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Ten‐year reinvestigation of ocular manifestations in Marfan syndrome
Importance Long‐term follow‐up of Marfan syndrome (MFS) patients. Background Investigate changes in ocular features in MFS patients fulfilling the Ghent‐2 criteria following a period of 10 years. Design Repeated cross‐sectional study with two observations. Participants Eighty‐four MFS patients were...
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Published in: | Clinical & experimental ophthalmology 2019-03, Vol.47 (2), p.212-218 |
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container_title | Clinical & experimental ophthalmology |
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creator | Sandvik, Gunhild F. Vanem, Thy T. Rand‐Hendriksen, Svend Cholidis, Symira Sæthre, Marit Drolsum, Liv |
description | Importance
Long‐term follow‐up of Marfan syndrome (MFS) patients.
Background
Investigate changes in ocular features in MFS patients fulfilling the Ghent‐2 criteria following a period of 10 years.
Design
Repeated cross‐sectional study with two observations.
Participants
Eighty‐four MFS patients were investigated in 2003‐2004 (baseline). Forty‐four of these patients (52%) were examined after 10 years.
Methods
A comprehensive ocular examination performed at baseline and follow‐up.
Main Outcome Measures
Development or progression of ectopia lentis (EL).
Results
At follow‐up, mean age was 50.1 ± 11.9 years (range: 30‐80 years), 74% were female and 70% of the patients were diagnosed with EL compared to 66% at baseline. Two patients (3 eyes) had developed EL over the decade, representing a 13% risk. Furthermore, one eye had progressed from a subtle tilt of the lens to dislocation. We found no significant change in the axial length (P = 0.96), the corneal curvature (P = 0.64) or the spherical equivalent (P = 0.23). Best corrected visual acuity was improved at follow‐up (P = 0.02). There were 7% and 33% risks for development of retinal detachment and cataract between baseline and follow‐up, respectively.
Conclusions and Relevance
Our study indicates that even though EL typically occurs at an early stage in most MFS patients, there is still a risk of developing EL in adulthood. The risk of developing vision‐threatening complications such as retinal detachment and cataract was much higher than in the normal population, but even so, the visual potential of the MFS patients was relatively good. |
doi_str_mv | 10.1111/ceo.13408 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2113266238</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2194010602</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3888-71d1aa44f1e096f249a627b450eccfb9391779f366b20986a3f7b5c75a28a8413</originalsourceid><addsrcrecordid>eNp1kLtOwzAYhS0EoqUw8AIoEgsMaX2LnYyoagEJ1KXMkePayFViF7sBZeMReEaeBNMUBiT-5b99Ojo6AJwjOEaxJlK5MSIU5gdgiCjFaQE5OtzPjEI6ACchrCGEGSbsGAwIxCwufAjmS2U_3z86JXzilbGvKmzNs9gaZxOnEyfbOn4aYY2On909JMYmj8JrYZPQ2ZV3jToFR1rUQZ3t-wg8zWfL6V36sLi9n948pJLkeZ5ytEJCUKqRggXTmBaCYV7RDCopdVWQAnFeaMJYhWGRM0E0rzLJM4FzkVNERuCq191499JGR2VjglR1LaxybSgxQgQzhkke0cs_6Nq13kZ3kSooRJBBHKnrnpLeheCVLjfeNMJ3JYLld7hlDLfchRvZi71iWzVq9Uv-pBmBSQ-8mVp1_yuV09mil_wC5tCCjQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2194010602</pqid></control><display><type>article</type><title>Ten‐year reinvestigation of ocular manifestations in Marfan syndrome</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Sandvik, Gunhild F. ; Vanem, Thy T. ; Rand‐Hendriksen, Svend ; Cholidis, Symira ; Sæthre, Marit ; Drolsum, Liv</creator><creatorcontrib>Sandvik, Gunhild F. ; Vanem, Thy T. ; Rand‐Hendriksen, Svend ; Cholidis, Symira ; Sæthre, Marit ; Drolsum, Liv</creatorcontrib><description>Importance
Long‐term follow‐up of Marfan syndrome (MFS) patients.
