Hypocortisolism in survivors of severe acute respiratory syndrome (SARS)
Summary Objective Following the severe acute respiratory syndrome (SARS) outbreak, many survivors were observed to suffer from psychosomatic symptoms reminiscent of various endocrine disorders. Hence, we sought to determine the existence of any chronic endocrine sequelae in SARS survivors. Design,...
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description | Summary
Objective Following the severe acute respiratory syndrome (SARS) outbreak, many survivors were observed to suffer from psychosomatic symptoms reminiscent of various endocrine disorders. Hence, we sought to determine the existence of any chronic endocrine sequelae in SARS survivors.
Design, patients, measurements Sixty‐one survivors of SARS prospectively recruited were analysed for hormonal derangements 3 months following recovery. Patients with pre‐existing endocrine disorders were excluded. Any endocrine abnormalities diagnosed were investigated and treated where indicated up to a year. Serial evaluation facilitated characterization of trends and prognostication of any endocrinological aberrations.
Results Twenty‐four (39·3%) patients had evidence of hypocortisolism. The hypothalamic–pituitary–adrenal (HPA) axis dysfunction of the majority resolved within a year. Two (3·3%) of the hypocortisolic cohort had transient subclinical thyrotoxicosis. Four (6·7%) were biochemically hypothyroid, being comprised of three with central hypothyroidism and one with primary hypothyroidism. Two of the three with central hypothyroidism had concomitant central hypocortisolism. Eight had subnormal DHEAS levels.
Conclusions These preliminary findings highlight a possible aetiologic role of SARS‐associated coronavirus in causing a reversible hypophysitis or direct hypothalamic effect, with the HPA axis affected more frequently than the HPT axis. |
doi_str_mv | 10.1111/j.1365-2265.2005.02325.x |
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Objective Following the severe acute respiratory syndrome (SARS) outbreak, many survivors were observed to suffer from psychosomatic symptoms reminiscent of various endocrine disorders. Hence, we sought to determine the existence of any chronic endocrine sequelae in SARS survivors.
Design, patients, measurements Sixty‐one survivors of SARS prospectively recruited were analysed for hormonal derangements 3 months following recovery. Patients with pre‐existing endocrine disorders were excluded. Any endocrine abnormalities diagnosed were investigated and treated where indicated up to a year. Serial evaluation facilitated characterization of trends and prognostication of any endocrinological aberrations.
Results Twenty‐four (39·3%) patients had evidence of hypocortisolism. The hypothalamic–pituitary–adrenal (HPA) axis dysfunction of the majority resolved within a year. Two (3·3%) of the hypocortisolic cohort had transient subclinical thyrotoxicosis. Four (6·7%) were biochemically hypothyroid, being comprised of three with central hypothyroidism and one with primary hypothyroidism. Two of the three with central hypothyroidism had concomitant central hypocortisolism. Eight had subnormal DHEAS levels.
Conclusions These preliminary findings highlight a possible aetiologic role of SARS‐associated coronavirus in causing a reversible hypophysitis or direct hypothalamic effect, with the HPA axis affected more frequently than the HPT axis.</description><identifier>ISSN: 0300-0664</identifier><identifier>EISSN: 1365-2265</identifier><identifier>DOI: 10.1111/j.1365-2265.2005.02325.x</identifier><identifier>PMID: 16060914</identifier><identifier>CODEN: CLECAP</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Adrenocorticotropic Hormone - blood ; Adult ; Anti-Inflammatory Agents - therapeutic use ; Biological and medical sciences ; Endocrinopathies ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Hydrocortisone - blood ; Hydrocortisone - therapeutic use ; Hypothalamo-Hypophyseal System - physiopathology ; Male ; Medical sciences ; Methylprednisolone - therapeutic use ; Middle Aged ; Original ; Pituitary-Adrenal System - physiopathology ; Prednisolone - therapeutic use ; Prospective Studies ; Severe Acute Respiratory Syndrome - blood ; Severe Acute Respiratory Syndrome - drug therapy ; Severe Acute Respiratory Syndrome - physiopathology ; Thyroid Diseases - blood ; Thyroid Diseases - complications ; Thyroid Diseases - physiopathology ; Vertebrates: endocrinology</subject><ispartof>Clinical endocrinology (Oxford), 2005-08, Vol.63 (2), p.197-202</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright Blackwell Publishing Aug 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6335-8abb729357f25ecf8123880ce0d98e133a08a7a646283b82026ab9562702fe593</citedby><cites>FETCH-LOGICAL-c6335-8abb729357f25ecf8123880ce0d98e133a08a7a646283b82026ab9562702fe593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2265.2005.02325.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2265.2005.02325.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16978309$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16060914$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leow, Melvin Khee-Shing</creatorcontrib><creatorcontrib>Kwek, Daniel Seow-Khee</creatorcontrib><creatorcontrib>Ng, Alan Wei-Keong</creatorcontrib><creatorcontrib>Ong, Kian-Chung</creatorcontrib><creatorcontrib>Kaw, Gregory Jon-Leng</creatorcontrib><creatorcontrib>Lee, Lawrence Soon-U</creatorcontrib><title>Hypocortisolism in survivors of severe acute respiratory syndrome (SARS)</title><title>Clinical endocrinology (Oxford)</title><addtitle>Clin Endocrinol (Oxf)</addtitle><description>Summary
Objective Following the severe acute respiratory syndrome (SARS) outbreak, many survivors were observed to suffer from psychosomatic symptoms reminiscent of various endocrine disorders. Hence, we sought to determine the existence of any chronic endocrine sequelae in SARS survivors.
