Risk assessment for aortic dissection in Turner syndrome: The role of the aortic growth rate

Objective The risk of aortic dissection (AoD) is increased in Turner syndrome (TS) but predicting those at risk is difficult. Based on scarce evidence, preventive aortic surgery is recommended when aortic diameter increases >5 mm/year. To investigate the aortic growth rate in TS and TS‐related co...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Clinical endocrinology (Oxford) 2024-03, Vol.100 (3), p.269-276
Hauptverfasser: Calanchini, Matilde, Bradley‐Watson, James, McMillan, Fiona, Myerson, Saul, Fabbri, Andrea, Turner, Helen E., Orchard, Elizabeth
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 276
container_issue 3
container_start_page 269
container_title Clinical endocrinology (Oxford)
container_volume 100
creator Calanchini, Matilde
Bradley‐Watson, James
McMillan, Fiona
Myerson, Saul
Fabbri, Andrea
Turner, Helen E.
Orchard, Elizabeth
description Objective The risk of aortic dissection (AoD) is increased in Turner syndrome (TS) but predicting those at risk is difficult. Based on scarce evidence, preventive aortic surgery is recommended when aortic diameter increases >5 mm/year. To investigate the aortic growth rate in TS and TS‐related conditions associated with aortic growth. We also reported our experience of women who suffered aortic dissection (AoD), and who had preventive aortic replacement. Methods 151 adult TS were retrospectively identified. Women who had more than one transthoracic echocardiogram (TTE) after age 16 years were included in the aortic growth study. Aortic diameters at sinuses of Valsalva (SoV) and ascending aorta (AA) were analysed by two experts. Results 70/151 women had more than one TTE (interscan interval 4.7 years). Mean aortic growth was 0.13 ± 0.59 mm/year at SoV and 0.23 ± 0.82 mm/year at AA. Known risk factors for aortic dilatation and TS‐related conditions were not associated with aortic growth. 4/151 women experienced AoD (age 25±8 years): two had paired scans for aortic growth, which was 0.67 mm/year at both SoV and AA in the first woman, and 11 mm/year (SoV) and 4 mm/year (AA) in the second. Only 1/4 of women with AoD survived; she used a TS cardiac‐alert card to inform emergency personnel about her risk of AoD. 5/151 had a preventive aortic replacement, but one died post‐operatively. Conclusions Mean aortic growth in our TS population was increased compared to non‐TS women and was not associated with currently known risk factors for AoD, suggesting that aortic growth rate itself could be a useful variable to stratify who is at risk for AoD.
doi_str_mv 10.1111/cen.15017
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2922448577</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2921989150</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3137-591413afcd38e6f2da550251aaebebaba717455bc7286d89c83050801de021933</originalsourceid><addsrcrecordid>eNp1kF1LwzAUhoMobk4v_AMS8EYvuuWjaVPvZMwPGAoy74SSpqeus21m0jL2783s9ELw3OQQnry8eRA6p2RM_Uw0NGMqCI0P0JDySASMReIQDQknJCBRFA7QiXMrQoiQJD5GAy4ZDSnjQ_T2UroPrJwD52poWlwYi5WxbalxXvpr3ZamwWWDF51twGK3bXJrarjBiyVgayrApsCt3_ev3q3ZtEtsVQun6KhQlYOz_TlCr3ezxfQhmD_fP05v54HmlMeBSHwZrgqdcwlRwXIlBGGCKgUZZCpTMY1DITIdMxnlMtGSE0EkoTkQRhPOR-iqz11b89mBa9O6dBqqSjVgOpeyhLEwlCKOPXr5B10Z_zHfbkfRRCZepKeue0pb45yFIl3bslZ2m1KS7pSnXnn6rdyzF_vELqsh_yV_HHtg0gObsoLt_0npdPbUR34BieyJXg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2921989150</pqid></control><display><type>article</type><title>Risk assessment for aortic dissection in Turner syndrome: The role of the aortic growth rate</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Calanchini, Matilde ; Bradley‐Watson, James ; McMillan, Fiona ; Myerson, Saul ; Fabbri, Andrea ; Turner, Helen E. ; Orchard, Elizabeth</creator><creatorcontrib>Calanchini, Matilde ; Bradley‐Watson, James ; McMillan, Fiona ; Myerson, Saul ; Fabbri, Andrea ; Turner, Helen E. ; Orchard, Elizabeth</creatorcontrib><description>Objective The risk of aortic dissection (AoD) is increased in Turner syndrome (TS) but predicting those at risk is