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Metabolic Mapping to Measure Retinal Metabolism

Primary Purpose

Macular Degeneration, Diabetic Retinopathy, Hippel-Landau Disease

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Feasibility Study - Imaging System
Sponsored by
National Eye Institute (NEI)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Macular Degeneration focused on measuring Mitochondrion, Retina, Mitochondria, Metabolism, In Vivo Imaging, Age-Related Macular Degeneration, AMD, Diabetic Retinopathy, DR, Hippel-Lindau Disease, VHL

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers
  • INCLUSION CRITERIA:

GENERAL INCLUSION CRITERIA:

  1. Ability and willingness to provide informed consent.
  2. Presence of a natural lens in the study eye(s).
  3. Media clarity, pupillary dilation, and cooperation sufficient to perform measurements.
  4. All participants will have the ability to read with at least 1 eye

AMD-SPECIFIC INCLUSION CRITERIA:

Participants will range from those with no AMD and little or no drusen in either eye through end stage AMD (geographic atrophic, retinal pigment epithelial detachment, or other signs of neovascular/exudative disease) in one eye. Participants will be classified with the AREDS System for Classifying Age-Related Macular Degeneration and will exhibit a range of severities of AMD with at least half exhibiting unilateral advanced AMD (geographic atrophy or neovascular AMD) and half at high risk of progression. Inclusion criteria are as follows:

  1. A diagnosis of AMD. We will use AREDS criteria and diagnostic scales for the definition of AMD.
  2. Men and women aged 60 years or older. Children are not included because AMD (by definition) is a disease afflicting adults.
  3. Eligible participants may have no evidence of AMD with little or no drusen in either eye, or may have any stage of AMD through end stage (geographic atrophic, retinal pigment epithelial detachment, or other signs of neovascular/exudative disease) in one eye.

DR-SPECIFIC INCLUSION CRITERIA:

  1. People with DR will be classified with the modified ETDRS scale; participants will have a range of severities of DR, with at least half classified in the severe non-proliferative DR category (SNPDR). Efforts will be made to recruit people with unilateral SNPDR.
  2. Participants will be men and women aged 18 years or older with diagnosis of diabetes mellitus (type 1 or type 2). Any one of the following will be considered sufficient evidence that diabetes is present:

    • Current regular use of insulin for the treatment of diabetes.
    • Current regular use of oral antihyperglycemia agents for the treatment of diabetes.
    • Documented diabetes by ADA guidelines.

VHL-SPECIFIC INCLUSION CRITERIA:

  1. Participants will be men and women aged 18 years or older with a genetic confirmation of VHL-disease.
  2. People with VHL disease exhibit a range of retinal lesions from none to severe.

EXCLUSION CRITERIA:

GENERAL EXCLUSION CRITERIA:

  1. Cataract surgery in the study eye.
  2. Glaucoma with evidence of optic nerve damage.
  3. Chronic requirement for any systemic or ocular medication for other eye diseases other than AMD, DR, or VHL-disease.
  4. Presence of implanted medical devices that may be affected by electromagnetic frequency (EMF) emissions. Although our equipment is CE or UL rated for EMF emissions it would be prudent to exclude people with implanted pacemakers, neural stimulators, and insulin pumps.
  5. Arrhythmia as indicated in medical records, as this may result in instability in measurements.
  6. History of seizures. The scanning mechanism of the system operates at 12 Hz, which may induce a seizure (n.b. a 12Hz scan rate is used in the Heidelberg HRTII and HRA).
  7. Presence of chronic obstructive pulmonary disease (COPD) or other lung disease that might make breathing 100% O2 unsafe.
  8. Ocular disease (other than AMD, DR, or VHL) that confounds assessment of the retina. These include but are not limited to central serous choroidopathy, optic atrophy, retinal vein occlusion, active uveitis, significant explained or unexplained visual field loss, or any other type of retinopathy or retinal degeneration.
  9. Vitreous hemorrhage.
  10. History of renal failure requiring dialysis or renal transplant.
  11. Existing condition that in the opinion of the investigator would preclude participation in the study (e.g., unstable medical status including blood pressure and glycemic control).

Sites / Locations

  • National Institutes of Health Clinical Center, 9000 Rockville Pike

Outcomes

Primary Outcome Measures

Fluorescence anisotropy

Secondary Outcome Measures

The difference in fluorescence anisotropy values within subjects under room air and 100% oxygen exposure (one minute exposure time).

