Mycophenolate sodium treatment in patients with primary Sjögren syndrome: a pilot trial
2007

Mycophenolate Sodium for Primary Sjögren Syndrome

Sample size: 11 publication Evidence: low

Author Information

Author(s): Willeke Peter, Schlüter Bernhard, Becker Heidemarie, Schotte Heiko, Domschke Wolfram, Gaubitz Markus

Primary Institution: Muenster University Hospital

Hypothesis

The study aims to evaluate the efficacy and safety of mycophenolate sodium (MPS) in patients with primary Sjögren syndrome (pSS) who are refractory to other treatments.

Conclusion

Mycophenolate sodium treatment may improve symptoms and some laboratory findings in patients with primary Sjögren syndrome, especially those with shorter disease duration.

Supporting Evidence

  • Eight out of eleven patients tolerated the treatment well.
  • Two patients dropped out due to side effects.
  • Significant improvement in subjective measures of ocular dryness was observed.
  • Laboratory tests showed a reduction in hypergammaglobulinemia and rheumatoid factors.

Takeaway

This study tested a medicine called mycophenolate sodium to see if it helps people with a condition that makes their eyes and mouth dry. It seems to help some people feel better.

Methodology

This was a single-center, open-label pilot trial with 11 patients treated with mycophenolate sodium for 6 months, with assessments at baseline, 3 months, and 6 months.

Potential Biases

Potential bias due to the open-label design and lack of a control group.

Limitations

The study had a small sample size and was not controlled.

Participant Demographics

All participants were women with a mean age of 50.1 years and a mean disease duration of 9.5 years.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/ar2322

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication