Development of plasma 21-deoxycortisol radioimmunoassay and application to the diagnosis of patients with 21-hydroxylase deficiency
Specific 21-deoxycortisol (21-DF) antiserum was raised in New Zealand white rabbits using a 21-DF-3,20-oxime-bovine serum albumin complex. Plasma radioimmunoassay of 21-DF was developed and used together with a radioimmunoassay of 17-hydroxyprogesterone (17-OH-P) for diagnosis of patients with 21-hy...
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Veröffentlicht in: | Journal of steroid biochemistry 1984-01, Vol.21 (2), p.185-191 |
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container_title | Journal of steroid biochemistry |
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creator | Milewicz, A. Vecsei, P. Korth-Schütz, S. Haack, D. Rösler, A. Lichtwald, K. Lewicka, S. Mittelstaedt, G.v. |
description | Specific 21-deoxycortisol (21-DF) antiserum was raised in New Zealand white rabbits using a 21-DF-3,20-oxime-bovine serum albumin complex. Plasma radioimmunoassay of 21-DF was developed and used together with a radioimmunoassay of 17-hydroxyprogesterone (17-OH-P) for diagnosis of patients with 21-hydroxylase deficiency of congenital and postpubertal forms. The assays were performed in plasma extracts after isolation by paper chromatography. The response of plasma 21-DF and 17-OH-P to i.v. ACTH (25 IU) was studied in 15 adult controls and compared to 8 women with the late onset form of 21-hydroxylase deficiency and 23 women with idiopathic hirsutism. Normal 21-DF values for women were 6.9 ± 3.6ng/dl and for men 9.71 ± 2.73 ng/dl. Newborn children (age: 3–10 days) had a value of 8.3 ± 4.8 ng/dl. These values are definitely lower than the lowest value ever published. This is possibly due to the specificity of the antibody. During the menstrual cycle the 21-DF values did not change. The baseline and post-stimulated concentrations of hormone were similar in controls and women with hirsutism but were significantly higher in women with the late onset form of 21-hydroxylase deficiency. In the congenital form of 21-hydroxylase deficiency the 21-DF values (baseline) were high. In general, the 21-DF and 17-OH-P values have shown parallel changes. However, one case of 21-hydroxylase deficiency with elevated 21-DF but normal 17-OH-P was observed. The use of 21-DF for the diagnosis of 21-hydroxylase deficiency is suggested. |
doi_str_mv | 10.1016/0022-4731(84)90382-0 |
format | Article |
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Plasma radioimmunoassay of 21-DF was developed and used together with a radioimmunoassay of 17-hydroxyprogesterone (17-OH-P) for diagnosis of patients with 21-hydroxylase deficiency of congenital and postpubertal forms. The assays were performed in plasma extracts after isolation by paper chromatography. The response of plasma 21-DF and 17-OH-P to i.v. ACTH (25 IU) was studied in 15 adult controls and compared to 8 women with the late onset form of 21-hydroxylase deficiency and 23 women with idiopathic hirsutism. Normal 21-DF values for women were 6.9 ± 3.6ng/dl and for men 9.71 ± 2.73 ng/dl. Newborn children (age: 3–10 days) had a value of 8.3 ± 4.8 ng/dl. These values are definitely lower than the lowest value ever published. This is possibly due to the specificity of the antibody. During the menstrual cycle the 21-DF values did not change. The baseline and post-stimulated concentrations of hormone were similar in controls and women with hirsutism but were significantly higher in women with the late onset form of 21-hydroxylase deficiency. In the congenital form of 21-hydroxylase deficiency the 21-DF values (baseline) were high. In general, the 21-DF and 17-OH-P values have shown parallel changes. However, one case of 21-hydroxylase deficiency with elevated 21-DF but normal 17-OH-P was observed. The use of 21-DF for the diagnosis of 21-hydroxylase deficiency is suggested.</description><identifier>ISSN: 0022-4731</identifier><identifier>DOI: 10.1016/0022-4731(84)90382-0</identifier><identifier>PMID: 6090811</identifier><identifier>CODEN: JSTBBK</identifier><language>eng</language><publisher>Oxford: Elsevier B.V</publisher><subject>17-alpha-Hydroxyprogesterone ; 17-Hydroxycorticosteroids - blood ; Adolescent ; Adrenals. Adrenal axis. Renin-angiotensin system (diseases) ; Adrenocorticotropic Hormone ; Adult ; Biological and medical sciences ; Child ; Child, Preschool ; Clinical Laboratory Techniques ; Cortodoxone - blood ; Endocrinopathies ; Female ; Hirsutism - blood ; Humans ; Hydroxyprogesterones - blood ; Infant ; Infant, Newborn ; Lipid Metabolism, Inborn Errors - blood ; Lipid Metabolism, Inborn Errors - diagnosis ; Male ; Malignant tumors ; Medical sciences ; Radioimmunoassay - methods ; Reference Values ; Steroid Hydroxylases - deficiency</subject><ispartof>Journal of steroid biochemistry, 1984-01, Vol.21 (2), p.185-191</ispartof><rights>1984</rights><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-be4f59679061ec7c1516b1009cf9e2879e45b59f3477c0f02b6e61bd50d59f563</citedby><cites>FETCH-LOGICAL-c417t-be4f59679061ec7c1516b1009cf9e2879e45b59f3477c0f02b6e61bd50d59f563</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9032397$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6090811$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Milewicz, A.