Evidence map›Paper›PMID 39185520›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Research Priorities of Individuals and Families with Sex Chromosome Aneuploidies.

Alexandra Carl, Samantha Bothwell, Fathia Farah, Karli Swenson, David Hong, Siddharth Prakash, John Strang, Nicole Tartaglia, Armin Raznahan, Judith Ross and 3 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Alexandra CarleXtraOrdinarY Kids Clinic and Research Team, Children's Hospital of Colorado, Aurora, Colorado.ORCID 0009-0006-1157-4554
Samantha BothwelleXtraOrdinarY Kids Clinic and Research Team, Children's Hospital of Colorado, Aurora, Colorado.ORCID 0000-0002-1616-8137
Fathia FarahDivision of Nutritional Sciences, College of Human Ecology, Cornell University, Ithaca, New York.
Karli SwensoneXtraOrdinarY Kids Clinic and Research Team, Children's Hospital of Colorado, Aurora, Colorado.ORCID 0000-0003-0513-7308
David HongDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California.
Siddharth PrakashDepartment of Internal Medicine, University of Texas Health Science Center at Houston, Houston, Texas.ORCID 0000-0001-6341-9624
John StrangDepartment of Pediatric Neuropsychology, Children's National Hospital, Washington, District of Columbia.
Nicole TartagliaeXtraOrdinarY Kids Clinic and Research Team, Children's Hospital of Colorado, Aurora, Colorado.ORCID 0000-0002-8529-6722
Armin RaznahanSection on Developmental Neurogenomics, Human Genetics Branch, National Institute of Mental Health, Bethesda, Maryland.ORCID 0000-0002-5622-1190
Judith RossDepartment of Pediatrics, Division of Endocrinology, Nemours/Alfred I. duPont Hospital for Children, Wilmington, Delaware.ORCID 0000-0002-8613-2498
INSIGHTS Consortium
GALAXY Consortium
Shanlee DaviseXtraOrdinarY Kids Clinic and Research Team, Children's Hospital of Colorado, Aurora, Colorado.ORCID 0000-0002-0304-9550

Funding

Colorado Clinical and Translational Sciences Institute (CCTSI)UM1TR004399 · NCATS · UNIVERSITY OF COLORADO DENVER · PI JANINE A HIGGINS, RONALD J. SOKOL · 2023 to 2026
$30.7M
The eXtraordinarY Babies Study: Natural History of Health and Neurodevelopment in Infants with Sex Chromosome TrisomyR01HD091251 · NICHD · UNIVERSITY OF COLORADO DENVER · PI Nicole Renee Tartaglia · 2017 to 2026
$5.6M
NCATS NIH HHS UM1 TR004399NCBDD CDC HHS U01 DD001298NICHD NIH HHS R01 HD091251
6 · The paper itself

Abstract

Sex chromosome aneuploidies (SCAs) are chromosomal variations that result from an atypical number of X and/or Y chromosomes. Combined, SCAs affect ~1/400 live births, including individuals with Klinefelter syndrome (47,XXY), Turner syndrome (45,X and variants), Double Y syndrome (47,XYY), Trisomy X (47,XXX), and rarer tetrasomies and pentasomies. Individuals with SCAs experience a wide variety of physical health, mental health, and healthcare experiences that differ from the standard population. To understand the priorities of the SCA community we surveyed participants in two large SCA registries, the Inspiring New Science in Guiding Healthcare in Turner Syndrome (INSIGHTS) Registry and the Generating Advancements in Longitudinal Analysis in X and Y Variations (GALAXY) Registry. 303/629 (48.1% response rate) individuals from 13 sites across the United States responded to the survey, including 251 caregivers and 52 self-advocates, with a range of ages from 3 weeks to 73 years old and represented SCAs including Turner syndrome, XXX, XXY, XYY, XXYY, and combined rare tetrasomies and pentasomies. Results demonstrate the priorities for physical health and emotional/behavioral health identified by the SCA community, as well as preferred types of research. All SCA subtypes indicated intervention studies as the top priority, emphasizing the need for researchers to focus on clinical treatments in response to priorities of the SCA community.

Indexed as

Klinefelter syndromeresearch prioritiesSex chromosome aneuploidiesTrisomy XTurner syndromeXXYXXYYXYY

Identifiers

PMID39185520
PMCPMC11343263

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.