ხუთშაბათი, აპრილი 30, 2026
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Global Ingredient Risk Index Weight Loss

Irvingia Gabonensis

Irvingia gabonensis

Also known as: African mango, Dika nut, Bush mango, Wild mango, Ogbono

LOW RISK 3.0/10 How?

Evidence Strength: MODERATE

This ingredient is classified as unclassified risk (GIRI score: 3.0/10). The classification is based on mechanistic and clinical evidence: irvingia gabonensis is thought to aid weight loss by affecting adipogenesis and….

02

Safety Profile

Common Adverse Effects

  • Headache
  • flatulence
  • sleep disturbances
  • dry mouth
  • gastrointestinal discomfort

Serious Adverse Effects

  • Allergic reactions
  • liver dysfunction
  • severe gastrointestinal distress

Contraindications

  • Liver disease
  • pregnancy
  • breastfeeding
  • hypersensitivity
  • People taking Antidiabetic drugs
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03

Interactions

Drug / Nutrient Interaction Mechanism Warning
Antidiabetic drugs potential additive effects — monitor blood glucose levels. Antihypertensive drugs: possible enhancement of effects — monitor blood pressure. Statins: potential interaction affecting lipid levels — clinical monitoring advised. Monitor
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04

Evidence and Scientific Findings

Overview

Ingredient Overview

Irvingia gabonensis, commonly known as African mango, is a tree native to West Africa. The seeds of this plant, often referred to as dika nuts, are used in dietary supplements for their purported weight loss benefits. These seeds are believed to influence metabolism and appetite regulation, making them popular in weight management products.
Classification

Biological and Chemical Classification

Chemical Class
Polyphenol
Biological Class
Plant extract
Natural Source
Irvingia gabonensis seeds
Scientific Name
Irvingia gabonensis
Chemical Formula
Not applicable
CAS Number
Not applicable
Mechanism

Mechanism of Action

Irvingia gabonensis is thought to aid weight loss by affecting adipogenesis and lipolysis. It may enhance the activity of adiponectin, a hormone involved in regulating glucose levels and fatty acid breakdown. Additionally, it is believed to inhibit the enzyme glycerol-3-phosphate dehydrogenase, which plays a role in the conversion of glucose to fat. The extract may also increase leptin sensitivity, potentially reducing appetite.
Clinical Evidence

Clinical Evidence of Effectiveness

Indication Evidence Level Summary
General Moderate Several small-scale clinical trials have suggested that Irvingia gabonensis can contribute to weight loss and improve metabolic parameters. However, the studies often have limitations such as small sample sizes and short durations. While some trials report significant reductions in body weight and waist circumference, the overall quality of evidence is moderate, and further research is needed to confirm these findings.
Evidence levels: Strong Moderate Limited Experimental
Pharmacokinetics

Pharmacokinetics

Absorption
The bioavailability of Irvingia gabonensis extract is not well-documented, but it is generally assumed to be absorbed in the gastrointestinal tract. The onset of effects is typically observed within a few weeks of consistent use. The exact Cmax and half-life are not clearly established.
Distribution
There is limited information on the distribution of Irvingia gabonensis in the body. It is presumed to be distributed via the bloodstream, but specific data on protein binding and blood-brain barrier penetration are lacking.
Metabolism
The metabolic pathways of Irvingia gabonensis are not fully understood. It is likely metabolized in the liver, but specific enzymes and metabolites have not been clearly identified in the literature.
Excretion
Excretion details for Irvingia gabonensis are not well-characterized. It is presumed to be eliminated primarily through the renal route, with urinary excretion of metabolites.
Dosage

Recommended Dosage

Condition / Use Typical Dose
Weight loss 150-300 mg twice daily.

Dosage ranges are based on clinical studies and commonly used supplement formulations. Individual requirements may vary.