Design, patients, measurements Sixty‐one survivors of SARS prospectively recruited were analysed for hormonal derangements 3 months following recovery. Patients with pre‐existing endocrine disorders were excluded. Any endocrine abnormalities diagnosed were investigated and treated where indicated up to a year. Serial evaluation facilitated characterization of trends and prognostication of any endocrinological aberrations.
Results Twenty‐four (39·3%) patients had evidence of hypocortisolism. The hypothalamic–pituitary–adrenal (HPA) axis dysfunction of the majority resolved within a year. Two (3·3%) of the hypocortisolic cohort had transient subclinical thyrotoxicosis. Four (6·7%) were biochemically hypothyroid, being comprised of three with central hypothyroidism and one with primary hypothyroidism. Two of the three with central hypothyroidism had concomitant central hypocortisolism. Eight had subnormal DHEAS levels.
Conclusions These preliminary findings highlight a possible aetiologic role of SARS‐associated coronavirus in causing a reversible hypophysitis or direct hypothalamic effect, with the HPA axis affected more frequently than the HPT axis.</description><subject>Adrenocorticotropic Hormone - blood</subject><subject>Adult</subject><subject>Anti-Inflammatory Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Hydrocortisone - blood</subject><subject>Hydrocortisone - therapeutic use</subject><subject>Hypothalamo-Hypophyseal System - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methylprednisolone - therapeutic use</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Pituitary-Adrenal System - physiopathology</subject><subject>Prednisolone - therapeutic use</subject><subject>Prospective Studies</subject><subject>Severe Acute Respiratory Syndrome - blood</subject><subject>Severe Acute Respiratory Syndrome - drug therapy</subject><subject>Severe Acute Respiratory Syndrome - physiopathology</subject><subject>Thyroid Diseases - blood</subject><subject>Thyroid Diseases - complications</subject><subject>Thyroid Diseases - physiopathology</subject><subject>Vertebrates: endocrinology</subject><issn>0300-0664</issn><issn>1365-2265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkd2L00AUxQdR3Fr9FyQIij4kzkfmIw8KS1m3QljBXdnHy2Q60alpps4k3ea_38SWuvrkvNyB-zuXczgIJQRnZHzv1xlhgqeUCp5RjHmGKaM82z9Cs9PiMZphhnGKhcjP0LMY13gkFZZP0RkRWOCC5DO0XA5bb3zoXPSNi5vEtUnsw87tfIiJr5NodzbYRJu-s0mwceuC7nwYkji0q-A3Nnl7ff71-t1z9KTWTbQvjnOOvn26uFks0_LL5efFeZkawRhPla4qSQvGZU25NbUilCmFjcWrQlnCmMZKSy1yQRWrFMVU6KrggkpMa8sLNkcfD3e3fbWxK2PbLugGtsFtdBjAawd_b1r3A777HUiiFMunA2-OB4L_1dvYwcZFY5tGt9b3EYTKmaA5HcFX_4Br34d2DAekGD0LMSaaI3WATPAxBlufnBAMU1ewhqkSmCqBqSv43RXsR-nLh0n-CI_ljMDrI6Cj0U0ddGtcfMAVUjE8Jfpw4O5cY4f_NgCLi6vpN-rTg97Fzu5Peh1-gpBMcri9ugRWMlneyhJu2D3gUL4X</recordid><startdate>200508</startdate><enddate>200508</enddate><creator>Leow, Melvin Khee-Shing</creator><creator>Kwek, Daniel Seow-Khee</creator><creator>Ng, Alan Wei-Keong</creator><creator>Ong, Kian-Chung</creator><creator>Kaw, Gregory Jon-Leng</creator><creator>Lee, Lawrence Soon-U</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</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><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200508</creationdate><title>Hypocortisolism in survivors of severe acute respiratory syndrome (SARS)</title><author>Leow, Melvin Khee-Shing ; Kwek, Daniel Seow-Khee ; Ng, Alan Wei-Keong ; Ong, Kian-Chung ; Kaw, Gregory Jon-Leng ; Lee, Lawrence Soon-U</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6335-8abb729357f25ecf8123880ce0d98e133a08a7a646283b82026ab9562702fe593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adrenocorticotropic Hormone - blood</topic><topic>Adult</topic><topic>Anti-Inflammatory Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Hydrocortisone - blood</topic><topic>Hydrocortisone - therapeutic use</topic><topic>Hypothalamo-Hypophyseal System - physiopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methylprednisolone - therapeutic use</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Pituitary-Adrenal