Does Mannose-Binding Lectin Gene Polymorphism in Pediatric Patients Undergoing Peritoneal Dialysis Cause Susceptibility to the Development of Peritonitis?
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Research Article
VOLUME: 11 ISSUE: 2
P: 133 - 138
2021

Does Mannose-Binding Lectin Gene Polymorphism in Pediatric Patients Undergoing Peritoneal Dialysis Cause Susceptibility to the Development of Peritonitis?

J Dr Behcet Uz Child Hosp 2021;11(2):133-138
1. Department Of Pediatric Intensive Care Unit, Faculty Of Medicine Dokuz Eylul University, Izmir, Turkey
2. Department Of Pediatric Nephrology, Dr. Behcet Uz Children’s Hospital, University Of Health Sciences, Izmir, Turkey
3. Departments Of Medical Genetics, Faculty Of Medicine Ege University, Izmir, Turkey
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Received Date: 2020-09-21T10:19:03
Accepted Date: 2021-08-03T17:08:13
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Abstract

Objective: This study aims to investigate the relationship between peritonitis attacks and mannose-binding lectin (MBL) gene polymorphism in patients undergoing peritoneal dialysis.

Method: Codon 54 polymorphism found in exon 1 of the MBL gene was investigated by polymerase chain reaction-restriction fragment length polymorphism method in 45 patients with chronic renal failure undergoing peritoneal dialysis.

Results: The frequency of the mutant B allele was not significantly higher in the patient group (4.4%) than the control group (2.1%). The AB genotype was found at a rate of 15.6% and 34% in the patient group and healthy control group, respectively. The AA genotype was found in 80% of children who underwent peritoneal dialysis and 63.8% of the healthy control group.

Conclusion: In our study, no relationship was found between peritonitis attacks and MBL gene polymorphism in patients undergoing peritoneal dialysis.

Keywords:
peritoneal dialysis, peritonitis, mannose-binding lectin, PCR