difficult. Based on scarce evidence, preventive aortic surgery is recommended when aortic diameter increases &gt;5 mm/year. To investigate the aortic growth rate in TS and TS‐related conditions associated with aortic growth. We also reported our experience of women who suffered aortic dissection (AoD), and who had preventive aortic replacement. Methods 151 adult TS were retrospectively identified. Women who had more than one transthoracic echocardiogram (TTE) after age 16 years were included in the aortic growth study. Aortic diameters at sinuses of Valsalva (SoV) and ascending aorta (AA) were analysed by two experts. Results 70/151 women had more than one TTE (interscan interval 4.7 years). Mean aortic growth was 0.13 ± 0.59 mm/year at SoV and 0.23 ± 0.82 mm/year at AA. Known risk factors for aortic dilatation and TS‐related conditions were not associated with aortic growth. 4/151 women experienced AoD (age 25±8 years): two had paired scans for aortic growth, which was 0.67 mm/year at both SoV and AA in the first woman, and 11 mm/year (SoV) and 4 mm/year (AA) in the second. Only 1/4 of women with AoD survived; she used a TS cardiac‐alert card to inform emergency personnel about her risk of AoD. 5/151 had a preventive aortic replacement, but one died post‐operatively. Conclusions Mean aortic growth in our TS population was increased compared to non‐TS women and was not associated with currently known risk factors for AoD, suggesting that aortic growth rate itself could be a useful variable to stratify who is at risk for AoD.</description><identifier>ISSN: 0300-0664</identifier><identifier>EISSN: 1365-2265</identifier><identifier>DOI: 10.1111/cen.15017</identifier><identifier>PMID: 38214123</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adolescent ; Adult ; Aorta ; aortic dilatation ; Aortic Diseases - complications ; Aortic Diseases - epidemiology ; Aortic Dissection ; aortic growth ; aortic replacement ; aortic surgery ; cardiovascular abnormalities ; Dissection ; Echocardiography ; Female ; Genetic disorders ; Growth rate ; Humans ; Retrospective Studies ; Risk Assessment ; Risk factors ; Turner syndrome ; Turner Syndrome - complications ; Turner Syndrome - epidemiology ; Turner's syndrome ; Young Adult</subject><ispartof>Clinical endocrinology (Oxford), 2024-03, Vol.100 (3), p.269-276</ispartof><rights>2024 John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3137-591413afcd38e6f2da550251aaebebaba717455bc7286d89c83050801de021933</cites><orcidid>0000-0002-3913-9988</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fcen.15017$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fcen.15017$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38214123$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Calanchini, Matilde</creatorcontrib><creatorcontrib>Bradley‐Watson, James</creatorcontrib><creatorcontrib>McMillan, Fiona</creatorcontrib><creatorcontrib>Myerson, Saul</creatorcontrib><creatorcontrib>Fabbri, Andrea</creatorcontrib><creatorcontrib>Turner, Helen E.</creatorcontrib><creatorcontrib>Orchard, Elizabeth</creatorcontrib><title>Risk assessment for aortic dissection in Turner syndrome: The role of the aortic growth rate</title><title>Clinical endocrinology (Oxford)</title><addtitle>Clin Endocrinol (Oxf)</addtitle><description>Objective The risk of aortic dissection (AoD) is increased in Turner syndrome (TS) but predicting those at risk is difficult. Based on scarce evidence, preventive aortic surgery is recommended when aortic diameter increases &gt;5 mm/year. To investigate the aortic growth rate in TS and TS‐related conditions associated with aortic growth. We also reported our experience of women who suffered aortic dissection (AoD), and who had preventive aortic replacement. Methods 151 adult TS were retrospectively identified. Women who had more than one transthoracic echocardiogram (TTE) after age 16 years were included in the aortic growth study. Aortic diameters at sinuses of Valsalva (SoV) and ascending aorta (AA) were analysed by two experts. Results 70/151 women had more than one TTE (interscan interval 4.7 years). Mean aortic growth was 0.13 ± 0.59 mm/year at SoV and 0.23 ± 0.82 mm/year at AA. Known risk factors for aortic dilatation and TS‐related conditions were not associated with aortic growth. 