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dc.date.accessioned2020-01-22T09:21:51Z
dc.date.available2020-01-22T09:21:51Z
dc.date.created2019-01-30T11:24:30Z
dc.date.issued2019
dc.identifier.citationAdil, Muhammed Yasin Xiao, J Olaffson, J.S. Chen, Xiangjun Lagali, Neil Ræder, Sten Utheim, Øygunn Aass Dartt, Darlene A. Utheim, Tor Paaske . Meibomian Gland Morphology is a Sensitive Early Indicator of Meibomian Gland Dysfunction. American Journal of Ophthalmology. 2018, 200, 16-25
dc.identifier.urihttp://hdl.handle.net/10852/72423
dc.description.abstractPurpose To investigate the relationship between meibomian gland (MG) morphology and clinical dry eye tests in patients with meibomian gland dysfunction (MGD). Design Cross-sectional study. Subjects Total 538 MGD patients and 21 healthy controls. Methods MG loss on meibography images of upper (UL) and lower lids (LL) was graded on a scale of 0 (lowest degree of MG loss) to 3. MG length, thickness, and interglandular space in the UL were measured. Clinical tests included meibum expression and quality, tear film break-up time, ocular staining, osmolarity, Schirmer I, blink interval timing, and Ocular Surface Disease Index (OSDI) questionnaire. Results Mean UL and LL meibogrades were significantly higher in MGD patients compared to controls (P < .001 for UL and LL). The sensitivity and specificity of the meibograde as a diagnostic parameter for MGD was 96.7% and 85%, respectively. Schirmer I was significantly increased in MGD patients with meibograde 1 compared to patients with meibograde 0, 2, and 3 in the UL (P < .05). MG thickness increased with higher meibograde (P < .001). MG morphology correlated significantly but weakly with several clinical parameters (P < .05). OSDI did not correlate with any MG morphologic parameter. Conclusions Grading of MG loss using meibograde effectively diagnoses MGD. Compensatory mechanisms such as increased aqueous tear production and dilation of MGs make early detection of MGD difficult by standard clinical measures of dry eye, whereas morphologic analysis of MGs reveals an early stage of MGD, and therefore represents a complementary clinical parameter with diagnostic potential.
dc.languageEN
dc.publisherElsevier Science
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleMeibomian Gland Morphology is a Sensitive Early Indicator of Meibomian Gland Dysfunction
dc.typeJournal article
dc.creator.authorAdil, Muhammed Yasin
dc.creator.authorXiao, J
dc.creator.authorOlaffson, J.S.
dc.creator.authorChen, Xiangjun
dc.creator.authorLagali, Neil
dc.creator.authorRæder, Sten
dc.creator.authorUtheim, Øygunn Aass
dc.creator.authorDartt, Darlene A.
dc.creator.authorUtheim, Tor Paaske
cristin.unitcode185,0,0,0
cristin.unitnameUniversitetet i Oslo
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1
dc.identifier.cristin1668522
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=American Journal of Ophthalmology&rft.volume=200&rft.spage=16&rft.date=2018
dc.identifier.jtitleAmerican Journal of Ophthalmology
dc.identifier.volume200
dc.identifier.startpage16
dc.identifier.endpage25
dc.identifier.doihttps://doi.org/10.1016/j.ajo.2018.12.006
dc.identifier.urnURN:NBN:no-75590
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0002-9394
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/72423/1/Manuscript_revision2.pdf
dc.type.versionAcceptedVersion


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