Plasma dehydroepiandrosterone and dehydroepiandrosterone sulfate in patients undergoing diagnostic coronary angiography

Herrington, David M.; Gordon, Gary B.; Achuff, Stephen C.; Trejo, Jorge F.; Weisman, Harlan F.; Kwiterovich, Peter O.; Pearson, Thomas A.

doi:10.1016/s0735-1097(10)80334-1

Cited by 147Hormonal and reproductive studiesAdrenal Hormones and DisordersLipoproteins and Cardiovascular Health

Plasma dehydroepiandrosterone and dehydroepiandrosterone sulfate in patients undergoing diagnostic coronary angiography

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Herrington, David M., Gordon, Gary B., Achuff, Stephen C., Trejo, Jorge F., Weisman, Harlan F., Kwiterovich, Peter O., Pearson, Thomas A.·1990·Journal of the American College of Cardiology

DOI 10.1016/s0735-1097(10)80334-1

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Abstract

Serum levels of DHEA sulfate are inversely associated with cardiovascular death in men, and urinary dehydroepiandrosterone (DHEA) levels are inversely associated with clinical manifestations of coronary artery disease. These observations may be related to the antiproliferative effects of DHEA, resulting in inhibition of atherosclerotic intimal hyperplasia. To examine the relation between these steroids and a direct measure of coronary atherosclerosis, plasma DHEA and DHEA sulfate levels were determined in 206 middle-aged patients (103 men, 103 women) undergoing elective coronary angiography. Plasma DHEA sulfate levels were lower in men with at least one stenosis greater than or equal to 50% compared with those without any stenosis greater than or equal to 50% (4.9 +/- 2.7 versus 6.1 +/- 3.5 nmol/ml, p = 0.05). Levels of DHEA sulfate were also inversely related to the number of diseased coronary vessels (r = -0.20, p = 0.05) and a continuous measure of the extent of coronary atherosclerosis (r = -0.25, p = 0.01) in men. The association between DHEA sulfate levels and extent of coronary artery disease was independent of age and other conventional risk factors for coronary disease. In women, there was no association between plasma DHEA or DHEA sulfate levels and coronary disease. These data demonstrate a consistent, independent, inverse, dose-response relation between plasma DHEA sulfate levels and angiographically defined coronary atherosclerosis in men. Plasma DHEA sulfate may be another important and potentially modifiable risk factor for the development and progression of coronary atherosclerosis.

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Low levels of DHEA and DHEA-S are associated with elevated risk of cardiovascular disease.
“Low levels of both DHEA and DHEA-S are associated with elevated risk of cardiovascular disease.98-100”
From Hormonal and Metabolic Changes of Aging and the Influence of Lifestyle Modifications (2021) · cites this paper as [100]