Background
Investigate changes in ocular features in MFS patients fulfilling the Ghent‐2 criteria following a period of 10 years.
Design
Repeated cross‐sectional study with two observations.
Participants
Eighty‐four MFS patients were investigated in 2003‐2004 (baseline). Forty‐four of these patients (52%) were examined after 10 years.
Methods
A comprehensive ocular examination performed at baseline and follow‐up.
Main Outcome Measures
Development or progression of ectopia lentis (EL).
Results
At follow‐up, mean age was 50.1 ± 11.9 years (range: 30‐80 years), 74% were female and 70% of the patients were diagnosed with EL compared to 66% at baseline. Two patients (3 eyes) had developed EL over the decade, representing a 13% risk. Furthermore, one eye had progressed from a subtle tilt of the lens to dislocation. We found no significant change in the axial length (P = 0.96), the corneal curvature (P = 0.64) or the spherical equivalent (P = 0.23). Best corrected visual acuity was improved at follow‐up (P = 0.02). There were 7% and 33% risks for development of retinal detachment and cataract between baseline and follow‐up, respectively.
Conclusions and Relevance
Our study indicates that even though EL typically occurs at an early stage in most MFS patients, there is still a risk of developing EL in adulthood. The risk of developing vision‐threatening complications such as retinal detachment and cataract was much higher than in the normal population, but even so, the visual potential of the MFS patients was relatively good.</description><identifier>ISSN: 1442-6404</identifier><identifier>EISSN: 1442-9071</identifier><identifier>DOI: 10.1111/ceo.13408</identifier><identifier>PMID: 30260057</identifier><language>eng</language><publisher>Melbourne: John Wiley & Sons Australia, Ltd</publisher><subject>Acuity ; Adult ; Aged ; Aged, 80 and over ; axial length ; Axial Length, Eye - pathology ; Cataract - diagnosis ; Cataracts ; Complications ; Cornea ; Cornea - pathology ; corneal curvature ; Cross-Sectional Studies ; Curvature ; Disease Progression ; Dislocation ; Dislocations ; ectopia lentis ; Ectopia Lentis - diagnosis ; Eye ; Female ; Follow-Up Studies ; Humans ; Male ; Marfan syndrome ; Marfan Syndrome - diagnosis ; Middle Aged ; Ophthalmology ; Retina ; Retinal Detachment - diagnosis ; Visual acuity ; Visual Acuity - physiology</subject><ispartof>Clinical & experimental ophthalmology, 2019-03, Vol.47 (2), p.212-218</ispartof><rights>2018 Royal Australian and New Zealand College of Ophthalmologists</rights><rights>2018 Royal Australian and New Zealand College of Ophthalmologists.</rights><rights>2019 Royal Australian and New Zealand College of Ophthalmologists</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3888-71d1aa44f1e096f249a627b450eccfb9391779f366b20986a3f7b5c75a28a8413</citedby><cites>FETCH-LOGICAL-c3888-71d1aa44f1e096f249a627b450eccfb9391779f366b20986a3f7b5c75a28a8413</cites><orcidid>0000-0001-5351-6834</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30260057$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sandvik, Gunhild F.</creatorcontrib><creatorcontrib>Vanem, Thy T.</creatorcontrib><creatorcontrib>Rand‐Hendriksen, Svend</creatorcontrib><creatorcontrib>Cholidis, Symira</creatorcontrib><creatorcontrib>Sæthre, Marit</creatorcontrib><creatorcontrib>Drolsum, Liv</creatorcontrib><title>Ten‐year reinvestigation of ocular manifestations in Marfan syndrome</title><title>Clinical & experimental ophthalmology</title><addtitle>Clin Exp Ophthalmol</addtitle><description>Importance
Long‐term follow‐up of Marfan syndrome (MFS) patients.
Background
Investigate changes in ocular features in MFS patients fulfilling the Ghent‐2 criteria following a period of 10 years.
Design
Repeated cross‐sectional study with two observations.
Participants
Eighty‐four MFS patients were investigated in 2003‐2004 (baseline). Forty‐four of these patients (52%) were examined after 10 years.
