PSAGN). Methods: sICAM-1 levels were measured (by ELISA) in 25 children with PSAGN during their initial presentation. Diagnosis of PSAGN was based on the presence of haematuria, transient hypocomplementaemia and positive laboratory evidences of recent Streptococcal infection. Patients were compared to 15 healthy children of matched age and sex. Results: Patients in the acute attack had significantly higher levels of sICAM-1 when compared to control [median (IQR) =45.17 (40.5-49.5) vs 32.5 (26.5-33.4), ng/ml, P ˂0.0001]. sICAM-1 levels correlated significantly with serum C3 (r = -0.58, p = 0.002), serum creatinine (r = 0.46, p = 0.02), and the severity of both systolic and diastolic hypertension (r = 0.64, p = 0.001 and r = 0.65, p ˂0.0001, respectively). No significant correlation was detected between sICAM-1 levels and the severity of proteinuria, haematuria, or oedema. Out of the studied 25 cases; 15 cases were reassessed 3 months after normalization of their complement level and a significant drop in sICAM-1 was found (p = 0.001). Conclusions: These results suggest that ICAM-1 may have a pathophysiologic role in PSAGN and that sICAM-1 may be used as a marker for the severity of the disease.      

DOI

10.21608/geget.2003.47774

Authors

First Name

Ayman

Last Name

Hammad

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Affiliation

Department of Pediatrics and Clinical Immunology, Mansoura Faculty of Medicine, Mansoura University, Egypt.

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First Name

Amr

Last Name

Sarhan

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Affiliation

Department of Pediatrics and Clinical Immunology, Mansoura Faculty of Medicine, Mansoura University, Egypt.

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First Name

Ashraf

Last Name

Bakr

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Affiliation

Department of Pediatrics and Clinical Immunology, Mansoura Faculty of Medicine, Mansoura University, Egypt.

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First Name

Hesham

Last Name

Abdel-Hady

MiddleName

-

Affiliation

Department of Pediatrics and Clinical Immunology, Mansoura Faculty of Medicine, Mansoura University, Egypt.

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Orcid

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First Name

Farha

Last Name

El-Chenawi

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Affiliation

Department of Pediatrics and Clinical Immunology, Mansoura Faculty of Medicine, Mansoura University, Egypt.

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Volume

3

Article Issue

1

Related Issue

7215

Issue Date

2003-08-01

Receive Date

2019-09-11

Publish Date

2003-08-01

Page Start

17

Page End

22

Print ISSN

1687-613X

Online ISSN

2636-3666

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https://geget.journals.ekb.eg/article_47774.html

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https://geget.journals.ekb.eg/service?article_code=47774

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3

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Original Article

Type Code

675

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Journal

Publication Title

GEGET

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https://geget.journals.ekb.eg/

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Article

Created At

22 Jan 2023