Urinary free cortisol and androgens in the population-Hormone interactions and the relationship with body composition and bone status.

Abstract:

OBJECTIVE:Abnormal secretion of thyroid hormones, growth hormone, cortisol and androgens influences body composition. We hypothesised that higher cortisol excretion, in combination with higher androgen and IGF-I concentrations, had a synergistic, favourable effect on body mass and bone. DESIGN, PATIENTS AND METHODS:This was a cross-sectional study on a population sample of 290 women and 93men. The mean age was 65.4±7.2yearsinwomen and 59.7±10.0yearsinmen. Body composition was assessed with bioimpedance, and skeletal health with calcaneal quantitative ultrasound and fracture rate. The influence of urinary free cortisol (UFC), serum DHEAs (women), testosterone (men), free T4andIGF-I on the outcome was studied with regression analyses adjusted for age and body mass index. RESULTS:In women, higher concentrations of UFC, DHEAs, IGF-I and lower free T4, were associated with higher fat-free mass. Only a higher UFC concentration was associated with favourable calcaneal measurements. In men, higher testosterone was associated with higher fat-free mass and lower fat mass. Higher IGF-I concentration, but not UFC, was independently associated with higher fat-free mass in men. Interaction analyses did not reveal any additive effects of hormones on body composition or bone in either sex. In both men and women, only age was associated with osteoporotic fractures. CONCLUSION:Serum concentrations of androgens together with IGF-I were positively associated with body composition in both sexes. Urinary cortisol was positively associated with fat-free mass and bone status in women only. Increasing age, but not hormones, was the major determinant of osteoporotic fractures in this population sample.

journal_name

Steroids

journal_title

Steroids

authors

Ragnarsson O,Trimpou P,Oleröd G,Landin-Wilhelmsen K

doi

10.1016/j.steroids.2016.09.006

subject

Has Abstract

pub_date

2016-11-01 00:00:00

pages

154-159

eissn

0039-128X

issn

1878-5867

pii

S0039-128X(16)30121-0

journal_volume

115

pub_type

杂志文章

相关文献

STEROIDS文献大全
  • An approach towards the development of progesterone antagonists: synthesis of 7 alpha/7 beta-aryl androstene derivatives.

    abstract::Synthesis of 3 beta,17 beta-dihydroxy-7 alpha/7 beta-(4-hydroxyphenyl)-androst-5-ene 3,17-diacetate (4 and 5, R = H) and 3 beta,17 beta-dihydroxy-7 alpha/7 beta-(4-methoxyphenyl)-androst-5-ene 3,17-diacetate (4 and 5, R = Me) have been carried out by Friedel-Crafts reaction on 3 beta,7,17 beta-trihydroxy-androst-5-ene...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/0039-128x(95)00007-d

    authors: Negi AS,Dwivedy I,Roy R,Ray S

    更新日期:1995-06-01 00:00:00

  • Effects of mifepristone on endometrial receptivity.

    abstract::At the development of receptivity the endometrium undergoes specific changes. Several factors have been suggested as markers of endometrial receptivity. A common feature for most of these factors is that they are directly, or indirectly, regulated by progesterone. The effect of various doses and regimens of mifepristo...

    journal_title:Steroids

    pub_type: 杂志文章,评审

    doi:10.1016/s0039-128x(03)00131-4

    authors: Danielsson KG,Marions L,Bygdeman M

    更新日期:2003-11-01 00:00:00

  • Long-acting contraceptive agents: bile acid esters of norethisterone.

    abstract::The synthesis of the esters of norethisterone (17 alpha-ethynyl-17 beta-hydroxyestr-4-en-3-one) with three bile acids and of the cholesteryl carbonate of norethisterone are described. :This article reports the synthesis of the esters of norethisterone (17 alpha-ethynl-17beta-hydroxyestr-4-en-3-one) with 3 bile acids ...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/0039-128x(83)90103-4

    authors: Herz JE,Sandoval J

    更新日期:1983-03-01 00:00:00

  • Trilostane, an orally active inhibitor of steroid biosynthesis.

