Testicular Sertoli cell function in male systemic lupus erythematosus
Objective. To assess the testicular Sertoli cell function in male SLE patients. Methods. Thirty-four consecutive patients were prospectively selected to evaluate serum inhibin B. Clinical features, treatment, semen analysis, urological evaluation, testicular ultrasound, hormones and anti-sperm antib...
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Veröffentlicht in: | Rheumatology (Oxford, England) England), 2008-11, Vol.47 (11), p.1692-1697 |
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description | Objective. To assess the testicular Sertoli cell function in male SLE patients. Methods. Thirty-four consecutive patients were prospectively selected to evaluate serum inhibin B. Clinical features, treatment, semen analysis, urological evaluation, testicular ultrasound, hormones and anti-sperm antibodies were determined. Results. Patients were subdivided into two groups: low serum inhibin B (Group 1, n = 8) and normal levels (Group 2, n = 26). The median sperm concentration (P = 0.024), total sperm count (P = 0.023) and total motile sperm count (P = 0.025) were lower in Group 1. Inhibin B levels were positively correlated with sperm concentration (r = 0.343), total motile sperm count (r = 0.357), and negatively correlated with follicule-stimulating hormone (FSH) (r = 0.699) and luteinizing hormone (r = 0.397). The median serum inhibin B was lower in SLE patients treated with intravenous cyclophosphamide (IVCYC) compared with those without this therapy (P = 0.031). Further evaluation of the 26 SLE patients with normal inhibin B and FSH levels revealed that medians of inhibin B/FSH ratio were lower in SLE patients with oligozoospermia compared with normozoospermia (P = 0.004). This ratio was also lower in SLE patients treated with IVCYC than those without this therapy (P = 0.04). In contrast, inhibin B serum level alone did not discriminate the later group of patients (P = 0.12). Conclusions. This is the first study to identify a high frequency of testicular Sertoli cell dysfunction in male SLE associated with semen abnormalities. Further prospective studies are necessary to determine if inhibin levels and inhibin B/FSH ratio will be an earlier and useful marker of IVCYC toxicity in these patients. |
doi_str_mv | 10.1093/rheumatology/ken338 |
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M. ; Borba, E. F. ; Bonfa, E. ; Okay, T. S. ; Cocuzza, M. ; Soares, P. M. F. ; Silva, C. A. A.</creator><creatorcontrib>Suehiro, R. M. ; Borba, E. F. ; Bonfa, E. ; Okay, T. S. ; Cocuzza, M. ; Soares, P. M. F. ; Silva, C. A. A.</creatorcontrib><description>Objective. To assess the testicular Sertoli cell function in male SLE patients. Methods. Thirty-four consecutive patients were prospectively selected to evaluate serum inhibin B. Clinical features, treatment, semen analysis, urological evaluation, testicular ultrasound, hormones and anti-sperm antibodies were determined. Results. Patients were subdivided into two groups: low serum inhibin B (Group 1, n = 8) and normal levels (Group 2, n = 26). The median sperm concentration (P = 0.024), total sperm count (P = 0.023) and total motile sperm count (P = 0.025) were lower in Group 1. Inhibin B levels were positively correlated with sperm concentration (r = 0.343), total motile sperm count (r = 0.357), and negatively correlated with follicule-stimulating hormone (FSH) (r = 0.699) and luteinizing hormone (r = 0.397). The median serum inhibin B was lower in SLE patients treated with intravenous cyclophosphamide (IVCYC) compared with those without this therapy (P = 0.031). Further evaluation of the 26 SLE patients with normal inhibin B and FSH levels revealed that medians of inhibin B/FSH ratio were lower in SLE patients with oligozoospermia compared with normozoospermia (P = 0.004). This ratio was also lower in SLE patients treated with IVCYC than those without this therapy (P = 0.04). In contrast, inhibin B serum level alone did not discriminate the later group of patients (P = 0.12). Conclusions. This is the first study to identify a high frequency of testicular Sertoli cell dysfunction in male SLE associated with semen abnormalities. Further prospective studies are necessary to determine if inhibin levels and inhibin B/FSH ratio will be an earlier and useful marker of IVCYC toxicity in these patients.