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...
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Veröffentlicht in: | Clinical endocrinology (Oxford) 2024-03, Vol.100 (3), p.269-276 |
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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 |
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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.</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 & 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 >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 & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & 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 >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> |
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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 |
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