    abstract::Trilostane is a competitive inhibitor of 3beta-hydroxysteroid dehydrogenase. In vitro, the drug inhibits conversion of pregnenolone to progesterone but does not alter conversion of cholesterol to pregnenolone nor progesterone to corticoid hormones. When given orally to rats, trilostane inhibits corticosterone and aldo...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/0039-128x(78)90010-7

    authors: Potts GO,Creange JE,Hardomg HR,Schane HP

    更新日期:1978-09-01 00:00:00

  • Steroids and genes related to steroid biosynthesis in the female giant freshwater prawn, Macrobrachium rosenbergii.

    abstract::The giant freshwater prawn, Macrobrachium rosenbergii, is important to many Asian countries due to its high economic value as an aquaculture product. With demand increasing, there is requirement for a better understanding of the biosynthetic components that regulate its growth and reproduction, including steroids, in ...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2016.01.006

    authors: Thongbuakaew T,Siangcham T,Suwansa-ard S,Elizur A,Cummins SF,Sobhon P,Sretarugsa P

    更新日期:2016-03-01 00:00:00

  • Estrogen and growth factor receptor interactions in human breast and non-small cell lung cancer cells.

    abstract::Extranuclear estrogen receptors may mediate rapid effects of estradiol that communicate with nuclear receptors and contribute to proliferation of human cancers bearing these signaling proteins. To assess these growth-promoting pathways, we undertook controlled homogenization and fractionation of NIH-H23 non-small cell...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2005.02.017

    authors: Pietras RJ,Márquez DC,Chen HW,Tsai E,Weinberg O,Fishbein M

    更新日期:2005-05-01 00:00:00

  • Androgen receptor isoforms AR-A and AR-B display functional differences in cultured human bone cells and genital skin fibroblasts.

    abstract::Two isoforms of the androgen receptor (AR-A and AR-B), differing by a lack of the first 187 amino acids in the NH2-terminal transactivation domain of AR-A, are expressed in connective tissue and bone. Transient transfections of normal human osteoblastic cells (HOB) and of genital skin fibroblasts defective in AR (GSF-...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2003.08.016

    authors: Liegibel UM,Sommer U,Boercsoek I,Hilscher U,Bierhaus A,Schweikert HU,Nawroth P,Kasperk C

    更新日期:2003-12-01 00:00:00

  • Synthesis of multiply deuterated 3- and 21-monosulfates of allo-tetrahydrocorticosteroids as internal standards for mass spectrometry.

    abstract::The accurate analysis of trace components in complex biological matrices requires the use of reliable internal standards. For liquid chromatography/mass spectrometry analysis, the stable isotope-labeled analogues of the analyte molecules are the most appropriate internal standards. In this paper the synthesis of the 3...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2012.08.007

    authors: Mitamura K,Mabuchi T,Nagae K,Nakajima M,Matsumoto R,Fujioka S,Sato K,Satoh née Okihara R,Iida T,Ogawa S,Hofmann AF,Ikegawa S

    更新日期:2012-11-01 00:00:00

  • The measurement of 4-androstene-3, 11, 17-trione (11-oxo-androstenedione) by radioimmunoassay in human plasma.

    abstract::A radioimmunoassay (RIA) method is described for the determination of 4-androstene-3, 11, 17-trione (11-oxo-androstenedione) in human plasma. 4-androstene-3, 11, 17-trione 3-(0-carboxymethyl) oxime-bovine serum albumin conjugate was used to generate highly specific antiserum in rabbits. Cross reactivities of several o...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/s0039-128x(84)80013-6

    authors: Schlaghecke R,Kley HK,Krüskemper HL

    更新日期:1984-07-01 00:00:00

  • In human T cells mifepristone antagonizes glucocorticoid non-genomic rapid responses in terms of Na(+)/H(+)-exchange 1 activity, but not ezrin/radixin/moesin phosphorylation.

