TY - JOUR T1 - Diastolic Filling Parameters Derived from Myocardial Perfusion Imaging Can Predict Left Ventricular End-Diastolic Pressure at Subsequent Cardiac Catheterization JF - Journal of Nuclear Medicine JO - J Nucl Med SP - 746 LP - 751 DO - 10.2967/jnumed.107.049395 VL - 49 IS - 5 AU - Dineshkumar Patel AU - Vincent J.B. Robinson AU - Roque B. Arteaga AU - John W. Thornton Y1 - 2008/05/01 UR - http://jnm.snmjournals.org/content/49/5/746.abstract N2 - Morbidity and mortality increase when diastolic dysfunction accompanies coronary artery disease (CAD). An elevated stress 201Tl lung-to-heart ratio (LHR) is a traditional marker of elevated left ventricular end-diastolic pressure (LVEDP), which adds prognostic value in CAD. Since the introduction of 99mTc-labeled agents, this valuable marker has been lost. Hence, there is only a limited ability to assess diastolic dysfunction by myocardial perfusion imaging (MPI). Methods: Fifty-two consecutive patients with an ejection fraction of ≥45% underwent MPI and cardiac catheterization within 15 d. Peak filling rate (PFR), time to PFR (TPFR), and filling rate during the first third of diastole (1/3FR) were obtained from MPI with SPECT software. Resting 201Tl LHR was calculated manually, and LVEDP was obtained at catheterization. Results: PFR, TPFR, and 1/3FR correlated significantly with LVEDP (r = −0.53, 0.45, and −0.45, respectively; P = 0.00005, 0.0009, and 0.0009, respectively), whereas resting 201Tl LHR did not (r = 0.10, P = 0.49). Receiver-operating-characteristic curve analysis of PFR, TPFR, and 1/3FR for detecting LVEDPs of ≥18 mm Hg showed areas under the curve of 0.83, 0.75, and 0.80, respectively. The combination of PFR and 1/3FR showed a negative predictive value of 84%, a positive predictive value of 86%, and a specificity of 94%. Conclusion: Diastolic filling variables obtained with the SPECT software showed a significant correlation with LVEDP. PFR, TPFR, and 1/3FR were superior to resting 201Tl LHR and showed good sensitivity, specificity, and predictive power for detecting LVEDPs of ≥18 mm Hg. Hence, combining data on the presence of perfusion defects with data on diastolic impairments can be achieved by adding these variables to MPI results. ER -