Rheumatoid arthritis

Efficacy and safety of first-line biological DMARDs in rheumatoid arthritis patients with chronic kidney disease

Ann Rheum DisPublished Retrospective cohort study

Authors' conclusion

bDMARDs demonstrated effective and safe profiles in patients with RA with CKD, even among patients on HD. In particular, IL-6is had a significantly higher drug retention rate in patients with an eGFR of <30 mL/min/1.73 m2 and fewer discontinuations due to ineffectiveness. IL-6is were more efficacious as monotherapy compared with the other bDMARDs.

Study context

Population
Patients with rheumatoid arthritis (RA) prescribed their first biological disease-modifying antirheumatic drugs (bDMARDs) at two hospitals, 2004–2021, including chronic kidney disease (CKD) and haemodialysis
Participants
425 patients
Exposure
First-line bDMARDs across kidney function categories
Outcome
Drug retention rate
Follow-up
36 months
Methodological detailstwo hospitals
  • Two hospitals

Main finding

As reported in the abstract

36-month drug retention rate, all bDMARDs

Observational data: associations, not effects.

Secondary outcomes

36-month drug retention rate, TNFαis

36-month drug retention rate, IL-6is

36-month drug retention rate, CTLA-4Ig

36-month drug retention rate, TNFαis

Retention of TNFαis significantly lower in estimated glomerular filtration rate (eGFR) <30

Discontinuation due to ineffectiveness, IL-6is in eGFR <30

IL-6is showed the highest retention rate and the lowest discontinuation rate due to ineffectiveness in this group: HR
0.11 (95% CI 0.02 to 0.85, p=0.03)

DAS28-CRP/erythrocyte sedimentation rate (ESR) and prednisolone dosage

All bDMARDs improved DAS28-CRP/ESR and reduced prednisolone dosage across all groups

Original publication

Efficacy and safety of first-line biological DMARDs in rheumatoid arthritis patients with chronic kidney disease. Ann Rheum Dis. Published 30 September 2024. doi:10.1136/ard-2024-225914

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

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.