</creatorcontrib><creatorcontrib>Vecsei, P.</creatorcontrib><creatorcontrib>Korth-Schütz, S.</creatorcontrib><creatorcontrib>Haack, D.</creatorcontrib><creatorcontrib>Rösler, A.</creatorcontrib><creatorcontrib>Lichtwald, K.</creatorcontrib><creatorcontrib>Lewicka, S.</creatorcontrib><creatorcontrib>Mittelstaedt, G.v.</creatorcontrib><title>Development of plasma 21-deoxycortisol radioimmunoassay and application to the diagnosis of patients with 21-hydroxylase deficiency</title><title>Journal of steroid biochemistry</title><addtitle>J Steroid Biochem</addtitle><description>Specific 21-deoxycortisol (21-DF) antiserum was raised in New Zealand white rabbits using a 21-DF-3,20-oxime-bovine serum albumin complex. Plasma radioimmunoassay of 21-DF was developed and used together with a radioimmunoassay of 17-hydroxyprogesterone (17-OH-P) for diagnosis of patients with 21-hydroxylase deficiency of congenital and postpubertal forms. The assays were performed in plasma extracts after isolation by paper chromatography. The response of plasma 21-DF and 17-OH-P to i.v. ACTH (25 IU) was studied in 15 adult controls and compared to 8 women with the late onset form of 21-hydroxylase deficiency and 23 women with idiopathic hirsutism. Normal 21-DF values for women were 6.9 ± 3.6ng/dl and for men 9.71 ± 2.73 ng/dl. Newborn children (age: 3–10 days) had a value of 8.3 ± 4.8 ng/dl. These values are definitely lower than the lowest value ever published. This is possibly due to the specificity of the antibody. During the menstrual cycle the 21-DF values did not change. The baseline and post-stimulated concentrations of hormone were similar in controls and women with hirsutism but were significantly higher in women with the late onset form of 21-hydroxylase deficiency. In the congenital form of 21-hydroxylase deficiency the 21-DF values (baseline) were high. In general, the 21-DF and 17-OH-P values have shown parallel changes. However, one case of 21-hydroxylase deficiency with elevated 21-DF but normal 17-OH-P was observed. The use of 21-DF for the diagnosis of 21-hydroxylase deficiency is suggested.</description><subject>17-alpha-Hydroxyprogesterone</subject><subject>17-Hydroxycorticosteroids - blood</subject><subject>Adolescent</subject><subject>Adrenals. Adrenal axis. Renin-angiotensin system (diseases)</subject><subject>Adrenocorticotropic Hormone</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Clinical Laboratory Techniques</subject><subject>Cortodoxone - blood</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Hirsutism - blood</subject><subject>Humans</subject><subject>Hydroxyprogesterones - blood</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Lipid Metabolism, Inborn Errors - blood</subject><subject>Lipid Metabolism, Inborn Errors - diagnosis</subject><subject>Male</subject><subject>Malignant tumors</subject><subject>Medical sciences</subject><subject>Radioimmunoassay - methods</subject><subject>Reference Values</subject><subject>Steroid Hydroxylases - deficiency</subject><issn>0022-4731</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTGP1DAQhVOAjuPgH4DkAiGuCNiO48QNEjo4QDqJBmrLscesURIHj_cgNX8cZ3e1JVSW5r35_DSvqp4x-ppRJt9Qynktuoa96sW1ok3Pa_qgujyPH1WPEX9QylQv-EV1IamiPWOX1Z_3cA9jXCaYM4meLKPByRDOagfx92pjygHjSJJxIYZp2s_RIJqVmNkRsyxjsCaHOJMcSd4BccF8nyMGPMCKVLhIfoW825i71aVCLX8UJ_hgi2zXJ9VDb0aEp6f3qvp2--Hrzaf67svHzzfv7morWJfrAYRvlewUlQxsZ1nL5MAoVdYr4H2nQLRDq3wjus5ST_kgQbLBtdSVaSubq-rlkbuk-HMPmPUU0MI4mhniHnXPuFR92_3XyEqepty2GMXRaFNETOD1ksJk0qoZ1VsxemtAbw3oXuhDMZqWtecn_n6YwJ2XTq0U_cVJN2jN6JOZbcCzrWB4o7aYb482KEe7D5A0Hg4KLiSwWbsY_p3jL6cerR8</recordid><startdate>19840101</startdate><enddate>19840101</enddate><creator>Milewicz, A.</creator><creator>Vecsei, P.</creator><creator>Korth-Schütz, S.</creator><creator>Haack, D.</creator><creator>Rösler, A.</creator><creator>Lichtwald, K.</creator><creator>Lewicka, S.</creator><creator>Mittelstaedt, G.v.</creator><general>Elsevier B.V</general><general>Pergamon</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>7SQ</scope><scope>7X8</scope></search><sort><creationdate>19840101</creationdate><title>Development of plasma 21-deoxycortisol radioimmunoassay and application to the diagnosis of patients with 21-hydroxylase deficiency</title><author>Milewicz, A. ; Vecsei, P. ; Korth-Schütz, S. ; Haack, D. ; Rösler, A. ; Lichtwald, K. ; Lewicka, S. ; Mittelstaedt, G.v.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-be4f59679061ec7c1516b1009cf9e2879e45b59f3477c0f02b6e61bd50d59f563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>17-alpha-Hydroxyprogesterone</topic><topic>17-Hydroxycorticosteroids - blood</topic><topic>Adolescent</topic><topic>Adrenals. Adrenal axis. Renin-angiotensin system (diseases)</topic><topic>Adrenocorticotropic Hormone</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Clinical Laboratory Techniques</topic><topic>Cortodoxone - blood</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Hirsutism - blood</topic><topic>Humans</topic><topic>Hydroxyprogesterones - blood</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Lipid Metabolism, Inborn Errors - blood</topic><topic>Lipid Metabolism, Inborn Errors - diagnosis</topic><topic>Male</topic><topic>Malignant tumors</topic><topic>Medical sciences</topic><topic>Radioimmunoassay - methods</topic><topic>Reference Values</topic><topic>Steroid Hydroxylases - deficiency</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Milewicz, A.</creatorcontrib><creatorcontrib>Vecsei, P.</creatorcontrib><creatorcontrib>Korth-Schütz, S.</creatorcontrib><creatorcontrib>Haack, D.</creatorcontrib><creatorcontrib>Rösler, A.</creatorcontrib><creatorcontrib>Lichtwald, K.</creatorcontrib><creatorcontrib>Lewicka, S.</creatorcontrib><creatorcontrib>Mittelstaedt, G.v.</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>Endocrinology Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of steroid biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Milewicz, A.</au><au>Vecsei, P.</au><au>Korth-Schütz, S.</au><au>Haack, D.</au><au>Rösler, A.</au><au>Lichtwald, K.</au><au>Lewicka, S.</au><au>Mittelstaedt, G.v.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of plasma 21-deoxycortisol radioimmunoassay and application to the diagnosis of patients with 21-hydroxylase deficiency</atitle><jtitle>Journal of steroid biochemistry</jtitle><addtitle>J Steroid Biochem</addtitle><date>1984-01-01</date><risdate>1984</risdate><volume>21</volume><issue>2</issue><spage>185</spage><epage>191</epage><pages>185-191</pages><issn>0022-4731</issn><coden>JSTBBK</coden><abstract>Specific 21-deoxycortisol (21-DF) antiserum was raised in New Zealand white rabbits using a 21-DF-3,20-oxime-bovine serum albumin complex. Plasma radioimmunoassay of 21-DF was developed and used together with a radioimmunoassay of 17-hydroxyprogesterone (17-OH-P) for diagnosis of patients with 21-hydroxylase deficiency of congenital and postpubertal forms. The assays were performed in plasma extracts after isolation by paper chromatography. The response of plasma 21-DF and 17-OH-P to i.v. ACTH (25 IU) was studied in 15 adult controls and compared to 8 women with the late onset form of 21-hydroxylase deficiency and 23 women with idiopathic hirsutism. Normal 21-DF values for women were 6.9 ± 3.6ng/dl and for men 9.71 ± 2.73 ng/dl. Newborn children (age: 3–10 days) had a value of 8.3 ± 4.8 ng/dl. These values are definitely lower than the lowest value ever published. This is possibly due to the specificity of the antibody. During the menstrual cycle the 21-DF values did not change. The baseline and post-stimulated concentrations of hormone were similar in controls and women with hirsutism but were significantly higher in women with the late onset form of 21-hydroxylase deficiency. In the congenital form of 21-hydroxylase deficiency the 21-DF values (baseline) were high. In general, the 21-DF and 17-OH-P values have shown parallel changes. However, one case of 21-hydroxylase deficiency with elevated 21-DF but normal 17-OH-P was observed. The use of 21-DF for the diagnosis of 21-hydroxylase deficiency is suggested.</abstract><cop>Oxford</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>6090811</pmid><doi>10.1016/0022-4731(84)90382-0</doi><tpages>7</tpages></addata></record> |
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subjects | 17-alpha-Hydroxyprogesterone 17-Hydroxycorticosteroids - blood Adolescent Adrenals. Adrenal axis. Renin-angiotensin system (diseases) Adrenocorticotropic Hormone Adult Biological and medical sciences Child Child, Preschool Clinical Laboratory Techniques Cortodoxone - blood Endocrinopathies Female Hirsutism - blood Humans Hydroxyprogesterones - blood Infant Infant, Newborn Lipid Metabolism, Inborn Errors - blood Lipid Metabolism, Inborn Errors - diagnosis Male Malignant tumors Medical sciences Radioimmunoassay - methods Reference Values Steroid Hydroxylases - deficiency |
title | Development of plasma 21-deoxycortisol radioimmunoassay and application to the diagnosis of patients with 21-hydroxylase deficiency |
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