    abstract::Glucocorticoids (GCs) and progesterone have been employed as immunosuppressive agents during pregnancy for many years. Intracellular acidification by GCs is due to a rapid non-genomic inhibition of membrane Na(+)/H(+)-exchange 1 (NHE1) activity and is followed by immunosuppression of PHA-stimulated proliferation. NHE1...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2016.01.004

    authors: Chien EJ,Hsu CH,Chang VH,Lin EP,Kuo TP,Chien CH,Lin HY

    更新日期:2016-07-01 00:00:00

  • The 1,25D3-MARRS protein: contribution to steroid stimulated calcium uptake in chicks and rats.

    abstract::There are currently two main candidates for the membrane receptor for 1,25(OH)2D3: the 1,25D3-MARRS protein/ERp57; and the classical VDR. The 1,25D3-MARRS protein is essential for hormone-stimulated phosphate and calcium uptake in chick intestinal cells, whereas the VDR is not. The 1,25D3-MARRS protein also shows a hi...

    journal_title:Steroids

    pub_type: 杂志文章,评审

    doi:10.1016/j.steroids.2005.02.005

    authors: Nemere I

    更新日期:2005-05-01 00:00:00

  • Synthesis and spectroscopic studies of Ru(II) complexes of steroidal thiosemicarbazones by multi step reaction: As anti-bacterial agents.

    abstract::Ru(II) steroidal metal complexes were synthesized by the reaction of dichlorodicarbonyl ruthenium(II) [Ru(CO)2Cl2]n with Steroidal thiosemicarbazones. Coordination via the thionic sulfur and the azomethine nitrogen atom of the thiosemicarbazone to the Ru(II) metal. Steroidal thiosemicarbazone derivatives were obtained...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2017.05.001

    authors: Khan SA,Asiri AM

    更新日期:2017-08-01 00:00:00

  • In vivo androgen retention in mouse kidney.

    abstract::The in vivo retention of 3-H-testosterone, dihydrotestosterone (DHT), 3alpha-androstanediol (3alpha-DIOL), 3beta-DIOL, androstenedione, progesterone and cortisol by renal cytoplasm and nuclei of male and female mice was studied. Testosterone was the major androgen isolated from cytoplasm and nuclei following testoster...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/s0039-128x(75)80011-0

    authors: Bullock LP,Bardin CW

    更新日期:1975-01-01 00:00:00

  • Induction of vaginal mucification in rats with testosterone and 17beta-hydroxy-5alpha-androstan-3-one.

    abstract::Based on histological criteria, Kingsley and Bogdanove (3) reported that the benzoate ester of 17beta-hydroxy-5alpha-androstan-3-one (5alpha-DHT), unlike testosterone propionate, is unable to induce vaginal mucification when given subcutaneously to rats. In contrats, Kennedy (4) found in estrogen-pretreated rats that ...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/0039-128x(76)90061-1

    authors: Kennedy TG,Armstrong DT

    更新日期:1976-03-01 00:00:00

  • Gene expression in endometrial cancer cells (Ishikawa) after short time high dose exposure to progesterone.

    abstract::The potent antiproliferative effect of progestins has been utilized in clinical regimens for treatment of endometrial proliferative disorders. The progestin infiltrated intrauterine device used as therapy for endometrial carcinoma as well as endometrial hyperplasia yields a hundred-fold increase of local progestin con...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2007.09.010

    authors: Paulssen RH,Moe B,Grønaas H,Orbo A

    更新日期:2008-01-01 00:00:00

  • Isolation fo 15alpha-hydroxypregnenolone and 15alpha-hydroxydehydroisoandrosterone from human pregnancy urine.

    abstract::15alpha-Hydroxydehydroisoandrosterone and 15alpha-hydroxypregnenolone were isolated from hydrolyzed extracts of human late pregnancy urine and identified by means of the isotope dilution technique. In two separate determinations the excretion rate of 15alpha-hydroxydehydroisoandrosterone was found to be 1.7 and 3.2 mi...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/s0039-128x(78)80002-6

    authors: Stanczyk FZ,Stern M,Solomon S

    更新日期:1978-05-01 00:00:00

  • Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids.

