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Meibomian Gland Morphology Is a Sensitive Early Indicator of Meibomian Gland Dysfunction
Univ Oslo, Norway; Norwegian Dry Eye Clin, Norway.
Univ Oslo, Norway; Norwegian Dry Eye Clin, Norway.
Univ Oslo, Norway.
Univ Oslo, Norway; Norwegian Dry Eye Clin, Norway; Arendal Hosp, Norway; Vestre Viken Hosp Trust, Norway; Univ Coll Southeast Norway, Norway.
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2019 (engelsk)Inngår i: American Journal of Ophthalmology, ISSN 0002-9394, E-ISSN 1879-1891, Vol. 200, s. 16-25Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

PURPOSE: 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 amp;lt; .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 amp;lt; .05 ). MG thickness increased with higher meibograde (P amp;lt; .001). MG morphology correlated significantly but weakly with several clinical parameters (P amp;lt; .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. (C) 2018 Elsevier Inc. All rights reserved.

sted, utgiver, år, opplag, sider
ELSEVIER SCIENCE INC , 2019. Vol. 200, s. 16-25
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URN: urn:nbn:se:liu:diva-157244DOI: 10.1016/j.ajo.2018.12.006ISI: 000464625600003PubMedID: 30578784OAI: oai:DiVA.org:liu-157244DiVA, id: diva2:1324083
Tilgjengelig fra: 2019-06-13 Laget: 2019-06-13 Sist oppdatert: 2019-06-13

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