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Statistical Methods
Snedecor, G. W., Cochran, W. G., & STOUT, B. B. (1939) · Soil Science · doi:10.1097/00010694-193902000-00006 · Cited by 19,423 · see citing works
Exploratory Data Analysis
David, F. N., & Tukey, J. W. (1977) · Biometrics · doi:10.2307/2529486 · Cited by 12,707 · see citing works
Exploratory Data Analysis.
Osborn, J. F., & Tukey, J. (1978) · Journal of the Royal Statistical Society Series A (General) · doi:10.2307/2344492 · Cited by 1,782 · see citing works
Estimation of the Probability of an Event as a Function of Several Independent Variables
Walker, S. H., & Duncan, D. B. (1967) · Biometrika · doi:10.1093/biomet/54.1-2.167 · Cited by 1,683 · see citing works
Age changes and sex differences in serum dehydroepiandrosterone sulfate concentrations throughout adulthood
ORENTREICH, N., BRIND, J. L., RIZER, R. L., & VOGELMAN, J. H. (1984) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-59-3-551 · Cited by 1,349 · see citing works
THE RELATIONSHIP OF PSYCHOSOCIAL FACTORS TO CORONARY HEART DISEASE IN THE FRAMINGHAM STUDY
Haynes, S., Levine, S., Scotch, N. A., Feinleib, M., & Kannel, W. B. (1978) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a112556 · Cited by 800 · see citing works
A prospective study of dehydroepiandrosterone sulfate, mortality and cardiovascular disease.
Barrett-Connor, E., Khaw, K.-T., & Yen, S. S. C. (1986) · New England Journal of Medicine · doi:10.1056/nejm198612113152405 · Cited by 681 · see citing works
Self-administration of a questionnaire on chest pain and intermittent claudication.
Rose, G., McCartney, P., & Reid, D. D. (1977) · Journal of Epidemiology & Community Health · doi:10.1136/jech.31.1.42 · Cited by 588 · see citing works
Dehydroepiandrosterone reduces serum low density lipoprotein levels and body fat but does not alter insulin sensitivity in normal men.
NESTLER, J. E., BARLASCINI, C. O., CLORE, J. N., & BLACKARD, W. G. (1988) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-66-1-57 · Cited by 414 · see citing works
Therapeutic effects of dehydroepiandrosterone (DHEA) in diabetic mice.
Coleman, D. L., Leiter, E. H., & Schwizer, R. W. (1982) · Diabetes · doi:10.2337/diab.31.9.830 · Cited by 317 · see citing works
Dehydroepiandrosterone and androsterone levels in human plasma. Effect of age and sex: day-to-day and diurnal variations.
MIGEON, C. J., KELLER, A. R., LAWRENCE, B., & SHEPARD, T. H. (1957) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-17-9-1051 · Cited by 260 · see citing works
Assessment methods for physical activity and physical fitness in population studies: Report of a NHLBI workshop
Wilson, P. W. F., Paffenbarger, R. S., Morris, J. N., & Havlik, R. J. (1986) · American Heart Journal · doi:10.1016/0002-8703(86)90022-0 · Cited by 244 · see citing works
Reduction of atherosclerosis by administration of dehydroepiandrosterone. A study in the hypercholesterolemic New Zealand white rabbit with aortic intimal injury.
Gordon, G., Bush, D. E., & Weisman, H. F. (1988) · Journal of Clinical Investigation · doi:10.1172/jci113652 · Cited by 241 · see citing works
Cigarette Smoking and Levels of Adrenal Androgens in Postmenopausal Women
Khaw, K.-T., Tazuke, S., & Barrett-Connor, E. (1988) · New England Journal of Medicine · doi:10.1056/nejm198806303182601 · Cited by 215 · see citing works
Pattern of Plasma Dehydroepiandrosterone Sulfate Levels in Humans from Birth to Adulthood: Evidence for Testicular Production*
PERETTI, E. D., & Forest, M. G. (1978) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-47-3-572 · Cited by 213 · see citing works
CIGARETTE SMOKING AND SERUM SEX HORMONES IN MEN
Dai, W. S., Gutai, J. P., Kuller, L. H., & Cauley, J. A. (1988) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a115033 · Cited by 166 · see citing works
Modulation of growth, differentiation and carcinogenesis by dehydroepiandrosterone.
Gordon, G. B., Shantz, L. M., & Talalay, P. (1987) · Advances in Enzyme Regulation · doi:10.1016/0065-2571(87)90023-9 · Cited by 159 · see citing works
Apolipoproteins and Coronary Artery Disease
Kottke, B. A., Zinsmeister, A. R., Holmes, D. R., KNELLER, R. W., Hallaway, B. J., & Mao, S. J. T. (1986) · Mayo Clinic Proceedings · doi:10.1016/s0025-6196(12)61947-8 · Cited by 156 · see citing works
Dehydroepiandrosterone feeding prevents aortic fatty streak formation and cholesterol accumulation in cholesterol-fed rabbit.
Arad, Y., Badimón, J. J., Badimón, L., Hembree, W. C., & Ginsberg, H. N. (1989) · Arteriosclerosis An Official Journal of the American Heart Association Inc · doi:10.1161/01.atv.9.2.159 · Cited by 134 · see citing works
Plasma Dehydroepiandrosterone Sulfate in Normal and Pathological Conditions
YAMAJI, T., & Ibayashi, H. (1969) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-29-2-273 · Cited by 133 · see citing works
Dehydroepiandrosterone and Structural Analogs: A New Class of Cancer Chemopreventive Agents
Schwartz, A. G., Whitcomb, J. M., Nyce, J. W., Lewbart, M. L., & Pashko, L. L. (1988) · Advances in cancer research · doi:10.1016/s0065-230x(08)60227-4 · Cited by 128 · see citing works
A comparison of direct adjustment and regression adjustment of epidemiologic measures
Wilcosky, T. C., & Chambless, L. E. (1985) · Journal of Chronic Diseases · doi:10.1016/0021-9681(85)90109-2 · Cited by 125 · see citing works
Cellular proliferation in atherosclerosis and hypertension
Schwartz, S. M., & Ross, R. (1984) · Progress in Cardiovascular Diseases · doi:10.1016/0033-0620(84)90010-0 · Cited by 116 · see citing works
Cigarette Advertising
Barrett-Connor, E., & Khaw, K. (1987) · New England Journal of Medicine · doi:10.1056/nejm198709103171116 · Cited by 75 · see citing works
Abnormal hormone levels in men with coronary artery disease.
