4.6 Article

Leukocyte telomere length is inversely associated with arterial wave reflection in 566 normotensive and never-treated hypertensive subjects

期刊

AGING-US
卷 12, 期 12, 页码 12376-12392

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/aging.103459

关键词

aging; circulatory system; hemodynamics; telomeres

资金

  1. Paivikki and Sakari Sohlberg Foundation
  2. Finnish Foundation of Cardiovascular Research
  3. Paavo Nurmi Foundation
  4. Pirkanmaa Regional Fund of the Finnish Cultural Foundation
  5. Aarne Koskelo Foundation
  6. Competitive State Research Financing of the Expert Responsibility Area of Tampere University Hospital [9X046, 9AA062, X51001]

向作者/读者索取更多资源

Telomeres are short segments in chromosome ends, the length of which is reduced during cell lifecycles. We examined the association of mean leukocyte telomere length (LTL) and short telomere proportion (STP) with hemodynamic variables in normotensive and never -treated hypertensive volunteers (n=566, 19-72 years). STP and mean LTL were determined using Southern blotting, and supine hemodynamics recorded using continuous tonometric pulse wave analysis and whole -body impedance cardiography. The analyses were adjusted for age, body mass index (BMI), alcohol use, smoking, plasma chemistry, and estimated glomerular filtration rate (eGFR). In univariate analyses, mean LTL and STP both correlated with age, BMI, eGFR, aortic blood pressure, augmentation index, and pulse wave velocity (p<0.05 for all). Mean LTL also correlated with systemic vascular resistance (p<0.05). In linear regression analyses of all hemodynamic variables, mean LTL was only an independent explanatory factor for augmentation index (Beta -0.006, p=0.032), while STP was not an explanatory factor for any of the hemodynamic variables, in contrast to age, BMI and several cardiovascular risk factors. To conclude, augmentation index was predominantly related with chronological aging, but also with mean LTL, suggesting that this variable of central wave reflection is a modest marker of vascular biological aging.

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