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NDT Advance Access published online on November 19, 2009

Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfp598
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© The Author 2009. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org



Association of inflammation and protein-energy wasting with endothelial dysfunction in peritoneal dialysis patients

Hoon Young Choi1,*, Jung Eun Lee2,*, Seung Hyeok Han3, Tae Hyun Yoo1, Beom Seok Kim1, Hyeong Cheon Park1, Shin-Wook Kang1, Kyu Hun Choi1, Sung Kyu Ha1, Ho Yung Lee1 and Dae-Suk Han1

1 Department of Internal Medicine, Institute of Kidney Disease, Yonsei University College of Medicine, Seoul, Korea 2 Department of Internal Medicine, Yong-In Severance Hospital, Yong-In, Korea 3 Department of Internal Medicine, National Health Insurance Corporation, Ilsan Hospital, Goyang, Korea

Correspondence and offprint requests to: Dae-Suk Han; E-mail: dshan{at}yuhs.ac



  Abstract

Background. Cardiovascular disease is the main cause of mortality in end-stage renal disease (ESRD) patients. Recent studies have indicated that non-traditional risk factors such as endothelial dysfunction (ED), chronic inflammation and protein-energy wasting (PEW) may contribute significantly to the increased cardiovascular mortality among dialysis patients. To further ascertain this association, we carried out a cross-sectional assessment of nutritional status, inflammatory markers and endothelial dysfunction in peritoneal dialysis (PD) patients.

Methods. We measured ED functionally by flow-mediated vasodilatation (FMD) using doppler ultrasonography and biochemically by soluble intercellular adhesion molecule-1 (sICAM-1) in 105 s\ PD patients and 32 age- and sex-matched healthy controls. We also simultaneously measured inflammatory markers and performed a subjective global assessment (SGA) of their nutritional status using a seven-point scoring scale. Subjects were subgrouped according to their nutritional and inflammatory status.

Results. In PD patients, FMD was markedly lower (9.9 ± 4.8% vs. 16.4 ± 4.8%, P < 0.05), and sICAM-1 was significantly higher than those in controls. The malnourished patients had significantly lower FMD (8.4±4.6% vs. 10.8±4.7%, P <0.05) and higher sICAM-1 than the nourished patients. The inflamed group had significantly lower FMD (7.1 ± 3.8 vs.11.1 ± 4.6%, P < 0.05) and higher sICAM-1 than the non-inflamed group. In all PD patients, lean body mass/body weight %, albumin and SGA correlated positively with FMD (r = +0.207, r = +0.224, r = +0.285, P < 0.05). However, age, log high sensitivity C-reactive protein (hsCRP), log IL-6 and sICAM-1 were negatively correlated with FMD (r = –0.275, r = –0.361, r = –0.360, r = –0.271, P < 0.05). A multiple regression analysis showed that log hsCRP was an independent factor affecting FMD. Endothelial function, demonstrated as FMD and sICAM-1 in the nourished PD patients without inflammation, was well preserved compared to other subgroups.

Conclusion. Our data suggest that chronic inflammation and PEW are closely linked to ED in PD patients.

Keywords: endothelial dysfunction; inflammation; peritoneal dialysis; protein-energy wasting


* These authors contributed equally to this work.


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