Key result
Heart failure was associated with an increase in liver mIBG activity over time (e.g., 2.85 to 2.93 in HF without DM, P=0.005), reversing the normal washout pattern.
Why the study?
123I-mIBG uptake in the liver was explored to assess the influence of heart failure and diabetes.
How does liver mIBG activity differ between heart failure patients with and without diabetes compared to normal controls?
Observational
How does liver mIBG activity differ between heart failure patients with and without diabetes compared to normal controls?
p-value: p=0.005
Liver mIBG activity increases over time in heart failure patients, reversing the normal washout pattern, with diabetes and abnormal liver function further decreasing uptake.
May reflect autonomic-metabolic interactions in HF; hypothesis-generating for liver mIBG as biomarker, needs prospective validation.
BACKGROUND AND AIM: I-meta-iodobenzylguanidine (mIBG) was explored in normal controls and patients with heart failure (HF). METHODS: ) was compared in three groups: HF with DM; HF without DM; and controls. Associations with plasma norepinephrine, liver function tests, and level of cardiac innervation were explored. RESULTS: , P < 0.0001); in HF subjects, activity increased during this interval (HF without DM: 2.85 vs 2.93 [P = 0.005]; HF with DM: 2.37 vs 2.43 [P = 0.054]). Early liver activity was lower in HF with DM subjects than in the other groups (P < 0.001); late liver activity was higher in HF without DM than in the other two groups (P < 0.01). Subjects with elevated plasma norepinephrine (> 520 pg/mL) or ≥ 1 abnormal liver function test had lower early and late liver activity. In subjects with preserved cardiac mIBG uptake, HF subjects had higher and control subjects lower liver activity than comparable subjects with decreased cardiac innervation. CONCLUSIONS: In HF subjects, liver mIBG activity increased over time, reversing the normal washout pattern, suggesting a compensatory change in sympathetic nerve function. DM, abnormal liver function tests, and decreased cardiac innervation were associated with decreased liver mIBG uptake in HF.
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Jacobson et al. (2020) conducted an observational in Heart failure and diabetes. Heart failure and diabetes vs. Normal controls was evaluated on Liver mIBG activity over time (p=0.005). Heart failure was associated with an increase in liver mIBG activity over time (e.g., 2.85 to 2.93 in HF without DM, P=0.005), reversing the normal washout pattern.
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