Effects of Dialysis Purity on Uremic Dyslipidemia

被引:19
作者
Schiffl, Helmut [1 ,3 ]
Lang, Susanne M. [1 ,2 ]
机构
[1] Univ Munich, Dept Internal Med, Munich, Germany
[2] SRH Wald Klinikum Gera, Dept Internal Med 2, Gera, Germany
[3] KfH Nierenzentrum Munchen Laim, D-80687 Munich, Germany
关键词
Maintenance dialysis; Ultrapure dialysis fluid; Uremic dyslipidemia; RISK-FACTORS; OXIDATIVE STRESS; PLASMA-LEVELS; HEMODIALYSIS; INFLAMMATION; DISEASE; HEMODIAFILTRATION; CONSEQUENCES; PATHOGENESIS; PENTOSIDINE;
D O I
10.1111/j.1744-9987.2009.00713.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dyslipidemia, a prominent feature of end-stage renal disease, is considered a risk factor for premature atherosclerosis in hemodialysis (HD) patients. Dyslipidemia is related to loss of kidney function as well as use of low-flux cellulosic dialyzer membranes, but the effects of dialysate purity are unknown. Forty-eight incident HD patients started high-flux polysulfone maintenance HD, either with conventional (potentially contaminated) or with on-line produced ultrapure dialysate. The quality of the dialysis fluid (CFU/mL, endotoxin concentration), markers of inflammation (C-reactive protein, Il-6), and parameters of the lipid profile and oxidative stress (oxidized low-density lipoprotein) were measured before initiation of HD, and after 6, 12 and 24 months on HD. Compared to baseline, treatment with conventional (mildly contaminated) dialysate significantly increased the uremic low-grade systemic inflammatory response syndrome (SIRS), augmented uremic dyslipidemia (triglycerides by +21%, and high-density lipoprotein (HDL) cholesterol by -10%) and enhanced oxidative stress. In contrast, the use of ultrapure dialysate significantly decreased uremia-associated SIRS, dyslipidemia (triglycerides -7% and HDL cholesterol +11%) and oxidative stress. Ultrapure dialysis fluid improves potential parameters of cardiovascular risk by decreasing inflammatory reactions, improving uremic dyslipidemia and lowering oxidative stress.
引用
收藏
页码:5 / 11
页数:7
相关论文
共 25 条
  • [1] Executive summary: Kidney Early Evaluation Program (KEEP) 2007 annual data report
    Bakris, George
    Collins, Allan J.
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2008, 51 (04) : S1 - S2
  • [2] Systemic lupus erythematosus and "lupus dyslipoproteinemia"
    de Carvalho, Jozelio Freire
    Bonfa, Eloisa
    Borba, Eduardo Ferreira
    [J]. AUTOIMMUNITY REVIEWS, 2008, 7 (03) : 246 - 250
  • [3] Ultrapure dialysate reduces plasma levels of β2-microglobulin and pentosidine in hemodialysis patients
    Furuya, R
    Kumagai, H
    Takahashi, M
    Sano, K
    Hishida, A
    [J]. BLOOD PURIFICATION, 2005, 23 (04) : 311 - 316
  • [4] Plasma levels of advanced glycation end products during haemodialysis, haemodiafiltration and haemofiltration: potential importance of dialysate quality
    Gerdemann, A
    Wagner, Z
    Solf, A
    Bahner, U
    Heidland, A
    Vienken, J
    Schinzel, R
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 2002, 17 (06) : 1045 - 1049
  • [5] Himmelfarb J, 2008, CONTRIB NEPHROL, V161, P132, DOI 10.1159/000130658
  • [6] IBELS LS, 1977, Q J MED, V46, P197
  • [7] Ultrapure dialysate decreases plasma pentosidine, a marker of "carbonyl stress"
    Izuhara, Y
    Miyata, T
    Saito, K
    Ishikawa, N
    Kakuta, T
    Nangaku, M
    Yoshida, H
    Saito, A
    Kurokawa, K
    de Strihou, CV
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2004, 43 (06) : 1024 - 1029
  • [8] Nontraditional risk factors for cardiovascular disease in patients with chronic kidney disease
    Kendrick, Jessica
    Chonchol, Michel B.
    [J]. NATURE CLINICAL PRACTICE NEPHROLOGY, 2008, 4 (12): : 672 - 681
  • [9] Effects of infection and inflammation on lipid and lipoprotein metabolism: mechanisms and consequences to the host
    Khovidhunkit, W
    Kim, MS
    Memon, RA
    Shigenaga, JK
    Moser, AH
    Feingold, KR
    Grunfeld, C
    [J]. JOURNAL OF LIPID RESEARCH, 2004, 45 (07) : 1169 - 1196
  • [10] Prevalence of dyslipidemic risk factors in hemodialysis and CAPD patients
    Kronenberg, F
    Lingenhel, A
    Neyer, U
    Lhotta, K
    König, P
    Auinger, M
    Wiesholzer, M
    Andersson, H
    Dieplinger, H
    [J]. KIDNEY INTERNATIONAL, 2003, 63 : S113 - S116