Key result
PET imaging revealed that the global mismatch score of cardiac sympathetic function was significantly greater in ischemic CHF patients than in healthy volunteers (50.3 vs 19.3, P=0.005).
Why the study?
Does PET imaging of pre- and postsynaptic cardiac sympathetic function identify a mismatch in patients with ischemic congestive heart failure compared to healthy volunteers?
Observational (n=38)
Does PET imaging of pre- and postsynaptic cardiac sympathetic function identify a mismatch in patients with ischemic congestive heart failure compared to healthy volunteers?
Patients with severe ischemic CHF exhibit a significant mismatch between pre- and postsynaptic left ventricular sympathetic function, which may be associated with adverse clinical outcomes.
Answers are grounded in this paper and cite their sources.
Elevated sympathetic mismatch on PET in ischemic CHF may signal higher risk; leaves open its prognostic or therapeutic utility.
UNLABELLED: Pre- and postsynaptic cardiac sympathetic function is altered in ischemic congestive heart failure (CHF). Whether there is a presynaptic-to-postsynaptic mismatch or whether mismatch is related to adverse cardiac events is unknown. METHODS: In 13 patients with ischemic CHF and 25 aged-matched healthy volunteers, presynaptic function was measured by PET of (11)C-meta-hydroxyephedrine ((11)C-mHED), a norepinephrine (NE) analog. Postsynaptic function, beta-adrenergic receptor (BAR) density (B'(max)), was measured by imaging (11)C-CGP12177. Myocardial blood flow (MBF) was measured by imaging (15)O-water. Each heart was analyzed both globally and regionally, excluding infarcted regions, and a mismatch score, defined as the ratio of B'(max) to NE uptake (PS(nt))(,) was used to indicate mismatch of post- and presynaptic function. RESULTS: Global and regional MBF was not different between CHF and healthy subjects. The global measure of PS(nt) was lower in CHF (0.32 +/- 0.34) than that in healthy subjects (0.81 +/- 0.33, P < 0.0001) and in all 12 regions. Global B'(max) tended to be lower in CHF than that in healthy subjects (10.0 +/- 6.4 pmol/mL vs. 13.4 +/- 4.2, P = 0.056) and in all 12 regions. The global mismatch score (B'(max):PS(nt)) in CHF patients was significantly greater than that in healthy subjects (50.3 +/- 50.7 vs. 19.3 +/- 9.7, P = 0.005) and also greater in 11 of 12 regions. After 1.5 y of follow-up, 4 individuals had an adverse outcome (CHF death, new or recurrent sudden death, or progressive CHF leading to transplantation). Three of the 4 had mismatch scores > 3 times that of the healthy subjects or the CHF patients without an adverse outcome. CONCLUSION: Mismatch between pre- and postsynaptic left ventricular sympathetic function is present in patients with severe CHF and may be more marked in those with adverse outcomes.
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Caldwell et al. (2008) conducted an observational in Ischemic congestive heart failure (n=38). PET imaging of pre- and postsynaptic cardiac sympathetic function vs. Aged-matched healthy volunteers was evaluated on Global mismatch score (ratio of B'max to NE uptake) (p=0.005). PET imaging revealed that the global mismatch score of cardiac sympathetic function was significantly greater in ischemic CHF patients than in healthy volunteers (50.3 vs 19.3, P=0.005).
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