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Elevated circulating levels and tissue expression of pentraxin 3 in uremia: a reflection of endothelial dysfunction.
- Source :
-
PloS one [PLoS One] 2013 May 03; Vol. 8 (5), pp. e63493. Date of Electronic Publication: 2013 May 03 (Print Publication: 2013). - Publication Year :
- 2013
-
Abstract
- Elevated systemic pentraxin 3 (PTX3) levels appear to be a powerful marker of inflammatory status and a superior outcome predictor in patients with chronic kidney disease (CKD). As previous data imply that PTX3 is involved in vascular pathology and that adipose tissue mass may influence circulating PTX3 levels, we aimed to study the importance of adipose tissue expression of PTX3 in the uremic milieu and its relation to endothelial dysfunction parameters. Plasma PTX3 and abdominal subcutaneous adipose tissue (SAT) PTX3 mRNA levels were quantified in 56 stage 5 CKD patients (median age 57 [range 25-75] years, 30 males) and 40 age and gender matched controls (median age 58 [range 20-79] years, 27 males). Associations between PTX3 measures and an extensive panel of clinical parameters, including surrogate markers of endothelial function, were assessed. Functional ex vivo studies on endothelial status and immunohistochemical staining for PTX3 were conducted in resistance subcutaneous arteries isolated from SAT. SAT PTX3 mRNA expression correlated with plasma PTX3 concentrations (rho = 0.54, p = 0.0001) and was increased (3.7 [0.4-70.3] vs. 1.2 [0.2-49.3] RQ, p = 0.02) in CKD patients with cardiovascular disease (CVD), but was not significantly different between patients and controls. The association to CVD was lost after adjustments. SAT PTX3 mRNA levels were independently correlated to asymmetric dimethylarginine and basal resistance artery tone developed after inhibition with nitric oxide synthase and cyclooxygenase (rho = -0.58, p = 0.002). Apparent positive PTX3 immunoreactivity was observed in both patient and control arteries. In conclusion, fat PTX3 mRNA levels are associated with measures of endothelial cell function in patients with CKD. PTX3 may be involved in adipose tissue-orchestrated mechanisms that are restricted to the uremic milieu and modify inflammation and vascular complications in CKD patients.
- Subjects :
- Adult
Aged
Arginine analogs & derivatives
Arginine metabolism
Biomarkers metabolism
C-Reactive Protein genetics
Cardiovascular Diseases complications
Cardiovascular Diseases physiopathology
Case-Control Studies
Endothelium physiopathology
Female
Gene Expression
Humans
Kidney physiopathology
Male
Middle Aged
Prognosis
RNA, Messenger genetics
Renal Insufficiency, Chronic complications
Renal Insufficiency, Chronic physiopathology
Serum Amyloid P-Component genetics
Subcutaneous Fat, Abdominal metabolism
Subcutaneous Fat, Abdominal pathology
Uremia etiology
Uremia physiopathology
Vascular Resistance
C-Reactive Protein metabolism
Cardiovascular Diseases metabolism
Endothelium metabolism
Kidney metabolism
RNA, Messenger metabolism
Renal Insufficiency, Chronic metabolism
Serum Amyloid P-Component metabolism
Uremia metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 8
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 23658833
- Full Text :
- https://doi.org/10.1371/journal.pone.0063493