5 research outputs found
Connection between Telomerase Activity in PBMC and Markers of Inflammation and Endothelial Dysfunction in Patients with Metabolic Syndrome
Metabolic syndrome (MS) is a constellation of metabolic derangements associated with vascular endothelial dysfunction and oxidative stress and is widely regarded as an inflammatory condition, accompanied by an increased risk for cardiovascular disease. The present study tried to investigate the implications of telomerase activity with inflammation and impaired endothelial function in patients with metabolic syndrome. Telomerase activity in circulating peripheral blood mononuclear cells (PBMC), TNF-α, IL-6 and ADMA were monitored in 39 patients with MS and 20 age and sex-matched healthy volunteers. Telomerase activity in PBMC, TNF-α, IL-6 and ADMA were all significantly elevated in patients with MS compared to healthy volunteers. PBMC telomerase was negatively correlated with HDL and positively correlated with ADMA, while no association between TNF-α and IL-6 was observed. IL-6 was increasing with increasing systolic pressure both in the patients with MS and in the healthy volunteers, while smoking and diabetes were positively correlated with IL-6 only in the patients' group. In conclusion, in patients with MS characterised by a strong dyslipidemic profile and low diabetes prevalence, significant telomerase activity was detected in circulating PBMC, along with elevated markers of inflammation and endothelial dysfunction. These findings suggest a prolonged activity of inflammatory cells in the studied state of this metabolic disorder that could represent a contributory pathway in the pathogenesis of atherosclerosis
Serum oxidized low-density lipoprotein is inversely correlated to telomerase activity in peripheral blood mononuclear cells of haemodialysis patients
Background. Telomerase preserves telomeres’ function and structure
preventing cellular senescence. Its activity is reduced in peripheral
blood mononuclear cells (PBMC) of haemodialysis (HD) patients. The
purpose of this study is to investigate the potential correlation
between increased oxidative stress/inflammation and telomerase activity
in PBMC of HD patients.
Methods: Telomerase activity was measured by PCR-ELISA in PBMC isolated
from a group of 42 HD patients and 39 subjects with estimated glomerular
filtration rate >= 80 mL/min (control group). Serum oxidized low-density
lipoprotein (ox-LDL), tumour necrosis factor-alpha (TNF-alpha) and
interleukin-10 (IL-10) were also measured in both groups by ELISA.
Results: Ox-LDL was negatively correlated to percentage telomerase
activity in PBMC (r = -0.506, P = 0.000 in the whole group of 81 HD and
normal subjects and r = -0.559, P < 0.001 in HD patients). TNF was also
inversely associated with percentage telomerase activity in the whole
group studied (r= -0.492, P= 0.000) while IL-10 was not. In stepwise
multiple linear regression, taking into consideration the most important
characteristics of the HD patients and control group, the only
significant predictors for percentage telomerase activity in PBMC were
ox-LDL and TNF (beta = -0.421, t= -4.083, P= 0.000 and beta= -0.381, t=
-3.691, P= 0.000, respectively) while examining separately HD patients,
the predictors for the same parameter were ox-LDL and HD duration (beta
= -0.671, t = -4.709, P = 0.000 and beta= -0.349, t = -2.447, P = 0.023,
respectively).
Conclusion: Ox-LDL serum level is inversely correlated to telomerase
activity in PBMC of HD patients. Our study proposes a new consequence of
increased oxidative stress in HD patients: the premature cellular
senescence potentially related to atherosclerosis through LDL oxidation