Circulating eNAMPT in Glaucoma: A Semi-Quantitative Plasma Analysis Before and After Nicotinamide Supplementation.
Antoni Vallbona-Garcia1,2,3, Simon T Gustavsson4, Theo G M F Gorgels1,3
1University Eye Clinic Maastricht, Maastricht University Medical Center, Maastricht, Netherlands.
Translational Vision Science & Technology
|January 28, 2026
Summary
This study developed a method to detect plasma extracellular nicotinamide phosphoribosyltransferase (eNAMPT) in glaucoma patients. Circulating eNAMPT levels did not differ between glaucoma patients and controls, nor did they change after nicotinamide supplementation.
Area of Science:
- Ophthalmology
- Neuroscience
- Biochemistry
Background:
- Glaucoma involves progressive retinal ganglion cell degeneration.
- Nicotinamide supplementation may offer neuroprotection by boosting NAD levels via the NAMPT salvage pathway.
- Extracellular NAMPT (eNAMPT) in blood may reflect NAD biosynthetic capacity and susceptibility to glaucoma.
Purpose of the Study:
- Develop a specific assay for plasma eNAMPT detection.
- Investigate plasma eNAMPT as a potential biomarker for glaucoma.
- Assess the impact of nicotinamide supplementation on circulating eNAMPT levels.
Main Methods:
- Developed a semiquantitative Western blotting assay for plasma eNAMPT.
- Utilized samples from a prospective clinical trial (30 controls, 90 glaucoma patients).
- Assessed intra- and inter-assay variability for the eNAMPT assay.
Main Results:
- Successfully detected plasma eNAMPT (52 kDa) and transferrin (77 kDa) using Western blotting.
- Intra-assay variability was 14.9%, and inter-assay variability was 37.9%.
- No significant differences in eNAMPT levels were observed between glaucoma patients and controls, or after nicotinamide supplementation.
Conclusions:
- Established a reliable method for detecting plasma eNAMPT in glaucoma and control subjects.
- The study provides a foundation for developing eNAMPT as a liquid biopsy biomarker.
- Further research is required to elucidate eNAMPT's role in glaucoma and response to nicotinamide therapy.
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