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Browse medicines, supplements, herbs, and health foods. Each profile brings community reports and linked research into one clear view.
Nicotinamide mononucleotide (NMN) and nicotinamide riboside (NR) are forms of vitamin B3 that the body turns into NAD+. The biochemical effect is proven: oral doses reliably raise blood NAD+. Clinical benefit in humans is not. Meta-analyses of randomised trials find no improvement in blood sugar, insulin, cholesterol, muscle mass or strength, and only a small diastolic blood-pressure signal so far.
3 of 21 results reported a benefit, from 4 published studies.
4 studies, including a review of trials
These are the figures the studies reported, not a prediction for any one person. Where several studies measured the same thing in the same unit, we show a simple average and say so. Every individual result is listed below.
See every resultInsulin resistance, pre-diabetes, type 2 diabetes, and metabolic syndrome.
Also known as: NMN, Nicotinamide mononucleotide, NR, Nicotinamide riboside
Every published result for this pair, extracted and audited.
These charts group published studies by what they reported and how they were run — green marks studies that reported a benefit for this pairing. Tiers run from pooled analyses of many trials (strongest) to one-off observational reports.
Direction of reported outcomes for NMN / NR (NAD+ precursors) in blood sugar control.
Study designs behind these findings.
Hand-selected PubMed studies, linked to the originals.
Ordered by strength of evidence, then result direction.
01Adjunctive berberine for schizophrenia with metabolic syndrome: a systematic review and meta-analysisXie K, et al. · Frontiers in psychiatry · 2026PMID 42433212 ↗02The Effect of Berberine Supplementation on Glycemic Control and Inflammatory Biomarkers in Metabolic Disorders: An Umbrella Meta-analysis of Randomized Controlled TrialsNazari A, et al. · Clinical therapeutics · 2024PMID 38016844 ↗03Effect of Fenugreek on Hyperglycemia: A Systematic Review and Meta-AnalysisShabil M, et al. · Medicina (Kaunas, Lithuania) · 2023PMID 36837450 ↗04Effect of saffron and fenugreek on lowering blood glucose: A systematic review with meta-analysisCorreia AGDS, et al. · Phytotherapy research : PTR · 2023PMID 36992660 ↗Be the first to share what you noticed with NMN / NR (NAD+ precursors) for blood sugar control. Why counts start empty.
Every measured outcome, one row per finding - numbers exactly as reported.
| Study | Design | n | Duration | Outcome measured | Reported result | Direction |
|---|---|---|---|---|---|---|
| PMID 39116016 2025 | Systematic review | 513 | - | blood NAD levels | reported qualitatively | Benefit |
| PMID 39116016 2025 | Systematic review | 513 | - | fasting glucose | reported qualitatively | No benefit |
| PMID 39116016 2025 | Systematic review | 513 | - | HDL-C | reported qualitatively | No benefit |
| PMID 39116016 2025 | Systematic review | 513 | - | LDL-C | reported qualitatively | No benefit |
| PMID 39116016 2025 | Systematic review | 513 | - | total cholesterol | reported qualitatively | No benefit |
| PMID 39116016 2025 | Systematic review | 513 | - | triglycerides | reported qualitatively | No benefit |
| PMID 39531138 2024 | Meta-analysis | 342 | 14 days to 12 weeks | fasting glucose | reported qualitatively | No benefit |
| PMID 39531138 2024 | Meta-analysis | 342 | 14 days to 12 weeks | fasting insulin | reported qualitatively | No benefit |
| PMID 39531138 2024 | Meta-analysis | 342 | 14 days to 12 weeks | glycated hemoglobin | reported qualitatively | No benefit |
| PMID 39531138 2024 | Meta-analysis | 342 | 14 days to 12 weeks | homeostatic model assessment for insulin resistance | reported qualitatively | No benefit |
| PMID 39531138 2024 | Meta-analysis | 342 | 14 days to 12 weeks | lipid profile | reported qualitatively | No benefit |
| PMID 33888596 2021 | Randomised trial | - | 10-week | Insulin-stimulated glucose disposal (hyperinsulinemic-euglycemic clamp) | reported qualitatively | Benefit |
| PMID 33888596 2021 | Randomised trial | - | 10-week | Skeletal muscle insulin signaling (phosphorylation of AKT and mTOR) | reported qualitatively | Benefit |
| PMID 29992272 2018 | Randomised trial | 40 | 12 wk | Body composition | reported qualitatively | No benefit |
| PMID 29992272 2018 | Randomised trial | 40 | 12 wk | Endogenous glucose production | reported qualitatively | No benefit |
| PMID 29992272 2018 | Randomised trial | 40 | 12 wk | Glucose disposal and oxidation | reported qualitatively | No benefit |
| PMID 29992272 2018 | Randomised trial | 40 | 12 wk | Insulin sensitivity | reported qualitatively | No benefit |
| PMID 29992272 2018 | Randomised trial | 40 | 12 wk | Intrahepatic lipid content | reported qualitatively | No benefit |
| PMID 29992272 2018 | Randomised trial | 40 | 12 wk | Lipolysis | reported qualitatively | No benefit |
| PMID 29992272 2018 | Randomised trial | 40 | 12 wk | Oxidation of lipids | reported qualitatively | No benefit |
| PMID 29992272 2018 | Randomised trial | 40 | 12 wk | Resting energy expenditure | reported qualitatively | No benefit |