ოთხშაბათი, აპრილი 15, 2026
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Global Ingredient Risk Index Metabolic

Chromium Picolinate

Chromium(III) picolinate

Also known as: Chromium(III) picolinate, CrPic, Chromax, CrP, Chromax II

LOW RISK 3.5/10 How?

Evidence Strength: MODERATE

This ingredient is classified as unclassified risk (GIRI score: 3.5/10). The classification is based on mechanistic and clinical evidence: chromium Picolinate enhances the action of insulin by facilitating the uptake of….

02

Safety Profile

Common Adverse Effects

  • Nausea
  • diarrhea
  • headache
  • dizziness
  • skin rash

Serious Adverse Effects

  • Renal impairment
  • liver dysfunction
  • hemolysis
  • rhabdomyolysis

Contraindications

  • Renal impairment
  • liver disease
  • type 1 diabetes
  • psychiatric disorders
  • People taking Insulin
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03

Interactions

Drug / Nutrient Interaction Mechanism Warning
Insulin enhanced hypoglycemic effect — monitor blood glucose levels. NSAIDs: increased chromium absorption — monitor for toxicity. Antacids: reduced chromium absorption — separate administration by 2 hours. Monitor
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04

Evidence and Scientific Findings

Overview

Ingredient Overview

Chromium Picolinate is a chemical compound often used in dietary supplements to improve glucose metabolism and enhance insulin sensitivity. It is derived from the combination of chromium and picolinic acid. This compound is popular in supplements aimed at weight management and blood sugar control, particularly for individuals with type 2 diabetes or metabolic syndrome.
Classification

Biological and Chemical Classification

Chemical Class
Coordination compound
Biological Class
Trace element
Natural Source
Endogenous source, trace mineral in foods
Scientific Name
Chromium(III) picolinate
Chemical Formula
C18H12CrN3O6
CAS Number
14639-25-9
Mechanism

Mechanism of Action

Chromium Picolinate enhances the action of insulin by facilitating the uptake of glucose into cells. It is believed to potentiate insulin signaling pathways, possibly through the activation of insulin receptor kinase and subsequent phosphorylation of insulin receptor substrates. Chromium may also modulate carbohydrate and lipid metabolism by influencing gene expression related to these pathways.
Clinical Evidence

Clinical Evidence of Effectiveness

Indication Evidence Level Summary
General Moderate Clinical studies on Chromium Picolinate have shown mixed results. Some trials suggest modest improvements in glucose control and insulin sensitivity in individuals with type 2 diabetes, while others show minimal or no effects. The quality of evidence varies, with some studies lacking rigorous design or having small sample sizes. Overall, the evidence supports a potential benefit in metabolic health, but further research is needed to confirm these effects.
Evidence levels: Strong Moderate Limited Experimental
Pharmacokinetics

Pharmacokinetics

Absorption
Chromium Picolinate is absorbed in the small intestine, but its bioavailability is relatively low, estimated at about 0.5-2%. Peak plasma concentrations (Cmax) are typically reached within 1-4 hours after oral administration. The compound has a half-life of approximately 24 hours.
Distribution
Chromium is distributed throughout the body, with higher concentrations in the liver, spleen, soft tissue, and bone. It binds moderately to plasma proteins and does not readily cross the blood-brain barrier.
Metabolism
Chromium Picolinate is not extensively metabolized. It remains largely in its original form in the bloodstream and tissues. The picolinate ligand may undergo some degree of metabolism, but the chromium ion itself is not significantly altered.
Excretion
Chromium is primarily excreted through the kidneys in urine. A small amount may also be eliminated via feces. Urinary excretion is the main route of elimination for absorbed chromium.
Half-Life
24 hours
Dosage

Recommended Dosage

Condition / Use Typical Dose
Type 2 Diabetes 200-1000 mcg daily. Metabolic Syndrome: 200-500 mcg daily. Weight Management: 200-400 mcg 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 Chromium Picolinate is a chemical compound often used in dietary supplements to improve glucose metabolism and enhance insulin…
Key Safety Concern Chromium Picolinate is generally considered safe at recommended doses, but high doses may lead to serious adverse effects such as renal and liver damage. Pregnant and breastfeeding women should use caution, as safety data in these populations are limited. Individuals with pre-existing kidney or liver conditions should avoid high doses due to potential exacerbation of these conditions.
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 Chromium Picolinate is a chemical compound often used in dietary supplements to improve glucose metabolism and enhance insulin…
Main Safety Concern Chromium Picolinate is generally considered safe at recommended doses, but high doses may lead to serious adverse effects such as renal and liver damage. Pregnant and breastfeeding women should use caution, as safety data in these populations are limited. Individuals with pre-existing kidney or liver conditions should avoid high doses due to potential exacerbation of these conditions.
Ingredient Chromium Picolinate
Scientific name Chromium(III) picolinate
Scientific Evidence Overview
  • 10 studies reviewed
  • 0 high-quality studies (meta-analysis or RCT)
  • Main clinical benefit observed: Chromium Picolinate is a chemical compound often used in dietary supplements to improve glucose metabolism and enhance insulin…
  • Evidence consistency: High consistency across studies (100%)
Safety Signals
  • Chromium Picolinate is generally considered safe at recommended doses, but high doses may lead to serious adverse effects such as renal and liver damage. Pregnant and breastfeeding women should use caution, as safety data in these populations are limited. Individuals with pre-existing kidney or liver conditions should avoid high doses due to potential exacerbation of these conditions.
Evidence Strength Limited
Regulatory Status
  • USA/FDA — Approved
Final Scientific Assessment

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

Ingredient Chromium Picolinate
Evidence reviewed 10 peer-reviewed studies (last 10 years)
Scientific name Chromium(III) picolinate
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, 12:00

