Effect of a single hemodialysis session on inflammatory markers

被引:12
作者
Bitla, Aparna R. [1 ]
Reddy, Prabhakar E. [1 ]
Manohar, Suchitra M. [1 ]
Vishnubhotla, Sivakumar V. [2 ]
Narasimha, Srinivasa Rao Pemmaraju Venkata Lakshmi [1 ]
机构
[1] Sri Venkateswara Inst Med Sci, Dept Biochem, Tirupati, Andhra Pradesh, India
[2] Sri Venkateswara Inst Med Sci, Dept Nephrol, Tirupati, Andhra Pradesh, India
关键词
Hemodialysis; inflammation; lipoprotein-associated phospholipase A2; PLATELET-ACTIVATING-FACTOR; C-REACTIVE PROTEIN; CHRONIC-RENAL-FAILURE; ACUTE-PHASE RESPONSE; FACTOR ACETYLHYDROLASE; PHOSPHOLIPASE A(2); HUMAN-PLASMA; ENDOTHELIAL DYSFUNCTION; LIPOPROTEIN; COHORT;
D O I
10.1111/j.1542-4758.2010.00491.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Inflammation is a common feature of end-stage renal disease. Although there is evidence for hemodialysis (HD)-induced inflammatory process, the effect of a dialysis session on changes in inflammatory markers is still unclear. Seventeen patients of end-stage renal disease on maintenance HD along with 20 age-matched and sex-matched healthy controls were recruited after informed consent. C-reactive protein (CRP) and lipoprotein-associated phospholipase A2 (LpPLA2) activity were measured in the study and control groups. Intradialytic in CRP and LpPLA2 were studied. Comparison of pre-HD vs. the control group and predialytic and postdialytic values was performed using the Mann-Whitney U test and Wilcoxon's test, respectively. Statistical evaluation of intradialytic changes in inflammatory markers was performed using Friedman's test. Hemodialysis patients had higher CRP levels compared with controls (P=0.001). Post-HD LpPLA2 activity (n=17) was higher (P=0.039) compared with the pre-HD activity. Intradialytic changes in inflammatory markers showed a significant increase (P=0.012) in LpPLA2 activity (n=7), while no change (P=0.133) was observed in CRP levels (n=17). Evidence on the pro-inflammatory state being initiated by dialysis is provided by increased LpPLA2 activity. This may add to the atherogenic mileu and cause endothelial dysfunction in this high-risk group. Drugs that inhibit the LpPLA2 pathway have been developed and may be effective in these patients.
引用
收藏
页码:411 / 417
页数:7
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