Evidence map›Paper›PMID 35568815›Full record

ArticleJournal of neurodevelopmental disorders2022

Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history study.

Caroline B Buchanan, Jennifer L Stallworth, Aubin E Joy, Rebekah E Dixon, Alexandra E Scott, Arthur A Beisang, Timothy A Benke, Daniel G Glaze, Richard H Haas, Peter T Heydemann and 11 more

2 registry-linked trialsOpen access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal of neurodevelopmental disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
7.9field-weighted citation impact, top 2% 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.

NCT00299312 completednot on this map

Rett Syndrome Natural History: Genetic and Physical Characteristics of Rett Syndrome

TypeobservationalSponsorUniversity of Alabama at BirminghamRan2006 to 2015Enrolled10ConditionsRett Syndrome, MECP2 Duplication Disorder, Rett-related Disorder
NCT02738281 completednot on this map

Rett Syndrome, MECP2 Duplication Disorder, and Rett- Related Disorders Natural History Protocol

TypeobservationalSponsorUniversity of Alabama at BirminghamRan2015 to 2021Enrolled1,044ConditionsRett Syndrome, MECP2 Duplication dIsorder, CDKL5 Disorder, FOXG1 Syndrome
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Reciprocal regulation of the HbioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Rett Syndrome Behaviour Questionnaire: Variability of Scores and Related Factors.Journal of child and adolescent psychopharmacology · 2025
    Article
  7. Article
  8. Review
  9. Rett syndrome: The Natural History Study journey.Annals of the Child Neurology Society · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Rett syndrome in Ireland: a demographic study.Orphanet journal of rare diseases · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

21 authors at 15 institutions in 1 country.

Caroline B Buchanan *Greenwood Genetic Center, 106 Gregor Mendel Circle, Greenwood, SC, 29649, USA. cbuchanan@ggc.org.
Jennifer L Stallworth *Greenwood Genetic Center, 106 Gregor Mendel Circle, Greenwood, SC, 29649, USA.
Aubin E JoyGreenwood Genetic Center, 106 Gregor Mendel Circle, Greenwood, SC, 29649, USA.
Rebekah E DixonGreenwood Genetic Center, 106 Gregor Mendel Circle, Greenwood, SC, 29649, USA.
Alexandra E ScottGreenwood Genetic Center, 106 Gregor Mendel Circle, Greenwood, SC, 29649, USA.
Arthur A BeisangGillette Children's Hospital, St. Paul, MN, USA.
Timothy A BenkeChildren's Hospital Colorado, University of Colorado at Denver, Denver, CO, USA.
Daniel G GlazeBaylor College of Medicine, Houston, TX, USA.
Richard H HaasRady Children's Hospital-San Diego, University of California, San Diego, CA, USA.
Peter T HeydemannRush University Medical Center, Chicago, IL, USA.
Mary D JonesUCSF Benioff Children's Hospital of Oakland, Oakland, CA, USA.
Jane B LaneCivitan International Research Center, University of Alabama at Birmingham, Birmingham, AL, USA.
David N LiebermanBoston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Eric D MarshChildren's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Jeffrey L NeulVanderbilt Kennedy Center, Vanderbilt University Medical Center, Nashville, TN, USA.
Sarika U PetersVanderbilt Kennedy Center, Vanderbilt University Medical Center, Nashville, TN, USA.
Robin C RytherWashington University School of Medicine in St. Louis, St. Louis, MO, USA.
Steve A SkinnerGreenwood Genetic Center, 106 Gregor Mendel Circle, Greenwood, SC, 29649, USA.
Shannon M StandridgeDivision of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Walter E KaufmannUniversity of South Carolina School of Medicine, Columbia, SC, USA. walter.e.kaufmann@emory.edu.
Alan K PercyCivitan International Research Center, University of Alabama at Birmingham, Birmingham, AL, USA.
Greenwood Genetic Center · USVanderbilt University Medical Center · USBaylor College of Medicine · USBoston Children's Hospital · USChildren's Hospital Colorado · USChildren's Hospital of Philadelphia · USCivitan International · USGillette Children's Specialty Healthcare · USRady Children's Hospital-San Diego · USRush University Medical Center · USUCSF Benioff Children's Hospital · USUniversity of Alabama at Birmingham · USUniversity of Cincinnati Medical Center · USUniversity of South Carolina · USWashington University in St. Louis · US

Funding

Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Jeffrey L Neul · 2020 to 2026
$10.3M
RARE DISEASE CRC FOR NEW THERAPIES AND NEW DIAGNOSTICSU54RR019478 · NCRR · BAYLOR COLLEGE OF MEDICINE · PI BEAUDET, ARTHUR L. · 2003 to 2008
$7.3M
NCRR NIH HHS U54 RR019478NICHD NIH HHS P50 HD103537NIH HHS RR019478
6 · The paper itself

Abstract

backgroundRett syndrome (RTT) is a neurodevelopmental disorder most often related to a pathogenic variant in the X-linked MECP2 gene. Internalizing behaviors appear to be common, but standard methods of diagnosing anxiety are not readily applied in this population which typically has cognitive impairment and limited expressive language. This study aims to describe the frequency of anxiety-like behavior and anxiolytic treatments along with associated clinical features in individuals with RTT.

methodsParental reports and medication logs provided data from 1380 females with RTT participating in two iterations of the multicenter U.S. RTT Natural History Study (RNHS) from 2006 to 2019.

resultsMost participants with RTT (77.5%) had at least occasional anxious or nervous behavior. Anxiety was reported to be the most troublesome concern for 2.6%, and within the top 3 concerns for 10.0%, of participants in the second iteration. Parents directly reported treatment for anxious or nervous behavior in 16.6% of participants in the second iteration with most reporting good control of the behavior (71.6%). In the medication logs of both RNHS iterations, the indication of anxiety was listed for a similar number of participants (15% and 14.5%, respectively). Increased use of anxiolytics and selective serotonin reuptake inhibitors (SSRIs) was related to more frequent anxiety-like behaviors (P < 0.001), older age (P < 0.001), and mild MECP2 variants (P = 0.002).

conclusionAnxiety-like behavior is frequent at all ages and is a significant parental concern in RTT. Older individuals and those with mild MECP2 variants are more likely to be treated with medications. Better diagnosis and treatment of anxiety in RTT should be a goal of both future studies and clinical care.

trial registrationNCT00299312 and NCT02738281.

Indexed as

Anti-Anxiety AgentsRett SyndromeAnxietyFemaleHumansAnti-Anxiety AgentsAnti-anxiety agentsAnxietyMethyl-CpG-binding protein 2Natural history studiesRett syndrome

Identifiers

PMID35568815
PMCPMC9107202
OpenAlexW4280517029

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.