Title of article :
Effect of Inflammatory Factors on B2-Microglobulin in Hemodialysis Patients.
Author/Authors :
Rahbar، M نويسنده Assistant Professor, Section of Nephrology, Department of Internal Medicine , , Mehdipour-Aghabagher، B نويسنده Research Assistant, Sina Research Development Center, Sina hospital, Tehran University of Medical Science, Tehran, Iran. ,
Issue Information :
فصلنامه با شماره پیاپی 50 سال 2012
Pages :
4
From page :
59
To page :
62
Abstract :
Introduction: Systemic inflammation is a common complication in patients with chronic renal dysfunction including hemodialysis patients. The aim of this study is evaluating association of inflammatory factors on B2-microglobulin (B2-m) in hemodialysis patients Materials and Methods: This is a single-center prospective study conducted on 39 hemodialysis patients in Sina hospital in 2009. All cases had well-functioning arteriovenous (AV) access or permanent venous catheter and were dialyzed thrice weekly. All patients were hemodialyzed using low flux membranes and Ferzinuce system. Blood samples were taken from the arterial line for the following assessments: Hct, hemoglobin, WBC, platelets, erythrocyte sedimentation rate (ESR), blood urea and serum creatinine, HDL cholesterol (HDL-C), total protein, albumin, CRP, and B2- microglobulin. The statistical analyses were performed using Chi-square test for relationships. All tests were two-tailed and with P < 0.05 were considered significant. Results: The cases included 28 females (71.8%) and 11 males (28.2%) with the mean age of 60.61±15.25 yrs. There was no significant relationship between CRP, HDL-C, Albumin and B2-microglobulin (P ? 0.05). Conclusion: Although the rise of inflammatory factors may increase B2-microglobulin levels, we found no significant relationship between inflammatory factors and B2-microglobulin when low-flux biocompatible membranes are used.
Journal title :
Shiraz Electronic Medical Journal
Serial Year :
2012
Journal title :
Shiraz Electronic Medical Journal
Record number :
2343845
Link To Document :
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