IP Library Granted Patent US 8,951,729
Granted Patent B2
US 8,951,729 · App. 13/349,877 · Granted Feb 10, 2015

Methods for diagnosing and treating eye-length related disorders

Inventors: Jay Neitz (Seattle, WA); Maureen Neitz (Seattle, WA)
Assignee: University of Washington Through its Center for Commercialization
C12Q1/6883C12Q2600/172
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Quick Facts
Patent No.
US 8,951,729
App. No.
13/349,877
Granted
Feb 10, 2015
Kind
B2
Abstract

The invention provides to methods for diagnosing eye-length related disorders, including myopia. The invention also provides methods for treating and limiting eye-length related disorders, including myopia. In addition, the invention provides certain haplotypes associated with eye-length related disorders, including myopia and Bornholm Eye Disease.

Claims (26)

1. A method of treating myopia comprising:

a) obtaining a biological sample comprising L-opsin and M-opsin nucleic acids from a human patient with an eye-length related disorder;

b) detecting in the biological sample the nucleotides encoding codons 153, 171, 178, 180, and 236 of the L-opsin gene and the nucleotides encoding codons 153, 171, 178, and 180 of the M-opsin gene and identifying a human patient with an L:M opsin haplotype encoded by the nucleotides detected in the biological sample selected from the group consisting of:

(i) (A) L-Opsin: methionine at position 153, isoleucine at position 171 and position 178, serine at position 180, and methionine at position 236; and (B) M-opsin: methionine at position 153, valine at position 171 and at position 178, and alanine at position 180;

(ii) (A) L-Opsin: methionine at position 153, valine at position 171, isoleucine at position 178, serine at position 180, and methionine at position 236; and (B) M-opsin: methionine at position 153, valine at position 171 and at position 178, and alanine at position 180;

(iii) (A) L-Opsin: leucine at position 153, valine at position 171, isoleucine at position 178, serine at position 180, and methionine at position 236; and (B) M-opsin: methionine at position 153, valine at position 171 and at position 178, and alanine at position 180;

(iv) (A) L-Opsin: methionine at position 153, valine at position 171, isoleucine at position 178, serine at position 180, and methionine at position 236; and (B) M-opsin: methionine at position 153, valine at position 171, isoleucine at position 178, and alanine at position 180;

(v) (A) L-Opsin: leucine at position 153, valine at position 171, isoleucine at position 178, alanine at position 180, and methionine at position 236; and (B) M-opsin: methionine at position 153, valine at position 171, isoleucine at position 178, and alanine at position 180;

(vi) (A) L-Opsin: methionine at position 153, valine at position 171, isoleucine at position 178, alanine at position 180, and methionine at position 236; and (B) M-opsin: methionine at position 153, valine at position 171, isoleucine at position 178, and alanine at position 180;

(vii) (A) L-Opsin: leucine at position 153, valine at position 171, isoleucine at position 178, serine at position 180, and methionine at position 236; and (B) M-opsin: leucine or methionine at position 153, valine at position 171, isoleucine at position 178, and alanine at position 180;

(viii) (A) L-Opsin: leucine at position 153, valine at position 171, isoleucine at position 178, serine at position 180, and methionine at position 236; and (B) M-opsin: methionine at position 153, valine at position 171, isoleucine at position 178, and alanine at position 180;

(ix) (A) L-Opsin: leucine at position 153, isoleucine at position 171, isoleucine at position 178, serine at position 180, and methionine at position 236; and (B) M-opsin: methionine at position 153, valine at position 171, valine at position 178, and alanine at position 180;

(x) (A) L-Opsin: methionine at position 153, valine at position 171, valine at position 178, alanine at position 180, and valine at position 236; and (B) M-opsin: methionine at position 153, valine at position 171, isoleucine at position 178, and alanine at position 180;

(xi) (A) L-Opsin: methionine at position 153, valine at position 171, isoleucine at position 178, serine at position 180, and valine at position 236; and (B) M-opsin: methionine at position 153, valine at position 171, valine at position 178, and alanine at position 180;

(xii) (A) L-Opsin: leucine at position 153, valine at position 171, isoleucine at position 178, serine at position 180, and methionine at position 236; and (B) M-opsin: leucine at position 153, valine at position 171, isoleucine at position 178, and serine at position 180; and

(xiii) (A) L-Opsin: leucine at position 153, valine at position 171, isoleucine at position 178, alanine at position 180, and methionine at position 236; and (B) M-opsin: leucine or methionine at position 153, valine at position 171, isoleucine at position 178, and alanine at position 180;

(c) determining the L:M cone ratio in an eye of the patient;

(d) calculating a predicted spherical equivalent refraction (SER) that is a negative diopter in the human patient by scaling a spherical equivalent refraction based on the L:M opsin haplotype according to the L:M cone ratio; and

(e) treating myopia in the human patient with a therapeutic device comprising a wavelength-dependent filter to treat the eye-length mediated disorder.

2. The method of claim 1 , wherein the wavelength-dependent filter blocks red light.

3. The method of claim 1 , wherein the wavelength-dependent filter blocks green light.

4. The method of claim 1 , wherein the wavelengths filtered by the wavelength-dependent filter are selected based on the predicted SER of the human patient.

5. The method of claim 1 , wherein the therapeutic device is a pair of spectacles comprising blur-inducing lenses.

6. The method of claim 5 , wherein the blur-inducing lenses induce blurring by one or more of: small bumps or depressions in one or both surfaces of the lenses; inclusions within the lenses of a material different from the lens material; incorporation of higher-level aberrations in the lenses; and coatings or films applied to one or both surfaces of the lenses that produce blur by diffraction scatter or diffusion.

7. The method of claim 1 , wherein the therapeutic device comprises blur-inducing contact lenses.

8. The method of claim 7 , wherein the blur-inducing contact lenses induce blurring by one or more of: inclusions within the lenses of a material different from the lens material; incorporation of higher-level aberrations in the lenses; and coatings or films applied to one or both surfaces of the lenses that produce blur by diffraction scatter or diffusion.

Assignments (3)
CONFIRMATORY LICENSE Recorded Mar 12, 2014
From: UNIVERSITY OF WASHINGTON / CENTER FOR COMMERCIALIZATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 032436/0519 →
CONFIRMATORY LICENSE Recorded Jul 6, 2012
From: UNIVERSITY OF WASHINGTON / CENTER FOR COMMERCIALIZATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 028503/0361 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2012
From: NEITZ, JAY; NEITZ, MAUREEN
To: UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR COMMERCIALIZATION
Reel/Frame 027709/0449 →
Continuity (2)
Provisional Application 61432984 · Jan 14, 2011
Related Publication 20120182520A1 · Jul 19, 2012