Key result
Premature CAD linked to ~54% fewer circulating endothelial progenitor cells and shorter telomeres versus controls.
Why the study?
Does premature coronary artery disease associate with accelerated senescence of circulating endothelial progenitor cells in young patients?
Case-Control (n=114)
No
Does premature coronary artery disease associate with accelerated senescence of circulating endothelial progenitor cells in young patients?
Premature coronary artery disease in young Indian patients is associated with accelerated vascular senescence, as evidenced by reduced numbers and shortened telomeres of circulating endothelial progenitor cells.
Answers are grounded in this paper and cite their sources.
May signal accelerated senescence in premature CAD; hypothesis-generating and requires prospective validation before clinical use.
BACKGROUND: The decreased number and senescence of circulating endothelial progenitor cells (EPCs) are considered markers of vascular senescence associated with aging, atherosclerosis, and coronary artery disease (CAD) in elderly. In this study, we explore the role of vascular senescence in premature CAD (PCAD) in a developing country by comparing the numerical status and senescence of circulating EPCs in PCAD patients to controls. METHODS: EPCs were measured by flow cytometry in 57 patients with angiographically documented CAD, and 57 controls without evidence of CAD, recruited from random patients ≤ 50 years of age at All India Institute of Medical Sciences. EPC senescence as determined by telomere length (EPC-TL) and telomerase activity (EPC-TA) was studied by real time polymerase chain reaction (q PCR) and PCR- ELISA respectively. RESULT: The number of EPCs (0.18% Vs. 0.039% of total WBCs, p < 0.0001), and EPC-TL (3.83 Vs. 5.10 kb/genome, p = 0.009) were markedly lower in PCAD patients compared to controls. These differences persisted after adjustment for age, sex, BMI, smoking and medications. EPC-TA was reduced in PCAD patients, but was statistically significant only after adjustment for confounding factors (1.81 Vs. 2.20 IU/cell, unadjusted p = 0.057, adjusted p = 0.044). CONCLUSIONS: We observed an association between increased vascular cell senescence with PCAD in a sample of young patients from India. This suggests that early accelerated vascular cell senescence may play an important mechanistic role in CAD epidemic in developing countries like India where PCAD burden is markedly higher compared to developed countries.
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Vemparala et al. (2013) conducted a case-control in Premature coronary artery disease (PCAD) (n=114). Premature coronary artery disease vs. Age-matched controls without coronary artery disease was evaluated on Circulating endothelial progenitor cell (EPC) number (% of total WBCs) (p=<0.001). Premature coronary artery disease was associated with lower numbers of circulating endothelial progenitor cells and shorter telomere lengths compared to controls.
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