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Identification of factors associated with the efficacy of atomoxetine in adult attention-deficit/hyperactivity disorder.
Nagai, Tsutomu; Kurihara, Tatsuya; Koya, Hiroaki; Nakano, Yukako; Sugisawa, Satoru; Sambe, Takehiko; Kishimoto, Keiko; Kogo, Mari; Ota, Haruhisa; Iwanami, Akira; Uchida, Naoki.
Affiliation
  • Nagai T; Department of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan.
  • Kurihara T; Division of Clinical Pharmacology, Department of Pharmacology, School of Medicine, Showa University, Tokyo, Japan.
  • Koya H; Division of Natural Medicine and Therapeutics, Department of Clinical Pharmacy, School of Pharmacy, Showa University, Tokyo, Japan.
  • Nakano Y; Department of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan.
  • Sugisawa S; Department of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan.
  • Sambe T; Department of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan.
  • Kishimoto K; Division of Clinical Pharmacology, Department of Pharmacology, School of Medicine, Showa University, Tokyo, Japan.
  • Kogo M; Division of Social Pharmacy, Department of Healthcare and Regulatory Sciences, School of Pharmacy, Showa University, Tokyo, Japan.
  • Ota H; Division of Pharmacotherapeutics, Department of Clinical Pharmacy, School of Pharmacy, Showa University, Tokyo, Japan.
  • Iwanami A; Medical Institute of Developmental Disabilities Research, Showa University, Tokyo, Japan.
  • Uchida N; Department of Psychiatry, School of Medicine, Showa University, Tokyo, Japan.
Neuropsychopharmacol Rep ; 42(3): 249-255, 2022 09.
Article in En | MEDLINE | ID: mdl-35485452
ABSTRACT

AIM:

Atomoxetine (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.

METHODS:

A 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.

RESULTS:

Of 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.

CONCLUSIONS:

Knowledge 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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Attention Deficit Disorder with Hyperactivity Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Humans Language: En Journal: Neuropsychopharmacol Rep Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Attention Deficit Disorder with Hyperactivity Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Humans Language: En Journal: Neuropsychopharmacol Rep Year: 2022 Document type: Article Affiliation country: