Evidence map›Paper›PMID 34214182›Full record

ReviewHeadache2021

A narrative review of the importance of pharmacokinetics and drug-drug interactions of preventive therapies in migraine management.

Shivang Joshi, Stewart J Tepper, Sylvia Lucas, Soeren Rasmussen, Rob Nelson

Open access · hybridAbstract readReview
In one paragraph

Review in Headache, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

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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

5 authors at 4 institutions in 1 country.

Shivang JoshiNeurology/Headache Medicine, DENT Neurologic Institute, Amherst, NY, USA.
Stewart J TepperDepartment of Neurology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
Sylvia LucasDepartment of Neurology, University of Washington Medical Centers, Seattle, WA, USA.
Soeren RasmussenGlobal Medical, Amgen Inc., Thousand Oaks, CA, USA.
Rob NelsonGlobal Medical, Amgen Inc., Thousand Oaks, CA, USA.
Amgen (United States) · USDartmouth College · USDent Neurologic Institute · USUniversity of Washington Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo review the pharmacokinetics of major classes of migraine preventives and the clinical implications of drug-drug interactions (DDIs) with the use of these therapies in migraine management.

backgroundPreventive treatments for migraine are recommended for a large proportion of patients with frequent migraine attacks. These patients often exhibit a number of comorbidities, which may lead to the introduction of multiple concomitant therapies. Potential DDIs must be considered when using polytherapy to avoid increased risk of adverse events (AEs) or inadequate treatment of comorbid conditions.

methodsA literature search was performed to identify pharmacokinetic properties and potential DDIs of beta-blockers, antiepileptic drugs, antidepressants, calcium channel blockers, gepants, and monoclonal antibody therapies targeting the calcitonin gene-related peptide pathway with medications that may be used for comorbid conditions.

resultsMost DDIs occur through alterations in cytochrome P450 isoenzyme activity and may be complicated by genetic polymorphism for metabolic enzymes. Additionally, drug metabolism may be altered by grapefruit juice ingestion and smoking. The use of migraine preventive therapies may exacerbate symptoms of comorbid conditions or increase the risk of AEs associated with comorbid conditions as a result of DDIs.

conclusionsDDIs are important to consider in patients with migraine who use multiple medications. The development of migraine-specific evidence-based preventive treatments allows for tailored clinical management that reduces the risk of DDIs and associated AEs in patients with comorbidities.

Indexed as

Adrenergic beta-AntagonistsAntibodies, MonoclonalAnticonvulsantsAntidepressive AgentsCalcitonin Gene-Related PeptideCalcitonin Gene-Related Peptide Receptor AntagonistsCalcium Channel BlockersComorbidityDrug InteractionsHumansMigraine DisordersAdrenergic beta-AntagonistsAntibodies, MonoclonalAnticonvulsantsAntidepressive AgentsCalcitonin Gene-Related PeptideCalcitonin Gene-Related Peptide Receptor AntagonistsCalcium Channel Blockersdrug-drug interactionsmigrainepharmacodynamicspharmacokineticspolytherapy

Identifiers

PMID34214182
PMCPMC8361687
OpenAlexW3176971103

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.