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Akkermansia muciniphila

Also called Akkermansia, pasteurized Akkermansia, A. muciniphila MucT, next-generation probiotic

By Kymata Labs EditorialMedical review pendingLast reviewed October 13, 2026 · What changed

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Summary

Akkermansia muciniphila is a gut bacterium sold live or pasteurized. A 2019 pilot found pasteurized cells improved insulin sensitivity, but a larger 142-person trial missed its insulin-sensitivity endpoint; a 2026 trial reported less weight regain after dieting (grade C). Benefits appeared mainly in people with low baseline Akkermansia. EFSA judged pasteurized cells safe up to 3.4 × 10^10 cells/day.

Top graded outcomes:C evidence grade Whole-body insulin sensitivity in metabolic syndromeC evidence grade Weight regain after a low-energy dietD evidence grade Insulin sensitivity, insulin and cholesterol in overweight insulin resistance

Key facts

What it is
A non-toxin-producing, avirulent bacterium reported as part of normal gut microbiota; products use live or pasteurized (inactivated) cells[6][1]
Insulin sensitivity
+28.6% versus placebo with pasteurized cells in a 32-person pilot; no difference on the primary endpoint in a 142-person trial[1][2]
Weight maintenance
1.2 kg regain versus 3.2 kg on placebo over 24 weeks after a low-energy diet (n = 90)[4]
Who responded
Two trials found benefits concentrated in people with low baseline gut Akkermansia[2][3]
EU safety assessment
Pasteurized A. muciniphila safe at 3.4 × 10^10 cells/day for adults; safety in pregnancy and breastfeeding not established[6][7]
Evidence base
5 graded human outcomes on this page
Last reviewed
October 13, 2026

How it works

ProposedLower Akkermansia abundance has been correlated with overweight, obesity, untreated type 2 diabetes and hypertension. Pasteurized MucT improved gut barrier function in preclinical models. In the 2019 human pilot, liver and inflammation markers fell while the overall microbiome was unchanged; how the bacterium acts in people is not established.[1][2]

What the human research says

Human trials only, one row per outcome. The form column shows what each trial actually tested. Grades follow our evidence-grading policy.

At a glance: strongest evidence per outcome

Evidence at a glance: strongest human evidence per outcome
OutcomeGradeEffectStrongest evidenceRows
Insulin sensitivityGrade CMixedRCT · n = 142 · 2026Form tested: Pasteurized A. muciniphila MucT2 rowsIncludes this form
WeightGrade CImprovedRCT · n = 90 · 2026Form tested: Pasteurized A. muciniphila MucT1 rowIncludes this form
Blood sugarGrade DImprovedRCT · n = 76 · 2020Form tested: WBF-011: inulin plus A. muciniphila, Clostridium beijerinckii, Clostridium butyricum, Bifidobacterium infantis and Anaerobutyricum hallii2 rowsIncludes this form

Every graded row

Outcome
Grade
Form tested
Sort

Showing 5 of 5 outcomes. Human trials only.

OutcomeEffectGradeBest evidencePMID
Whole-body insulin sensitivity in metabolic syndromeMixedGrade C

RCT · n = 142 · 2026

Adults with metabolic syndrome, with or without prediabetes (Ireland and Germany)

Form: Pasteurized A. muciniphila MucT · Dose: 30 billion cells/day · Duration: 4 months

The primary endpoint (Matsuda index) did not differ from placebo. Exploratory analyses found improvements in prediabetic, older and low-baseline-Akkermansia subgroups, including GLP-1 response.

42343233 (opens PubMed)Source [2]
Weight regain after a low-energy dietImprovedGrade C

RCT · n = 90 · 2026

Adults with overweight or obesity who lost at least 8% of body weight on an 8-week low-energy diet

Form: Pasteurized A. muciniphila MucT · Dose: Daily (amount not stated in the abstract) · Duration: 24 weeks

Weight regain was 1.2 kg versus 3.2 kg on placebo (P = 0.012), and net loss from baseline was 3.1 kg greater. No serious treatment-related adverse events.