</description><identifier>ISSN: 1462-0324</identifier><identifier>EISSN: 1462-0332</identifier><identifier>DOI: 10.1093/rheumatology/ken338</identifier><identifier>PMID: 18786967</identifier><identifier>CODEN: BJRHDF</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adolescent ; Adult ; Autoantibodies - blood ; Biological and medical sciences ; Chi-Square Distribution ; Cyclophosphamide - therapeutic use ; Diseases of the osteoarticular system ; Follicle Stimulating Hormone - blood ; Hormone ; Humans ; Immunosuppressive Agents - therapeutic use ; Inhibin B ; Inhibins - blood ; Lupus Erythematosus, Systemic - blood ; Lupus Erythematosus, Systemic - drug therapy ; Lupus Erythematosus, Systemic - pathology ; Luteinizing Hormone - blood ; Male ; Medical sciences ; Middle Aged ; Prospective Studies ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Sertoli cell ; Sertoli Cells - metabolism ; Sertoli Cells - pathology ; Sertoli Cells - physiology ; Sperm ; Sperm Count ; Sperm Motility ; Spermatozoa - immunology ; Statistics, Nonparametric ; Systemic lupus erythematosus ; Testis - diagnostic imaging ; Ultrasonography</subject><ispartof>Rheumatology (Oxford, England), 2008-11, Vol.47 (11), p.1692-1697</ispartof><rights>The Author 2008. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2008</rights><rights>2009 INIST-CNRS</rights><rights>The Author 2008. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c482t-f163f0ecfeaf0cdb2e9de3dfb37d9ea189a4ec338f116228b39f9e053d7830273</citedby><cites>FETCH-LOGICAL-c482t-f163f0ecfeaf0cdb2e9de3dfb37d9ea189a4ec338f116228b39f9e053d7830273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,1585,27928,27929</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20838762$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18786967$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suehiro, R. M.</creatorcontrib><creatorcontrib>Borba, E. F.</creatorcontrib><creatorcontrib>Bonfa, E.</creatorcontrib><creatorcontrib>Okay, T. S.</creatorcontrib><creatorcontrib>Cocuzza, M.</creatorcontrib><creatorcontrib>Soares, P. M. F.</creatorcontrib><creatorcontrib>Silva, C. A. A.</creatorcontrib><title>Testicular Sertoli cell function in male systemic lupus erythematosus</title><title>Rheumatology (Oxford, England)</title><addtitle>Rheumatology (Oxford)</addtitle><description>Objective. To assess the testicular Sertoli cell function in male SLE patients. Methods. Thirty-four consecutive patients were prospectively selected to evaluate serum inhibin B. Clinical features, treatment, semen analysis, urological evaluation, testicular ultrasound, hormones and anti-sperm antibodies were determined. Results. Patients were subdivided into two groups: low serum inhibin B (Group 1, n = 8) and normal levels (Group 2, n = 26). The median sperm concentration (P = 0.024), total sperm count (P = 0.023) and total motile sperm count (P = 0.025) were lower in Group 1. Inhibin B levels were positively correlated with sperm concentration (r = 0.343), total motile sperm count (r = 0.357), and negatively correlated with follicule-stimulating hormone (FSH) (r = 0.699) and luteinizing hormone (r = 0.397). The median serum inhibin B was lower in SLE patients treated with intravenous cyclophosphamide (IVCYC) compared with those without this therapy (P = 0.031). Further evaluation of the 26 SLE patients with normal inhibin B and FSH levels revealed that medians of inhibin B/FSH ratio were lower in SLE patients with oligozoospermia compared with normozoospermia (P = 0.004). This ratio was also lower in SLE patients treated with IVCYC than those without this therapy (P = 0.04). In contrast, inhibin B serum level alone did not discriminate the later group of patients (P = 0.12). Conclusions. This is the first study to identify a high frequency of testicular Sertoli cell dysfunction in male SLE associated with semen abnormalities. Further prospective studies are necessary to determine if inhibin levels and inhibin B/FSH ratio will be an earlier and useful marker of IVCYC toxicity in these patients.