Literature DB >> 22712469

Dehydroepiandrosterone replacement therapy in older adults improves indices of arterial stiffness.

Edward P Weiss1, Dennis T Villareal, Ali A Ehsani, Luigi Fontana, John O Holloszy.   

Abstract

Serum dehydroepiandrosterone (DHEA) concentrations decrease approximately 80% between ages 25 and 75 year. Aging also results in an increase in arterial stiffness, which is an independent predictor of cardiovascular disease (CVD) risk and mortality. Therefore, it is conceivable that DHEA replacement in older adults could reduce arterial stiffness. We sought to determine whether DHEA replacement therapy in older adults reduces carotid augmentation index (AI) and carotid-femoral pulse wave velocity (PWV) as indices of arterial stiffness. A randomized, double-blind trial was conducted to study the effects of 50 mg day(-1) DHEA replacement on AI (n = 92) and PWV (n = 51) in women and men aged 65-75 year. Inflammatory cytokines and sex hormones were measured in fasting serum. AI decreased in the DHEA group, but not in the placebo group (difference between groups, -6 ± 2 AI units, P = 0.002). Pulse wave velocity also decreased (difference between groups, -3.5 ± 1.0 m s(-1), P = 0.001); however, after adjusting for baseline values, the between-group comparison became nonsignificant (P = 0.20). The reductions in AI and PWV were accompanied by decreases in inflammatory cytokines (tumor necrosis factor α and IL-6, P < 0.05) and correlated with increases in serum DHEAS (r = -0.31 and -0.37, respectively, P < 0.05). The reductions in AI also correlated with free testosterone index (r = -0.23, P = 0.03). In conclusion, DHEA replacement in elderly men and women improves indices of arterial stiffness. Arterial stiffness increases with age and is an independent risk factor for CVD. Therefore, the improvements observed in this study suggest that DHEA replacement might partly reverse arterial aging and reduce CVD risk.
© 2012 The Authors. Aging Cell © 2012 Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland.

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Year:  2012        PMID: 22712469      PMCID: PMC3444670          DOI: 10.1111/j.1474-9726.2012.00852.x

Source DB:  PubMed          Journal:  Aging Cell        ISSN: 1474-9718            Impact factor:   9.304


  43 in total

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Authors:  L Mazat; S Lafont; C Berr; B Debuire; J F Tessier; J F Dartigues; E E Baulieu
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8.  Dehydroepiandrosterone increases endothelial cell proliferation in vitro and improves endothelial function in vivo by mechanisms independent of androgen and estrogen receptors.

Authors:  Maro R I Williams; Tye Dawood; Shanhong Ling; Aozhi Dai; Robert Lew; Kathy Myles; John W Funder; Krishnankutty Sudhir; Paul A Komesaroff
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10.  Dehydroepiandrosterone (DHEA) replacement decreases insulin resistance and lowers inflammatory cytokines in aging humans.

Authors:  Edward P Weiss; Dennis T Villareal; Luigi Fontana; Dong-Ho Han; John O Holloszy
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  9 in total

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Review 2.  Dehydroepiandrosterone on metabolism and the cardiovascular system in the postmenopausal period.

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Review 4.  In vivo and in vitro evidences of dehydroepiandrosterone protective role on the cardiovascular system.

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Journal:  Int J Endocrinol Metab       Date:  2015-04-30

5.  Multiple dietary supplements do not affect metabolic and cardio-vascular health.

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6.  Relationship Between Serum Total Testosterone Concentration and Augmentation Index at Radial Artery in Japanese Postmenopausal Patients.

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Journal:  J Clin Med Res       Date:  2017-09-01

7.  Novel associations between sex hormones and diabetic vascular complications in men and postmenopausal women: a cross-sectional study.

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8.  Low Serum Dehydroepiandrosterone and Dehydroepiandrosterone Sulfate Are Associated With Coronary Heart Disease in Men With Type 2 Diabetes Mellitus.

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9.  Experimental design of the Effects of Dehydroepiandrosterone in Pulmonary Hypertension (EDIPHY) trial.

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  9 in total

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