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Research summary ·
AI summary · not yet reviewedSubjects not reportedNot reportedPeer review unconfirmed

MMP Genotype Associations with MS in Humans

A study with 200 participants found a strong association between the MMP2 rs243865 (-1306) TT genotype and multiple sclerosis (MS), with about 10 times higher odds of the disease. The MMP3 rs3025058 5A/6A genotype was also linked to 2.45 times higher odds of MS. Additionally, specific combinations of genotypes indicated even greater risks.

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This plain-English summary was written by AI from a published abstract and may contain errors. It is not medical advice. Read the original study and talk to your MS team before making decisions about treatment.
Human efficacy
Not yet assessed
Mechanism
Not yet assessed
Evidence strength
Not yet assessed
Outcome
Not yet assessed

Why it matters

These findings highlight the potential genetic factors influencing MS susceptibility, suggesting a need for personalized approaches in MS management.

What this does not prove

The study did not find significant links between the genotypes and clinical factors such as attack frequency or disease duration, indicating that while genetics may influence susceptibility, they do not appear to directly affect disease progression.

Next milestone

No next milestone was established from the available source.

Study facts
Study design
Not reported
Participants / samples
200 · basis not reported
Randomised
No
Controlled
Not reported
Primary endpoint met
No
Relevant MS type
Not reported
Publication date
2026-10-02
Evidence reviewed
Abstract only
Regulatory approval
Not reported
Research areas
Not classified

Original sources

Supporting passages (6)
sample sizeMethods: The study included 100 MS patients and 100 healthy controls.
randomizedNo
primary endpoint metNo
publication date2026-10-02
findingsThe MMP2 rs243865 (-1306) TT genotype showed a strong positive association with MS, exhibiting approximately 10-fold higher odds of the disease (p < 0.001).
limitationsNo statistically significant association was found between the examined genotypes or haplotypes and clinical parameters, including attack frequency and disease duration (p > 0.05).

AI assessment, not yet reviewed by a person · version 1 · Community votes are separate from evidence review.

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