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05

SETI — Scientific Evidence Transparency Index

SETI Score 50/100
Risk Level High risk
Scientific Confidence Low
Evidence Strength Limited
Key Benefit Irvingia gabonensis, commonly known as African mango, is a tree native to West Africa.
Key Safety Concern Irvingia gabonensis is generally considered safe for short-term use in healthy adults. However, caution is advised for individuals with liver conditions due to potential hepatotoxicity. Pregnant and breastfeeding women should avoid its use due to insufficient safety data. Regulatory agencies have not issued specific warnings, but users should consult healthcare providers before starting supplementation.
Evidence Reviewed 10 PubMed studies
Scientific Confidence Low
Based on study quality, consistency, and recency

Executive Summary — Ingredient Assessment

SETI Score 50/100
Risk Level High risk
Evidence Strength Limited
Main Benefit Irvingia gabonensis, commonly known as African mango, is a tree native to West Africa.
Main Safety Concern Irvingia gabonensis is generally considered safe for short-term use in healthy adults. However, caution is advised for individuals with liver conditions due to potential hepatotoxicity. Pregnant and breastfeeding women should avoid its use due to insufficient safety data. Regulatory agencies have not issued specific warnings, but users should consult healthcare providers before starting supplementation.
Ingredient Irvingia Gabonensis
Scientific name Irvingia gabonensis
Scientific Evidence Overview
  • 10 studies reviewed
  • 0 high-quality studies (meta-analysis or RCT)
  • Main clinical benefit observed: Irvingia gabonensis, commonly known as African mango, is a tree native to West Africa.
  • Evidence consistency: High consistency across studies (100%)
Safety Signals
  • Irvingia gabonensis is generally considered safe for short-term use in healthy adults. However, caution is advised for individuals with liver conditions due to potential hepatotoxicity. Pregnant and breastfeeding women should avoid its use due to insufficient safety data. Regulatory agencies have not issued specific warnings, but users should consult healthcare providers before starting supplementation.
Evidence Strength Limited
Regulatory Status
  • USA/FDA — Approved
Final Scientific Assessment

The available scientific evidence for Irvingia Gabonensis indicates notable safety signals that warrant caution. Use should be considered carefully and monitored, particularly in sensitive populations or alongside other medications.

Ingredient Irvingia Gabonensis
Evidence reviewed 10 peer-reviewed studies (last 10 years)
Scientific name Irvingia gabonensis
50 /100

Total SETI Score

High risk
Evidence quality 10/40
Evidence consistency 20/20
Safety signals 0/20
Study recency 10/10
Evidence transparency 10/10

Evidence Summary

  • 10 studies reviewed
  • 0 high-quality studies (meta-analysis or systematic review)
  • 0 studies identified benefits or no safety concern (GREEN)
  • 10 studies reported limited or advisory safety evidence (YELLOW)

Evidence Policy

Only peer-reviewed scientific literature indexed in PubMed or comparable databases is included in this evaluation. Commercial websites, blogs, and marketing materials are excluded. All references include direct traceable links to source documents.

