ხუთშაბათი, აპრილი 16, 2026
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Global Ingredient Risk Index Weight Loss

CLA

Conjugated Linoleic Acid

Also known as: CLA, Linoleic Acid, Conjugated Linoleic Acid, Tonalin, Clarinol

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: cLA is thought to influence body composition by modulating lipid metabolism. It….

02

Safety Profile

Common Adverse Effects

  • Nausea
  • diarrhea
  • stomach upset
  • fatigue
  • headache

Serious Adverse Effects

  • Insulin resistance
  • increased inflammation
  • liver dysfunction

Contraindications

  • Diabetes
  • metabolic syndrome
  • liver disease
  • People taking Warfarin
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03

Interactions

Drug / Nutrient Interaction Mechanism Warning
Warfarin increased bleeding risk — monitor INR closely. Antidiabetic drugs: potential for altered glucose control — adjust medication as needed. Statins: possible additive effects on lipid levels — monitor lipid profile. Monitor
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04

Evidence and Scientific Findings

Overview

Ingredient Overview

Conjugated Linoleic Acid (CLA) is a type of polyunsaturated fatty acid found primarily in meat and dairy products. It is commonly used in dietary supplements for its purported benefits in weight management and body composition improvement. CLA is believed to aid in reducing body fat and increasing lean muscle mass, making it a popular choice among individuals seeking weight loss solutions.
Classification

Biological and Chemical Classification

Chemical Class
Fatty Acid
Biological Class
Lipid
Natural Source
Ruminant animals, dairy products
Scientific Name
Conjugated Linoleic Acid
Chemical Formula
C18H32O2
CAS Number
2420-56-6
Mechanism

Mechanism of Action

CLA is thought to influence body composition by modulating lipid metabolism. It may reduce body fat by inhibiting lipoprotein lipase, an enzyme involved in fat storage. Additionally, CLA is believed to enhance energy expenditure and increase fat oxidation. It may also promote the apoptosis of adipocytes, thereby reducing fat cell numbers.
Clinical Evidence

Clinical Evidence of Effectiveness

Indication Evidence Level Summary
General Moderate The clinical evidence for CLA's effectiveness in weight loss is mixed. Some studies suggest modest reductions in body fat and improvements in lean muscle mass, while others show minimal to no effect. The variability in results may be due to differences in study design, dosage, and duration. Overall, the evidence suggests that CLA may offer some benefits for body composition, but its impact on weight loss is not consistently significant.
Evidence levels: Strong Moderate Limited Experimental
Pharmacokinetics

Pharmacokinetics

Absorption
CLA is absorbed in the small intestine, with bioavailability influenced by the form of CLA and dietary fat content. Peak plasma concentrations are typically reached within 4-6 hours after ingestion. The half-life of CLA in the body is approximately 36 hours.
Distribution
CLA is distributed throughout the body, with a preference for adipose tissue. It is transported in the blood bound to albumin and other plasma proteins. CLA can cross the blood-brain barrier, although its effects in the central nervous system are not well understood.
Metabolism
CLA is metabolized primarily in the liver through beta-oxidation pathways. It is converted into various metabolites, including conjugated dienes and hydroxylated derivatives. The enzymes involved include acyl-CoA oxidase and enoyl-CoA hydratase.
Excretion
CLA and its metabolites are primarily excreted via the biliary route into the feces. A small proportion is eliminated through the urine. The excretion rate can vary depending on dietary intake and individual metabolic differences.
Half-Life
36 hours
Dosage

Recommended Dosage

Condition / Use Typical Dose
Weight management 3-6 grams per day. Body composition improvement: 3-4 grams per day.

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 Conjugated Linoleic Acid (CLA) is a type of polyunsaturated fatty acid found primarily in meat and dairy products.
Key Safety Concern CLA is generally considered safe for most adults when used at recommended dosages. However, individuals with diabetes or metabolic syndrome should exercise caution due to potential effects on insulin sensitivity. Pregnant and breastfeeding women should consult healthcare providers before use. There are no significant regulatory warnings associated with CLA.
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 Conjugated Linoleic Acid (CLA) is a type of polyunsaturated fatty acid found primarily in meat and dairy products.
Main Safety Concern CLA is generally considered safe for most adults when used at recommended dosages. However, individuals with diabetes or metabolic syndrome should exercise caution due to potential effects on insulin sensitivity. Pregnant and breastfeeding women should consult healthcare providers before use. There are no significant regulatory warnings associated with CLA.
Ingredient CLA
Scientific name Conjugated Linoleic Acid
Scientific Evidence Overview
  • 10 studies reviewed
  • 0 high-quality studies (meta-analysis or RCT)
  • Main clinical benefit observed: Conjugated Linoleic Acid (CLA) is a type of polyunsaturated fatty acid found primarily in meat and dairy products.
  • Evidence consistency: High consistency across studies (100%)
Safety Signals
  • CLA is generally considered safe for most adults when used at recommended dosages. However, individuals with diabetes or metabolic syndrome should exercise caution due to potential effects on insulin sensitivity. Pregnant and breastfeeding women should consult healthcare providers before use. There are no significant regulatory warnings associated with CLA.
Evidence Strength Limited
Regulatory Status
  • USA/FDA — Approved
Final Scientific Assessment