System - physiopathology</topic><topic>Prednisolone - therapeutic use</topic><topic>Prospective Studies</topic><topic>Severe Acute Respiratory Syndrome - blood</topic><topic>Severe Acute Respiratory Syndrome - drug therapy</topic><topic>Severe Acute Respiratory Syndrome - physiopathology</topic><topic>Thyroid Diseases - blood</topic><topic>Thyroid Diseases - complications</topic><topic>Thyroid Diseases - physiopathology</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leow, Melvin Khee-Shing</creatorcontrib><creatorcontrib>Kwek, Daniel Seow-Khee</creatorcontrib><creatorcontrib>Ng, Alan Wei-Keong</creatorcontrib><creatorcontrib>Ong, Kian-Chung</creatorcontrib><creatorcontrib>Kaw, Gregory Jon-Leng</creatorcontrib><creatorcontrib>Lee, Lawrence Soon-U</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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical endocrinology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leow, Melvin Khee-Shing</au><au>Kwek, Daniel Seow-Khee</au><au>Ng, Alan Wei-Keong</au><au>Ong, Kian-Chung</au><au>Kaw, Gregory Jon-Leng</au><au>Lee, Lawrence Soon-U</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypocortisolism in survivors of severe acute respiratory syndrome (SARS)</atitle><jtitle>Clinical endocrinology (Oxford)</jtitle><addtitle>Clin Endocrinol (Oxf)</addtitle><date>2005-08</date><risdate>2005</risdate><volume>63</volume><issue>2</issue><spage>197</spage><epage>202</epage><pages>197-202</pages><issn>0300-0664</issn><eissn>1365-2265</eissn><coden>CLECAP</coden><abstract>Summary
Objective Following the severe acute respiratory syndrome (SARS) outbreak, many survivors were observed to suffer from psychosomatic symptoms reminiscent of various endocrine disorders. Hence, we sought to determine the existence of any chronic endocrine sequelae in SARS survivors.
Design, patients, measurements Sixty‐one survivors of SARS prospectively recruited were analysed for hormonal derangements 3 months following recovery. Patients with pre‐existing endocrine disorders were excluded. Any endocrine abnormalities diagnosed were investigated and treated where indicated up to a year. Serial evaluation facilitated characterization of trends and prognostication of any endocrinological aberrations.
Results Twenty‐four (39·3%) patients had evidence of hypocortisolism. The hypothalamic–pituitary–adrenal (HPA) axis dysfunction of the majority resolved within a year. Two (3·3%) of the hypocortisolic cohort had transient subclinical thyrotoxicosis. Four (6·7%) were biochemically hypothyroid, being comprised of three with central hypothyroidism and one with primary hypothyroidism. Two of the three with central hypothyroidism had concomitant central hypocortisolism. Eight had subnormal DHEAS levels.
Conclusions These preliminary findings highlight a possible aetiologic role of SARS‐associated coronavirus in causing a reversible hypophysitis or direct hypothalamic effect, with the HPA axis affected more frequently than the HPT axis.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>16060914</pmid><doi>10.1111/j.1365-2265.2005.02325.x</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adrenocorticotropic Hormone - blood Adult Anti-Inflammatory Agents - therapeutic use Biological and medical sciences Endocrinopathies Female Fundamental and applied biological sciences. Psychology Humans Hydrocortisone - blood Hydrocortisone - therapeutic use Hypothalamo-Hypophyseal System - physiopathology Male Medical sciences Methylprednisolone - therapeutic use Middle Aged Original Pituitary-Adrenal System - physiopathology Prednisolone - therapeutic use Prospective Studies Severe Acute Respiratory Syndrome - blood Severe Acute Respiratory Syndrome - drug therapy Severe Acute Respiratory Syndrome - physiopathology Thyroid Diseases - blood Thyroid Diseases - complications Thyroid Diseases - physiopathology Vertebrates: endocrinology |
title | Hypocortisolism in survivors of severe acute respiratory syndrome (SARS) |
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