Methods
A comprehensive ocular examination performed at baseline and follow‐up.
Main Outcome Measures
Development or progression of ectopia lentis (EL).
Results
At follow‐up, mean age was 50.1 ± 11.9 years (range: 30‐80 years), 74% were female and 70% of the patients were diagnosed with EL compared to 66% at baseline. Two patients (3 eyes) had developed EL over the decade, representing a 13% risk. Furthermore, one eye had progressed from a subtle tilt of the lens to dislocation. We found no significant change in the axial length (P = 0.96), the corneal curvature (P = 0.64) or the spherical equivalent (P = 0.23). Best corrected visual acuity was improved at follow‐up (P = 0.02). There were 7% and 33% risks for development of retinal detachment and cataract between baseline and follow‐up, respectively.
Conclusions and Relevance
Our study indicates that even though EL typically occurs at an early stage in most MFS patients, there is still a risk of developing EL in adulthood. The risk of developing vision‐threatening complications such as retinal detachment and cataract was much higher than in the normal population, but even so, the visual potential of the MFS patients was relatively good.</description><subject>Acuity</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>axial length</subject><subject>Axial Length, Eye - pathology</subject><subject>Cataract - diagnosis</subject><subject>Cataracts</subject><subject>Complications</subject><subject>Cornea</subject><subject>Cornea - pathology</subject><subject>corneal curvature</subject><subject>Cross-Sectional Studies</subject><subject>Curvature</subject><subject>Disease Progression</subject><subject>Dislocation</subject><subject>Dislocations</subject><subject>ectopia lentis</subject><subject>Ectopia Lentis - diagnosis</subject><subject>Eye</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Male</subject><subject>Marfan syndrome</subject><subject>Marfan Syndrome - diagnosis</subject><subject>Middle Aged</subject><subject>Ophthalmology</subject><subject>Retina</subject><subject>Retinal Detachment - diagnosis</subject><subject>Visual acuity</subject><subject>Visual Acuity - physiology</subject><issn>1442-6404</issn><issn>1442-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kLtOwzAYhS0EoqUw8AIoEgsMaX2LnYyoagEJ1KXMkePayFViF7sBZeMReEaeBNMUBiT-5b99Ojo6AJwjOEaxJlK5MSIU5gdgiCjFaQE5OtzPjEI6ACchrCGEGSbsGAwIxCwufAjmS2U_3z86JXzilbGvKmzNs9gaZxOnEyfbOn4aYY2On909JMYmj8JrYZPQ2ZV3jToFR1rUQZ3t-wg8zWfL6V36sLi9n948pJLkeZ5ytEJCUKqRggXTmBaCYV7RDCopdVWQAnFeaMJYhWGRM0E0rzLJM4FzkVNERuCq191499JGR2VjglR1LaxybSgxQgQzhkke0cs_6Nq13kZ3kSooRJBBHKnrnpLeheCVLjfeNMJ3JYLld7hlDLfchRvZi71iWzVq9Uv-pBmBSQ-8mVp1_yuV09mil_wC5tCCjQ</recordid><startdate>201903</startdate><enddate>201903</enddate><creator>Sandvik, Gunhild F.</creator><creator>Vanem, Thy T.</creator><creator>Rand‐Hendriksen, Svend</creator><creator>Cholidis, Symira</creator><creator>Sæthre, Marit</creator><creator>Drolsum, Liv</creator><general>John Wiley & Sons Australia, Ltd</general><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>7TK</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5351-6834</orcidid></search><sort><creationdate>201903</creationdate><title>Ten‐year reinvestigation of ocular manifestations in Marfan syndrome</title><author>Sandvik, Gunhild F. ; Vanem, Thy T. ; Rand‐Hendriksen, Svend ; Cholidis, Symira ; Sæthre, Marit ; Drolsum, Liv</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3888-71d1aa44f1e096f249a627b450eccfb9391779f366b20986a3f7b5c75a28a8413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acuity</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>axial length</topic><topic>Axial Length, Eye - pathology</topic><topic>Cataract - diagnosis</topic><topic>Cataracts</topic><topic>Complications</topic><topic>Cornea</topic><topic>Cornea - pathology</topic><topic>corneal curvature</topic><topic>Cross-Sectional Studies</topic><topic>Curvature</topic><topic>Disease Progression</topic><topic>Dislocation</topic><topic>Dislocations</topic><topic>ectopia lentis</topic><topic>Ectopia Lentis - diagnosis</topic><topic>Eye</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Male</topic><topic>Marfan syndrome</topic><topic>Marfan Syndrome - diagnosis</topic><topic>Middle Aged</topic><topic>Ophthalmology</topic><topic>Retina</topic><topic>Retinal Detachment - diagnosis</topic><topic>Visual acuity</topic><topic>Visual Acuity - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sandvik, Gunhild F.