Zumoff, B., Troxler, R. G., O'Connor, J., Rosenfeld, R. S., Kream, J., Levin, J., Hickman, J. R., Sloan, A., Walker, W. J., Cook, R. L., et al. (1982) · Arteriosclerosis An Official Journal of the American Heart Association Inc · doi:10.1161/01.atv.2.1.58 · Cited by 73 · see citing works
Hyperapobetalipoproteinemia in a kindred with familial combined hyperlipidemia and familial hypercholesterolemia.
Kwiterovich, P. O., White, S., Forte, T. M., Bachorik, P. S., Smith, H., & Sniderman, A. D. (1987) · Arteriosclerosis An Official Journal of the American Heart Association Inc · doi:10.1161/01.atv.7.3.211 · Cited by 57 · see citing works
Inhibition of the conversion of 3T3 fibroblast clones to adipocytes by dehydroepiandrosterone and related anticarcinogenic steroids.
Gordon, G., Newitt, J. A., Shantz, L. M., Weng, D. E., & Talalay, P. (1986) · PubMed · Cited by 57 · see citing works
Sex Difference in the Metabolism of Dehydroisoandrosterone Sulfate*
Zumoff, B., & Bradlow, H. L. (1980) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-51-2-334 · Cited by 53 · see citing works
Influence of a Low-Calorie Diet and Fasting on the Metabolism of Dehydroepiandrosterone Sulfate in Adult Obese Subjects1
Hendrikx, A., Heyns, W., & MOOR, P. D. (1968) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-28-11-1525 · Cited by 50 · see citing works
Absence of an Inverse Relation of Dehydroepiandrosterone Sulfate with Cardiovascular Mortality in Postmenopausal Women
(1987) · New England Journal of Medicine · doi:10.1056/nejm198709103171115 · Cited by 48 · see citing works
17-Ketosteroids and Arteriosclerosis*t
Kask, E. (1959) · Angiology · doi:10.1177/000331975901000504 · Cited by 44 · see citing works
A POSSIBLE INTERRELATION BETWEEN GLUCOSE-6-PHOSPHATE DEHYDROGENASE AND DEHYDROEPIANDROSTERONE IN OBESITY
Lopez‐S, A., & Krehl, W. A. (1967) · The Lancet · doi:10.1016/s0140-6736(67)91654-6 · Cited by 44 · see citing works
Excretion of urinary steroids by men and women with myocardial infarction.
Marmorston, J., Jj, L., Bernstein, J. L., Sobel, H., Kuzma, O. T., ALEXANDER, R., Magidson, O., & Fj, M. (1957) · PubMed · Cited by 36 · see citing works
URINARY STEROID-EXCRETION PATTERNS AFTER ACUTE MYOCARDIAL INFARCTION
RAO, L. G. S. (1970) · The Lancet · doi:10.1016/s0140-6736(70)90005-x · Cited by 33 · see citing works
Further evidence of altered adrenocortical function in hypertension. Dehydroepiandrosterone excretion rate
Nowaczynski, W. J., Fragachán, F., Silah, J. G., Millette, B., & Genest, J. (1968) · Canadian Journal of Biochemistry · doi:10.1139/o68-155 · Cited by 31 · see citing works
Serum Dehydroepiandrosterone Sulfate and Dehydroepiandrosterone Levels in Essential Hypertension
Sekihara, H., Ohsawa, N., & Kosáka, K. (1975) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-40-1-156 · Cited by 29 · see citing works
Neuroendocrine Correlates of the Type a Behavior Pattern: A Review and New Hypotheses
Fava, M., Littman, A. B., & Halperin, P. (1988) · The International Journal of Psychiatry in Medicine · doi:10.2190/27le-67ju-0453-jd27 · Cited by 28 · see citing works
Serum lipids and dehydroepiandrosterone excretion in normal subjects
Sonka, J., Fassati, M., Fassati, P., Gregorova, I., & Picek, K. (1968) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)42691-4 · Cited by 28 · see citing works
Total serum cholesterol and urinary dehydroepiandrosterone in humans
Lopez‐S, A., Wingo, C., Hebert, J. A., Johnson, W. D., & Troendle, D. A. (1976) · Atherosclerosis · doi:10.1016/0021-9150(76)90139-8 · Cited by 25 · see citing works
Inhibitory action of dehydroepiandrosterone (DHEA) on fibroblast growth
Saenger, P. H., & New, M. I. (1977) · Cellular and Molecular Life Sciences · doi:10.1007/bf01951309 · Cited by 24 · see citing works
Secretion rate of dehydroepiandrosterone and dehydroepiandrosterone sulfate in benign essential hypertension as compared to normal subjects
Shao, A.-H., Nowaczynski, W. J., Kuchel, O., & Genest, J. (1970) · Canadian Journal of Biochemistry · doi:10.1139/o70-203 · Cited by 20 · see citing works
Plasma Lipids and Steroid Hormones in Patients with Hypercholesterolaemia or Hyperlipaemia during Dehydroepiandrosterone Sulphate Administration*
Adlebcreutz, H., Kerstell, J., Schauman, K. O., Svanborg, A., & Vihko, R. (1972) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.1972.tb00575.x · Cited by 19 · see citing works
Urinary Steroids in the Measurement of Aging and of Atherosclerosis†
Marmorston, J., Griffith, G. C., Geller, P. J., Fishman, E. L., Welsch, F., & Weiner, J. M. (1975) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1975.tb00894.x · Cited by 17 · see citing works
Measurement of serum levels of dehydroepiandrosterone sulfate: A comparison of radioimmunoassay and enzymatic analysis
Holtzclaw, W. D., & Gordon, G. (1989) · Steroids · doi:10.1016/0039-128x(89)90050-0 · Cited by 15 · see citing works
PATTERN OF PLASMA LEVELS OF CORTISOL, DEHYDROEPIANDROSTERONE AND PREGNENOLONE SULPHATE IN NORMAL SUBJECTS AND IN PATIENTS WITH HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLAEMIA DURING ACTH INFUSION
Boizel, R., PERETTI, E. D., Cathiard, A. M., Halimi, S., BOST, M., Berthezène, F., & Saez, J. M. (1986) · Clinical Endocrinology · doi:10.1111/j.1365-2265.1986.tb01702.x · Cited by 14 · see citing works
STATISTICAL TECHNIQUES OF DIFFERENCE*
Weiner, J. M., & Marmorston, J. (1969) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1969.tb34096.x · Cited by 10 · see citing works
Quenching of hexafluoroacetone phosphorescence by mercury
Lang, N. C., & Kutschke, K. O. (1968) · Canadian Journal of Chemistry · doi:10.1139/v68-170 · Cited by 4 · see citing works
Plasma androsterone, dehydroepiandrosterone and 11-hydroxycorticoids in obesity. Effects of diet and physical activity.
Sonka, J., Gregorova, I., Tomsová, Z., Pavlova, A., Zhirková, A., Rath, R., Urbánek, J., & Josífko, M. (1972) · PubMed · Cited by 4 · see citing works

