MISO: Metabolomics in Surgical Ophthalmological Patients

Sponsor
Universitaire Ziekenhuizen Leuven (Other)
Overall Status
Unknown status
CT.gov ID
NCT03098316
Collaborator
FRO (Funds for Research in Ophthalmology, Belgium) (Other)
90
1
19.9
4.5

Study Details

Study Description

Brief Summary

Metabolomics consists in the study of metabolites in body fluids or tissues. It investigates the consequences of the activity of genes and proteins. One of its advantages is that it is able to do a simultaneous measurement of metabolic changes in living organisms as a response to a disturbance (disease, diet, environment, others) and because a metabolic profile is summative of all the biochemical processes occurring in the body at a given time, it makes no presumption about the relative importance of these processes. Ultimately it is a fingerprint of the organism's health status, at a given time.

Metabolomic analysis of serum, plasma and urine has revealed panels of metabolites that distinguish patients with cardiovascular disease, breast cancer, Parkinson disease, Alzheimer's disease and diabetes from control patients. Regarding ocular diseases only few studies have been published, related to diabetic retinopathy, retinal detachment, age-related macular degeneration, uveitis and glaucoma.

Glaucoma is one of the leading causes of blindness in the world, according to the World Health Organization, and there are still no biomarkers that can provide an early diagnosis. Nowadays, glaucoma classification relies substantially in the measurement of intraocular pressure (IOP), which can be rather artificial and also unreliable since IOP values can fluctuate during the day. Moreover, patients with normal IOP values can also develop glaucomatous neuropathy (normal-tension glaucoma, NTG) and progress even when IOP is decreased. Several studies have shown that NTG patients suffer from a systemic vascular dysregulation, with higher rates of systemic hypotension, Raynaud phenomenon and migraine. Hence, other mechanisms than an increased IOP are of importance in the development and progression of glaucoma.

Only one metabolome-wide study has been made in glaucoma (Burgess, I.; 2015). In a sample of 72 american patients with primary open angle glaucoma (POAG), the authors found significant differences in comparison to controls.

The hypothesis for this study is that glaucoma patients will differ from controls, and POAG patients will differ from NTG patients. The investigators will look into metabolomics as a way to create a method to diagnose and stratify patients, as an add-on or alternative to the currently available diagnostic tools like IOP, functional and structural measurement.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Metabolomics analysis of patient samples

Detailed Description

This is a cross sectional study built to compare samples from glaucoma patients undergoing surgery (open-angle glaucoma and normal-tension glaucoma, age and gender matched) with age and gender-matched controls (healthy patients undergoing cataract surgery). For this the investigators will collect plasma, urine and aqueous humor to be analyzed through mass spectrometry and nuclear magnetic resonance spectroscopy. Patients have a night fasting period prior to sample collection, and a lifestyle and food frequency questionnaire is filled to control for nutritional influence on metabolites. Diabetic patients are excluded, since it would confound our analysis.

Study Design

Study Type:
Observational
Anticipated Enrollment :
90 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Metabolomics in Surgical Ophthalmological Patients
Actual Study Start Date :
Jan 31, 2017
Anticipated Primary Completion Date :
Sep 30, 2017
Anticipated Study Completion Date :
Sep 30, 2018

Arms and Interventions

Arm Intervention/Treatment
POAG

Primary open angle glaucoma patients

Diagnostic Test: Metabolomics analysis of patient samples
Metabolomics analysis of patient samples by mass spectrometry and nuclear magnetic resonance spectroscopy.

NTG

Normal/Low tension glaucoma patients

Diagnostic Test: Metabolomics analysis of patient samples
Metabolomics analysis of patient samples by mass spectrometry and nuclear magnetic resonance spectroscopy.

Control

Patients with cataract and without glaucoma or other eye diseases

Diagnostic Test: Metabolomics analysis of patient samples
Metabolomics analysis of patient samples by mass spectrometry and nuclear magnetic resonance spectroscopy.

Outcome Measures

Primary Outcome Measures

  1. Metabolomics profile of each group [Morning of the surgery]

    un-targeted metabolomics and identification of metabolites based on exact mass using metabolomics library

Secondary Outcome Measures

  1. Surgical success of glaucoma patients [12 months]

    Success is defined as an IOP between 6 and 18 mmHg with a reduction of 30% from baseline, and was sub-categorized as complete success if accomplished without glaucoma medication, qualified success with glaucoma medication, and total success as a combination of both complete and qualified. Eyes needing further glaucoma surgery, IOP ≤5 or > 18 mmHg on two consecutive visits, or loss of light perception due to glaucoma were considered as failures. Needling of encysted blebs is not considered a failure.

Eligibility Criteria

Criteria

Ages Eligible for Study:
60 Years to 90 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • glaucoma patients (POAG/NTG): undergoing trabeculectomy, XEN® implantation or cataract surgery

  • Controls (non glaucoma): undergoing cataract surgery

  • Caucasian

Exclusion Criteria:
  • Diabetes mellitus

  • any intra ocular surgery on study eye, other than clear cornea cataract surgery more than one year before

  • other eye pathologies than the one the surgery is intended for (except refractive error and cataract in glaucoma patients), namely retinopathies, uveitis and other causes for neuropathy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospitals Leuven Leuven Belgium 3000

Sponsors and Collaborators

  • Universitaire Ziekenhuizen Leuven
  • FRO (Funds for Research in Ophthalmology, Belgium)

Investigators

  • Principal Investigator: Ingeborg Stalmans, MD, PhD, Universitaire Ziekenhuizen Leuven

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Prof. Dr. Stalmans Ingeborg, Head of the glaucoma department, Universitaire Ziekenhuizen Leuven
ClinicalTrials.gov Identifier:
NCT03098316
Other Study ID Numbers:
  • MISO Study
First Posted:
Mar 31, 2017
Last Update Posted:
Apr 4, 2017
Last Verified:
Mar 1, 2017
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Prof. Dr. Stalmans Ingeborg, Head of the glaucoma department, Universitaire Ziekenhuizen Leuven
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 4, 2017