Full Information

First Posted
October 6, 2006
Last Updated
June 30, 2017
Sponsor
National Eye Institute (NEI)
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1. Study Identification

Unique Protocol Identification Number
NCT00385333
Brief Title
Metabolic Mapping to Measure Retinal Metabolism
Official Title
A Novel Non-Invasive In Vivo Imaging System to Measure Retinal Metabolism
Study Type
Interventional

2. Study Status

Record Verification Date
September 16, 2010
Overall Recruitment Status
Completed
Study Start Date
September 29, 2006 (undefined)
Primary Completion Date
June 1, 2008 (Actual)
Study Completion Date
September 16, 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Eye Institute (NEI)

4. Oversight

5. Study Description

Brief Summary
This study will test whether a new non-invasive technique can quickly and precisely measure retinal metabolism (the amount of energy retinal cells use). The retina is the part of the eye that sends information to the brain. Participants in current NEI studies who have age-related macular degeneration (AMD), diabetic retinopathy, or von Hippel-Landau disease may be eligible for this study. Healthy volunteers will participate as controls. Patients with AMD must be 60 years of age or older; those with VHL disease or diabetic retinopathy must be 18 or older. Participants undergo the tests and procedures required in the NEI study in which they previously enrolled. In addition, for the current study, they undergo metabolic mapping. For this procedure, the subject's eyes are dilated, and different amounts of low-level light are shone into the eye to see how different cells respond with changes in metabolism. Measurements are taken while the subject breathes room air and while he or she breathes medical grade oxygen for about 1 minute. The entire procedure takes about 15 minutes.
Detailed Description
Background. Alterations in retinal metabolism are associated with blinding conditions and vision loss. We propose to apply a non-invasive in vivo retinal imaging system to investigate key physiologic processes affecting retinal metabolism. The imaging system is designed to quantify and characterize the topology of retinal metabolism in 3-dimensional space across 40--130 picosecond time periods and allows dynamic measurement of physiologically relevant events. Objectives. The primary objectives of our study are to: (1) evaluate the utility of this system in a clinical setting; and (2) examine variation in retinal metabolism within retinal cell subtypes under environmental conditions optimized to support this metabolism. The working hypothesis of our first objective is that the imaging system will be easily and efficiently implemented in a clinical setting and will yield stable and repeatable results. The working hypothesis for our second objective is that people with or at high risk for progression to sight threatening retinal disease will exhibit different metabolic profiles than an age- and sex-matched disease-free comparison group. Their peers with less severe disease may exhibit differences with severe diseased and non-diseased groups. The long-term goal of the project is to address the following research questions: Are metabolic profiles generated by the imaging system effective for determining presence and severity of retinal diseases?; and if so, are these metabolic profiles useful in identifying people at risk for progression to sight threatening forms of retinal diseases? Study Population. We will first apply the systems in 3 groups of 10 people exhibiting a range of severity in retinal diseases that influence retinal metabolism; these diseases are: age-related macular degeneration (AMD); diabetic retinopathy (DR); and von-Hippel-Lindau (VHL) disease. Design. Cross-sectional sampling design. If the system yields accurate, stable, and repeatable results it will be applied in longitudinal studies to evaluate prognostic utility for estimating the risk of progression to sight-threatening AMD, DR, or VHL disease. Outcome Measures. The magnitude and 3-D topographic profile of fluorescence anisotropy values across physiologically meaningful time periods for a 20 degree field centered on the macula. Fluorescence anisotropy of our system provides a measure of retinal metabolism.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Macular Degeneration, Diabetic Retinopathy, Hippel-Landau Disease, Mitochondria
Keywords
Mitochondrion, Retina, Mitochondria, Metabolism, In Vivo Imaging, Age-Related Macular Degeneration, AMD, Diabetic Retinopathy, DR, Hippel-Lindau Disease, VHL

