Evidence map›Paper›PMID 35485452›Full record

ArticleNeuropsychopharmacology reports2022

Identification of factors associated with the efficacy of atomoxetine in adult attention-deficit/hyperactivity disorder.

Tsutomu Nagai, Tatsuya Kurihara, Hiroaki Koya, Yukako Nakano, Satoru Sugisawa, Takehiko Sambe, Keiko Kishimoto, Mari Kogo, Haruhisa Ota, Akira Iwanami and 1 more

Open access · goldAbstract read
In one paragraph

Article in Neuropsychopharmacology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. 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

11 authors at 2 institutions in 1 country.

Tsutomu NagaiDepartment of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan.ORCID 0000-0002-6501-2702
Tatsuya KuriharaDivision of Natural Medicine and Therapeutics, Department of Clinical Pharmacy, School of Pharmacy, Showa University, Tokyo, Japan.ORCID 0000-0002-6145-452X
Hiroaki KoyaDepartment of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan.
Yukako NakanoDepartment of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan.
Satoru SugisawaDepartment of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan.ORCID 0000-0002-4066-8545
Takehiko SambeDivision of Clinical Pharmacology, Department of Pharmacology, School of Medicine, Showa University, Tokyo, Japan.
Keiko KishimotoDivision of Social Pharmacy, Department of Healthcare and Regulatory Sciences, School of Pharmacy, Showa University, Tokyo, Japan.ORCID 0000-0001-6341-8138
Mari KogoDivision of Pharmacotherapeutics, Department of Clinical Pharmacy, School of Pharmacy, Showa University, Tokyo, Japan.ORCID 0000-0001-7553-0872
Haruhisa OtaMedical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.
Akira IwanamiDepartment of Psychiatry, School of Medicine, Showa University, Tokyo, Japan.
Naoki UchidaDivision of Clinical Pharmacology, Department of Pharmacology, School of Medicine, Showa University, Tokyo, Japan.
Showa University · JPShowa University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimAtomoxetine (ATX) is a non-central stimulant and a standard treatment for adult attention-deficit/hyperactivity disorder (ADHD). The long-term efficacy of Atomoxetine is about 40% at 6 months. The variability in efficacy between individuals is thought to be related to patient-specific factors, but no detailed research has been conducted. In this retrospective cohort study, we aimed to identify the factors associated with Atomoxetine efficacy.

methodsA total of 147 patients with attention-deficit/hyperactivity disorder aged ≥18 years who were using Atomoxetine for the first time were included in this study. The outcome was treatment success (treatment maintained for at least 6 months and improvement in symptoms). Symptom assessment was based on the overall improvement in symptoms judged by an expert physician.

resultsOf the patient sample, 103 (70.1%) achieved the outcome. Logistic regression analysis identified "the maximum dose of ATX" and "gambling habit" as factors associated with efficacy ( P  < 0.05). In the process of Atomoxetine titration, the larger the maximum dose, the higher the efficacy was shown to be. Gambling habits may be indicative of impulsivity, which is among the core symptoms of attention-deficit/hyperactivity disorder. Thus, a gambling habit may be considered a surrogate marker for impulsivity.

conclusionsKnowledge of these factors will help healthcare professionals to predict the likely efficacy of Atomoxetine in a given patient before subscribing it, facilitating individualized pharmacotherapy for adult attention-deficit/hyperactivity disorder.

Indexed as

Attention Deficit Disorder with HyperactivityAdolescentAdrenergic Uptake InhibitorsAdultAtomoxetine HydrochlorideHumansRetrospective StudiesTreatment OutcomeAdrenergic Uptake InhibitorsAtomoxetine Hydrochlorideadrenergic uptake inhibitorsatomoxetine hydrochlorideattention-deficit disorder with hyperactivitycohort studiesmultivariate analysis

Identifiers

PMID35485452
PMCPMC9515700
OpenAlexW4225125886

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.