Last updated: 06 მარ 2026, 12:01

Evidence Distribution

1 Animal studies
9 Other / unclassified
  1. Observational / other LOW evidence YELLOW
    Technological innovations in margarine production: Current trends and future perspectives on trans-fat removal and saturated fat replacement. ↗
    Journal Compr Rev Food Sci Food Saf
    Year 2025
    Study type Observational / other
    Evidence strength LOW evidence
    Bihola A et al.. Technological innovations in margarine production: Current trends and future perspectives on trans-fat removal and saturated fat replacement.. Compr Rev Food Sci Food Saf. 2025. PMID:39699296.
  2. Observational / other LOW evidence YELLOW
    Antibacterial activities, PASS prediction and ADME analysis of phytochemicals from Curcubita moschata, Curcubita maxima, and Irvingia gabonensis: insights from in silico studies. ↗
    Journal In Silico Pharmacol
    Year 2024
    Study type Observational / other
    Evidence strength LOW evidence
    Abdul-Hammed M et al.. Antibacterial activities, PASS prediction and ADME analysis of phytochemicals from Curcubita moschata, Curcubita maxima, and Irvingia gabonensis: insights from in silico studies.. In Silico Pharmacol. 2024. PMID:39035102.
  3. Animal study LOW evidence YELLOW
    Anti-diabetic, anti-pancreatic lipase, and anti-protein glycation potential of Irvingia gabonensis stem bark extracts: in vitro and in silico studies. ↗
    Journal In Silico Pharmacol
    Year 2024
    Study type Animal study
    Evidence strength LOW evidence
    Omonkhua AA et al.. Anti-diabetic, anti-pancreatic lipase, and anti-protein glycation potential of Irvingia gabonensis stem bark extracts: in vitro and in silico studies.. In Silico Pharmacol. 2024. PMID:38751710.
  4. Observational / other LOW evidence YELLOW
    Evaluation of microstructure evolution and mechanical properties of Al-10Zn-1.63Si/Irvingia gabonensis particulates alloy composites. ↗
    Journal J Appl Biomater Funct Mater
    Year 2024
    Study type Observational / other
    Evidence strength LOW evidence
    Jeremiah Lekwuwa C et al.. Evaluation of microstructure evolution and mechanical properties of Al-10Zn-1.63Si/Irvingia gabonensis particulates alloy composites.. J Appl Biomater Funct Mater. 2024. PMID:38488249.
  5. Observational / other LOW evidence YELLOW
    Irvingia gabonensis baill. (African Mango): A comprehensive review of its ethnopharmacological significance, unveiling its long-standing history and therapeutic potential. ↗
    Journal J Ethnopharmacol
    Year 2024
    Study type Observational / other
    Evidence strength LOW evidence
    Hassan YR et al.. Irvingia gabonensis baill. (African Mango): A comprehensive review of its ethnopharmacological significance, unveiling its long-standing history and therapeutic potential.. J Ethnopharmacol. 2024. PMID:38395180.
  6. Observational / other LOW evidence YELLOW
    A mechanistic exploration of the metabolome of African mango seeds and its potential to alleviate cognitive impairment induced by high-fat/high-carbohydrate diets: Involvement… ↗
    Journal J Ethnopharmacol
    Year 2024
    Study type Observational / other
    Evidence strength LOW evidence
    Hassan YR et al.. A mechanistic exploration of the metabolome of African mango seeds and its potential to alleviate cognitive impairment induced by high-fat/high-carbohydrate diets: Involvement of PI3K/AKT/GSK-3u03b2/CREB, PERK/CHOP/Bcl-2, and AMPK/SIRT-1/mTOR Axes.. J Ethnopharmacol. 2024. PMID:38218500.
  7. Observational / other LOW evidence YELLOW
    A comprehensive review on clinically proven medicinal plants in the treatment of overweight and obesity, with mechanistic insights. ↗
    Journal Heliyon
    Year 2023
    Study type Observational / other
    Evidence strength LOW evidence
    Aziz MA et al.. A comprehensive review on clinically proven medicinal plants in the treatment of overweight and obesity, with mechanistic insights.. Heliyon. 2023. PMID:36816319.
  8. Observational / other LOW evidence YELLOW
    Flavonoid glycosides and ellagic acid cognates from defatted African mango (Irvingia gabonensis) seed kernel. ↗
    Journal Nat Prod Res
    Year 2023
    Study type Observational / other
    Evidence strength LOW evidence
    Zulfiqar F et al.. Flavonoid glycosides and ellagic acid cognates from defatted African mango (Irvingia gabonensis) seed kernel.. Nat Prod Res. 2023. PMID:36318869.
  9. Observational / other LOW evidence YELLOW
    Dietary supplements for obesity. ↗
    Journal J Prev Med Hyg
    Year 2022
    Study type Observational / other
    Evidence strength LOW evidence
    Bonetti G et al.. Dietary supplements for obesity.. J Prev Med Hyg. 2022. PMID:36479472.
  10. Observational / other LOW evidence YELLOW
    Effects of Irvingia gabonensis Extract on Metabolism, Antioxidants, Adipocytokines, Telomere Length, and Aerobic Capacity in Overweight/Obese Individuals. ↗
    Journal Nutrients
    Year 2022
    Study type Observational / other
    Evidence strength LOW evidence
    Nonsa-Ard R et al.. Effects of Irvingia gabonensis Extract on Metabolism, Antioxidants, Adipocytokines, Telomere Length, and Aerobic Capacity in Overweight/Obese Individuals.. Nutrients. 2022. PMID:36364907.
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06

Score Transparency

Q × L × D × S × 10 = 3.0 / 10

The GIRI Score is the product of four independently computed evidence components, each normalised to 0–1, then scaled to 0–10. Every component is derived exclusively from peer-reviewed references and regulatory data — no editorial judgement is applied.

