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Abstract
To develop and validate a non-invasive method for measuring myocardial iron in order
to allow diagnosis and treatment before overt cardiomyopathy and failure develops.
We have developed a new magnetic resonance T2-star (T2*) technique for the measurement
of tissue iron, with validation to chemical estimation of iron in patients undergoing
liver biopsy. To assess the clinical value of this technique, we subsequently correlated
myocardial iron measured by this T2* technique with ventricular function in 106 patients
with thalassaemia major. There was a significant, curvilinear, inverse correlation
between iron concentration by biopsy and liver T2* (r=0.93, P<0.0001). Inter-study
cardiac reproducibility was 5.0%. As myocardial iron increased, there was a progressive
decline in ejection fraction (r=0.61, P<0.001). All patients with ventricular dysfunction
had a myocardial T2* of <20 ms. There was no significant correlation between myocardial
T2* and the conventional parameters of iron status, serum ferritin and liver iron.
Multivariate analysis of clinical parameters to predict the requirement for cardiac
medication identified myocardial T2* as the most significant variable (odds ratio
0.79, P<0.002).
Myocardial iron deposition can be reproducibly quantified using myocardial T2* and
this is the most significant variable for predicting the need for ventricular dysfunction
treatment. Myocardial iron content cannot be predicted from serum ferritin or liver
iron, and conventional assessments of cardiac function can only detect those with
advanced disease. Early intensification of iron chelation therapy, guided by this
technique, should reduce mortality from this reversible cardiomyopathy.