    abstract::A new synthesis of both epimeric forms of 26-cholestanoic acids and 26-alcohols containing a 3beta-hydroxy-Delta(5)- or a Delta(4)-3-keto-functionality in ring A is described starting from stigmasterol or (20S)-3beta-acetoxy-pregn-5-en-20-carboxylic acid. The obtained compounds are useful as standards for studies of c...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2005.02.014

    authors: Khripach VA,Zhabinskii VN,Konstantinova OV,Khripach NB,Antonchick AV,Antonchick AP,Schneider B

    更新日期:2005-07-01 00:00:00

  • Chromatographic patterns of urinary ethynyl estrogen metabolites in various populations.

    abstract::Radioactive mestranol (ME) and/or ethynylestradiol (EE) were administered to women in Nigeria, Sri Lanka, and the USA, and the types and patterns of radioactive urinary conjugates examined by Sephadex LH-20 chromatography. There are no differences in the total excretion of urinary radioactivity over 3 days. Consistent...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/0039-128x(80)90001-x

    authors: Williams MC,Goldzieher JW

    更新日期:1980-09-01 00:00:00

  • Antigen-specific T cell functions are suppressed over the estrogen-dendritic cell-indoleamine 2,3-dioxygenase axis.

    abstract::Estrogen results in the suppression of experimental allergic encephalomyelitis (EAE), a frequently used experimental animal model of multiple sclerosis (MS). The mechanism by which estrogen acts in diseases with an autoimmune background is less clear. Here, we used splenic dendritic cells (DC) from the Lewis rats EAE ...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2004.05.019

    authors: Xiao BG,Liu X,Link H

    更新日期:2004-09-01 00:00:00

  • The effects of dehydroepiandrosterone (DHEA) supplementation on body composition and blood pressure: A meta-analysis of randomized clinical trials.

    abstract::Dehydroepiandrosterone (DHEA) supplementation has been anecdotally considered as a tool to improve body composition and health status. We aimed to verify the impact of DHEA supplementation on traditional measurements of body composition and blood pressure (BP) due to their clinical applicability. A meta-analysis of ra...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2020.108710

    authors: Wang F,He Y,O Santos H,Sathian B,C Price J,Diao J

    更新日期:2020-11-01 00:00:00

  • Occurrence and seasonal variation of 19-norcholest-4-en-3-one and 3 beta-monohydroxy sterols in the Californian gorgonian, Muricea californica.

    abstract::The first natural occurrence of 19-norcholestenone is reported, together with 17 sterols and one other delta 4-3-ketone in the extracts of the Californian gorgonian, Muricea californica (Aurivillius). Six additional demethyl sterols and five additional 4-monomethyl sterols which remain unidentified were also detected....

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/0039-128x(83)90093-4

    authors: Popov S,Carlson RM,Djerassi C

    更新日期:1983-04-01 00:00:00

  • Formation and isolation of delta 5-3-ketosteroids using a purified rat liver alcohol dehydrogenase.

    abstract::3 beta-Hydroxy-5-androsten-17-one is converted to 5-androstene-3, 17-dione by rat liver alcohol dehydrogenase (ADH). We have reported on the purity of the enzyme which is eluted with pyrazole as a single homogeneous protein using an AMP-agarose affinity column. Rat liver ADH can oxidize hydroxyl groups not only at 3 b...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/0039-128x(82)90079-4

    authors: Knutson VP,Ungar F

    更新日期:1982-11-01 00:00:00

  • Expression of estrogen receptor alpha in developing brain, ovary and shell gland of Gallus gallus domesticus: Impact of stress and estrogen.

    abstract::Estrogen plays a central role in the control of reproductive behaviour and in the regulation of neuroendocrine system. To elucidate the mechanism by which it controls the stress-modulated functions, it is important to understand how estrogenic effects are mediated. The distribution of estrogen receptor alpha (ERα) pro...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2019.03.002

    authors: Niranjan MK,Srivastava R

    更新日期:2019-06-01 00:00:00

  • The synthesis and in vitro activity of some delta 7,9(11)-lanostadienes.