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Autoantibodies - blood</subject><subject>Biological and medical sciences</subject><subject>Chi-Square Distribution</subject><subject>Cyclophosphamide - therapeutic use</subject><subject>Diseases of the osteoarticular system</subject><subject>Follicle Stimulating Hormone - blood</subject><subject>Hormone</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Inhibin B</subject><subject>Inhibins - blood</subject><subject>Lupus Erythematosus, Systemic - blood</subject><subject>Lupus Erythematosus, Systemic - drug therapy</subject><subject>Lupus Erythematosus, Systemic - pathology</subject><subject>Luteinizing Hormone - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Prospective Studies</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Sertoli cell</subject><subject>Sertoli Cells - metabolism</subject><subject>Sertoli Cells - pathology</subject><subject>Sertoli Cells - physiology</subject><subject>Sperm</subject><subject>Sperm Count</subject><subject>Sperm Motility</subject><subject>Spermatozoa - immunology</subject><subject>Statistics, Nonparametric</subject><subject>Systemic lupus erythematosus</subject><subject>Testis - diagnostic imaging</subject><subject>Ultrasonography</subject><issn>1462-0324</issn><issn>1462-0332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtLAzEUhYMovn-BIIPgcjTJbTOZpRRfWBG0SnET0syNjs6jJhOw_96UKdWlq2TxnfMlh5AjRs8YzeHcvWOodddW7dvi_BMbALlBdtlA8JQC8M31nQ92yJ73H5TSIQO5TXaYzKTIRbZLLifou9KESrvkCV1sKxODVZXY0JiubJukbJJaV5j4he-wLk1ShXnwCbpF945Lvw_-gGxZXXk8XJ375PnqcjK6SccP17eji3FqBpJ3qWUCLEVjUVtqihnHvEAo7AyyIkfNZK4HaOI_LGOCczmD3OZIh1BkEijPYJ-c9L1z136F-HL10QbXRKVi-VAIEJRHCHrIuNZ7h1bNXVlrt1CMquVy6u9yql8upo5X1WFWY_GbWU0VgdMVoL3RlXW6MaVfc5xKkJlY6s96rg3zf5rTPlDGgb_XEe0-VdRmQ3UzfVV30_vHl-noSo3gB9x1nOQ</recordid><startdate>20081101</startdate><enddate>20081101</enddate><creator>Suehiro, R. M.</creator><creator>Borba, E. F.</creator><creator>Bonfa, E.</creator><creator>Okay, T. S.</creator><creator>Cocuzza, M.</creator><creator>Soares, P. M. F.</creator><creator>Silva, C. A. A.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><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>7QP</scope><scope>K9.</scope><scope>NAPCQ</scope></search><sort><creationdate>20081101</creationdate><title>Testicular Sertoli cell function in male systemic lupus erythematosus</title><author>Suehiro, R. M. ; Borba, E. F. ; Bonfa, E. ; Okay, T. S. ; Cocuzza, M. ; Soares, P. M. F. ; Silva, C. A. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c482t-f163f0ecfeaf0cdb2e9de3dfb37d9ea189a4ec338f116228b39f9e053d7830273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Autoantibodies - blood</topic><topic>Biological and medical sciences</topic><topic>Chi-Square Distribution</topic><topic>Cyclophosphamide - therapeutic use</topic><topic>Diseases of the osteoarticular system</topic><topic>Follicle Stimulating Hormone - blood</topic><topic>Hormone</topic><topic>Humans</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Inhibin B</topic><topic>Inhibins - blood</topic><topic>Lupus Erythematosus, Systemic - blood</topic><topic>Lupus Erythematosus, Systemic - drug therapy</topic><topic>Lupus Erythematosus, Systemic - pathology</topic><topic>Luteinizing Hormone - blood</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Prospective Studies</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Sertoli cell</topic><topic>Sertoli Cells - metabolism</topic><topic>Sertoli Cells - pathology</topic><topic>Sertoli Cells - physiology</topic><topic>Sperm</topic><topic>Sperm Count</topic><topic>Sperm Motility</topic><topic>Spermatozoa - immunology</topic><topic>Statistics, Nonparametric</topic><topic>Systemic lupus erythematosus</topic><topic>Testis - diagnostic imaging</topic><topic>Ultrasonography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suehiro, R. M.