Flagged first, then by citations

1 of the 49 references couldn’t be matched to a known paper.

Research works printed but not linked: 2

Lopez-S A. Metabolic and endocrine factors in aging. In: Rothschild H. Chapman CF. eds. Risk Factors for Senility. New York: Oxford Univer- sity Press. 1984:210-9.
Pearson TA. Risk Factors for Arteriographically Defined Coronary Ar- tery Disease (PhD dissertation). Baltimore: The Johns Hopkins School of Hygiene and Public Health. Department of Epidemiology. 1983.

Sorted by citations

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Wu, F. C. W., & von Eckardstein, A. (2003) · Endocrine Reviews · doi:10.1210/er.2001-0025 · Cited by 592 · see citing works
DHEA and DHEA‐S: A Review
Kroboth, P. D., Salek, F. S., Pittenger, A. L., Fabian, T. J., & Frye, R. F. (1999) · The Journal of Clinical Pharmacology · doi:10.1177/00912709922007903 · Cited by 523 · see citing works
Relationships Among Plasma Dehydroepiandrosterone Sulfate and CortisolLevels, Symptoms of Dissociation, and Objective Performance in Humans Exposedto Acute Stress
Morgan, C. A., Southwick, S., Hazlett, G., Rasmusson, A., Hoyt, G., Zimolo, Z., & Charney, D. (2004) · Archives of General Psychiatry · doi:10.1001/archpsyc.61.8.819 · Cited by 304 · see citing works
The relationship of natural androgens to coronary heart disease in males: a review
Alexandersen, P., Haarbo, J., & Christiansen, C. (1996) · Atherosclerosis · doi:10.1016/0021-9150(96)05864-9 · Cited by 239 · see citing works
Decreased testosterone and dehydroepiandrosterone sulfate concentrations are associated with increased insulin and glucose concentrations in nondiabetic men.
Haffner, S. M., Valdez, R. A., Mykkänen, L., Stern, M. P., & Katz, M. S. (1994) · Metabolism · doi:10.1016/0026-0495(94)90202-x · Cited by 226 · see citing works
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Pataky, M. W., Young, W. F., & Nair, K. S. (2021) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2020.07.033 · Cited by 207 · see citing works
Endogenous Sex Hormones in Relation to Age, Sex, Lifestyle Factors, and Chronic Diseases in a General Population: The Tromsø Study
Bjørnerem, Å., Straume, B., Midtby, M., Fønnebø, V., Sundsfjord, J., Svartberg, J., Acharya, G., Øian, P., & Berntsen, G. K. R. (2004) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2004-0735 · Cited by 199 · see citing works
Dehydroepiandrosterone Modulates Endothelial Nitric Oxide Synthesis Via Direct Genomic and Nongenomic Mechanisms
Simoncini, T., Mannella, P., Fornari, L., Varone, G. L., Caruso, A., & Genazzani, A. R. (2003) · Endocrinology · doi:10.1210/en.2003-0044 · Cited by 185 · see citing works
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Labrie, F. (2010) · Progress in brain research · doi:10.1016/s0079-6123(10)82004-7 · Cited by 183 · see citing works
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Mazat, L., Lafont, S., Berr, C., Debuire, B., Tessier, J.-F., Dartigues, J., & Baulieu, É.-É. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.121177998 · Cited by 172 · see citing works
The Epidemiology of DHEAS and Cardiovascular Disease
Barrett-Connor, E. L., & Goodman‐Gruen, D. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb17386.x-i1 · Cited by 167 · see citing works
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Svartberg, J. B., von Mühlen, D. G., Mathiesen, E. B., Joakimsen, O., Bønaa, K. H., & Stensland-Bugge, E. (2006) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2006.01637.x · Cited by 163 · see citing works
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BERNINI, G. P., Sgrò, M., Moretti, A., Argenio, G. F., BARLASCINI, C. O., Cristofani, R., & Salvetti, A. (1999) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.84.6.5824 · Cited by 156 · see citing works
Low dehydroepiandrosterone and ischemic heart disease in middle-aged men: prospective results from the Massachusetts Male Aging Study
Feldman, H. A., Johannes, C. B., Araujo, A. B., Mohr, B. A., Longcope, C., & McKinlay, J. B. (2001) · American Journal of Epidemiology · doi:10.1093/aje/153.1.79 · Cited by 141 · see citing works
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Liu, D., & Dillon, J. S. (2004) · Steroids · doi:10.1016/j.steroids.2004.02.004 · Cited by 132 · see citing works
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Araghi‐Niknam, M., Chung, S., Nelson-White, T. M., Eskelson, C. D., & WATSON, R. R. (1996) · Life Sciences · doi:10.1016/0024-3205(96)00396-7 · Cited by 128 · see citing works
Inhibition of accelerated coronary atherosclerosis with dehydroepiandrosterone in the heterotopic rabbit model of cardiac transplantation.
Eich, D., Nestler, J. E., Johnson, D. E., Dworkin, G. H., Ko, D., Wechsler, A. S., & Hess, M. L. (1993) · Circulation · doi:10.1161/01.cir.87.1.261 · Cited by 126 · see citing works
Dehydroepiandrosterone (DHEA)–the Multifunctional Steroid
Regelson, W., & Kalimi, M. (1994) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1994.tb56860.x · Cited by 126 · see citing works
Relationship between androgenic hormones and arterial stiffness, based on longitudinal hormone measurements
Hougaku, H., Fleg, J. L., Najjar, S. S., Lakatta, E. G., Harman, S. M., Blackman, M. R., & Metter, E. J. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00059.2005 · Cited by 123 · see citing works
DHEA-S Levels and Cardiovascular Disease Mortality in Postmenopausal Women: Results from the National Institutes of Health—National Heart, Lung, and Blood Institute (NHLBI)-Sponsored Women’s Ischemia Syndrome Evaluation (WISE)
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Identification of the fetal liver cytochrome CYP3A7 in human endometrium and placenta.
Schuetz, J. D., Kauma, S. W., & Guzelian, P. S. (1993) · Journal of Clinical Investigation · doi:10.1172/jci116607 · Cited by 119 · see citing works
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Mitchell, L. E., Sprecher, D. L., Borecki, I. B., Rice, T., Laskarzewski, P. M., & Rao, D. C. (1994) · Circulation · doi:10.1161/01.cir.89.1.89 · Cited by 116 · see citing works
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Metherall, J. E., Li, H., & Waugh, K. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.5.2634 · Cited by 108 · see citing works
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Lasco, A., Frisina, N., Morabito, N., Gaudio, A., Morini, E., Trifiletti, A., Basile, G., Nicita-Mauro, V., & Cucinotta, D. (2001) · European Journal of Endocrinology · doi:10.1530/eje.0.1450457 · Cited by 103 · see citing works
