Herb Profile

Cinnamon

Cinnamomum verum

Cinnamon is the aromatic bark of Cinnamomum trees; this profile covers Cinnamomum verum, the Ceylon or 'true' cinnamon, which is low in coumarin compared with the more common cassia types.

Last reviewed: 3 sources citedReport a correctionProfile-wide ·B Moderate

Use extra caution Hepatotoxicity risk lower than cassia Details

Evidence
Moderate Evidence
Typical onset
Varies by prep
Safety rating
Moderate caution
Best for
Metabolic
Avoid / review if
Antidiabetic Drugs (Additive Hypoglycemia)
Cinnamon monograph visual
Generated profile category visual

At a glance

From this profile's structured data
Evidence
Grade B
Safety
Hepatotoxicity risk lower than cassia
Profile context
metabolic
Next steps

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Safety

Safety & Cautions

Hepatotoxicity risk lower than cassia

Elevated caution

Caution level: Elevated. One caution category applies — read it before use.

  • Liver-SensitiveLiver-related caution language appears in the profile.
Detailed safety fields

Pregnancy, breastfeeding, and contraindications

  • Antidiabetic Drugs (Additive Hypoglycemia)

Safety classifications

  • Liver-Sensitive: Liver-related caution language appears in the profile.

Full safety note

  • Hepatotoxicity risk lower than cassia

Safety labels

  • Liver-Sensitive

Evidence-based safety

Caution when combined

Severity and certainty are shown separately. A high-priority caution can still be theoretical: these pairings are screened from shared contraindication mechanisms and are not automatically documented clinical interactions. Provenance identifies the source fields that produced each flag; it does not upgrade the certainty of the pairwise claim.

Evidence

Evidence Summary

Evidence lens

Useful signal, but study design, dose, and population still matter.

ModerateModerate Evidence

Human clinical evidence: Present in source signals

Mechanistic / preclinical: Mechanism mappedMetabolic Regulation · Glucose Metabolism Support

Research maturity: Established researchLong Term Human Evidence May Be Limited.

Safety boundary: Safety note availableHepatotoxicity risk lower than cassia

This profile cites 3 human studies.

Study design details
Evidence Grade

Grade B: Moderate Evidence

Evaluation of methodological rigor, population reach, and evidence alignment.

Design Match
Meta-analysis
Risk of Bias
Low
Consistency
Consistent
Strongest recorded design is a meta-analysis, drawn from 9 recorded studies, 7 in people. No disagreement is recorded across them.
How evidence grades work

Each grade reflects the strength and consistency of published human evidence — not marketing claims. Grades are based on study count, design quality, effect size, consistency, and recency.

Strong
Multiple RCTs, consistent direction, adequate effect size
Moderate
Some RCTs or consistent observational data in humans
Preliminary / Mixed
Animal or in-vitro only, or conflicting human data
Traditional / Theoretical
Traditional use only; no controlled human trials
Clinical Study Summaries (8)4 human evidence sources · 0 human trials · Participant totals not consistently reported · Consistency not yet classifiable

Filter by study class

Showing 8 of 8 studies.

What the evidence actually shows

This table contains 8 structured sources, including 4 human evidence sources; 0 are human trials. A reliable participant total cannot be calculated because sample size is not consistently structured in the cited sources. Source-to-conclusion relationships are not classified in this structured set, so consistency is not yet classifiable.

Profile-wide evidence grade: see the profile grade above · Confidence: not separately assigned

What would change our conclusion?

Larger, well-controlled human trials using comparable populations, doses, preparations, and clinically meaningful outcomes could materially strengthen or weaken this conclusion. Replication in a different population or a high-quality synthesis resolving current disagreement could also materially change confidence.

StudyDesignNDoseDurationPopulationOutcomeResult & magnitudeSource

The effect of cinnamon supplementation on glycemic control in patients with type 2 diabetes mellitus: An updated systematic review and dose-response meta-analysis of randomized controlled trials

Moridpour AH et al. · Phytother Res · 2024

Background
Meta-analysis

Statistically combines results from multiple eligible studies; confidence still depends on the quality, consistency, and directness of those studies.

PubMed

The effect of cinnamon supplementation on cardiovascular risk factors in adults: a GRADE assessed systematic review, dose-response and meta-analysis of randomized controlled trials

Background
Meta-analysis

Statistically combines results from multiple eligible studies; confidence still depends on the quality, consistency, and directness of those studies.

Pooled RCT evidence showed reductions across waist circumference, blood pressure, fasting glucose, insulin, HbA1c, HOMA-IR, CRP, LDL, total cholesterol, triglycerides, and MDA.PubMed

Effects of Cinnamon Supplementation on Lipid Profile: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

Background
Meta-analysis

Statistically combines results from multiple eligible studies; confidence still depends on the quality, consistency, and directness of those studies.