</creatorcontrib><creatorcontrib>Borba, E. F.</creatorcontrib><creatorcontrib>Bonfa, E.</creatorcontrib><creatorcontrib>Okay, T. S.</creatorcontrib><creatorcontrib>Cocuzza, M.</creatorcontrib><creatorcontrib>Soares, P. M. F.</creatorcontrib><creatorcontrib>Silva, C. A. A.</creatorcontrib><collection>Istex</collection><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>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><jtitle>Rheumatology (Oxford, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suehiro, R. M.</au><au>Borba, E. F.</au><au>Bonfa, E.</au><au>Okay, T. S.</au><au>Cocuzza, M.</au><au>Soares, P. M. F.</au><au>Silva, C. A. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Testicular Sertoli cell function in male systemic lupus erythematosus</atitle><jtitle>Rheumatology (Oxford, England)</jtitle><addtitle>Rheumatology (Oxford)</addtitle><date>2008-11-01</date><risdate>2008</risdate><volume>47</volume><issue>11</issue><spage>1692</spage><epage>1697</epage><pages>1692-1697</pages><issn>1462-0324</issn><eissn>1462-0332</eissn><coden>BJRHDF</coden><abstract>Objective. To assess the testicular Sertoli cell function in male SLE patients. Methods. Thirty-four consecutive patients were prospectively selected to evaluate serum inhibin B. Clinical features, treatment, semen analysis, urological evaluation, testicular ultrasound, hormones and anti-sperm antibodies were determined. Results. Patients were subdivided into two groups: low serum inhibin B (Group 1, n = 8) and normal levels (Group 2, n = 26). The median sperm concentration (P = 0.024), total sperm count (P = 0.023) and total motile sperm count (P = 0.025) were lower in Group 1. Inhibin B levels were positively correlated with sperm concentration (r = 0.343), total motile sperm count (r = 0.357), and negatively correlated with follicule-stimulating hormone (FSH) (r = 0.699) and luteinizing hormone (r = 0.397). The median serum inhibin B was lower in SLE patients treated with intravenous cyclophosphamide (IVCYC) compared with those without this therapy (P = 0.031). Further evaluation of the 26 SLE patients with normal inhibin B and FSH levels revealed that medians of inhibin B/FSH ratio were lower in SLE patients with oligozoospermia compared with normozoospermia (P = 0.004). This ratio was also lower in SLE patients treated with IVCYC than those without this therapy (P = 0.04). In contrast, inhibin B serum level alone did not discriminate the later group of patients (P = 0.12). Conclusions. This is the first study to identify a high frequency of testicular Sertoli cell dysfunction in male SLE associated with semen abnormalities. Further prospective studies are necessary to determine if inhibin levels and inhibin B/FSH ratio will be an earlier and useful marker of IVCYC toxicity in these patients.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>18786967</pmid><doi>10.1093/rheumatology/ken338</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Autoantibodies - blood Biological and medical sciences Chi-Square Distribution Cyclophosphamide - therapeutic use Diseases of the osteoarticular system Follicle Stimulating Hormone - blood Hormone Humans Immunosuppressive Agents - therapeutic use Inhibin B Inhibins - blood Lupus Erythematosus, Systemic - blood Lupus Erythematosus, Systemic - drug therapy Lupus Erythematosus, Systemic - pathology Luteinizing Hormone - blood Male Medical sciences Middle Aged Prospective Studies Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Sertoli cell Sertoli Cells - metabolism Sertoli Cells - pathology Sertoli Cells - physiology Sperm Sperm Count Sperm Motility Spermatozoa - immunology Statistics, Nonparametric Systemic lupus erythematosus Testis - diagnostic imaging Ultrasonography |
title | Testicular Sertoli cell function in male systemic lupus erythematosus |
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