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

Ingredient CLA
Evidence reviewed 10 peer-reviewed studies (last 10 years)
Scientific name Conjugated Linoleic Acid
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

2 Animal studies
8 Other / unclassified
  1. Observational / other LOW evidence YELLOW
    There may be a differential mechanistic impact on colorectal cancer of lactose-containing foods between lactase persistent and lactase non-persistent populations. ↗
    Journal Front Nutr
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Szilagyi A et al.. There may be a differential mechanistic impact on colorectal cancer of lactose-containing foods between lactase persistent and lactase non-persistent populations.. Front Nutr. 2026. PMID:41756623.
  2. Animal study LOW evidence YELLOW
    The Effects of Supplemented Conjugated Linoleic Acid on Lipid Metabolism in Cattle. ↗
    Journal Animals (Basel)
    Year 2026
    Study type Animal study
    Evidence strength LOW evidence
    Xiao C et al.. The Effects of Supplemented Conjugated Linoleic Acid on Lipid Metabolism in Cattle.. Animals (Basel). 2026. PMID:41751012.
  3. Observational / other LOW evidence YELLOW
    The Effect of Diet Acid Detergent Fiber Content on Finishing Lamb Meat Fatty Acid Composition, Tenderness and Stability. ↗
    Journal Food Sci Nutr
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Einkamerer OB et al.. The Effect of Diet Acid Detergent Fiber Content on Finishing Lamb Meat Fatty Acid Composition, Tenderness and Stability.. Food Sci Nutr. 2026. PMID:41704731.
  4. Observational / other LOW evidence YELLOW
    Lipidomic Insight into Eggs and Meat of Quail (Coturnix japonica) as Potential 'Superfoods'. ↗
    Journal Molecules
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Biau0142ek M et al.. Lipidomic Insight into Eggs and Meat of Quail (Coturnix japonica) as Potential 'Superfoods'.. Molecules. 2026. PMID:41683387.
  5. Observational / other LOW evidence YELLOW
    c9, t11-Conjugated linoleic acid supplementation improves cognitive memory in u03c9-3 polyunsaturated fatty acid-deficient mice. ↗
    Journal Food Funct
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Ji W et al.. c9, t11-Conjugated linoleic acid supplementation improves cognitive memory in u03c9-3 polyunsaturated fatty acid-deficient mice.. Food Funct. 2026. PMID:41622908.
  6. Observational / other LOW evidence YELLOW
    A Comprehensive Review on Medium- and Long-Chain Fatty Acid-Derived Metabolites: From Energy Sources to Metabolic Signals. ↗
    Journal Metabolites
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Park JB et al.. A Comprehensive Review on Medium- and Long-Chain Fatty Acid-Derived Metabolites: From Energy Sources to Metabolic Signals.. Metabolites. 2026. PMID:41590653.
  7. Animal study LOW evidence YELLOW
    Fabrication and characterization of Idesia polycarpa-derived conjugated linoleic acid microcapsules by spray drying: In vitro digestion and release kinetics. ↗
    Journal Food Chem X
    Year 2026
    Study type Animal study
    Evidence strength LOW evidence
    Yang H et al.. Fabrication and characterization of Idesia polycarpa-derived conjugated linoleic acid microcapsules by spray drying: In vitro digestion and release kinetics.. Food Chem X. 2026. PMID:41551806.
  8. Observational / other LOW evidence YELLOW
    Effects of dietary supplementation of safflower seed oil (Carthamus tinctorius) on rainbow trout growth and physiological parameters (Oncorhynchus mykiss W.). ↗
    Journal J Fish Biol
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Bayir H. Effects of dietary supplementation of safflower seed oil (Carthamus tinctorius) on rainbow trout growth and physiological parameters (Oncorhynchus mykiss W.).. J Fish Biol. 2026. PMID:41539651.
  9. Observational / other LOW evidence YELLOW
    Grazing versus housing in native dairy goats: Impacts on milk yield, composition, and conjugated linoleic acid enrichment under arid conditions. ↗
    Journal Vet World
    Year 2025
    Study type Observational / other
    Evidence strength LOW evidence
    Trejo-Lu00f3pez MT et al.. Grazing versus housing in native dairy goats: Impacts on milk yield, composition, and conjugated linoleic acid enrichment under arid conditions.. Vet World. 2025. PMID:41716174.
  10. Observational / other LOW evidence YELLOW
    The Safety of Nebulized Conjugated Linoleic Acid for COVID-19 Respiratory Tract Infections. ↗
    Journal Cureus
    Year 2025
    Study type Observational / other
    Evidence strength LOW evidence
    Jonsson ST et al.. The Safety of Nebulized Conjugated Linoleic Acid for COVID-19 Respiratory Tract Infections.. Cureus. 2025. PMID:41567914.
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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 CLA. 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 CLA

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.