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Steven J. Hoff
James R. Stewart
William H. Frist
John A. Carey
Walter H. Merrill
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Ann Thorac Surg 1992;53:572-577
© 1992 The Society of Thoracic Surgeons


Articles

Noninvasive detection of heart transplant rejection with positron emission scintigraphy

Steven J. Hoff, MD1, James R. Stewart, MD*, William H. Frist, MD, Robert M. Kessler, MD, Martin P. Sandler, MD, James B. Atkinson, MD, PhD, John Votaw, PhD, John A. Carey, FRCSI, M.Sib Ansari, MS, Walter H. Merrill, MD

Departments of Cardiac and Thoracic Surgery, Pathology, and Radiology, Vanderbilt University Medical Center, Nashville, Tennesee, USA

* Address reprint requests to Dr Stewart, Department of Cardiac and Thoracic Surgery, The Vanderbilt Clinic, Rm 2973, Nashville, TN 37232-5734.

Positron emission tomography has recently been used to evaluate ischemic heart disease through changes in myocardial blood flow and carbohydrate metabolism. Positron-emitting tracers were evaluated for their ability to detect acute allograft rejection after heterotopic cardiac transplantation in the rat. Sham-operated controls, non-rejecting isografts, and rejecting allografts were evaluated. Decay-corrected uptake of 13NH3 and 18F 2-fluoro 2-deoxyglucose (FDG) reflects blood flow and glucose flux, respectively. Histologic examination of rejecting allografts documented mild rejection at 4 days and severe acute rejection by 8 days. All isografts were free from rejection. Uptake of FDG is greater in rejecting allografts than in nonrejecting isografts during both severe rejection (2.4% ± 0.8% versus 0.77% ± 0.4%; p < 0.02) and mild rejection (2.1% ± 0.6% versus 0.4% ± 0.1%; p < 0.02). Uptake of NH3 in severely rejected grafts is reduced compared with nonrejecting grafts (0.6% ± 0.3% versus 1.7% ± 1.1%; p < 0.02). There is no difference in NH3 uptake during mild rejection (1.8% ± 0.7% versus 1.3% ± 0.3%; p > 0.05). Uptake of FDG and NH3 in native hearts of animals from all experimental groups is not significantly different from that in sham-operated controls. Glucose may be a preferred metabolic substrate during rejection. Our data support a humoral mechanism for substrate preference during transplant rejection and a potential diagnostic role for positron emission tomography.




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