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WATSON, R. R., Huls, A., Araghinikuam, M., & Chung, S. (1996) · Drugs & Aging · doi:10.2165/00002512-199609040-00005 · Cited by 103 · see citing works
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Jansson, J.-H., Nilsson, T., & Johnson, O. (1998) · Heart · doi:10.1136/hrt.80.4.334 · Cited by 100 · see citing works
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Schneider, R. H., Nidich, S. I., Salerno, J. W., Sharma, H. M., Robinson, C. E., Nidich, R., & Alexander, C. N. (1998) · Psychosomatic Medicine · doi:10.1097/00006842-199801000-00008 · Cited by 95 · see citing works
Prevalence of hyperapobetalipoproteinemia and other lipoprotein phenotypes in men (aged ≤50 years) and women (≤60 years) with coronary artery disease
Kwiterovich, P. O., Coresh, J., & Bachorik, P. S. (1993) · The American Journal of Cardiology · doi:10.1016/0002-9149(93)91002-y · Cited by 91 · see citing works
Association of Dehydroepiandrosterone Sulfate, Body Composition, and Physical Fitness in Independent Community‐Dwelling Older Men and Women
Abbasi, A. A., Duthie, E. H., Sheldahl, L. M., Wilson, C. R., Sasse, E. A., Rudman, I. W., & Mattson, D. E. (1998) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1998.tb01036.x · Cited by 88 · see citing works
Low Dehydroepiandrosterone Sulfate and Heart Disease in Middle-Aged Men: Cross-Sectional Results from the Massachusetts Male Aging Study
Feldman, H. A., Johannes, C. B., McKinlay, J. B., & Longcope, C. (1998) · Annals of Epidemiology · doi:10.1016/s1047-2797(97)00199-3 · Cited by 84 · see citing works
Longitudinal changes in dehydroepiandrosterone concentrations in men and women
Nafziger, A. N., Bowlin, S. J., Jenkins, P. L., & Pearson, T. A. (1998) · Journal of Laboratory and Clinical Medicine · doi:10.1016/s0022-2143(98)90181-0 · Cited by 82 · see citing works
Role of DHEA in cardiovascular diseases
Savineau, J., Marthan, R., & de la Roque, E. D. (2012) · Biochemical Pharmacology · doi:10.1016/j.bcp.2012.12.004 · Cited by 78 · see citing works
CARDIOVASCULAR CONSEQUENCES OF POLYCYSTIC OVARY SYNDROME
Amowitz, L. L., & Sobel, B. E. (1999) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/s0889-8529(05)70079-7 · Cited by 76 · see citing works
Adrenal Androgen Secretion and Biologic Effects
Meikle, A. W., Daynes, R. A., & Araneo, B. A. (1991) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/s0889-8529(18)30274-3 · Cited by 76 · see citing works
Dehydroepiandrosterone and coronary atherosclerosis
HERRINGTON, D. M. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb17387.x-i1 · Cited by 75 · see citing works
Effects of a reduction in circulating insulin by metformin on serum dehydroepiandrosterone sulfate in nondiabetic men
Nestler, J. E., Beer, N., Jakubowicz, D. J., & Beer, R. M. (1994) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.78.3.8126125 · Cited by 74 · see citing works
Dehydroepiandrosterone Inhibits Human Platelet Aggregation in Vitro and in Vivoa
Jesse, R. L., Loesser, K. E., Eich, D., Qian, Y. Z., Hess, M. L., & Nestler, J. E. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb17388.x-i1 · Cited by 71 · see citing works
Sex Hormones and Incident Heart Failure in Men and Postmenopausal Women: The Atherosclerosis Risk in Communities Study
Zhao, D., Güallar, E., Ballantyne, C. M., Post, W. S., Ouyang, P., Vaidya, D. M., Jia, X., Ying, W., Subramanya, V., Ndumele, C. E., et al. (2020) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaa500 · Cited by 69 · see citing works
Relation of Dehydroepiandrosterone and Dehydroepiandrosterone Sulfate with Cardiovascular Disease Risk Factors in Women
Johannes, C. B., Stellato, R. K., Feldman, H. A., Longcope, C., & McKinlay, J. B. (1999) · Journal of Clinical Epidemiology · doi:10.1016/s0895-4356(98)00144-9 · Cited by 67 · see citing works
No Association Between Dehydroepiandrosterone Sulfate and Development of Atherosclerosis in a Prospective Population Study (Bruneck Study)
Kiechl, S. J., Willeit, J., Bonora, E., Schwarz, S., & Xu, Q. (2000) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.20.4.1094 · Cited by 64 · see citing works
Expression and Cyclic Variability of CYP3A4 and CYP3A7 Isoforms in Human Endometrium and Cervix During the Menstrual Cycle
Sarkar, M. A., Vadlamuri, S. V., Ghosh, S., & Glover, D. D. (2003) · Drug Metabolism and Disposition · doi:10.1124/dmd.31.1.1 · Cited by 61 · see citing works
Dehydroepiandrosterone sulfate, diseases and mortality in a general aged population
Tilvis, R. S., Kähönen, M. A. P., & Härkönen, M. (1999) · Aging Clinical and Experimental Research · doi:10.1007/bf03399633 · Cited by 57 · see citing works
Dehydroepiandrosterone (DHEA) and systemic lupus erythematosus
Derksen, R. H. W. M. (1998) · Seminars in Arthritis and Rheumatism · doi:10.1016/s0049-0172(98)80013-9 · Cited by 55 · see citing works
Inhibition of Macrophage Superoxide Generation by Dehydroepiandrosterone
Mohan, P. F., & Jacobson, M. S. (1993) · The American Journal of the Medical Sciences · doi:10.1097/00000441-199307000-00004 · Cited by 55 · see citing works
Effects of replacement dose of dehydroepiandrosterone in men and women of advancing age.
Morales, A. J., Nolan, J. J., Nelson, J. C., & Yen, S. S. (1994) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.78.6.7515387 · Cited by 841 · see citing works
Pharmacology And Therapeutic Effects of Dehydroepiandrosterone In Older Subjects
Legrain, S., & Girard, L. (2003) · Drugs & Aging · doi:10.2165/00002512-200320130-00001 · Cited by 54 · see citing works
Dehydroepiandrosterone Reduces Plasma Plasminogen Activator Inhibitor Type 1 and Tissue Plasminogen Activator Antigen in Men
Beer, N., Jakubowicz, D. J., Matt, D. W., Beer, R. M., & Nestler, J. E. (1996) · The American Journal of the Medical Sciences · doi:10.1097/00000441-199605000-00002 · Cited by 53 · see citing works
Dehydroepiandrosterone protects low density lipoproteins against peroxidation by free radicals produced by γ-radiolysis of ethanol–water mixtures
Khalil, A., Lehoux, J., Wagner, J. R., Lesur, O., Cruz, S., Dupont, É., Jay‐Gerin, J., Wallach, J., & Fülöp, T. (1998) · Atherosclerosis · doi:10.1016/s0021-9150(97)00194-9 · Cited by 53 · see citing works
Dehydroepiandrosterone replacement in healthy men with age-related decline of DHEA-S: effects on fat distribution, insulin sensitivity and lipid metabolism
Jędrzejuk, D., Mędraś, M., Milewicz, A., & Demissie, M. (2003) · The Aging Male · doi:10.1080/tam.6.3.151.156 · Cited by 53 · see citing works
Plasma Dehydroepiandrosterone Sulfate and Cardiovascular Disease Risk in Older Men and Women