Evidence Distribution

2 Animal studies
8 Other / unclassified
  1. Observational / other LOW evidence YELLOW
    Dietary nanou2011chromium picolinate enhances interferon-gamma expression in heat-stressed broilers vaccinated against Newcastle disease. ↗
    Journal Res Vet Sci
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Hajializadeh F et al.. Dietary nanou2011chromium picolinate enhances interferon-gamma expression in heat-stressed broilers vaccinated against Newcastle disease.. Res Vet Sci. 2026. PMID:41468791.
  2. Animal study LOW evidence YELLOW
    Impact of Chromium Picolinate on Leydig Cell Steroidogenesis and Antioxidant Balance Using an In Vitro Insulin Resistance Model. ↗
    Journal Antioxidants (Basel)
    Year 2023
    Study type Animal study
    Evidence strength LOW evidence
    Moreira R et al.. Impact of Chromium Picolinate on Leydig Cell Steroidogenesis and Antioxidant Balance Using an In Vitro Insulin Resistance Model.. Antioxidants (Basel). 2023. PMID:38247463.
  3. Observational / other LOW evidence YELLOW
    Dietary Effects of Chromium Picolinate and Chromium Nanoparticles in Wistar Rats Fed with a High-Fat, Low-Fiber Diet: The Role of Fat Normalization. ↗
    Journal Nutrients
    Year 2022
    Study type Observational / other
    Evidence strength LOW evidence
    Majewski M et al.. Dietary Effects of Chromium Picolinate and Chromium Nanoparticles in Wistar Rats Fed with a High-Fat, Low-Fiber Diet: The Role of Fat Normalization.. Nutrients. 2022. PMID:36501167.
  4. Observational / other LOW evidence YELLOW
    Oxidative, epigenetic changes and fermentation processes in the intestine of rats fed high-fat diets supplemented with various chromium forms. ↗
    Journal Sci Rep
    Year 2022
    Study type Observational / other
    Evidence strength LOW evidence
    Dworzau0144ski W et al.. Oxidative, epigenetic changes and fermentation processes in the intestine of rats fed high-fat diets supplemented with various chromium forms.. Sci Rep. 2022. PMID:35701510.
  5. Observational / other LOW evidence YELLOW
    Determination of chromium(III) picolinate in dietary supplements by flow injection - electrospray ionization - tandem mass spectrometry, using cobalt(II) picolinate as internal… ↗
    Journal Talanta
    Year 2022
    Study type Observational / other
    Evidence strength LOW evidence
    Arroyo Negrete MA et al.. Determination of chromium(III) picolinate in dietary supplements by flow injection - electrospray ionization - tandem mass spectrometry, using cobalt(II) picolinate as internal standard.. Talanta. 2022. PMID:34953383.
  6. Observational / other LOW evidence YELLOW
    Effect of a high-fat diet and chromium on hormones level and Cr retention in rats. ↗
    Journal J Endocrinol Invest
    Year 2022
    Study type Observational / other
    Evidence strength LOW evidence
    Stu0119pniowska A et al.. Effect of a high-fat diet and chromium on hormones level and Cr retention in rats.. J Endocrinol Invest. 2022. PMID:34550535.
  7. Observational / other LOW evidence YELLOW
    Effects of Supplemental Chromium Nanoparticles on IFN-u03b3 expression of Heat Stress Broilers. ↗
    Journal Biol Trace Elem Res
    Year 2022
    Study type Observational / other
    Evidence strength LOW evidence
    Hamidi O et al.. Effects of Supplemental Chromium Nanoparticles on IFN-u03b3 expression of Heat Stress Broilers.. Biol Trace Elem Res. 2022. PMID:33598892.
  8. Observational / other LOW evidence YELLOW
    Effects of Different Chromium Compounds on Hematology and Inflammatory Cytokines in Rats Fed High-Fat Diet. ↗
    Journal Front Immunol
    Year 2021
    Study type Observational / other
    Evidence strength LOW evidence
    Dworzau0144ski W et al.. Effects of Different Chromium Compounds on Hematology and Inflammatory Cytokines in Rats Fed High-Fat Diet.. Front Immunol. 2021. PMID:33717096.
  9. Animal study LOW evidence YELLOW
    Assessment of DNA Methylation and Oxidative Changes in the Heart and Brain of Rats Receiving a High-Fat Diet Supplemented with Various Forms… ↗
    Journal Animals (Basel)
    Year 2020
    Study type Animal study
    Evidence strength LOW evidence
    Dworzau0144ski W et al.. Assessment of DNA Methylation and Oxidative Changes in the Heart and Brain of Rats Receiving a High-Fat Diet Supplemented with Various Forms of Chromium.. Animals (Basel). 2020. PMID:32825649.
  10. Observational / other LOW evidence YELLOW
    Chromium(III) Glycinate Complex Supplementation Improves the Blood Glucose Level and Attenuates the Tissular Copper to Zinc Ratio in Rats with Mild Hyperglycaemia. ↗
    Journal Biol Trace Elem Res
    Year 2020
    Study type Observational / other
    Evidence strength LOW evidence
    Kru00f3l E et al.. Chromium(III) Glycinate Complex Supplementation Improves the Blood Glucose Level and Attenuates the Tissular Copper to Zinc Ratio in Rats with Mild Hyperglycaemia.. Biol Trace Elem Res. 2020. PMID:30826908.
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06

Score Transparency

Q × L × D × S × 10 = 3.5 / 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 = 3.5 / 10

Final GIRI Score for Chromium Picolinate. 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 3.5/10

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
3.5

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

What drove the Low classification for Chromium Picolinate

GIRI Score 3.5 / 10

A score of 3.5 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.