Q
Evidence Quantity 0 / 10
0%

0 of 10 approved references (score saturates at 10). More peer-reviewed studies = stronger evidence base.

Method: Q = number of approved references ÷ 10 (capped at 1.0)

L
Evidence Quality 5 / 10
50%

Limited — mostly case reports or animal studies

Method: L = mean study-level weight across approved references. Level 1 (meta-analysis / systematic review) = 1.0; Level 2 (RCT) = 0.8; Level 3 (cohort/case-control) = 0.6; Level 4 (case report) = 0.4; Level 5 (animal / in-vitro) = 0.2.

D
Evidence Direction 5 / 10
Benefit
Risk
50%

Mixed or neutral — roughly equal benefit and risk signals

Method: D = (sum of risk-scored references − sum of benefit-scored references) ÷ total evidence score, then scaled from [−1, 1] to [0, 1]. 0.0 = pure benefit; 0.5 = neutral; 1.0 = pure risk.

S
Safety Signals 5 / 10
50%

One or more monitoring-level safety signals active

Method: S = 0.5 (neutral baseline) + sum of active signal severity deltas ÷ 10. Severity deltas: Critical = +2.0, High = +1.5, Moderate = +1.0, Low = +0.5. Capped at 1.0.

0Q × 5L × 5D × 5S = 3.0 / 10

Final GIRI Score for Irvingia Gabonensis. Risk level thresholds: Low 0–3.0 · Moderate 3.0–5.5 · High 5.5–7.5 · Critical 7.5–10.

Full methodology & data sources

The GIRI Score is computed entirely from structured data — no editorial scoring or subjective weighting is applied at any step.

  • References: Only approved references are counted. Each reference is assigned an evidence level (L1–L5) and a direction (risk / neutral / benefit) by the reference manager or AI classifier.
  • Safety Signals: Sourced from regulatory agencies (FDA, EMA, Health Canada, TGA, and others) and pharmacovigilance databases. Only active signals count toward the score.
  • Formula version: GIRI Score v3.7.0 — Q × L × D × S × 10.
  • Limitations: The score reflects published evidence and recorded signals as of the last update date. It is not a clinical risk assessment and should not replace advice from a qualified healthcare professional.
07

Risk Level Classification

LOW RISK 3.0/10

Based on available regulatory signals and scientific evidence, this ingredient presents a low safety concern under normal conditions of use.

LOW
0–3.0
MODERATE
3.0–5.5
HIGH
5.5–7.5
CRITICAL
7.5–10
3.0

The score pin shows exactly where this ingredient falls on the fixed risk scale.

What drove the Low classification for Irvingia Gabonensis

GIRI Score 3.0 / 10

A score of 3.0 places this ingredient in the Low band. Thresholds: Low 0–3.0 · Moderate 3.0–5.5 · High 5.5–7.5 · Critical 7.5–10.

Evidence Quantity (Q) 0 / 10 refs

0 approved references.

Evidence Quality (L) 50%

Limited — mostly case reports or animal studies (Level 4–5).

Evidence Direction (D) 50% toward risk

Neutral or mixed — benefit and risk signals roughly balanced.

Safety Signals (S) 0 active signals

No active signals — S component is at neutral baseline (0.5), contributing no extra risk weight.

Regulatory Status 1 jurisdiction with restrictions

1 jurisdiction has active restrictions or advisories. Regulatory signals are recorded as Safety Signals and raise the S component.

How are the Low / Moderate / High / Critical thresholds defined?

The four risk levels are fixed score bands. A score is assigned to exactly one level based on where it falls:

LevelScoreMeaning
LOW0.0 – 2.9Sparse or predominantly beneficial evidence. No active safety alerts.
MODERATE3.0 – 5.4Mixed signals — some risk alongside benefit. Caution at high doses or in sensitive groups.
HIGH5.5 – 7.4Multiple studies or regulatory alerts documenting adverse effects. Professional oversight recommended.
CRITICAL7.5 – 10Regulatory restrictions in one or more major jurisdictions. Serious documented harm. Avoid without specialist supervision.

Thresholds are fixed constants (GIRI_Score_Utils::LEVEL_THRESHOLDS). They do not change per ingredient and are never subject to editorial adjustment.

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