Jia, X., Sun, C., Tang, O., Gorlov, I. P., Nambi, V., Virani, S. S., Villareal, D. T., Taffet, G. E., Yu, B., Bressler, J., et al. (2020) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaa518 · Cited by 50 · see citing works
Hyperinsulinaemia and decreased plasma levels of dehydroepiandrosterone sulfate in premenopausal women with coronary heart disease
Slowinska-Srzednicka, J., Malczewska, B., Srzednicki, M., Chotkowska, E., Brzezińska, A., Zgliczyński, W., Ossowski, M., Jeske, W., Zgliczyński, S., & SADOWSKI, Z. (1995) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.1995.tb00871.x · Cited by 50 · see citing works
Metabolism of DHEA by Cytochromes P450 in Rat and Human Liver Microsomal Fractions
Fitzpatrick, J. L., Ripp, S. L., Smith, N. B., Pierce, W. M. J., & Prough, R. A. (2001) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2341 · Cited by 50 · see citing works
Association of insulin resistance with lipid profile, metabolic syndrome, and hormonal aberrations in overweight or obese women with polycystic ovary syndrome.
Ebrahimi-Mameghani, M., Saghafi‐Asl, M., Pirouzpanah, S., Aliasgharzadeh, A., Aliashrafi, S., Rezayi, N., & Sadaghiani, M. M. (2015) · PubMed Central · Cited by 49 · see citing works
Effect of DHEA-sulfate on adiponectin gene expression in adipose tissue from different fat depots in morbidly obese humans
Morante, J. J. H., Milagro, F. I., Gabaldón, J. A., Martínez, J. A., Zamora, S., & Garaulet, M. (2006) · European Journal of Endocrinology · doi:10.1530/eje.1.02256 · Cited by 48 · see citing works
Effects of insulin reduction with benfluorex on serum dehydroepiandrosterone (DHEA), DHEA sulfate, and blood pressure in hypertensive middle-aged and elderly men
Nestler, J. E., Beer, N., Jakubowicz, D. J., Colombo, C., & Beer, R. M. (1995) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.80.2.7852539 · Cited by 48 · see citing works
Disparate effects of weight reduction by diet on serum dehydroepiandrosterone-sulfate levels in obese men and women
Jakubowicz, D. J., Beer, N., Beer, R. M., & Nestler, J. E. (1995) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.80.11.7593454 · Cited by 46 · see citing works
Senescent Decline in Serum Dehydroepiandrosterone Sulfate Concentrations in a Population of Wild Baboons
Sapolsky, R., Vogelman∥, J. H., Orentreich∥, N., & Jeanne Altmann, A. (1993) · Journal of Gerontology · doi:10.1093/geronj/48.5.b196 · Cited by 44 · see citing works
Sex-specific action of insulin to acutely increase the metabolic clearance rate of dehydroepiandrosterone in humans.
Nestler, J. E., & Kahwash, Z. (1994) · Journal of Clinical Investigation · doi:10.1172/jci117487 · Cited by 43 · see citing works
Effects of nitrendipine on glucose tolerance and serum insulin and dehydroepiandrosterone sulfate levels in insulin-resistant obese and hypertensive men
Beer, N., Jakubowicz, D. J., Beer, R. M., Arocha, I., & Nestler, J. E. (1993) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.76.1.8421087 · Cited by 43 · see citing works
Stress, Well-Being and Reproductive Success
Edwards, K. L., Edes, A. N., & Brown, J. L. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-23633-5_5 · Cited by 43 · see citing works
The cincinnati myocardial infarction and hormone family study: Family resemblance for dehydroepiandrosterone sulfate in control and myocardial infarction families
Rice, T., Sprecher, D. L., Borecki, I. B., Mitchell, L. E., Laskarzewski, P. M., & Rao, D. C. (1993) · Metabolism · doi:10.1016/0026-0495(93)90126-9 · Cited by 39 · see citing works
Dehydroepiandrosterone-Mediated Stimulation of Sigma-1 Receptor Activates Akt-eNOS Signaling in the Thoracic Aorta of Ovariectomized Rats with Abdominal Aortic Banding
Bhuiyan, M. S., Tagashira, H., & Fukunaga, K. (2010) · Cardiovascular Therapeutics · doi:10.1111/j.1755-5922.2010.00196.x · Cited by 40 · see citing works
Perceived Stigmatization, Ingroup Pride, and Immune and Endocrine Activity
Ratner, K. G., Halim, M. L., & Amodio, D. M. (2012) · Social Psychological and Personality Science · doi:10.1177/1948550612443715 · Cited by 40 · see citing works
Effect of DHEA on endocrine functions of adipose tissue, the involvement of PPARγ
Karbowska, J., & Kochan, Z. (2005) · Biochemical Pharmacology · doi:10.1016/j.bcp.2005.04.022 · Cited by 38 · see citing works
Dehydroepiandrosterone pretreatment protects rats against the pro-oxidant and necrogenic effects of carbon tetrachloride
Aragno, M., Tamagno, E., Boccuzzi, G., Brignardello, E., Chiarpotto, E., Pizzini, A., & Danni, O. (1993) · Biochemical Pharmacology · doi:10.1016/0006-2952(93)90572-e · Cited by 38 · see citing works
Functional characterization of a human organic anion transporter hOAT4 in placental BeWo cells
Zhou, F., Illsley, N. P., & You, G. (2005) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2005.09.008 · Cited by 36 · see citing works
Are low dehydroepiandrosterone sulphate levels predictive for cardiovascular diseases?
Thijs, L., Fagard, R., Forette, F., Nawrot, T. S., & Staessen, J. A. (2003) · Acta Cardiologica · doi:10.2143/ac.58.5.2005304 · Cited by 35 · see citing works
DHEAS and POMS measures identify cocaine dependence treatment outcome
WILKINS, J. N., Majewska, M., van Gorp, W. G., Li, S. H., Hinken, C., Plotkin, D., & Setoda, D. (2004) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2004.04.006 · Cited by 34 · see citing works
Role of Endogenous Androgen Against Insulin Resistance and Athero-sclerosis in Men with Type 2 Diabetes
Fukui, M., Kitagawa, Y., Ose, H., Hasegawa, G., Yoshikawa, T., & Nakamura, N. (2007) · Current Diabetes Reviews · doi:10.2174/157339907779802094 · Cited by 33 · see citing works
Effect of dehydroepiandrosterone on bone mass, serum lipids, and dimethylbenz(a)anthracene-induced mammary carcinoma in the rat.
Luo, S., Labrie, C., Bélanger, A., & Labrie, F. (1997) · Endocrinology · doi:10.1210/endo.138.8.5345 · Cited by 34 · see citing works
Dehydroepiandrosterone on metabolism and the cardiovascular system in the postmenopausal period
Teixeira, C. J., Veras, K. M. D. A., & Carvalho, C. R. D. O. (2019) · Journal of Molecular Medicine · doi:10.1007/s00109-019-01842-5 · Cited by 32 · see citing works
The Dehydroepiandrosterone And WellNess (DAWN) study: Research design and methods
von Mühlen, D. G., Laughlin, G. A., Kritz‐Silverstein, D. C., & Barrett-Connor, E. L. (2006) · Contemporary Clinical Trials · doi:10.1016/j.cct.2006.04.009 · Cited by 31 · see citing works
Effects of DHEA on metabolic and endocrine functions of adipose tissue
Karbowska, J., & Kochan, Z. (2013) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci-2013-0009 · Cited by 30 · see citing works
