JAK2 Mutation May Predict Response and Guide First Line Treatment in Rheumatoid Arthritis

Sponsor
Mansoura University (Other)
Overall Status
Completed
CT.gov ID
NCT04667988
Collaborator
(none)
76
1
2
16
4.8

Study Details

Study Description

Brief Summary

This study included 76 newly diagnosed RA patients and 50 matched controls. Basal JAK2 mutation was assessed by PCR in blood samples, TNF-α and IL 6 were measured by ELISA in serum of patients and controls. All patients started therapy with conventional synthetic DMARDs (including methotrexate). Response assessment at 3rd month was evaluated by DAS28 and ACR response criteria. JAK2 mutation was correlated with different clinical and laboratory parameters of patients.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: JAK expression
N/A

Detailed Description

PCR detection of the JAK-2 V617F mutation using ASO specific PCR Genetic marker:
The detection of jak2 V617F mutation were done by using the following primers (JAK2 Reverse:

5' CTGAATAGTCCTACAGTGTTTTCAGTTTCA 3', JAK2 Forward (specific): 5' AGCATTTGGTTTTAAATTATGGAGTATATT 3' and JAK2 Forward (internal control): 5' ATCTATAGTCATGCTGAAAGTAGGAGAAAG 3'). Cycling conditions were 35 cycles with annealing temperature 58.5oC flowed by agarose gel 2% electrophoresis for bands detections.

All patients started treatment by conventional synthetic DMARDs (including methotrexate). Response assessment at 3rd month was evaluated by DAS28 and ACR response criteria. JAK2 mutation was correlated with different clinical and laboratory parameters of patients.

The Disease Activity Score (DAS) and the DAS28 have been developed to measure disease activity in RA both in daily clinical practice as well as in clinical trials on a group as well as individual level. The DAS/DAS28 is a continuous measure of RA disease activity that combines information from swollen joints, tender joints, acute phase response and general health The DAS28 is a measure of disease activity in rheumatoid arthritis (RA). DAS stands for 'disease activity score' and the number 28 refers to the 28 joints that are examined in this assessment. questionnaires (e.g. the HAQ which assesses function), X-rays, and newer imaging techniques such as ultrasound and MRI.

The ACR20 is a composite measure defined as both improvement of 20% in the number of tender and number of swollen joints, and a 20% improvement in three of the following five criteria: patient global assessment, physician global assessment, functional ability measure [most often Health Assessment Questionnaire (HAQ)], visual analog pain scale, and erythrocyte sedimentation rate or C-reactive protein (CRP). ACR50 and ACR70 are the same instruments with improvement levels defined as 50% and 70% respectively versus 20% for ACR20.

Study Design

Study Type:
Interventional
Actual Enrollment :
76 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
Single (Investigator)
Primary Purpose:
Other
Official Title:
JAK2 Mutation May Predict Response and Guide First Line Treatment in Rheumatoid Arthritis
Actual Study Start Date :
Jan 1, 2019
Actual Primary Completion Date :
Apr 1, 2020
Actual Study Completion Date :
May 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: RA patients

newly diagnosed RA will started therapy with conventional synthetic DMARDs (including methotrexate)

Diagnostic Test: JAK expression
JAK2 assessment in blood by PCR

Experimental: control

JAK2 mutation assesment by PCR

Diagnostic Test: JAK expression
JAK2 assessment in blood by PCR

Outcome Measures

Primary Outcome Measures

  1. JAK2 mutation expression in newly diagnosed RA patients [6 months]

    Impact of pretreatment JAK2 mutation on response of Rheumatoid Arthritis patients to first line csDMARDS.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • New case RA patients

  • good liver and renal function

Exclusion Criteria:
  • Other autoimmune diss

  • Malignancy

  • Active viral infection

  • pregnancy and lactation

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mansoura University Hospital Mansoura Egypt

Sponsors and Collaborators

  • Mansoura University

Investigators

  • Study Chair: Mohamed Elbaiomy, MD, Mansoura University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mansoura University
ClinicalTrials.gov Identifier:
NCT04667988
Other Study ID Numbers:
  • R.20.11.1075
First Posted:
Dec 16, 2020
Last Update Posted:
Dec 16, 2020
Last Verified:
Jan 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 16, 2020