Glaucoma
Conditions
Brief summary
The investigators will include different subgroups of open-angle glaucoma and healthy controls. The participants will attend two visits with two weeks apart. At each visit the participants will have blood drawn and will undergo OCT examination. In between the two visits, participants will receive a treatment of Nicotinamide 1,5g/day for one week and 3.0g/day for the second week.
Detailed description
The investigators plan to recruit four groups, each containing 30 subjects: 1) pseudoexfoliative glaucoma, 2) High tension open-angle glaucoma, 3) Normal tension glaucoma 4) Age-matched controls. Those enrolled will undergo two visits including an ophthalmic exam, blood sampling, and at the first visit, distribution of nicotinamide tablets. We plan to recruit participants amongst glaucoma patients already followed at the Eye Clinic at Umeå University Hospital. Furthermore, age-matched controls will be recruited through lists from the population register at Statistics Sweden. Before enrolling any subject, they will receive both oral and written information as well as sign a consent form. Furthermore, they will be evaluated to make sure that they fulfill the inclusion- and exclusion criteria prior to inclusion. The ophthalmic exam includes measurement of IOP, perimetry, and OCT/A. Between visits, the participants will receive 1,5 grams of NAM per day the first week and 3 grams per day the second week. The blood drawn will initially be sent to Biobanken Norr for storage. Samples will then be sent to the Swedish Metabolomics Centre, Umeå University and Department of Medical Biochemistry and Biophysics, Karolinska University for analysis using high-resolution mass spectrometry.
Interventions
DIETARY_SUPPLEMENTNicotinamide
Tabletts of 500mg Nicotinamide (B3-vitamin)
Sponsors
Umeå University
Study design
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
for glaucoma patients: * Manifest glaucoma (PEXG, HTG, NTG) in one or two eyes, * age \> 18 years, * replicable visual field defects that cannot be explained by any other disease or insult, * suspect/anomalous optic nerve head or abnormalities in the retinal nerve fiber layer. Inclusion criteria for age-matched controls: -A normal visual field and optic nerve, age \> 18 years.
Exclusion criteria
for all: * Any disease affecting retinal function (such as more than mild macular degeneration or diabetic retinopathy), neurological or other non-glaucomatous conditions that may affect the visual field, * inability to perform a perimetric exam, * resistance in quitting intake of multivitamins or B-vitamins, * allergy to NAM or niacin, previous eye surgery involving the central retina, * pregnant or breast-feeding women, * fertile women not using reliable contraception, * diagnosis of cancer in the last five years (not including treated squamous cell carcinoma), anamnesis of liver-disease or peptic ulcer, * not able to speak and understand either Swedish or English.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Plasma level of NAM before and after NAM treatment in all groups | Two weeks | Are NAM levels in plasma lower in patients with glaucoma compared to healthy controls and will a short-term treatment with NAM raise the plasma concentration of NAM? |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Perfusion density and flow index in macula and optic nerve head before and after NAM treatment in all gropus | Two weeks | Will a short-term treatment with NAM influence the retinal vasculature measured with OCTA? |
Countries
Sweden
Outcome results
None listed