Genetics of Serum Dehydroepiandrosterone Sulfate and Its Relationship to Insulin in a Population-Based Cohort of Twin Subjects
Nestler, J. E., Whitfield, J. B., Williams, T. Y., Zhu, G., Condon, J., Kirk, K. M., Heath, A. C., Montgomery, G. W., & Martin, N. G. (2002) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.87.2.8240 · Cited by 30 · see citing works
Effects of gonadal androgens and oestrogens on adrenal androgen levels
Polderman, K. H., Gooren, L. J., & van der Veen, E. A. (1995) · Clinical Endocrinology · doi:10.1111/j.1365-2265.1995.tb02611.x · Cited by 30 · see citing works
The Relationships of Testosterone, Estradiol, Dehydroepiandrosterone-sulfate and Sex Hormone-binding Globulin to Lipid and Glucose Metabolism in Healthy Men
Shono, N., Kumagai, S., Higaki, Y., Nishizumi, M., & Sasaki, H. (1996) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat1994.3.45 · Cited by 30 · see citing works
Research on the Age-Related Changes in the Nitric Oxide Pathway in the Arteries of Rats and the Intervention Effect of Dehydroepiandrosterone
Wu, S., Ruan, Y., Yin, M.-Z., & Lai, W. (2007) · Gerontology · doi:10.1159/000100961 · Cited by 29 · see citing works
Marked attenuation of production of collagen type I from cardiac fibroblasts by dehydroepiandrosterone
Iwasaki, T., Mukasa, K., Yoneda, M., Ito, S., Yamada, Y., Mori, Y., Fujisawa, N., Fujisawa, T., Wada, K., Sekihara, H., et al. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00370.2004 · Cited by 29 · see citing works
Effects of the Long-acting Calcium Channel Blockers, Amlodipine, Manidipine and Cilnidipine on Steroid Hormones and Insulin Resistance in Hypertensive Obese Patients
Ueshiba, H., & Miyachi, Y. (2004) · Internal Medicine · doi:10.2169/internalmedicine.43.561 · Cited by 29 · see citing works
Serum dehydroepiandrosterone sulfate concentration and carotid atherosclerosis in men with type 2 diabetes
Fukui, M., Kitagawa, Y., Nakamura, N., Kadono, M., Yoshida, M., Hirata, C., Wada, K., Hasegawa, G., & Yoshikawa, T. (2005) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2005.01.014 · Cited by 28 · see citing works
Plasma Dehydroepiandrosterone and Risk of Myocardial Infarction in Women
Page, J. H., Ma, J., Rexrode, K. M., Rifai, N., Manson, J. E., & Hankinson, S. E. (2008) · Clinical Chemistry · doi:10.1373/clinchem.2007.099291 · Cited by 25 · see citing works
Prevention of Carbon Tetrachloride-Induced Lipid Peroxidation in Liver Microsomes from Dehydroepiandrosterone-Pretreated Rats
Aragno, M., Tamagno, E., Poli, G., Boccuzzi, G., Brignardello, E., & Danni, O. (1994) · Free Radical Research · doi:10.3109/10715769409056595 · Cited by 24 · see citing works
Effect of Dehydroepiandrosterone on Cyclic‐Guanosine Monophosphate in Men of Advancing Age
Jakubowicz, D. J., Beer, N., & Rengifo, R. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb17395.x-i1 · Cited by 23 · see citing works
Dehydroepiandrosterone sulfate levels in women. Relationships with age, body mass index and insulin levels
Mazza, E., Maccario, M., Ramunni, J., Gauna, C., Bertagna, A., Barberis, A., Patroncini, S., Messina, M., & Ghigo, E. (1999) · Journal of Endocrinological Investigation · doi:10.1007/bf03343629 · Cited by 23 · see citing works
Association of dehydroepiandrosterone-sulfate with endothelial function in young women with polycystic ovary syndrome
Dagre, A. G., Lekakis, J., Mihas, C. C., Protogerou, A. D., Thalassinou, L., Tryfonopoulos, D. J., Douridas, G. N., Papamichael, C. M., & Alevizaki, M. K. (2006) · European Journal of Endocrinology · doi:10.1530/eje.1.02153 · Cited by 22 · see citing works
Association Between Urinary Albumin Excretion and Serum Dehydroepiandrosterone Sulfate Concentration in Male Patients With Type 2 Diabetes
Fukui, M., Kitagawa, Y., Nakamura, N., Kadono, M., Hasegawa, G., & Yoshikawa, T. (2004) · Diabetes Care · doi:10.2337/diacare.27.12.2893 · Cited by 22 · see citing works
A Close Association between Insulin Resistance and Dehydroepiandrosterone Sulfate in Subjects with Essential Hypertension.
Suzuki, M., Kanazawa, A., HASEGAWA, M., Hattori, Y., & Harano, Y. (1999) · Endocrine Journal · doi:10.1507/endocrj.46.521 · Cited by 22 · see citing works
Effects of Prasterone (dehydroepiandrosterone) on markers of cardiovascular risk and bone turnover in premenopausal women with systemic lupus erythematosus: a pilot study
Marder, W., Somers, E. C., Kaplan, M. J., Anderson, M. D., Lewis, E., & McCune, W. J. (2010) · Lupus · doi:10.1177/0961203310371156 · Cited by 21 · see citing works
Changes in Serum Sex Hormone Profiles after Short-term Low-dose Administration of Dehydroepiandrosterone (DHEA) to Young and Elderly Persons
Yamada, Y., Sekihara, H., Omura, M., Yanase, T., Takayanagi, R., Mune, T., Yasuda, K., Ishizuka, T., Ueshiba, H., Miyachi, Y., et al. (2007) · Endocrine Journal · doi:10.1507/endocrj.k05-132 · Cited by 20 · see citing works
Effects of dehydroepiandrosterone (DHEA) supplementation on the lipid profile: A systematic review and dose-response meta-analysis of randomized controlled trials
Qin, Y., Santos, H. O., Khani, V., Tan, S. C., & Zhi, Y. (2020) · Nutrition Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2020.05.015 · Cited by 19 · see citing works
Relationship Between Dehydroepiandrosterone Sulfate and Serum Lipid Levels in Japanese Men
Okamoto, K. (1996) · Journal of Epidemiology · doi:10.2188/jea.6.63 · Cited by 19 · see citing works
Testosterone and Dehydroepiandrosterone Treatment in Ageing Men: Are We All Set?
Walther, A., & Seuffert, J. (2019) · The World Journal of Men s Health · doi:10.5534/wjmh.190006 · Cited by 19 · see citing works
Physiologic benefits of a stress reduction program for healthy middle-aged army officers
Littman, A. B., D, M. F. M., Halperin, P., Lamon‐Fava, S., Drews, F. R., Oleshansky, M. A., Bielenda, C. C., & MacLaughlin, R. A. (1993) · Journal of Psychosomatic Research · doi:10.1016/0022-3999(93)90136-4 · Cited by 18 · see citing works
Dehydroepiandrosterone Sulfate Induces Acute Vasodilation of Porcine Coronary Arteries In Vitro and In Vivo
Hutchison, S. J., Browne, A., Ko, E., Chou, T. M., Zellner, C., Komesaroff, P. A., Chatterjee, K., & Sudhir, K. (2005) · Journal of Cardiovascular Pharmacology · doi:10.1097/01.fjc.0000175434.64412.9d · Cited by 18 · see citing works
Cincinnati myocardial infarction and hormone family study: Family resemblance for testosterone in random and MI families
Rice, T., Sprecher, D. L., Borecki, I. B., Mitchell, L. E., Laskarzewski, P. M., & Rao, D. C. (1993) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320470421 · Cited by 15 · see citing works

