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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
Main Authors: Sandvik, Gunhild F., Vanem, Thy T., Rand‐Hendriksen, Svend, Cholidis, Symira, Sæthre, Marit, Drolsum, Liv
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container_title Clinical & experimental ophthalmology
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creator Sandvik, Gunhild F.
Vanem, Thy T.
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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
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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 &amp; 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 &amp; 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 &amp; experimental ophthalmology</title><addtitle>Clin Exp Ophthalmol</addtitle><description>Importance Long‐term follow‐up of Marfan syndrome (MFS) patients. 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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). 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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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