Inflammatory myopathies

Tacrolimus personalized therapy based on CYP3A5 genotype in Chinese patients with idiopathic inflammatory myopathies

Rheumatology (Oxford)Published Cohort study

Authors' conclusion

TAC treatment may elicit favorable outcome in patients with IIM and MDA5+ DM when Cmin exceeded 5.35 and 5.85 ng/ml, which is crucial to a lower relapse rate.

Study context

Population
Chinese patients with idiopathic inflammatory myopathies (IIM) treated with tacrolimus (TAC), including MDA5+ DM467 Cmin
Participants
134 patients
Exposure
CYP3A5 expressers vs nonexpressers; TAC Cmin vs relapse
Outcome
Relationship between TAC Cmin and relapses; optimal Cmin by ROC analysis
Methodological detailsROC analysis, CYP3A5 genotype-based dosing
  • ROC analysis
  • CYP3A5 genotype-based dosing

Main finding

As reported in the abstract

Optimal TAC Cmin cutoff for relapse, IIM

Optimal cutoff, acute IIM (P = 0.001)

5.30 ng/ml

Optimal cutoff, subacute IIM (P = 0.013)

5.85 ng/ml

Optimal cutoff, chronic IIM (P = 0.002)

4.85 ng/ml

Optimal cutoff, all-phase IIM (P <0.001)

5.35 ng/ml

Observational data: associations, not effects.

Further findings

TAC dose required to attain target Cmin

P = 0.019

Optimal TAC Cmin cutoff for relapse, MDA5+ DM

Ng/ml

Acute MDA5+ DM (P = 0.007)
5.35
Subacute MDA5+ DM (P = 0.001)
5.85
Chronic MDA5+ DM (P = 0.036)
5.55
All-phase MDA5+ DM (P <0.001)
5.85

TAC dose required to attain target Cmin

CYP3A5 genotype one of the significant factors influencing TAC Cmin

Original publication

Tacrolimus personalized therapy based on CYP3A5 genotype in Chinese patients with idiopathic inflammatory myopathies. Rheumatology (Oxford). Published 18 June 2024. doi:10.1093/rheumatology/keae316

Composed by AI from the published abstract and checked against it. How Briefs are made →

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