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AQP-9, KCNJ11 and ABCC8 Gene Variants in Open Angle Glaucoma: A Hypothesis

Author(s): Gabriele Thumann, Nino Sorgente

Importance: Primary open angle glaucoma, an age-related, retinal neurodegenerative disease of unknown etiology, is treated by lowering intraocular pressure, even though elevated intraocular pressure is present in only about 60% of patients. Since we found that tolbutamide, which inhibits the opening of ATP-sensitive potassium channels, modulates aqueous dynamics with a significant increase in outflow, and since aquaporin-9 is essential for retinal ganglion cells survival, gene variants coding for the ATP-sensitive potassium channels and aquaporin-9 may participate in the development and progression of glaucoma.

Objective: To identify gene variants involved in ion and water transport in the trabecular meshwork of glaucoma donors.

Design: The study is a gene association study; since gene variants can be somatic or germline, the following genes KCNJ8, KCNJ11, ABCC8, and ABCC9, QP1, AQP4, AQP9, ATP1A1, KCNMA11, and CLCN3 associated to ATP-sensitive potassium channels and water transport in the trabecular meshwork were sequenced from DNA isolated from trabecular meshwork of glaucoma donors.

Setting: The study is a gene association study carried out with samples obtained through the Cooperative Human Tissue Network of which the DNA was isolated by the technical personnel at the Lions Vision Gift eye bank and analyzed by Admera Health LLC.

Participants: The only criteria for the ten donors (5 male, 5 females; 70-91 years of age) in the study was a diagnosis of primary open angle glaucoma and a consent form signed at their lifetime or by responsible relatives.

Main Outcomes and Measures: Of several missense variants, one was found in all 10 and three were found in nine trabecular meshwork samples. All variants, whether synonymous or missense, were germline.

Results: The AQP9 missense variant, rs1867380 (Aca/Gca, 279T/A), was found in all 10 trabecular meshwork samples. Two common missense variants in the KCNJ11 gene, rs5215 (Gtc/Atc, 337V/I) and 5219 (Aag/Gag, 23K/E), and one missense variant in the ABCC8 gene, rs757110 (Gcc/Tcc, 1369AS), were found in the same nine trabecular meshwork samples. Several other missense variants were found in some, but not in the majority of trabecular meshwork samples.

Conclusions and Relevance: Variants of the KCNJ11 and ABCC8 genes that code for subunits of ATP-sensitive potassium channels and a variant of the AQP9 gene may be implicated in the development of elevated intraocular pressure and glaucoma. Understanding how these genes impact the energetics of the neural retina may provide further insights into the pathogenic nature of these variants, as well as offer clues for developing novel therapeutic targets.

    Editor In Chief

    Dr. Jui-Teng Lin

  • New Vision Inc
    Taipei, Taiwan

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