</creatorcontrib><creatorcontrib>Vanem, Thy T.</creatorcontrib><creatorcontrib>Rand‐Hendriksen, Svend</creatorcontrib><creatorcontrib>Cholidis, Symira</creatorcontrib><creatorcontrib>Sæthre, Marit</creatorcontrib><creatorcontrib>Drolsum, Liv</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical & experimental ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sandvik, Gunhild F.</au><au>Vanem, Thy T.</au><au>Rand‐Hendriksen, Svend</au><au>Cholidis, Symira</au><au>Sæthre, Marit</au><au>Drolsum, Liv</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ten‐year reinvestigation of ocular manifestations in Marfan syndrome</atitle><jtitle>Clinical & experimental ophthalmology</jtitle><addtitle>Clin Exp Ophthalmol</addtitle><date>2019-03</date><risdate>2019</risdate><volume>47</volume><issue>2</issue><spage>212</spage><epage>218</epage><pages>212-218</pages><issn>1442-6404</issn><eissn>1442-9071</eissn><abstract>Importance
Long‐term follow‐up of Marfan syndrome (MFS) patients.
Background
Investigate changes in ocular features in MFS patients fulfilling the Ghent‐2 criteria following a period of 10 years.
Design
Repeated cross‐sectional study with two observations.
Participants
Eighty‐four MFS patients were investigated in 2003‐2004 (baseline). Forty‐four of these patients (52%) were examined after 10 years.
Methods
A comprehensive ocular examination performed at baseline and follow‐up.
Main Outcome Measures
Development or progression of ectopia lentis (EL).
Results
At follow‐up, mean age was 50.1 ± 11.9 years (range: 30‐80 years), 74% were female and 70% of the patients were diagnosed with EL compared to 66% at baseline. Two patients (3 eyes) had developed EL over the decade, representing a 13% risk. Furthermore, one eye had progressed from a subtle tilt of the lens to dislocation. We found no significant change in the axial length (P = 0.96), the corneal curvature (P = 0.64) or the spherical equivalent (P = 0.23). Best corrected visual acuity was improved at follow‐up (P = 0.02). There were 7% and 33% risks for development of retinal detachment and cataract between baseline and follow‐up, respectively.
Conclusions and Relevance
Our study indicates that even though EL typically occurs at an early stage in most MFS patients, there is still a risk of developing EL in adulthood. The risk of developing vision‐threatening complications such as retinal detachment and cataract was much higher than in the normal population, but even so, the visual potential of the MFS patients was relatively good.</abstract><cop>Melbourne</cop><pub>John Wiley & Sons Australia, Ltd</pub><pmid>30260057</pmid><doi>10.1111/ceo.13408</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-5351-6834</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acuity Adult Aged Aged, 80 and over axial length Axial Length, Eye - pathology Cataract - diagnosis Cataracts Complications Cornea Cornea - pathology corneal curvature Cross-Sectional Studies Curvature Disease Progression Dislocation Dislocations ectopia lentis Ectopia Lentis - diagnosis Eye Female Follow-Up Studies Humans Male Marfan syndrome Marfan Syndrome - diagnosis Middle Aged Ophthalmology Retina Retinal Detachment - diagnosis Visual acuity Visual Acuity - physiology |
title | Ten‐year reinvestigation of ocular manifestations in Marfan syndrome |
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