42120725 (opens PubMed)Source [4]
Post-meal glucose in type 2 diabetes (multi-strain product with Akkermansia)ImprovedGrade D

RCT · n = 76 · 2020

Adults with type 2 diabetes

Form: WBF-011: inulin plus A. muciniphila, Clostridium beijerinckii, Clostridium butyricum, Bifidobacterium infantis and Anaerobutyricum hallii · Dose: Twice daily (counts not stated in the abstract) · Duration: 12 weeks

Glucose area under the curve fell by 36.1 mg/dL/180 min versus placebo (P = 0.05), and HbA1c by 0.6 points; no safety or tolerability issues.

32675291 (opens PubMed)Source [5]
Weight and HbA1c in type 2 diabetes with overweightNo effectGrade D

RCT · n = 58 · 2025

Adults with type 2 diabetes and overweight or obesity

Form: Live A. muciniphila strain AKK-WST01 · Dose: Not stated in the abstract · Duration: 12 weeks

Weight and HbA1c fell in both groups with no between-group difference; in people with low baseline Akkermansia, the strain colonized well and lowered weight, fat mass and HbA1c.

39879980 (opens PubMed)Source [3]
Insulin sensitivity, insulin and cholesterol in overweight insulin resistanceImprovedGrade D

Pilot RCT · n = 32 · 2019

Adults with overweight or obesity and insulin resistance

Form: Live or pasteurized A. muciniphila · Dose: 10^10 bacteria/day · Duration: 3 months

Pasteurized cells improved insulin sensitivity (+28.6%) and lowered insulin (−34%) and total cholesterol (−8.7%) versus placebo; weight fell 2.3 kg (P = 0.09). Both forms were safe and well tolerated.

31263284 (opens PubMed)Source [1]

Forms

FormElemental %Absorption (human data)GI toleranceStudied for
Pasteurized (heat-inactivated) A. muciniphilaVaries[6]Not applicable (whole compound or extract; no elemental fraction)Not absorbed; acts in the gut. The EU-assessed product must have no detectable viable cells (<10 CFU/g).[6]Safe and well tolerated at 10^10 cells/day for 3 months; no serious treatment-related adverse events over 24 weeks in the 2026 weight trial.[1][4]Insulin sensitivity and weight maintenance
Live A. muciniphilaVaries[1][3]Not applicable (whole compound or extract; no elemental fraction)Colonization was efficient in people with low baseline Akkermansia and poor in those with high levels.[3]Safe and well tolerated at 10^10 cells/day for 3 months in the 2019 pilot.[1]Insulin resistance and type 2 diabetes

Studied doses

Doses studied in human trials ranged from 10^10 to 3 × 10^10 cells/day for 3 to 4 months, plus a 24-week weight-maintenance trial whose abstract does not state the cell count.[1][2][4]

These are amounts used in research, not personal advice. Your clinician or pharmacist can say what fits you.

Interactions

Published interactions only: each row cites a source. No row means none was found in our sources, not that a combination is safe.

None found in our sources.

Who should be careful

Pregnancy and breastfeeding
EFSA concluded in 2025 that safety of pasteurized A. muciniphila in pregnant and breastfeeding women has not been established.[7]
Children and adolescents
EFSA set lower safe intakes for adolescents (2.1 × 10^10 cells/day at 12–13 years; 3.0 × 10^10 at 14–17); no assessment covers younger children.[7]
Live products
The EU safety opinion covers pasteurized cells with no detectable viable bacteria; it does not assess live-cell products.[6]

Talk to your pharmacist or clinician before starting a supplement, especially if you take prescription medicines.

How to read the label

  1. Live or pasteurizedThe best-studied product is pasteurized; the 2019 pilot reported its insulin-sensitivity improvement for the pasteurized form.[1]
  2. Count cells, not milligramsTrials dosed 10^10 to 3 × 10^10 cells/day; EFSA's adult safe level is 3.4 × 10^10 cells/day.[1][2][6]
  3. Single strain vs blendSome products mix Akkermansia with other bacteria and inulin; results from blends do not describe Akkermansia alone.[5]

Frequently asked questions

What is Akkermansia muciniphila?

