Plasma pentraxin 3 in patients with chronic kidney disease: associations with renal function, protein-energy wasting, cardiovascular disease, and mortality

Clin J Am Soc Nephrol. 2007 Sep;2(5):889-97. doi: 10.2215/CJN.00870207. Epub 2007 Aug 16.

Abstract

Background and objectives: Plasma protein pentraxin 3 concentrations are elevated in a wide range of diseased states. However, no study has evaluated protein pentraxin 3 in patients with chronic kidney disease.

Design, setting, participants, & measurements: Plasma protein pentraxin 3 concentrations were analyzed in relation to GFR, inflammation, cardiovascular disease, and protein-energy wasting in 71 patients with stages 3 to 4 chronic kidney disease, 276 patients with stage 5 chronic kidney disease, and 61 control subjects. Survival (5 yr) in patients with stage 5 chronic kidney disease was analyzed in relation to protein pentraxin 3 levels.

Results: Both patient groups with chronic kidney disease had higher protein pentraxin 3 concentrations than control subjects, with the highest concentration in patients with stage 5 chronic kidney disease. In all patients with chronic kidney disease, protein pentraxin 3 correlated negatively with GFR and positively with inflammatory markers. Patients with protein-energy wasting, inflammation, and cardiovascular disease had higher concentrations of protein pentraxin 3 than their counterparts. Patients with high protein pentraxin 3 levels had higher all-cause and cardiovascular mortality. After adjustment for age, gender, C-reactive protein, and cardiovascular disease, all-cause mortality was still significantly higher in patients with high protein pentraxin 3. Finally, protein pentraxin 3 showed a predictive value of mortality similar to that of IL-6 and better than C-reactive protein.

Conclusion: Plasma protein pentraxin 3 increases as GFR declines and is associated with the presence of cardiovascular disease and protein-energy wasting. Furthermore, in patients with chronic kidney disease, elevated protein pentraxin 3 predicted all-cause mortality.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • C-Reactive Protein / analysis*
  • Cardiovascular Diseases / etiology
  • Chronic Disease
  • Cohort Studies
  • Cross-Sectional Studies
  • Energy Metabolism*
  • Female
  • Humans
  • Kidney / physiopathology
  • Kidney Diseases / blood
  • Kidney Diseases / complications
  • Kidney Diseases / metabolism*
  • Kidney Diseases / mortality*
  • Kidney Diseases / physiopathology
  • Male
  • Middle Aged
  • Proteins / metabolism*
  • Serum Amyloid P-Component / analysis*

Substances

  • Proteins
  • Serum Amyloid P-Component
  • PTX3 protein
  • C-Reactive Protein