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Br J Ophthalmol 2005;89:684-688 doi:10.1136/bjo.2004.056804
  • Clinical science
    • Extended reports

Lactoferrin Glu561Asp facilitates secondary amyloidosis in the cornea

  1. K Araki-Sasaki1,
  2. Y Ando2,
  3. M Nakamura2,
  4. K Kitagawa3,
  5. S Ikemizu4,
  6. T Kawaji1,
  7. T Yamashita5,
  8. M Ueda5,
  9. K Hirano6,
  10. M Yamada7,
  11. K Matsumoto1,
  12. S Kinoshita8,
  13. H Tanihara1
  1. 1Department of Ophthalmology, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto 860-0811, Japan
  2. 2Department of Diagnostic Medicine, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto 860-0811, Japan
  3. 3Department of Ophthalmology, Kanazawa Medical University Hospital, 1-1 Daigaku, Uchinada-machi, Kahoku-gun, Ishikawa 920-0293, Japan
  4. 4Department of Structural Biology, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto 860-0811, Japan
  5. 5Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto 860-0811, Japan
  6. 6Department of Ophthalmology, Japanese Red Cross Nagoya First Hospital, 3-35 Michishita-cho, Nagoya 453-8511, Japan
  7. 7Division for Vision Research, National Institute of Sensory Organs, National Tokyo Medical Center, 2-5-1 Higashigaoka, Meguro 152-8902, Tokyo, Japan
  8. 8Department of Ophthalmology, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kawaramachidori Noboru, Kamigyoku, Kyoto 602-8566, Japan
  1. Correspondence to: Yukio Ando MD, PhD, Department of Diagnostic Medicine, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto 860-0811, Japan; yukiokaiju.medic.kumamoto-u.ac.jp
  • Accepted 5 October 2004

Abstract

Aim: To elucidate the pathogenic mechanism of amyloid formation in corneal amyloidosis with trichiasis.

Methods: Ophthalmological examination was performed in nine patients to determine secondary corneal amyloidosis with trichiasis. Congo red staining and immunohistochemistry using anti-human lactoferrin antibody were used for biopsied corneal samples. For genetic analyses, single strand conformation polymorphism (SSCP), direct DNA sequence analysis, and polymerase chain reaction (PCR) induced mutation restriction analysis (IMRA) were employed to detect lactoferrin gene polymorphism.

Results: All patients had had trichiasis at least for 1 year, and all amyloid-like deposits were found in one eye with trichiasis. Ophthalmological examination revealed that eight patients showed gelatinous type of amyloid deposition and one showed lattice type of amyloid deposition. Studies of biopsied corneal samples with Congo red stain revealed positive staining just under the corneal epithelial cells. Immunoreactivity of anti-human lactoferrin antibodies was recognised in all tissues with positive Congo red staining. Lactoferrin gene analysis revealed that seven patients were heterozygotic and two were homozygotic for lactoferrin Glu561Asp. The frequency of the polymorphism in the patients was significantly different from that in 56 healthy control subjects.

Conclusion: Lactoferrin Glu561Asp is a key polymorphism related to facilitating amyloid formation in corneal amyloidosis with trichiasis.

Footnotes

  • Competing interests: The authors have no proprietary, financial, or commercial interests in any of the companies or products mentioned in this paper.

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