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Faecal Analyses in Rheumatoid Arthritis Therapy

Completed
Conditions
Rheumatoid Arthritis
Interventions
Registration Number
NCT03775824
Lead Sponsor
Region Skane
Brief Summary

This study evaluates the intestinal microbiome and disease activity in patients with rheumatoid arthritis receiving immunosuppressive therapy. Patients will be analysed at two time points in reference to two predefined primary endpoints:

* Changes in intestinal microbiome

* Response to therapy

The investigators want to evaluate if successful treatment of rheumatoid arthritis coincide with specific changes in the gut flora.

Detailed Description

Methotrexate (MTX) and tumor necrosis factor (TNF) -inhibitors are two efficient medications for the treatment of rheumatoid arthritis. In a substantial number of cases however, these medications remain ineffective. At present, the scientific community has limited understanding of why some patients are resistant to these medications. The purpose of this study is to understand if the gut flora may associate with treatment response.

Recent studies have associated rheumatoid arthritis with intestinal dysbiosis. Specifically, the bacteria Prevotella copri, has been associated with this disease, an observation that has been supported also by mechanistic studies. In patients receiving methotrexate, normalization of dysbiosis has been associated with successful treatment.

This study is of observational character and integrated in the routine clinical care of patients with rheumatoid arthritis at the Rheumatology Clinic, Skane University Hospital, Lund, Sweden. Study participants are asked to deliver blood and fecal sampling at two time-points together with clinical evaluation of disease activity. With an estimated inclusion of 50 patients, at least 20 responders and 20 non-responders are expected to be included and to be compared to each other.

If successful treatment response in rheumatoid arthritis is associated with specific alterations of the gut flora, these results may guide future studies on the impact of dysbiosis and probiotics on this disease.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Rheumatoid arthritis according to the 2010 classification criteria
  • About to start methotrexate or TNF-inhibitor because of active disease
Exclusion Criteria
  • Failure to understand protocol
  • A history of alcohol abuse
  • Concomitant inflammatory bowel disease
  • Any history of diverticulitis
  • A history of failure to comply with prescribed medication
  • Ongoing biological therapy

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
TNF startTNF startPatients with active rheumatoid arthritis who are either naive to TNF-inhibitors, or have not used this medicine in the last year and who are about to start therapy with any of the following (biosimilars included); infliximab, adalimumab, etanercept, certolizumab or golimumab
MTX startMTX startPatients with active rheumatoid arthritis who are either naive to methotrexate, or have not used this medicine in the last year and who are about to start therapy with methotrexate i.v. or s.c.
Primary Outcome Measures
NameTimeMethod
Intestinal gut flora in rheumatoid arthritisAnalysis made at study start/baseline

Intestinal gut flora based on DNA-based microbial analysis of fecal samples

Change in gut floraChange from baseline Dysbiosis Index Score at 6 months

Change in Dysbiosis Index Score at follow up compared to baseline.

The Dysbiosis Index Score measures degree of intestinal dysbiosis on a scale from 1 to 5, where 5 indicates dysbiosis. The Index has been extensively described at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029765/

Change in disease activity/treatment response at follow upChange from baseline DAS-28 at 6 months

Change in Disease Activity Score 28 (DAS-28), an established index of disease activity in rheumatoid arthritis between 0-10, where 10 equals maximum activity.

Secondary Outcome Measures
NameTimeMethod
Adherance to immunosuppressive therapyAnalysis made at 6 months follow up

Is the patient still prescribed the same immunosuppressant compared to baseline?

Change in intestinal concentration PrevotellaChange from baseline concentration at 6 months

Alterations in intestinal concentrations of Prevotella bacteria according to polymerase chain reaction (PCR)-based analysis

Change in intestinal concentration ClostridiaChange from baseline concentration at 6 months

Alterations in intestinal concentrations of Clostridia bacteria according to PCR-based analysis

Change in intestinal concentration LactobacillusChange from baseline concentration at 6 months

Alterations in intestinal concentrations of Lactobacillus bacteria according to PCR-based analysis

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