TY - JOUR
T1 - Calibration of myocardial T2 and T1 against iron concentration
AU - Carpenter, J.P.
AU - He, T.
AU - Kirk, P.
AU - Roughton, M.
AU - Anderson, L.J.
AU - De Noronha, S.V.
AU - Baksi, A.J.
AU - Sheppard, M.N.
AU - Porter, J.B.
AU - Walker, J.M.
AU - Wood, J.C.
AU - Forni, G.L.
AU - Catani, G.S.A.
AU - Matta, G.
AU - Fucharoen, S.
AU - Fleming, Adam
AU - House, Mike
AU - Black, Gregory
AU - Firmin, D.N.
AU - St. Pierre, Tim
AU - Pennell, D.J.
PY - 2014/8/12
Y1 - 2014/8/12
N2 - © 2014 Carpenter et al.; licensee BioMed Central. Background: The assessment of myocardial iron using T2∗ cardiovascular magnetic resonance (CMR) has been validated and calibrated, and is in clinical use. However, there is very limited data assessing the relaxation parameters T1 and T2 for measurement of human myocardial iron. Methods. Twelve hearts were examined from transfusion-dependent patients: 11 with end-stage heart failure, either following death (n = 7) or cardiac transplantation (n = 4), and 1 heart from a patient who died from a stroke with no cardiac iron loading. Ex-vivo R1 and R2 measurements (R1 = 1/T1 and R2 = 1/T2) at 1.5 Tesla were compared with myocardial iron concentration measured using inductively coupled plasma atomic emission spectroscopy. Results: From a single myocardial slice in formalin which was repeatedly examined, a modest decrease in T2 was observed with time, from mean (±SD) 23.7 ± 0.93 ms at baseline (13 days after death and formalin fixation) to 18.5 ± 1.41 ms at day 566 (p <0.001). Raw T2 values were therefore adjusted to correct for this fall over time. Myocardial R2 was correlated with iron concentration [Fe] (R20.566, p <0.001), but the correlation was stronger between LnR2 and Ln[Fe] (R20.790, p <0.001). The relation was [Fe] = 5081•(T2)-2.22between T2 (ms) and myocardial iron (mg/g dry weight). Analysis of T1 proved challenging with a dichotomous distribution of T1, with very short T1 (mean 72.3 ± 25.8 ms) that was independent of iron concentration in all hearts stored in formalin for greater than 12 months. In the remaining hearts stored for
AB - © 2014 Carpenter et al.; licensee BioMed Central. Background: The assessment of myocardial iron using T2∗ cardiovascular magnetic resonance (CMR) has been validated and calibrated, and is in clinical use. However, there is very limited data assessing the relaxation parameters T1 and T2 for measurement of human myocardial iron. Methods. Twelve hearts were examined from transfusion-dependent patients: 11 with end-stage heart failure, either following death (n = 7) or cardiac transplantation (n = 4), and 1 heart from a patient who died from a stroke with no cardiac iron loading. Ex-vivo R1 and R2 measurements (R1 = 1/T1 and R2 = 1/T2) at 1.5 Tesla were compared with myocardial iron concentration measured using inductively coupled plasma atomic emission spectroscopy. Results: From a single myocardial slice in formalin which was repeatedly examined, a modest decrease in T2 was observed with time, from mean (±SD) 23.7 ± 0.93 ms at baseline (13 days after death and formalin fixation) to 18.5 ± 1.41 ms at day 566 (p <0.001). Raw T2 values were therefore adjusted to correct for this fall over time. Myocardial R2 was correlated with iron concentration [Fe] (R20.566, p <0.001), but the correlation was stronger between LnR2 and Ln[Fe] (R20.790, p <0.001). The relation was [Fe] = 5081•(T2)-2.22between T2 (ms) and myocardial iron (mg/g dry weight). Analysis of T1 proved challenging with a dichotomous distribution of T1, with very short T1 (mean 72.3 ± 25.8 ms) that was independent of iron concentration in all hearts stored in formalin for greater than 12 months. In the remaining hearts stored for
U2 - 10.1186/s12968-014-0062-4
DO - 10.1186/s12968-014-0062-4
M3 - Article
SN - 1097-6647
VL - 16
JO - Journal of Cardiovascular Magnetic Resonance
JF - Journal of Cardiovascular Magnetic Resonance
IS - 1
M1 - 62
ER -