Abstract
BACKGROUND: (123)I-metaiodo-benzylguanidine (MIBG) scintigraphy is considered a
valid imaging test to evaluate the cardiac sympathetic nervous system. However,
scientific literature showed that some drugs are able to or are expected to
interfere with MIBG uptake. Thirty years after introduction of the method and
over 15 years since the appearance of the first document on pharmacological
interference with MIBG, an update on this issue has become necessary.
AIM: The aims of this review paper are: (1) to identify the pharmacological basis
of interference of a variety of substances with MIBG uptake; and (2) to update
the list of drugs that definitely interfere with MIBG on the grounds of evidence
in the literature.
MATERIALS AND METHODS: A MEDLINE search was conducted. Scientific studies, case
report and review articles were collected. Papers published demonstrating drugs
interfering with MIBG uptake were evaluated.
RESULTS: Drugs may interact with MIBG uptake by 5 mechanism: (1) type-1 uptake
inhibition; (2) inhibition of active transport to vesicles; (3) competition in
transport to vesicles; (4) depletion of neurosecretory vesicle content; (5)
calcium-mediated mechanism. We find that drugs like cocaine, antidepressants,
some antipsychotic, tramadol, labetalol, sympatho-mimetics, reserpine and some
calcium antagonists (as diltiazem, verapamil and nifedipine) do interfere with
MIBG uptake. On the other hand, we find that controversial data are available on
scientific literature regarding digoxin and amiodarone.
CONCLUSIONS: A compiled statement of MIBG interfering medicines is now
recommended to help nuclear medicine physicians in clinical practice to avoid
potential pitfalls and improve the efficacy of (123)I-MIBG scintigraphy as a
diagnostic tool.
| Original language | English |
|---|---|
| Pages (from-to) | 1326-1333 |
| Number of pages | 8 |
| Journal | European Review for Medical and Pharmacological Sciences |
| Volume | 2013 / N/A |
| DOIs | |
| Publication status | Published - 2013 |
Keywords
- MIBG
- pharmacologic intervention
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