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Published on: December 13, 2017
High-sensitivity cardiac troponin T in infants exposed to anti-Ro antibodies
Julie Barsalou1, Edgar Jaeggi2, Lars Grosse-Wortmann2,3
1Division of Pediatric Rheumatology, The Hospital for Sick Children, University of Toronto, Toronto, Canada.
Insights
High-sensitivity cardiac troponin T (hs-cTnT) levels are not routinely indicated for infants exposed to anti-Ro antibodies, as they often fall within normal ranges and do not reliably predict cardiac involvement in neonatal lupus erythematosus (NLE). Further research is needed to clarify its role as a biomarker.
Area of Science:
- Pediatrics
- Cardiology
- Immunology
Background:
- Neonatal lupus erythematosus (NLE) can manifest as cardiac involvement, including myocarditis and endocardial fibroelastosis (EFE).
- The utility of high-sensitivity cardiac troponin T (hs-cTnT) in detecting subclinical myocardial inflammation in infants exposed prenatally to anti-Ro antibodies remains unclear.
Purpose of the Study:
- To investigate hs-cTnT levels in infants exposed to anti-Ro antibodies, with or without cardiac NLE.
- To correlate hs-cTnT levels with cardiac magnetic resonance imaging (CMR) findings in a subset of these infants.
Main Methods:
- A cohort of 45 infants exposed prenatally to anti-Ro antibodies were assessed.
- hs-cTnT levels were measured, and CMR was performed in select infants with elevated levels (≥30 ng/l).
Main Results:
- Only 3 out of 45 infants had hs-cTnT levels outside the reference range for healthy infants.
- No subclinical myocarditis or EFE was detected by CMR in any of the 12 infants who underwent the procedure.
- Elevated hs-cTnT levels were observed in infants with and without cardiac NLE, with some levels guiding treatment adjustments.
Conclusions:
- Routine hs-cTnT measurement is not recommended for all infants exposed to anti-Ro antibodies.
- The role of hs-cTnT as a biomarker for cardiac NLE requires further investigation.
Objectives:
Cardiac involvement in neonatal lupus erythematosis (NLE) can present as myocarditis/endocardial fibroelastosis (EFE). It is unknown whether high-sensitivity cardiac troponin T (hs-cTnT) is useful in identifying subclinical myocardial inflammation in infants exposed prenatally to anti-Ro antibodies. This study reports hs-cTnT levels in infants exposed to anti-Ro antibodies with/without cardiac NLE and reports cardiac MRI (CMR) findings in a subset of these children.
Methods:
The study included 45 consecutive infants exposed prenatally to anti-Ro antibodies with (n = 7) or without (n = 38) cardiac NLE, who were seen at the SickKids NLE Clinic between 2012 and 2014. Hs-cTnT levels were measured at least once, and those infants with values of ≥30 ng/l were offered the opportunity to undergo CMR. Descriptive statistics were performed.
Results:
Of 38 infants without cardiac NLE, 25 had a hs-cTnT level of ≥30 ng/l (including 1 of >113 ng/l); of these, 8 underwent CMR (all without myocarditis/EFE). All 7 infants with cardiac NLE had at least one hs-cTnT level of ≥30 ng/l, but only 2/7 had a level of >113 ng/l; 4/7 infants with cardiac NLE had CMR (all without myocarditis/EFE); 6/7 infants with cardiac NLE had their steroid treatment adjusted based on the trend in their hs-cTnT levels.
Conclusion:
Only 3/45 anti-Ro antibodies-exposed infants had hs-cTnT values outside the reference range reported in healthy infants. None of 12 infants who had CMR had subclinical myocarditis/EFE. Routine measurement of hs-cTnT in every anti-Ro antibody-exposed infant is not indicated. Further studies are needed to define the role of hs-cTnT as a biomarker for cardiac NLE.
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