Pituitary-adrenocortical function in abdominal obesity of males: Evidence for decreased 21-hydroxylase activity
Certain differences in regional fat distribution might be explicable by subtle hyperactivity of the hypothalamic-pituitary-adrenal (HPA) axis. We examined prospectively PA function relative to abdominal obesity defined by waist-to-hip circumference ratio (WHR) in 71 normotensive men aged 30–55 years...
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Veröffentlicht in: | The Journal of steroid biochemistry and molecular biology 1996-04, Vol.58 (1), p.123-133 |
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description | Certain differences in regional fat distribution might be explicable by subtle hyperactivity of the hypothalamic-pituitary-adrenal (HPA) axis. We examined prospectively PA function relative to abdominal obesity defined by waist-to-hip circumference ratio (WHR) in 71 normotensive men aged 30–55 years. Basal PA activity was assessed by measurements of serum cortisol and plasma corticotropin (ACTH) concentrations during the oral glucose tolerance test (OGTT). Functional activity was examined by dexamethasone suppression and ACTH stimulation tests; responses of 17-hydroxyprogesterone (17-OHP), 11-deoxycortisol (S), cortisol, dehydroepiandrosterone (DHEA), and androstenedione were determined. When the subjects were divided into tertiles for the WHR, the ratio of mean ACTH to mean cortisol during the OGTT was increased (
p < 0.05), and the ratio of urinary cortisol to body-mass index was decreased (
p < 0.01), whilst the net increments of cortisol (
p < 0.05) and 17-OHP (
p < 0.05) from 0 to 60 min, as well as the ratio of 17-OHP to S increments (
p < 0.05) after ACTH were elevated in the highest vs lowest WHR tertile. The ratio of mean ACTH to mean cortisol (
r = 0.495;
p < 0.001) during the OGTT, the ratio of net 17-OHP to S increments (
r = 0.404;
p < 0.001), and the net DHEA (
r = 0.276;
p = 0.020) and 17-OHP (
r = 0.336;
p = 0.005) responses to ACTH at 60 min correlated with WHR. In multivariate analyses the ratio of mean ACTH to cortisol, cortisol response to ACTH, and the ratio of net 17-OHP to S increments were all significant predictors of WHR independent of smoking, physical activity, and BMI explaining 49.0% of the variance in WHR. Thus, abdominal obesity may be associated with decreased activity of adrenal 21-hydroxylase. Either obesity-related functional alteration of 21-hydroxylase activity or the high carrier prevalence of genetic defects of this enzyme may explain these findings. |
doi_str_mv | 10.1016/0960-0760(96)00013-1 |
format | Article |
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p < 0.05), and the ratio of urinary cortisol to body-mass index was decreased (
p < 0.01), whilst the net increments of cortisol (
p < 0.05) and 17-OHP (
p < 0.05) from 0 to 60 min, as well as the ratio of 17-OHP to S increments (
p < 0.05) after ACTH were elevated in the highest vs lowest WHR tertile. The ratio of mean ACTH to mean cortisol (
r = 0.495;
p < 0.001) during the OGTT, the ratio of net 17-OHP to S increments (
r = 0.404;
p < 0.001), and the net DHEA (
r = 0.276;
p = 0.020) and 17-OHP (
r = 0.336;
p = 0.005) responses to ACTH at 60 min correlated with WHR. In multivariate analyses the ratio of mean ACTH to cortisol, cortisol response to ACTH, and the ratio of net 17-OHP to S increments were all significant predictors of WHR independent of smoking, physical activity, and BMI explaining 49.0% of the variance in WHR. Thus, abdominal obesity may be associated with decreased activity of adrenal 21-hydroxylase. Either obesity-related functional alteration of 21-hydroxylase activity or the high carrier prevalence of genetic defects of this enzyme may explain these findings.]]></description><identifier>ISSN: 0960-0760</identifier><identifier>EISSN: 1879-1220</identifier><identifier>DOI: 10.1016/0960-0760(96)00013-1</identifier><identifier>PMID: 8809194</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>17-alpha-Hydroxyprogesterone ; Adrenocorticotropic Hormone - blood ; Adrenocorticotropic Hormone - pharmacology ; Adult ; Androstenedione - blood ; Biological and medical sciences ; Body Constitution ; Cortodoxone - blood ; Dehydroepiandrosterone - blood ; Dexamethasone - pharmacology ; Glucose Tolerance Test ; Humans ; Hydrocortisone - blood ; Hydrocortisone - urine ; Hydroxyprogesterones - blood ; Male ; Medical sciences ; Metabolic diseases ; Middle Aged ; Obesity ; Obesity - blood ; Obesity - enzymology ; Obesity - physiopathology ; Pituitary-Adrenal System - enzymology ; Pituitary-Adrenal System - physiopathology ; Prospective Studies ; Regression Analysis ; Smoking ; Steroid 21-Hydroxylase - metabolism</subject><ispartof>The Journal of steroid biochemistry and molecular biology, 1996-04, Vol.58 (1), p.123-133</ispartof><rights>1996</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-3440ec54179f324329c0451038d201daf4f6f581d71d9966204712de428078f33</citedby><cites>FETCH-LOGICAL-c386t-3440ec54179f324329c0451038d201daf4f6f581d71d9966204712de428078f33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/0960076096000131$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3223329$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8809194$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hautanen, Aarno</creatorcontrib><creatorcontrib>Adlercreutz, Herman</creatorcontrib><title>Pituitary-adrenocortical function in abdominal obesity of males: Evidence for decreased 21-hydroxylase activity</title><title>The Journal of steroid biochemistry and molecular biology</title><addtitle>J Steroid Biochem Mol Biol</addtitle><description><![CDATA[Certain differences in regional fat distribution might be explicable by subtle hyperactivity of the hypothalamic-pituitary-adrenal (HPA) axis. We examined prospectively PA function relative to abdominal obesity defined by waist-to-hip circumference ratio (WHR) in 71 normotensive men aged 30–55 years. Basal PA activity was assessed by measurements of serum cortisol and plasma corticotropin (ACTH) concentrations during the oral glucose tolerance test (OGTT). Functional activity was examined by dexamethasone suppression and ACTH stimulation tests; responses of 17-hydroxyprogesterone (17-OHP), 11-deoxycortisol (S), cortisol, dehydroepiandrosterone (DHEA), and androstenedione were determined. When the subjects were divided into tertiles for the WHR, the ratio of mean ACTH to mean cortisol during the OGTT was increased (
p < 0.05), and the ratio of urinary cortisol to body-mass index was decreased (
p < 0.01), whilst the net increments of cortisol (
p < 0.05) and 17-OHP (
p < 0.05) from 0 to 60 min, as well as the ratio of 17-OHP to S increments (
p < 0.05) after ACTH were elevated in the highest vs lowest WHR tertile. The ratio of mean ACTH to mean cortisol (
r = 0.495;
p < 0.001) during the OGTT, the ratio of net 17-OHP to S increments (
r = 0.404;
p < 0.001), and the net DHEA (
r = 0.276;
p = 0.020) and 17-OHP (
r = 0.336;
p = 0.005) responses to ACTH at 60 min correlated with WHR. In multivariate analyses the ratio of mean ACTH to cortisol, cortisol response to ACTH, and the ratio of net 17-OHP to S increments were all significant predictors of WHR independent of smoking, physical activity, and BMI explaining 49.0% of the variance in WHR. Thus, abdominal obesity may be associated with decreased activity of adrenal 21-hydroxylase. Either obesity-related functional alteration of 21-hydroxylase activity or the high carrier prevalence of genetic defects of this enzyme may explain these findings.]]></description><subject>17-alpha-Hydroxyprogesterone</subject><subject>Adrenocorticotropic Hormone - blood</subject><subject>Adrenocorticotropic Hormone - pharmacology</subject><subject>Adult</subject><subject>Androstenedione - blood</subject><subject>Biological and medical sciences</subject><subject>Body Constitution</subject><subject>Cortodoxone - blood</subject><subject>Dehydroepiandrosterone - blood</subject><subject>Dexamethasone - pharmacology</subject><subject>Glucose Tolerance Test</subject><subject>Humans</subject><subject>Hydrocortisone - blood</subject><subject>Hydrocortisone - urine</subject><subject>Hydroxyprogesterones - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Middle Aged</subject><subject>Obesity</subject><subject>Obesity - blood</subject><subject>Obesity - enzymology</subject><subject>Obesity - physiopathology</subject><subject>Pituitary-Adrenal System - enzymology</subject><subject>Pituitary-Adrenal System - physiopathology</subject><subject>Prospective Studies</subject><subject>Regression Analysis</subject><subject>Smoking</subject><subject>Steroid 21-Hydroxylase - metabolism</subject><issn>0960-0760</issn><issn>1879-1220</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE2LFDEQhoMo67j6DxRykEUPvVYlme6OB2FZ1g9YWA96DpmkgpHuzpp0D86_N80Mc_QUKvV-FA9jrxGuEbD9ALqFBroW3un2PQCgbPAJ22Df6QaFgKdsc5Y8Zy9K-V1FUmJ3wS76HjRqtWHpe5yXONt8aKzPNCWX8hydHXhYJjfHNPE4cbvzaYxT_U07KnE-8BT4aAcqH_ndPnqaHPGQMvfkMtlCngtsfh18Tn8PQ525rVn7anzJngU7FHp1ei_Zz893P26_NvcPX77d3tw3Tvbt3EilgNxWYaeDFEoK7UBtEWTvBaC3QYU2bHv0HXqt21aA6lB4UqKHrg9SXrKrY-5jTn8WKrMZY3E0DHaitBTT9VJKIXQVqqPQ5VRKpmAecxwrD4NgVs5mhWhWiEbXYeVssNrenPKX3Uj-bDqBrfu3p70tlWbIdnKxnGW1utav7Z-OMqos9pGyKS6uNH3M5GbjU_z_Hf8AQymYxw</recordid><startdate>19960401</startdate><enddate>19960401</enddate><creator>Hautanen, Aarno</creator><creator>Adlercreutz, Herman</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19960401</creationdate><title>Pituitary-adrenocortical function in abdominal obesity of males: Evidence for decreased 21-hydroxylase activity</title><author>Hautanen, Aarno ; Adlercreutz, Herman</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-3440ec54179f324329c0451038d201daf4f6f581d71d9966204712de428078f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>17-alpha-Hydroxyprogesterone</topic><topic>Adrenocorticotropic Hormone - blood</topic><topic>Adrenocorticotropic Hormone - pharmacology</topic><topic>Adult</topic><topic>Androstenedione - blood</topic><topic>Biological and medical sciences</topic><topic>Body Constitution</topic><topic>Cortodoxone - blood</topic><topic>Dehydroepiandrosterone - blood</topic><topic>Dexamethasone - pharmacology</topic><topic>Glucose Tolerance Test</topic><topic>Humans</topic><topic>Hydrocortisone - blood</topic><topic>Hydrocortisone - urine</topic><topic>Hydroxyprogesterones - blood</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Middle Aged</topic><topic>Obesity</topic><topic>Obesity - blood</topic><topic>Obesity - enzymology</topic><topic>Obesity - physiopathology</topic><topic>Pituitary-Adrenal System - enzymology</topic><topic>Pituitary-Adrenal System - physiopathology</topic><topic>Prospective Studies</topic><topic>Regression Analysis</topic><topic>Smoking</topic><topic>Steroid 21-Hydroxylase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hautanen, Aarno</creatorcontrib><creatorcontrib>Adlercreutz, Herman</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of steroid biochemistry and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hautanen, Aarno</au><au>Adlercreutz, Herman</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pituitary-adrenocortical function in abdominal obesity of males: Evidence for decreased 21-hydroxylase activity</atitle><jtitle>The Journal of steroid biochemistry and molecular biology</jtitle><addtitle>J Steroid Biochem Mol Biol</addtitle><date>1996-04-01</date><risdate>1996</risdate><volume>58</volume><issue>1</issue><spage>123</spage><epage>133</epage><pages>123-133</pages><issn>0960-0760</issn><eissn>1879-1220</eissn><abstract><![CDATA[Certain differences in regional fat distribution might be explicable by subtle hyperactivity of the hypothalamic-pituitary-adrenal (HPA) axis. We examined prospectively PA function relative to abdominal obesity defined by waist-to-hip circumference ratio (WHR) in 71 normotensive men aged 30–55 years. Basal PA activity was assessed by measurements of serum cortisol and plasma corticotropin (ACTH) concentrations during the oral glucose tolerance test (OGTT). Functional activity was examined by dexamethasone suppression and ACTH stimulation tests; responses of 17-hydroxyprogesterone (17-OHP), 11-deoxycortisol (S), cortisol, dehydroepiandrosterone (DHEA), and androstenedione were determined. When the subjects were divided into tertiles for the WHR, the ratio of mean ACTH to mean cortisol during the OGTT was increased (
p < 0.05), and the ratio of urinary cortisol to body-mass index was decreased (
p < 0.01), whilst the net increments of cortisol (
p < 0.05) and 17-OHP (
p < 0.05) from 0 to 60 min, as well as the ratio of 17-OHP to S increments (
p < 0.05) after ACTH were elevated in the highest vs lowest WHR tertile. The ratio of mean ACTH to mean cortisol (
r = 0.495;
p < 0.001) during the OGTT, the ratio of net 17-OHP to S increments (
r = 0.404;
p < 0.001), and the net DHEA (
r = 0.276;
p = 0.020) and 17-OHP (
r = 0.336;
p = 0.005) responses to ACTH at 60 min correlated with WHR. In multivariate analyses the ratio of mean ACTH to cortisol, cortisol response to ACTH, and the ratio of net 17-OHP to S increments were all significant predictors of WHR independent of smoking, physical activity, and BMI explaining 49.0% of the variance in WHR. Thus, abdominal obesity may be associated with decreased activity of adrenal 21-hydroxylase. Either obesity-related functional alteration of 21-hydroxylase activity or the high carrier prevalence of genetic defects of this enzyme may explain these findings.]]></abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>8809194</pmid><doi>10.1016/0960-0760(96)00013-1</doi><tpages>11</tpages></addata></record> |
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subjects | 17-alpha-Hydroxyprogesterone Adrenocorticotropic Hormone - blood Adrenocorticotropic Hormone - pharmacology Adult Androstenedione - blood Biological and medical sciences Body Constitution Cortodoxone - blood Dehydroepiandrosterone - blood Dexamethasone - pharmacology Glucose Tolerance Test Humans Hydrocortisone - blood Hydrocortisone - urine Hydroxyprogesterones - blood Male Medical sciences Metabolic diseases Middle Aged Obesity Obesity - blood Obesity - enzymology Obesity - physiopathology Pituitary-Adrenal System - enzymology Pituitary-Adrenal System - physiopathology Prospective Studies Regression Analysis Smoking Steroid 21-Hydroxylase - metabolism |
title | Pituitary-adrenocortical function in abdominal obesity of males: Evidence for decreased 21-hydroxylase activity |
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