Plasma variation of corticosteroid-binding globulin and sex hormone-binding globulin

Sex hormone-binding globulin (SHBG) and corticosteroid-binding globulin (CBG) circulate in plasma and bind their cognate ligands with high affinity, offering a steroid delivery system to target tissues by a variety of mechanisms. Analysis of these steroid-binding proteins is gaining importance in th...

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Published inHormone and metabolic research Vol. 38; no. 4; p. 241
Main Authors Lewis, J G, Möpert, B, Shand, B I, Doogue, M P, Soule, S G, Frampton, C M, Elder, P A
Format Journal Article
LanguageEnglish
Published Germany 01.04.2006
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Abstract Sex hormone-binding globulin (SHBG) and corticosteroid-binding globulin (CBG) circulate in plasma and bind their cognate ligands with high affinity, offering a steroid delivery system to target tissues by a variety of mechanisms. Analysis of these steroid-binding proteins is gaining importance in the clinical setting, although more information is warranted on their diurnal and biological variation. This study shows that plasma SHBG (in normal subjects) exhibits little diurnal or biological variation over the 30 day period studied, in contrast to CBG, where plasma levels peak in the early afternoon. This leads to attenuation of the diurnal free cortisol level rhythm compared to total cortisol. We also show that plasma CBG is significantly lower in male subjects with the metabolic syndrome compared to age-matched lean counterparts, and may therefore act as a surrogate marker of insulin resistance. The consequence of lower levels of CBG in these obese male subjects is reflected by higher levels of circulating free cortisol, potentially offering a more favourable environment for adipogenesis.
AbstractList Sex hormone-binding globulin (SHBG) and corticosteroid-binding globulin (CBG) circulate in plasma and bind their cognate ligands with high affinity, offering a steroid delivery system to target tissues by a variety of mechanisms. Analysis of these steroid-binding proteins is gaining importance in the clinical setting, although more information is warranted on their diurnal and biological variation. This study shows that plasma SHBG (in normal subjects) exhibits little diurnal or biological variation over the 30 day period studied, in contrast to CBG, where plasma levels peak in the early afternoon. This leads to attenuation of the diurnal free cortisol level rhythm compared to total cortisol. We also show that plasma CBG is significantly lower in male subjects with the metabolic syndrome compared to age-matched lean counterparts, and may therefore act as a surrogate marker of insulin resistance. The consequence of lower levels of CBG in these obese male subjects is reflected by higher levels of circulating free cortisol, potentially offering a more favourable environment for adipogenesis.
Author Lewis, J G
Frampton, C M
Shand, B I
Elder, P A
Möpert, B
Doogue, M P
Soule, S G
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/16700005$$D View this record in MEDLINE/PubMed
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Snippet Sex hormone-binding globulin (SHBG) and corticosteroid-binding globulin (CBG) circulate in plasma and bind their cognate ligands with high affinity, offering a...
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StartPage 241
SubjectTerms Adult
Circadian Rhythm
Cohort Studies
Female
Humans
Hydrocortisone - blood
Male
Metabolic Syndrome - blood
Middle Aged
Sex Hormone-Binding Globulin - metabolism
Transcortin - metabolism
Title Plasma variation of corticosteroid-binding globulin and sex hormone-binding globulin
URI https://www.ncbi.nlm.nih.gov/pubmed/16700005
Volume 38
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