Fundus Autofluorescence Imaging in Macular Telangiectasia Type 2: MacTel Study Report Number 9

  • Laurenz Pauleikhoff
  • Tjebo F C Heeren
  • Martin Gliem
  • Ernest Lim
  • Daniel Pauleikhoff
  • Frank G Holz
  • Traci Clemons
  • Konstantinos Balaskas
  • MACTEL STUDY GROUP
  • Catherine A Egan
  • Peter Charbel Issa

Abstract

PURPOSE: To investigate the role of fundus autofluorescence (FAF) imaging in the diagnosis of macular telangiectasia type 2 (MacTel) and to describe disease-associated FAF patterns and their origin.

DESIGN: Cross-sectional multicenter study METHODS: FAF images were collected from the multicenter MacTel Natural History Observation and Registry Study. In a first qualitative approach, common FAF phenotypes were defined and correlated with multimodal imaging. We then evaluated how many eyes showed FAF changes, and temporal vs nasal asymmetry of FAF changes was graded. Finally, 100 eyes of MacTel patients and 100 control eyes (50 normal eyes and 50 eyes with other macular diseases) were combined and 2 masked graders assessed the presence of MacTel based on FAF images alone.

RESULTS: The study included 807 eyes of 420 patients (33 eyes were excluded owing to poor image quality). Loss of macular pigment, cystoid spaces, pigment plaques, neovascular membranes, and ectatic vascular changes commonly caused characteristic changes on FAF images. All MacTel patients had macular FAF changes in at least 1 eye. In 95% of eyes, these changes were more pronounced temporally than nasally. Common FAF patterns were increased (60%) and mixed/decreased FAF (38%) and/or visibility of vascular changes such as blunted vessels or ectatic capillaries (79%). Based on those features, high diagnostic performance was achieved for detection of the disease based on FAF alone (Youden index up to 0.91).

CONCLUSIONS: The study demonstrates that MacTel is consistently associated with disease-specific changes on FAF imaging. Those changes are typically more pronounced in the temporal parafovea.

Bibliografische Daten

OriginalspracheEnglisch
ISSN0002-9394
DOIs
StatusVeröffentlicht - 08.2021
Extern publiziertJa

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PubMed 33775659