Literature DB >> 20395357

Oxidized high-density lipoprotein is associated with protein-energy wasting in maintenance hemodialysis patients.

Hirokazu Honda1, Masashi Ueda, Shiho Kojima, Shinichi Mashiba, Hiroki Suzuki, Nozomu Hosaka, Yuki Hirai, Mari Nakamura, Hisako Nagai, Noriyuki Kato, Masanori Mukai, Makoto Watanabe, Keiko Takahashi, Kanji Shishido, Tadao Akizawa.   

Abstract

BACKGROUND AND OBJECTIVES: Oxidized HDL (oxHDL) may behave as proinflammatory HDL because of reduced anti-inflammatory capacity and is considered a risk factor for mortality in patients on maintenance hemodialysis (MHD). The study presented here assessed the effect of oxHDL on protein-energy wasting (PEW) in MHD patients. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: This prospective study examined a cohort of MHD patients (n = 176) who were not taking lipid-lowering drugs. Blood samples were obtained to measure albumin, lipids, high-sensitivity C-reactive protein (hsCRP), oxidized LDL (oxLDL), and oxHDL. PEW was assessed by subjective global assessment (SGA) and geriatric nutritional risk index (GNRI). Measurements and assessment of nutritional status were followed up 1 year later.
RESULTS: OxHDL was significantly increased in patients with PEW at baseline. High oxHDL and high hsCRP were significantly associated with PEW, and receiver operating characteristic curves for oxHDL and hsCRP showed statistically similar accuracy for predicting SGA-positive status. According to multivariate regression models, high oxHDL had a significant influence on PEW in patients, particularly those with high hsCRP. Decreased changes in GNRI and high prevalence of SGA-positive status at 1 year were more common in patients with high oxHDL at baseline and 1 year later than in patients with low oxHDL at both time points.
CONCLUSIONS: A high oxHDL state may be associated with PEW estimated by GNRI and SGA, particularly concomitant with inflammation in MHD patients.

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Year:  2010        PMID: 20395357      PMCID: PMC2879312          DOI: 10.2215/CJN.06110809

Source DB:  PubMed          Journal:  Clin J Am Soc Nephrol        ISSN: 1555-9041            Impact factor:   8.237


  31 in total

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