The relationship between renal function and plasma concentration of the cachectic factor zinc-alpha2-glycoprotein (ZAG) in adult patients with chronic kidney disease

PLoS One. 2014 Jul 30;9(7):e103475. doi: 10.1371/journal.pone.0103475. eCollection 2014.

Abstract

Zinc-α2-glycoprotein (ZAG), a potent cachectic factor, is increased in patients undergoing maintenance dialysis. However, there is no data for patients before initiation of renal replacement therapy. The purpose of the present study was to assess the relationship between plasma ZAG concentration and renal function in patients with a large range of glomerular filtration rate (GFR). Plasma ZAG concentration and its relationship to GFR were investigated in 71 patients with a chronic kidney disease (CKD) stage 1 to 5, 17 chronic hemodialysis (HD), 8 peritoneal dialysis (PD) and 18 non-CKD patients. Plasma ZAG concentration was 2.3-fold higher in CKD stage 5 patients and 3-fold higher in HD and PD patients compared to non-CKD controls (P<0.01). The hemodialysis session further increased plasma ZAG concentration (+39%, P<0.01). An inverse relationship was found between ZAG levels and plasma protein (rs = -0.284; P<0.01), albumin (rs = -0.282, P<0.05), hemoglobin (rs = -0.267, P<0.05) and HDL-cholesterol (rs = -0.264, P<0.05) and a positive correlation were seen with plasma urea (rs = 0.283; P<0.01). In multiple regression analyses, plasma urea and HDL-cholesterol were the only variables associated with plasma ZAG (r2 = 0.406, P<0.001). In CKD-5 patients, plasma accumulation of ZAG was not correlated with protein energy wasting. Further prospective studies are however needed to better elucidate the potential role of ZAG in end-stage renal disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Female
  • Glomerular Filtration Rate
  • Humans
  • Kidney Failure, Chronic / blood
  • Kidney Failure, Chronic / diagnosis
  • Kidney Failure, Chronic / therapy
  • Kidney Failure, Chronic / urine
  • Kidney Function Tests
  • Male
  • Middle Aged
  • Renal Dialysis
  • Renal Insufficiency, Chronic / blood*
  • Renal Insufficiency, Chronic / diagnosis
  • Renal Insufficiency, Chronic / therapy
  • Renal Insufficiency, Chronic / urine*
  • Risk Factors
  • Seminal Plasma Proteins / blood*
  • Severity of Illness Index
  • Zn-Alpha-2-Glycoprotein

Substances

  • Seminal Plasma Proteins
  • Zn-Alpha-2-Glycoprotein

Grants and funding

This study was supported by two governmental institutions from France, INSERM and INSA-Lyon, and by the Fédération Nationale d’Aide aux Insuffisants Rénaux (FNAIR). CC.PELLETIER and PM. ALIX held grants from “Société Française de Néphrologie,” E KALBACHER was the recipient of a grant from “Académie de Médecine” and L. KOPPE held a fellowship from “Fondation pour la Recherche Médicale”. ML CROZE held a grant from the French “Ministère de l’Enseignement Supérieur et de la Recherche." The authors have no competing financial interests to disclose. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.