Evidence map›Paper›PMID 36160443›Full record

ArticleFrontiers in pharmacology2022

Psychotropic drugs interaction with the lipid nanoparticle of COVID-19 mRNA therapeutics.

Adonis Sfera, Sabine Hazan, Jonathan J Anton, Dan O Sfera, Christina V Andronescu, Sarvin Sasannia, Leah Rahman, Zisis Kozlakidis

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

8 authors at 6 institutions in 3 countries.

Adonis SferaPatton State Hospital, San Bernardino, CA, United States.
Sabine HazanDepartment of Psychiatry, University of California, Riverside, Riverside, CA, United States.
Jonathan J AntonPatton State Hospital, San Bernardino, CA, United States.
Dan O SferaPatton State Hospital, San Bernardino, CA, United States.
Christina V AndronescuDepartment of Anthropology, Stanford University, Stanford, CA, United States.
Sarvin SasanniaShiraz University of Medical Sciences, Shiraz, Iran.
Leah RahmanDepartment of Medicine, University of Oregon, Eugene, OR, United States.
Zisis KozlakidisInternational Agency For Research On Cancer (IARC), Lyon, France.
Patton State Hospital · USCentre International de Recherche sur le Cancer · FRShiraz University of Medical Sciences · IRStanford University · USUniversity of California, Riverside · USUniversity of Oregon · US

Funding

World Health Organization 001
6 · The paper itself

Abstract

The messenger RNA (mRNA) vaccines for COVID-19, Pfizer-BioNTech and Moderna, were authorized in the US on an emergency basis in December of 2020. The rapid distribution of these therapeutics around the country and the world led to millions of people being vaccinated in a short time span, an action that decreased hospitalization and death but also heightened the concerns about adverse effects and drug-vaccine interactions. The COVID-19 mRNA vaccines are of particular interest as they form the vanguard of a range of other mRNA therapeutics that are currently in the development pipeline, focusing both on infectious diseases as well as oncological applications. The Vaccine Adverse Event Reporting System (VAERS) has gained additional attention during the COVID-19 pandemic, specifically regarding the rollout of mRNA therapeutics. However, for VAERS, absence of a reporting platform for drug-vaccine interactions left these events poorly defined. For example, chemotherapy, anticonvulsants, and antimalarials were documented to interfere with the mRNA vaccines, but much less is known about the other drugs that could interact with these therapeutics, causing adverse events or decreased efficacy. In addition, SARS-CoV-2 exploitation of host cytochrome P450 enzymes, reported in COVID-19 critical illness, highlights viral interference with drug metabolism. For example, patients with severe psychiatric illness (SPI) in treatment with clozapine often displayed elevated drug levels, emphasizing drug-vaccine interaction.

Indexed as

cell-cell fusioncholesterol analogsDSPCionizable lipidsLNPPEGylated lipidspsychotropic drugs

Identifiers

PMID36160443
PMCPMC9503827
OpenAlexW4295027734

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.