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Feasibility Study - Imaging System
Primary Outcome Measure Information:
Title
Fluorescence anisotropy
Secondary Outcome Measure Information:
Title
The difference in fluorescence anisotropy values within subjects under room air and 100% oxygen exposure (one minute exposure time).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA: GENERAL INCLUSION CRITERIA: Ability and willingness to provide informed consent. Presence of a natural lens in the study eye(s). Media clarity, pupillary dilation, and cooperation sufficient to perform measurements. All participants will have the ability to read with at least 1 eye AMD-SPECIFIC INCLUSION CRITERIA: Participants will range from those with no AMD and little or no drusen in either eye through end stage AMD (geographic atrophic, retinal pigment epithelial detachment, or other signs of neovascular/exudative disease) in one eye. Participants will be classified with the AREDS System for Classifying Age-Related Macular Degeneration and will exhibit a range of severities of AMD with at least half exhibiting unilateral advanced AMD (geographic atrophy or neovascular AMD) and half at high risk of progression. Inclusion criteria are as follows: A diagnosis of AMD. We will use AREDS criteria and diagnostic scales for the definition of AMD. Men and women aged 60 years or older. Children are not included because AMD (by definition) is a disease afflicting adults. Eligible participants may have no evidence of AMD with little or no drusen in either eye, or may have any stage of AMD through end stage (geographic atrophic, retinal pigment epithelial detachment, or other signs of neovascular/exudative disease) in one eye. DR-SPECIFIC INCLUSION CRITERIA: People with DR will be classified with the modified ETDRS scale; participants will have a range of severities of DR, with at least half classified in the severe non-proliferative DR category (SNPDR). Efforts will be made to recruit people with unilateral SNPDR. Participants will be men and women aged 18 years or older with diagnosis of diabetes mellitus (type 1 or type 2). Any one of the following will be considered sufficient evidence that diabetes is present: Current regular use of insulin for the treatment of diabetes. Current regular use of oral antihyperglycemia agents for the treatment of diabetes. Documented diabetes by ADA guidelines. VHL-SPECIFIC INCLUSION CRITERIA: Participants will be men and women aged 18 years or older with a genetic confirmation of VHL-disease. People with VHL disease exhibit a range of retinal lesions from none to severe. EXCLUSION CRITERIA: GENERAL EXCLUSION CRITERIA: Cataract surgery in the study eye. Glaucoma with evidence of optic nerve damage. Chronic requirement for any systemic or ocular medication for other eye diseases other than AMD, DR, or VHL-disease. Presence of implanted medical devices that may be affected by electromagnetic frequency (EMF) emissions. Although our equipment is CE or UL rated for EMF emissions it would be prudent to exclude people with implanted pacemakers, neural stimulators, and insulin pumps. Arrhythmia as indicated in medical records, as this may result in instability in measurements. History of seizures. The scanning mechanism of the system operates at 12 Hz, which may induce a seizure (n.b. a 12Hz scan rate is used in the Heidelberg HRTII and HRA). Presence of chronic obstructive pulmonary disease (COPD) or other lung disease that might make breathing 100% O2 unsafe. Ocular disease (other than AMD, DR, or VHL) that confounds assessment of the retina. These include but are not limited to central serous choroidopathy, optic atrophy, retinal vein occlusion, active uveitis, significant explained or unexplained visual field loss, or any other type of retinopathy or retinal degeneration. Vitreous hemorrhage. History of renal failure requiring dialysis or renal transplant. Existing condition that in the opinion of the investigator would preclude participation in the study (e.g., unstable medical status including blood pressure and glycemic control).
Facility Information:
Facility Name
National Institutes of Health Clinical Center, 9000 Rockville Pike
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
15078664
Citation
Congdon N, O'Colmain B, Klaver CC, Klein R, Munoz B, Friedman DS, Kempen J, Taylor HR, Mitchell P; Eye Diseases Prevalence Research Group. Causes and prevalence of visual impairment among adults in the United States. Arch Ophthalmol. 2004 Apr;122(4):477-85. doi: 10.1001/archopht.122.4.477.
Results Reference
background
PubMed Identifier
11033038
Citation
Beatty S, Koh H, Phil M, Henson D, Boulton M. The role of oxidative stress in the pathogenesis of age-related macular degeneration. Surv Ophthalmol. 2000 Sep-Oct;45(2):115-34. doi: 10.1016/s0039-6257(00)00140-5.
Results Reference
background
PubMed Identifier
15504974
Citation
Nyengaard JR, Ido Y, Kilo C, Williamson JR. Interactions between hyperglycemia and hypoxia: implications for diabetic retinopathy. Diabetes. 2004 Nov;53(11):2931-8. doi: 10.2337/diabetes.53.11.2931.
Results Reference
background

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Metabolic Mapping to Measure Retinal Metabolism

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