    abstract::The synthesis of delta 7,9(11)-lanostadiene derivatives functionalized at C(32) starting from 3 beta-acetoxy-7 alpha,32-epoxylanostan-11-one has been presented. The delta 7,9(11) moiety was efficiently introduced in three steps in 71% yield by the regioselective abstraction of allylic 8 beta hydrogen. The formyl group...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/s0039-128x(97)00075-5

    authors: Solaja BA,Dermanović M,Lim DM,Paik YK,Tinant B,Declerq JP

    更新日期:1997-11-01 00:00:00

  • Binding specificity of medroxyprogesterone acetate and proligestone for the progesterone and glucocorticoid receptor in the dog.

    abstract::The use of the synthetic progestin medroxyprogesterone acetate (MPA) for estrus prevention in the dog can result in overproduction of growth hormone, suppression of plasma glucocorticoid levels, and the induction of mammary tumors. Proligestone (PROL) was claimed to be devoid of these unwanted side effects. In the pre...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/0039-128x(95)00216-d

    authors: Selman PJ,Wolfswinkel J,Mol JA

    更新日期:1996-03-01 00:00:00

  • Progesterone inhibition of voltage-gated calcium channels is a potential neuroprotective mechanism against excitotoxicity.

    abstract::The therapeutic use of progesterone following traumatic brain injury has recently entered phase III clinical trials as a means of neuroprotection. Although it has been hypothesized that progesterone protects against calcium overload following excitotoxic shock, the exact mechanisms underlying the beneficial effects of...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2011.02.013

    authors: Luoma JI,Kelley BG,Mermelstein PG

    更新日期:2011-08-01 00:00:00

  • Phytoestrogens as inhibitors of fungal 17beta-hydroxysteroid dehydrogenase.

    abstract::Different phytoestrogens were tested as inhibitors of 17beta-hydroxysteroid dehydrogenase from the fungus Cochliobolus lunatus (17beta-HSDcl), a member of the short-chain dehydrogenase/reductase superfamily. Phytoestrogens inhibited the oxidation of 100microM 17beta-hydroxyestra-4-en-3-one and the reduction of 100micr...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2005.02.022

    authors: Kristan K,Krajnc K,Konc J,Gobec S,Stojan J,Lanisnik Rizner T

    更新日期:2005-08-01 00:00:00

  • Sterols of the cultured euglenid Eutreptia viridis: a novel delta 23-unsaturated sterol.

    abstract::The sterol mixture isolated from the marine alga Eutreptia viridis consists mainly of delta 5,7-dienes which account for 80% of the free sterols. Eighteen different sterols were detected, including a novel sterol with the rare delta 23-unsaturation, viz. 24-ethylcholesta-5,7,23Z-trien-3 beta-o1. ...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/0039-128x(82)90018-6

    authors: Zielinski J,Kokke WC,Fenical W,Djerassi C

    更新日期:1982-10-01 00:00:00

  • Glucocorticosteroids as antioxidants in treatment of asthma and COPD. New application for an old medication?

    abstract::Inhaled corticosteroids (ICS) are the standard of care in asthma and are widely used in the treatment of patients with COPD. The influence of steroids on inflammatory processes has long been established since glucocorticoids and their receptor belong to the regulatory network involved in inhibition of several inflamma...

    journal_title:Steroids

    pub_type: 杂志文章,评审

    doi:10.1016/j.steroids.2006.10.007

    authors: Sadowska AM,Klebe B,Germonpré P,De Backer WA

    更新日期:2007-01-01 00:00:00

  • Characterization of ligands for thyroid receptor subtypes and their interactions with co-regulators.

    abstract::Thyroid hormone receptors (TRs) are nuclear receptors that are activated by thyroid hormone ligands and co-regulator proteins. Two receptor subtypes, TRalpha and TRbeta, have been suggested to play a role in numerous physiological functions. However, specificity of receptor subtype function and co-regulator interactio...

    journal_title:Steroids

    pub_type: 杂志文章

    doi:10.1016/j.steroids.2008.11.014

    authors: Koury EJ,Pawlyk AC,Berrodin TJ,Smolenski CL,Nagpal S,Deecher DC

    更新日期:2009-02-01 00:00:00