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      Telomere Length as an Indicator of Biological Aging : The Gender Effect and Relation With Pulse Pressure and Pulse Wave Velocity

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          Abstract

          Chronological age is the primary determinant of stiffness of central arteries. Increased stiffness is an independent indicator of cardiovascular risk. The aim of this study was to determine whether telomere length, a possible index of biological aging, provides a better account than chronological age for variation in arterial stiffness, evaluated by measuring pulse pressure and aortic pulse wave velocity. The study population included 193 French subjects (120 men, 73 women), with a mean age of 56±11 years, who were not on any antihypertensive medications. Telomere length was evaluated in white blood cells by measuring the mean length of the terminal restriction fragments. Age-adjusted telomere length was longer in women than in men (8.67±0.09 versus 8.37±0.07 kb; P =0.016). In both genders, telomere length was inversely correlated with age ( P <0.01). Multivariate analysis showed that in men, but not in women, telomere length significantly contributed to pulse pressure and pulse wave velocity variations. In conclusion, telomere length provides an additional account to chronological age of variations in both pulse pressure and pulse wave velocity among men, such that men with shorter telomere length are more likely to exhibit high pulse pressure and pulse wave velocity, which are indices of large artery stiffness. The longer telomere length in women suggests that for a given chronological age, biological aging of men is more advanced than that of women.

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          A simple salting out procedure for extracting DNA from human nucleated cells

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            PLEIOTROPY, NATURAL SELECTION, AND THE EVOLUTION OF SENESCENCE

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              The rate of telomere sequence loss in human leukocytes varies with age.

              A gradual loss of telomeric repeat sequences with aging previously has been noted in normal adult tissues, and this process has been implicated in cell senescence. No data exist that address the rate of telomere shortening in normal human cells within families or early in life. To address these questions, we measured telomere lengths in peripheral blood leukocytes (PBLs) from 75 members of 12 families and in a group of unrelated healthy children who were 5-48 months old. Here we report the surprising observation that rates of telomere attrition vary markedly at different ages. Telomeric repeats are lost rapidly (at a rate of >1 kilobase per year) from the PBLs of young children, followed by an apparent plateau between age 4 and young adulthood, and by gradual attrition later in life. These data suggest that the loss of telomeric repeats in hematopoietic cells is a dynamic process that is differentially regulated in young children and adults. Our results have implications for current models of how telomeric sequences are lost in normal somatic cells and suggest that PBLs are an excellent tissue to investigate how this process is controlled.
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                Author and article information

                Journal
                Hypertension
                Hypertension
                Ovid Technologies (Wolters Kluwer Health)
                0194-911X
                1524-4563
                February 2001
                February 2001
                : 37
                : 2
                : 381-385
                Affiliations
                [1 ]From the Center “Investigations Preventives et Cliniques” (IPC) (A.B., F.T., K.B.), and INSERM U337 (A.B., M.L., C.L.), Paris, France, and Hypertension Research Center (K.O., M.K., A.A.), University of Medicine and Dentistry of New Jersey (UMDNJ), and Department of Preventive Medicine and Community Health UMDNJ (J.S.), Newark, New Jersey.
                Article
                10.1161/01.HYP.37.2.381
                11230304
                d08c3fee-c6a3-420b-b5cf-7b5341ff0b46
                © 2001
                History

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