4/151 women experienced AoD (age 25±8 years): two had paired scans for aortic growth, which was 0.67 mm/year at both SoV and AA in the first woman, and 11 mm/year (SoV) and 4 mm/year (AA) in the second. Only 1/4 of women with AoD survived; she used a TS cardiac‐alert card to inform emergency personnel about her risk of AoD. 5/151 had a preventive aortic replacement, but one died post‐operatively. Conclusions Mean aortic growth in our TS population was increased compared to non‐TS women and was not associated with currently known risk factors for AoD, suggesting that aortic growth rate itself could be a useful variable to stratify who is at risk for AoD.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aorta</subject><subject>aortic dilatation</subject><subject>Aortic Diseases - complications</subject><subject>Aortic Diseases - epidemiology</subject><subject>Aortic Dissection</subject><subject>aortic growth</subject><subject>aortic replacement</subject><subject>aortic surgery</subject><subject>cardiovascular abnormalities</subject><subject>Dissection</subject><subject>Echocardiography</subject><subject>Female</subject><subject>Genetic disorders</subject><subject>Growth rate</subject><subject>Humans</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Risk factors</subject><subject>Turner syndrome</subject><subject>Turner Syndrome - complications</subject><subject>Turner Syndrome - epidemiology</subject><subject>Turner's syndrome</subject><subject>Young Adult</subject><issn>0300-0664</issn><issn>1365-2265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kF1LwzAUhoMobk4v_AMS8EYvuuWjaVPvZMwPGAoy74SSpqeus21m0jL2783s9ELw3OQQnry8eRA6p2RM_Uw0NGMqCI0P0JDySASMReIQDQknJCBRFA7QiXMrQoiQJD5GAy4ZDSnjQ_T2UroPrJwD52poWlwYi5WxbalxXvpr3ZamwWWDF51twGK3bXJrarjBiyVgayrApsCt3_ev3q3ZtEtsVQun6KhQlYOz_TlCr3ezxfQhmD_fP05v54HmlMeBSHwZrgqdcwlRwXIlBGGCKgUZZCpTMY1DITIdMxnlMtGSE0EkoTkQRhPOR-iqz11b89mBa9O6dBqqSjVgOpeyhLEwlCKOPXr5B10Z_zHfbkfRRCZepKeue0pb45yFIl3bslZ2m1KS7pSnXnn6rdyzF_vELqsh_yV_HHtg0gObsoLt_0npdPbUR34BieyJXg</recordid><startdate>202403</startdate><enddate>202403</enddate><creator>Calanchini, Matilde</creator><creator>Bradley‐Watson, James</creator><creator>McMillan, Fiona</creator><creator>Myerson, Saul</creator><creator>Fabbri, Andrea</creator><creator>Turner, Helen E.</creator><creator>Orchard, Elizabeth</creator><general>Wiley Subscription Services, Inc</general><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><orcidid>https://orcid.org/0000-0002-3913-9988</orcidid></search><sort><creationdate>202403</creationdate><title>Risk assessment for aortic dissection in Turner syndrome: The role of the aortic growth rate</title><author>Calanchini, Matilde ; Bradley‐Watson, James ; McMillan, Fiona ; Myerson, Saul ; Fabbri, Andrea ; Turner, Helen E. ; Orchard, Elizabeth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3137-591413afcd38e6f2da550251aaebebaba717455bc7286d89c83050801de021933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aorta</topic><topic>aortic dilatation</topic><topic>Aortic Diseases - complications</topic><topic>Aortic Diseases - epidemiology</topic><topic>Aortic Dissection</topic><topic>aortic growth</topic><topic>aortic replacement</topic><topic>aortic surgery</topic><topic>cardiovascular abnormalities</topic><topic>Dissection</topic><topic>Echocardiography</topic><topic>Female</topic><topic>Genetic disorders</topic><topic>Growth rate</topic><topic>Humans</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Risk factors</topic><topic>Turner syndrome</topic><topic>Turner Syndrome - complications</topic><topic>Turner Syndrome - epidemiology</topic><topic>Turner's syndrome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Calanchini, Matilde</creatorcontrib><creatorcontrib>Bradley‐Watson, James</creatorcontrib><creatorcontrib>McMillan, Fiona</creatorcontrib><creatorcontrib>Myerson, Saul</creatorcontrib><creatorcontrib>Fabbri, Andrea</creatorcontrib><creatorcontrib>Turner, Helen E.