Overview
Flushing form of B3 — historically used for dyslipidemia at gram doses.
Forms & variants of Niacin (Flush)
Different chemical forms of Niacin (Flush) behave differently. Browse each form's mechanism, bioavailability, and best-use context.
NAD+ precursor that bypasses the flush — studied for cellular aging.
Direct NAD+ precursor — popular longevity supplement with growing human data.
Non-flushing B3 — used for deficiency, skin health, and at high doses in dermatology.
Mechanism of action
Activates GPR109A on adipocytes → reduces FFA flux → lowers VLDL/triglycerides.
Effects on the body
Organ system effects
Evidence-based benefits
Raises HDL and lowers LDL/TG
Strong evidenceOutcome benefit unclear (AIM-HIGH/HPS2-THRIVE).
Potential side effects
- · Flushing
- · Itching
- · Headache
- · Hepatotoxicity (sustained-release)
- · Hyperglycemia
Drug interactions
No notable interactions reported.
Supplement interactions
None listed.
No specific avoidances listed.
Dosing & bioavailability
Where to buy
Affiliate-style search links to reputable retailers. We don't endorse specific brands — verify third-party testing (USP, NSF, Informed Sport) before purchase.
Scientific evidence (8)
Niacin on lipid profile (AIM-HIGH)
AIM-HIGH Investigators
RCT of niacin in patients on statin therapy.
Raised HDL but no incremental clinical benefit on statin.
PubMed: Niacin (Flush) — Raises HDL and lowers LDL/TG
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PubMed: Niacin (Flush) — randomized controlled trial
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PubMed: Niacin (Flush) — meta-analysis
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PubMed: Niacin (Flush) — pharmacokinetics
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PubMed: Niacin (Flush) — safety adverse events
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PubMed: Niacin (Flush) — dose response
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Google Scholar: Niacin (Flush) — clinical evidence
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Cross-database citation index for Niacin (Flush) as it relates to "clinical evidence".
Includes preprints, theses, and journal articles. Useful for tracking citation counts and follow-on work.