Evidence map›Paper›PMID 32857933›Full record

Trial reportThe Journal of clinical psychiatry2020

Escitalopram in Adolescents With Generalized Anxiety Disorder: A Double-Blind, Randomized, Placebo-Controlled Study.

Jeffrey R Strawn, Jeffrey A Mills, Heidi Schroeder, Sarah A Mossman, Sara T Varney, Laura B Ramsey, Ethan A Poweleit, Zeruesenay Desta, Kim Cecil, Melissa P DelBello

Registry-linked trialOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02818751 (Neurofunctional Predictors of Escitalopram Treatment Response in Adolescents With Anxiety), which is not on this map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 5% 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.

NCT02818751 nacompletednot on this map

Neurofunctional Predictors of Escitalopram Treatment Response in Adolescents With Anxiety

TypeinterventionalSponsorUniversity of CincinnatiRan2015 to 2020Enrolled84ConditionsAnxietyArmsEscitalopram, Placebo
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Circulating endocannabinoids in children and adolescents: associations with anxiety and the impact of selective serotonin reuptake inhibitors.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Trial
  5. Trial
  6. Acute Neurofunctional Effects of Escitalopram in Pediatric Anxiety: A Double-Blind, Placebo-Controlled Trial.Journal of the American Academy of Child and Adolescent Psychiatry · 2021
    Trial
  7. Article
  8. Observational
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Influence ofCanadian journal of psychiatry. Revue canadienne de psychiatrie · 2024
    Article
  16. Journal of child and adolescent psychopharmacology · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. Review
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

10 authors at 4 institutions in 1 country.

Jeffrey R StrawnUniversity of Cincinnati, Department of Psychiatry, Box 670559, Cincinnati, OH 45267-0559. strawnjr@uc.edu.
Jeffrey A MillsDepartment of Economics, Lindner College of Business, University of Cincinnati, Cincinnati, Ohio, USA.
Heidi SchroederDepartment of Psychiatry, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
Sarah A MossmanDepartment of Psychiatry, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
Sara T VarneyDepartment of Psychiatry, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
Laura B RamseyDepartment of Pediatrics, Divisions of Clinical Pharmacology & Research in Patient Services, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Ethan A PoweleitDepartment of Pediatrics, Divisions of Clinical Pharmacology & Research in Patient Services, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Zeruesenay DestaDivision of Clinical Pharmacology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana,.
Kim CecilImaging Research Center, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Melissa P DelBelloDepartment of Psychiatry, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
University of Cincinnati Medical Center · USCincinnati Children's Hospital Medical Center · USIndiana University School of MedicineUniversity of Cincinnati · US

Funding

Neurofunctional Predictors of Treatment Response in Adolescents with GADK23MH106037 · NIMH · UNIVERSITY OF CINCINNATI · PI STRAWN, JEFFREY ROBERT · 2014 to 2017
$745k
NIMH NIH HHS K23 MH106037
6 · The paper itself

Abstract

backgroundSelective serotonin reuptake inhibitors (SSRIs) are commonly used to treat pediatric anxiety disorders, including generalized anxiety disorder (GAD); however, their efficacy and tolerability are difficult to predict. This study evaluated the efficacy and tolerability of escitalopram in adolescents with GAD (DSM-IV-TR) and the impact of variants in HTR2A and serotonin transporter (SLC6A4) genes and cytochrome P450 2C19 (CYP2C19) phenotypes on response as well as CYP2C19 phenotype on escitalopram pharmacokinetics from February 2015 through November 2018.

methodsPatients were treated with escitalopram (forced titration to 15 mg/d, then flexible titration to 20 mg/d) (n = 26, mean ± SD age: 14.8 ± 1.7 years) or placebo (n = 25, mean ± SD age: 14.9 ± 1.6 years) for 8 weeks. Outcomes were the change in scores on the Pediatric Anxiety Rating Scale (PARS) and Clinical Global Impressions (CGI) scales as well as vital signs and adverse events. Plasma escitalopram and desmethylcitalopram area under the curve during 24 hours (AUC0-24) and maximum concentration (Cmax) were determined and compared across CYP2C19 phenotypes.

resultsEscitalopram was superior to placebo for mean ± SD baseline-to-endpoint change in PARS (-8.65 ± 1.3 vs -3.52 ± 1.1, P = .005) and CGI scores, and increasing CYP2C19 metabolism was associated with decreases in escitalopram Cmax (P = .07) and AUC0-24 (P < .05). Vital signs, corrected QT interval, and adverse events were similar in patients who received escitalopram and placebo.

conclusionsEscitalopram reduces anxiety symptoms, and pharmacogenetics variables influence the trajectory and magnitude of improvement. Variation in CYP2C19 metabolism accounts for significant differences in escitalopram pharmacokinetics, raising the possibility that CYP2C19 phenotype should be considered when prescribing escitalopram.

trial registrationClinicalTrials.gov identifier: NCT02818751.

Indexed as

AdolescentAnti-Anxiety AgentsAnxiety DisordersArea Under CurveChildCitalopramCytochrome P-450 CYP2C19Double-Blind MethodFemaleHumansMalePsychiatric Status Rating ScalesSelective Serotonin Reuptake InhibitorsTreatment OutcomeAnti-Anxiety AgentsCitalopramCytochrome P-450 CYP2C19desmethylcitalopramSelective Serotonin Reuptake Inhibitors

Identifiers

PMID32857933
PMCPMC7504974
OpenAlexW3080184330

What OpenQuestion holds

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Registered trials

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.