Correlation between Serum Dehydroepiandrosterone Sulfate and Coronary Artery Disease in Middle-Aged and Elderly Men
Sumino, H., Ichikawa, S., Kasama, S., Ichikawa, A., Araki, Y., Kanai, H., Itoh, T., Iwasaki, T., Sawada, Y., Takahashi, T., et al. (2016) · The Kitakanto Medical Journal · doi:10.2974/kmj.66.111
Dehydroepiandrosterone and coronary atherosclerosis
HERRINGTON, D. M. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb17387.x-i1 · Cited by 75 · see citing works
Association of serum dehydroepiandrosterone levels with the severity of coronary artery lesions in male patients
Ma, H. (2008) · Zhejiang Journal of Laboratory Medicine
Analysis of serum concentration of dehydroepiandrosterone in male patients with coronary heart disease
Wen-yue, X. (2004) · Chinese Journal of Geriatric Cardiovascular and Cerebrovascular Disease
Dehydroepiandrosterone Sulfate and the Risk of Myocardial Infarction in US Male Physicians: A Prospective Study
Newcomer, L. M., Manson, J. E., Barbieri, R. L., Hennekens, C. H., & Stampfer, M. J. (1994) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a117175 · Cited by 53 · see citing works

Authors: Herrington, D. M., Gordon, G. B., Achuff, S. C., Trejo, J. F., Weisman, H. F., Kwiterovich, P. O., & Pearson, T. A.
Affiliations: Johns Hopkins University (US)
Corresponding author: Herrington, David M.
ORCID: Herrington, David M.
Venue: Journal of the American College of Cardiology
Publisher: Elsevier BV
Published: 1990-10
Volume: 16
Issue: 4
Pages: 862-870
ISSN: 0735-1097 (ISSN-L)
DOI: 10.1016/s0735-1097(10)80334-1
OpenAlex: W2091187697
Cited by: 147
References: 49
Citations by year: 2026: 1 · 2025: 1 · 2023: 1 · 2022: 1 · 2021: 1 · 2020: 4 · 2019: 4 · 2016: 1 · 2015: 2 · 2014: 2 · 2013: 2 · 2012: 3
FWCI: 3.78
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/open-access/userlicense/1.0/ (vor, 8324 d)
Locations: Journal of the American College of Cardiology (publishedVersion)
PubMed (publishedVersion)
Funders: Andrew W. Mellon Foundation
Johns Hopkins University
National Institutes of Health (7t32hl007642-03, 5p01ca044530-13)
U.S. Public Health Service (31497)
National Heart, Lung, and Blood Institute (HL07642)
National Cancer Institute (P01CA44530, CA 44530)
Topics: Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
Keywords: dehydroepiandrosterone sulfate, dehydroepiandrosterone, coronary artery disease, coronary artery stenosis, sex differences, cardiovascular risk factors, middle-aged adults, coronary angiography
MeSH terms: Adult, Coronary Artery Disease, Coronary Vessels, Dehydroepiandrosterone, Female, Humans, Male, Middle Aged, Regression Analysis, Risk Factors, Sex Factors, Stroke Volume, Coronary Angiography, Dehydroepiandrosterone Sulfate

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Plasma dehydroepiandrosterone and dehydroepiandrosterone sulfate in patients undergoing diagnostic coronary angiography

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