See the associated article on page 784.Hear t failure (HF) is a major public health problem that affects more than 5.8 million people in the United States and 23 million people worldwide (1). HF is a clinical syndrome, rather than a disease, and can occur in patients with reduced and preserved left ventricular (LV) ejection fraction. Community-based studies indicate that approximately 50% of patients with the clinical diagnosis of HF have preserved EF (HFpEF), whereas the remaining patient population presents with HF with reduced EF (HFrEF) (2,3). The values used to define preserved EF range in the literature from 40% to 55%, but current guidelines recommend an EF of more than 50% with elevated natriuretic peptide (BNP or NTproBNP) levels and relevant structural heart disease, such as left atrial enlargement or LV diastolic dysfunction, as criteria for HFpEF (4,5). Although clinical symptoms and mortality are similar among patients with HFpEF and HErEF, there are pronounced differences between these HF phenotypes in patient demographics, responses to therapy, and underlying pathophysiology of LV remodeling (6,7). Importantly, the prevalence of HFpEF relative to HFrEF is rising at a rate of 1% per year and will thus dominate as the prevalent HF phenotype over the next decade (8). Despite the rising prevalence, there are limited data to support effective therapies for HFpEF, and the role of diagnostic strategies and prognostic biomarkers remain ambiguous (4,9).Excessive cardiac sympathetic nervous system (SNS) activation is a hallmark of HF progression in patients with HFrEF (10-12). A compensatory increase in adrenergic drive causes desensitization/ downregulation of the norepinephrine transporter (or uptake-1 mechanism) on the cardiac presynaptic nerve terminal due to excess norepinephrine in the synaptic cleft. The downregulation of uptake-1 exposes the heart and postsynaptic adrenergic receptors to greater concentrations of norepinephrine, which in turn causes desensitization/downregulation of b-adrenergic receptors, cardiac remodeling, and worsening of HF and prognosis (10). Importantly, in vivo noninvasive assessment of sympathetic innervation with SPECT and PET imaging using radiolabeled analogs of norepinephrine have provided valuable prognostic information in patients with HFrEF beyond currently available biomarkers, such as BNP and LV ejection fraction. The most commonly used SPECT tracer to assess cardiac sympathetic innervation is 123 Imetaiodobenzylguanadine ( 123 I-mIBG), whereas the most commonly used PET tracer is 11 C-hydroxyephedrine ( 11 C-HED). Both of these tracers are norepinephrine radioanalogs, and their uptake primarily represents presynaptic nerve function (or density) in the heart.LV diastolic dysfunction is a characteristic finding in patients with HFpEF, and increasing severity of diastolic dysfunction is related to HF progression and a worse prognosis in these patients (13,14). Several lines of evidence suggest that dysregulated SNS activity plays an important role in the pathophysiol...