Evidence map›Paper›PMID 40277101›Full record

ReviewCurrent protein & peptide science2025

A2 Milk: The Impact of Genetic Variation in Milk Protein on Human Health.

Leila Ben Farhat, Hiba Selmi, Violetta Toth, Amanda Hoarau, Agnes Suli, Kata Sara Labas, Abidi Ferid, Edit Miko

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current protein & peptide science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Leila Ben FarhatLaboratory of Protein Engineering and Bioactive Molecules (LR11ES24), INSAT (National Institute of Applied Science and Technology, University of Carthage, Tunis, BP 676-1080, Tunisia.ORCID 0000-0002-6912-6088
Hiba SelmiLaboratory of Protein Engineering and Bioactive Molecules (LR11ES24), INSAT (National Institute of Applied Science and Technology, University of Carthage, Tunis, BP 676-1080, Tunisia.ORCID 0000-0002-4446-5657
Violetta TothFaculty of Agriculture, University of Szeged, H-6800 Hódmezovásárhely, Hungary.ORCID 0000-0002-1394-716X
Amanda HoarauFaculty of Sciences and Technology, Engineering School (Esiroi), University of Reunion Island's, Agri-Food, St Pierre, Reunion Island.ORCID 0000-0001-9665-4110
Agnes SuliFaculty of Agriculture, University of Szeged, H-6800 Hódmezovásárhely, Hungary.ORCID 0000-0003-4939-2423
Kata Sara LabasFaculty of Agriculture, University of Szeged, H-6800 Hódmezovásárhely, Hungary.ORCID 0009-0007-7439-7994
Abidi FeridLaboratory of Protein Engineering and Bioactive Molecules (LR11ES24), INSAT (National Institute of Applied Science and Technology, University of Carthage, Tunis, BP 676-1080, Tunisia.ORCID 0000-0002-7896-1624
Edit MikoFaculty of Agriculture, University of Szeged, H-6800 Hódmezovásárhely, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, a new type of cow's milk has been commercialized in the markets, called A2 milk. It is derived from a specific allelic composition on chromosome 6. The only difference between A1 and A2 milk results from the polymorphism at the 67 amino acid chain. In this position, A2 milk has a proline amino acid, while A1 milk has a histidine amino acid. Proteins are one of the most important components of milk, especially casein, and have received significant attention as they are the source of bioactive opioid peptides called beta-casomorphin-7. Peptides are released through enzymatic digestion of casein and whey proteins. More precisely, this bioactive peptide is produced by sequential gastrointestinal digestion of bovine A1 variants proteins, while this phenomenon is not present in variant A2. Studies have reported that A1 milk can be harmful to health not only for adults but also for infants and that β-casein A2 becomes a safer choice following the relationship between disease risk and consumption of the beta-casomorphin-7 peptide. Indeed, epidemiological studies suggest that the released beta-casomorphin-7 peptide is a risk factor for the development of diseases in humans, but this has not yet been validated by other studies. In contrast, A2 milk has been suggested as an appropriate substitute for A1 milk since populations consuming milk containing high levels of the A2 beta-casein variant have lower rates of diseases, such as diabetes, coronary heart disease, autism, and schizophrenia.

Indexed as

CaseinsGenetic VariationMilkMilk ProteinsAnimalsCattleDiabetes MellitusEndorphinsHumansPeptide FragmentsWhey Proteinsbeta-casomorphin 7CaseinsEndorphinsMilk ProteinsPeptide FragmentsWhey ProteinsA1 milkA2 milkCowgenetic variation.health claimspolymorphism

Identifiers

PMID40277101

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.