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Granular and Lattice Deposits in Corneal Dystrophy Caused by R124C Mutation of TGFBIp

Patel, Dhara A PhD*; Chang, Shu-Hong MD*; Harocopos, George J MD*†; Vora, Smita C BS*; Thang, Diep Huu MD‡; Huang, Andrew J W MD, MPH*

doi: 10.1097/ICO.0b013e3181d4f737
Clinical Science

Purpose: Both granular and lattice deposits are present in Avellino corneal dystrophy (ACD), primarily associated with the R124H mutation of transforming growth factor-β-induced (TGFBIp). We investigated the presence of these deposits in other TGFBI mutations and the use of Thioflavin-T (ThT), a fluorescent amyloid stain for characterizing corneal amyloid deposits.

Methods: Surgical corneal specimens of 3 unrelated patients clinically diagnosed with ACD were studied. Corneal sections from normal individuals and patients with prior lattice corneal dystrophy (LCD) were used as controls. Histochemical studies were performed with Congo red and Masson trichrome stains, and fluorescent imaging with scanning laser confocal microscopy was performed for ThT and anti-TGFBIp antibody staining.

Results: Clinical and histopathological findings supported the diagnoses of ACD in these 3 cases in whom granular deposits stained with Masson trichrome and lattice deposits stained with ThT and Congo red showed birefringence and dichroism as expected. However, genotyping revealed a heterozygous R124C mutation in each case. In addition to classical stromal deposits, unique subepithelial TGFBIp aggregates, which stain with neither ThT nor trichrome, were observed. In control LCD sections, stromal deposits were stained with ThT but not with trichrome, confirming lack of granular deposits.

Conclusions: Our results demonstrate that both granular and lattice corneal deposits can be associated with R124C mutation in addition to the more common R124H mutation. An additional feature of nonhyaline, nonamyloid, TGFBIp subepithelial deposits might substantiate the categorization of such cases as a variant form of ACD. This study further validates ThT staining for detection of amyloid TGFBIp deposits.

From the Departments of *Ophthalmology and Visual Sciences and †Pathology and Immunology, Washington University School of Medicine, Saint Louis, MO; and ‡Eye Hospital of Ho Chi Minh City, Ho Chi Minh City, Vietnam.

Received for publication April 30, 2009; revision received January 14, 2010; accepted January 18, 2010.

Supported by grants from National Institutes of Health R01EY017609 (AJWH), NRSA 5-T32-EY13360-09 (DAP), a RPB Physician Scientist Award (AJWH), and an unrestricted grant from Horncrest Foundation, Inc (AJWH). This work was also supported in part by awards to the Department of Ophthalmology and Visual Sciences at Washington University from a Research to Prevent Blindness, Inc unrestricted grant and the NIH Vision Core Grant P30 EY 02687.

Disclosure of funding received: Refer to sources of support that require acknowledgement above.

Reprints: Andrew J.W. Huang, Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, 660 S. Euclid Avenue, Campus box 8096, Saint Louis, MO 63110 (e-mail: huanga@vision.wustl.edu).

© 2010 Lippincott Williams & Wilkins, Inc.