Updated pooled evidence supports favorable changes in selected lipid-profile measures with cinnamon supplementation.PubMed

Effect of cinnamon as a Chinese herbal medicine on markers of cardiovascular risk in women with polycystic ovary syndrome: A systematic review and meta-analysis of randomized controlled trials

Background
Meta-analysis

Statistically combines results from multiple eligible studies; confidence still depends on the quality, consistency, and directness of those studies.

Cinnamon modestly reduced weight and improved HOMA-IR, fasting glucose, total cholesterol, and LDL in women with PCOS.PubMed

Antibacterial mechanisms of cinnamon and its constituents: A review

Vasconcelos NG et al. · Microb Pathog · 2018

Background
Narrative review

Summarizes selected literature without the full prespecified search and selection methods of a systematic review.

PubMed

Cinnamon as a Complementary Therapeutic Approach for Dysglycemia and Dyslipidemia Control in Type 2 Diabetes Mellitus and Its Molecular Mechanism of Action: A Review

Silva ML et al. · Nutrients · 2022

Background
Narrative review

Summarizes selected literature without the full prespecified search and selection methods of a systematic review.

PubMed
Show 2 more studies

The effects of cinnamon on patients with metabolic diseases: an umbrella review of meta-analyses of randomized controlled trials

Background
Narrative review

Summarizes selected literature without the full prespecified search and selection methods of a systematic review.

Cinnamon was associated with improvements in fasting glucose and lipid profiles, with stronger effects in diabetes/metabolic-syndrome populations.PubMed

Effect of cinnamon supplementation on blood pressure, oxidative stress, and inflammatory biomarkers in adults: An umbrella review of the meta-analyses of randomized controlled trials

Background
Narrative review

Summarizes selected literature without the full prespecified search and selection methods of a systematic review.

Higher-level evidence suggests possible improvements in blood pressure, oxidative-stress markers, and some inflammatory markers.PubMed

Dosing & Timing

Dose guidance
1 3 g/day powder or equivalent extract
How Cinnamon works

Simplified mechanism pathway based on preclinical and pharmacological evidence. Does not confirm clinical efficacy.

Mechanism Pathway — How Cinnamon Works

How Cinnamon WorksCinnamon acts on biological target pathways via metabolic (regulation), leading to metabolic.CinnamonBiological TargetBiological pathwayMetabolicRegulationMetabolicObservable outcomeGlucoseRegulation
CompoundTarget / ReceptorMechanismEffect / Outcome
Mechanisms & biological pathways

Preclinical pathways. Proposed mechanisms from in vitro and animal research; these do not confirm clinical outcomes in humans.

  • Metabolic Regulation
  • Glucose Metabolism Support

Active Compounds

Key constituents studied in Cinnamon, with full pharmacology and safety profiles.

Compare related active botanicals

Explore botanicals with similar chemistry, effects, or safety considerations in the Botanical Activity Atlas.

Guides that use Cinnamon

Compare & Sourcing

Compare side-by-side tradeoffs or verify active marker guidelines.

Review available sources for Cinnamon

Independent database mapping — evaluated separately from safety and efficacy scores.

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Safety first · Harm reduction

This information is educational and not medical advice. Start low, avoid risky combinations, and consult a licensed clinician before making health decisions—especially if you use medications, have diagnosed conditions, or are pregnant/breastfeeding.

Learn how we evaluate confidence, safety, and intensity on the methodology page.

Editorial Review

Checked against primary sources, cited evidence, and contraindication language before publication. Evidence claims, safety language, and affiliate modules are reviewed independently. Not personal medical advice.

Editorial Standards →

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Botanical profile context

How to interpret Cinnamon

Cinnamon herb profile with evidence context, key research topics, source notes, safety context, and references presented in an evidence-first format. Use this herb profile as a starting point for evidence review, not as a recommendation to start a new supplement. Botanical products can vary by plant part, extract ratio, standardization, dose, and contaminant testing, so two labels with the same common name may not behave the same way.

When reviewing Cinnamon, compare the traditional-use context against the human evidence, mechanism notes, and safety cautions. Pay special attention to pregnancy, breastfeeding, liver or kidney disease, blood-pressure effects, sedation, stimulation, anticoagulant use, antidepressants, and any prescription medication overlap.

For product decisions, prefer transparent labels, named extracts, clear serving sizes, and third-party quality testing. Avoid treating a long list of possible mechanisms as proof that an herb will solve a specific condition.