</creatorcontrib><creatorcontrib>Orchard, Elizabeth</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical endocrinology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Calanchini, Matilde</au><au>Bradley‐Watson, James</au><au>McMillan, Fiona</au><au>Myerson, Saul</au><au>Fabbri, Andrea</au><au>Turner, Helen E.</au><au>Orchard, Elizabeth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk assessment for aortic dissection in Turner syndrome: The role of the aortic growth rate</atitle><jtitle>Clinical endocrinology (Oxford)</jtitle><addtitle>Clin Endocrinol (Oxf)</addtitle><date>2024-03</date><risdate>2024</risdate><volume>100</volume><issue>3</issue><spage>269</spage><epage>276</epage><pages>269-276</pages><issn>0300-0664</issn><eissn>1365-2265</eissn><abstract>Objective The risk of aortic dissection (AoD) is increased in Turner syndrome (TS) but predicting those at risk is difficult. Based on scarce evidence, preventive aortic surgery is recommended when aortic diameter increases &gt;5 mm/year. To investigate the aortic growth rate in TS and TS‐related conditions associated with aortic growth. We also reported our experience of women who suffered aortic dissection (AoD), and who had preventive aortic replacement. Methods 151 adult TS were retrospectively identified. Women who had more than one transthoracic echocardiogram (TTE) after age 16 years were included in the aortic growth study. Aortic diameters at sinuses of Valsalva (SoV) and ascending aorta (AA) were analysed by two experts. Results 70/151 women had more than one TTE (interscan interval 4.7 years). Mean aortic growth was 0.13 ± 0.59 mm/year at SoV and 0.23 ± 0.82 mm/year at AA. Known risk factors for aortic dilatation and TS‐related conditions were not associated with aortic growth. 4/151 women experienced AoD (age 25±8 years): two had paired scans for aortic growth, which was 0.67 mm/year at both SoV and AA in the first woman, and 11 mm/year (SoV) and 4 mm/year (AA) in the second. Only 1/4 of women with AoD survived; she used a TS cardiac‐alert card to inform emergency personnel about her risk of AoD. 5/151 had a preventive aortic replacement, but one died post‐operatively. Conclusions Mean aortic growth in our TS population was increased compared to non‐TS women and was not associated with currently known risk factors for AoD, suggesting that aortic growth rate itself could be a useful variable to stratify who is at risk for AoD.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38214123</pmid><doi>10.1111/cen.15017</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-3913-9988</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0300-0664
ispartof Clinical endocrinology (Oxford), 2024-03, Vol.100 (3), p.269-276
issn 0300-0664
1365-2265
language eng
recordid cdi_proquest_miscellaneous_2922448577
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adolescent
Adult
Aorta
aortic dilatation
Aortic Diseases - complications
Aortic Diseases - epidemiology
Aortic Dissection
aortic growth
aortic replacement
aortic surgery
cardiovascular abnormalities
Dissection
Echocardiography
Female
Genetic disorders
Growth rate
Humans
Retrospective Studies
Risk Assessment
Risk factors
Turner syndrome
Turner Syndrome - complications
Turner Syndrome - epidemiology
Turner's syndrome
Young Adult
title Risk assessment for aortic dissection in Turner syndrome: The role of the aortic growth rate
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T23%3A54%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Risk%20assessment%20for%20aortic%20dissection%20in%20Turner%20syndrome:%20The%20role%20of%20the%20aortic%20growth%20rate&rft.jtitle=Clinical%20endocrinology%20(Oxford)&rft.au=Calanchini,%20Matilde&rft.date=2024-03&rft.volume=100&rft.issue=3&rft.spage=269&rft.epage=276&rft.pages=269-276&rft.issn=0300-0664&rft.eissn=1365-2265&rft_id=info:doi/10.1111/cen.15017&rft_dat=%3Cproquest_cross%3E2921989150%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2921989150&rft_id=info:pmid/38214123&rfr_iscdi=true