Falsely elevated cardiac troponin-I in patients with seropositive rheumatoid arthritis
Patrick R Kenny1, David R Finger
1Rheumatology Service, Department of Medicine, Tripler Army Medical Center, Honolulu, HI 96859-5000, USA. david.finger@haw.tamc.amedd.army.mil
Insights
Patients with rheumatoid arthritis (RA) and positive rheumatoid factor (RF) do not show falsely elevated cardiac troponin-I (cTnI) levels. This study confirms that RF does not interfere with cTnI assays in RA patients.
Area of Science:
- Cardiology
- Immunology
- Clinical Chemistry
Background:
- Elevated cardiac troponin-I (cTnI) is a marker for myocardial infarction.
- Previous reports suggest serum rheumatoid factor (RF) may interfere with cTnI assays, causing false elevations.
- The impact of RF in rheumatoid arthritis (RA) patients on cTnI assays is not well-defined.
Purpose of the Study:
- To investigate if seropositive rheumatoid arthritis (RA) patients exhibit abnormally elevated cardiac troponin-I (cTnI) concentrations.
- To assess the potential interference of rheumatoid factor (RF) with cTnI assays in RA patients.
Main Methods:
- Serum samples were collected from 60 patients diagnosed with seropositive RA.
- Rheumatoid factor (RF) and cardiac troponin-I (cTnI) levels were measured using both Abbott AxSYM and Bayer ADVIA Centaur assays.
Main Results:
- None of the 60 RA patients with RF levels ranging from 15 to 2724 IU/ml showed elevated cTnI.
- No falsely elevated cTnI levels were detected by either the Abbott or Bayer assay in this cohort.
Conclusions:
- This study demonstrates that seropositive RA patients do not have falsely elevated serum cTnI levels when tested with two commercial assays.
- Rheumatoid factor (RF) does not appear to interfere with cTnI measurements in RA patients using these assays.
Objective:
To determine if patients with seropositive rheumatoid arthritis (RA) have abnormally elevated concentrations of cardiac troponin-I (cTnI). Reports suggest the presence of serum rheumatoid factor (RF) may interfere with the cTnI assay, leading to falsely elevated cTnI levels. One study reported a falsely elevated cTnI in 15 out of 100 serum samples with elevated RF using the Abbott assay, but no elevated level using the Bayer assay. It is unclear how many of these samples came from patients with RA.
Methods:
Serum samples were drawn from 60 patients with seropositive RA. We measured RF and cTnI levels using both the Abbott AxSYM assay and the Bayer ADVIA Centaur assay.
Results:
Of 60 RA patients with RF ranging from 15 to 2724 IU/ml, none was found to have an elevated cTnI on either assay.
Conclusion:
Using 2 commercial assays for cTnI, we found that patients with seropositive RA do not have falsely elevated serum cTnI levels.
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