Evidence map›Paper›PMID 36425231›Full record

ArticleHealth psychology research2022

Clinically Relevant Drug Interactions with Monoamine Oxidase Inhibitors.

Amber N Edinoff, Connor R Swinford, Amira S Odisho, Caroline R Burroughs, Cain W Stark, Walid A Raslan, Elyse M Cornett, Adam M Kaye, Alan D Kaye

Open access · goldAbstract read
In one paragraph

Article in Health psychology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.3field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 54 citations in OpenAlex.

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  16. Antidepressant-like Effects of Chinese Quince (International journal of molecular sciences · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Amber N EdinoffDepartment of Psychiatry, Harvard Medical School, Massachusetts General Hospital.
Connor R SwinfordDepartment of Psychiatry and Behavioral Medicine, Louisiana State University Health Science Center Shreveport.
Amira S OdishoDepartment of Psychiatry and Behavioral Medicine, Louisiana State University Health Science Center Shreveport.
Caroline R BurroughsSchool of Medicine, Louisiana State University Health Science Center Shreveport.
Cain W StarkSchool of Medicine, Louisiana State University Health Science Center Shreveport.
Walid A RaslanCollege of Medicine-Tucson, University of Arizona.
Elyse M CornettDepartment of Anesthesiology, Louisiana State University Health Science Center Shreveport.
Adam M KayeDepartment of Pharmacy Practice, Thomas J. Long School of Pharmacy and Health Sciences, University of the Pacific.
Alan D KayeDepartment of Anesthesiology, Louisiana State University Health Science Center Shreveport.
Louisiana State University Health Sciences Center Shreveport · USLouisiana State University in Shreveport · USMassachusetts General Hospital · USUniversity of Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoamine oxidase inhibitors (MAOI) are a class of drugs that were originally developed for the treatment of depression but have since been expanded to be used in management of affective and neurological disorders, as well as stroke and aging-related neurocognitive changes. Ranging from irreversible to reversible and selective to non-selective, these drugs target the monoamine oxidase (MAO) enzyme and prevent the oxidative deamination of various monoamines and catecholamines such as serotonin and dopamine, respectively. Tyramine is a potent releaser of norepinephrine (NE) and is found in high concentrations in foods such as aged cheeses and meats. Under normal conditions, NE is unable to accumulate to toxic levels due to the presence of MAO-A, an enzyme that degrades neurotransmitters, including NE. When MAO-A is inhibited, the capacity to handle tyramine intake from the diet is significantly reduced causing the brain to be vulnerable to overstimulation of postsynaptic adrenergic receptors with as little as 8-10 mg of tyramine ingested and can result in life-threatening blood pressure elevations. In addition to adverse reactions with certain foods, both older and newer MAOIs can negatively interact with both sympathomimetic and serotonergic drugs. In general, patients on a MAOI want to avoid two types of medications: those that can elevate blood pressure via sympathomimetic actions (e.g., phenylephrine and oxymetazoline) and those that can increase serotonin levels via 5-HT reuptake inhibition (e.g., dextromethorphan, chlorpheniramine, and brompheniramine). Illicit drugs that stimulate the central nervous system such as ecstasy (MDMA, 3,4-methylenedioxymethamphetamine) act as serotonin releasers. Patient involvement is also crucial to ensure any interaction within the healthcare setting includes making other providers aware of a MAOI prescription as well as avoiding certain OTC medications that can interact adversely with MAOIs.

Indexed as

bleedingdrug interactionsecstasyheadachehypertensive crisisinsomniaMonoamine oxidase inhibitorssexual dysfunctionweight gain

Identifiers

PMID36425231
PMCPMC9680847
OpenAlexW4308117869

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.