A bacterium reported as part of normal human gut microbiota. Supplements contain live or pasteurized cells.[6][1]

Does Akkermansia help weight loss?

In a 2026 trial of 90 adults, pasteurized cells reduced weight regain after dieting (1.2 vs 3.2 kg). Weight changes in earlier trials were small or not significant.[4][1]

Does Akkermansia improve insulin sensitivity?

A 32-person pilot said yes for the pasteurized form, but a 142-person trial found no difference on its primary measure.[1][2]

Why is pasteurized Akkermansia used?

In the 2019 pilot, the insulin-sensitivity and cholesterol improvements were reported for pasteurized cells, and the EU safety opinion covers pasteurized cells.[1][6]

How much Akkermansia was studied?

Trials used 10^10 to 3 × 10^10 cells per day; EFSA considers up to 3.4 × 10^10 pasteurized cells/day safe for adults.[1][2][6]

Is Akkermansia safe?

Trials of 3 to 6 months reported it safe and well tolerated. Safety in pregnancy and breastfeeding has not been established.[1][4][7]

Sources

  1. [1]Supplementation with Akkermansia muciniphila in overweight and obese human volunteers: a proof-of-concept exploratory study.. Nat Med, 2019. RCT PMID 31263284
  2. [2]Effect of pasteurized Akkermansia muciniphila MucT on insulin sensitivity, body composition, and GLP-1 production in subjects with metabolic syndrome: impact of low baseline gut Akkermansia levels.. Gut Microbes, 2026. RCT PMID 42343233
  3. [3]Akkermansia muciniphila supplementation in patients with overweight/obese type 2 diabetes: Efficacy depends on its baseline levels in the gut.. Cell Metab, 2025. RCT PMID 39879980
  4. [4]Pasteurized Akkermansia muciniphila Muc(T) for weight loss maintenance in people with overweight and obesity: a controlled randomized trial.. Nat Med, 2026. RCT PMID 42120725
  5. [5]Improvements to postprandial glucose control in subjects with type 2 diabetes: a multicenter, double blind, randomized placebo-controlled trial of a novel probiotic formulation.. BMJ Open Diabetes Res Care, 2020. RCT PMID 32675291
  6. [6]Safety of pasteurised Akkermansia muciniphila as a novel food pursuant to Regulation (EU) 2015/2283.. EFSA J, 2021. guideline PMID 34484452
  7. [7]Safety of an extension of use of pasteurised Akkermansia muciniphila as a novel food pursuant to Regulation (EU) 2015/2283.. EFSA J, 2025. guideline PMID 41018002

What changed

  1. October 13, 2026 · evidence · independent reviewIndependent review: 2019 pilot (32 completers across three arms) regraded C to D, a single small trial under the grading rubric. All PMIDs re-checked.Writer: Kymata Labs Editorial · No credentialed reviewer yet
  2. October 13, 2026 · all · reviewStrict second-pass self-review (no separate reviewer could be dispatched for this batch): all 7 PMIDs re-verified by NCBI esummary (titles and years match the record) and efetch checked for retraction, expression-of-concern and erratum flags (none flagged); every evidence row, key fact, form, dose, label line, FAQ and insight re-read against its abstract, and against PMC full text where the dose or count lives. Fixes: removed mucus-layer and mouse-study statements not supported by the cited sources, unverified countries, and a live-versus-pasteurized comparison the abstract does not make. Page set indexable.Writer: Kymata Labs Editorial · No credentialed reviewer yet
  3. October 13, 2026 · all · new pageFirst draft. Every PMID checked against NCBI E-utilities esummary (title and year from the record) and abstracts read for each cited row, including the 2021 and 2025 EFSA novel-food opinions. No NIH ODS or NCCIH fact sheet covers Akkermansia.Writer: Kymata Labs Editorial · No credentialed reviewer yet

How we write, grade and correct these pages: editorial and evidence policy.

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