Evidence map›Paper›PMID 39228695›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Genetic Testing History in Adults with Autism Spectrum Disorder.

Susanna B Mierau, Robyn P Thom, Caitlin T Ravichandran, Amanda Nagy, Cashel Rice, Christina Macenski, Christopher J Keary, Michelle L Palumbo, Christopher J McDougle, Ann M Neumeyer

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

10 authors.

Susanna B MierauMassachusetts General Hospital Lurie Center for Autism, Lexington, MA, USA.ORCID 0000-0002-1220-6423
Robyn P ThomMassachusetts General Hospital Lurie Center for Autism, Lexington, MA, USA.
Caitlin T RavichandranMassachusetts General Hospital Lurie Center for Autism, Lexington, MA, USA.
Amanda NagyMassachusetts General Hospital Lurie Center for Autism, Lexington, MA, USA.
Cashel RiceMassachusetts General Hospital Lurie Center for Autism, Lexington, MA, USA.
Christina MacenskiMassachusetts General Hospital Lurie Center for Autism, Lexington, MA, USA.
Christopher J KearyMassachusetts General Hospital Lurie Center for Autism, Lexington, MA, USA.
Michelle L PalumboMassachusetts General Hospital Lurie Center for Autism, Lexington, MA, USA.
Christopher J McDougleMassachusetts General Hospital Lurie Center for Autism, Lexington, MA, USA.
Ann M NeumeyerMassachusetts General Hospital Lurie Center for Autism, Lexington, MA, USA.

Funding

RESTORING CORTICAL NETWORK FUNCTION IN RETT SYNDROMEK02NS131521 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI Susanna Mierau · 2024 to 2026
$773k
NINDS NIH HHS K02 NS131521
6 · The paper itself

Abstract

Background & Objectives: Many genes have been identified in autism spectrum disorder (ASD). Yet little is known about how many adults with ASD receive recommended genetic testing and their outcomes. We investigated the percentage of adults with ASD who received genetic testing using recommended methods in our ASD specialty clinic and the percentage with positive findings. Methods: Potentially eligible adults were identified through search of our health system data repository and ASD diagnoses confirmed using review of relevant medical records by consensus of psychiatrists specializing in ASD. Patients were included (N=630) who had at least one visit with a qualifying clinician between 5/1/2010 and 12/15/2020 and demographic data available. Data were collected through manual retrospective review of the electronic health record. Results: Only 41% of the adults with ASD (261/630) had a history of genetic testing documented in the medical record. Genetic testing was declined by patients or families for 11% (72) of records and not recorded in 47% (297). Mean (SD; range) age for the 261 adults with testing documented was 28.5 (5.3; 22-58) years. Sixty-seven (26%) were identified as female, 14 (6%) as Asian, 8 (3%) as Black or African American, 226 (89%) as White, 6 (2%) as other race, and 2 (1%) as Hispanic. 189 (73%) had intellectual disability. Ninety-one percent (236) had the genetic testing method recorded. Only 54% (95% CI: 46%, 61%) of patients had testing using a recommended method (chromosomal array, autism/intellectual disability sequencing panel, or exome sequencing). Few adults had received testing with sequencing technologies. A genetic cause of ASD was found in 28% (95% CI: 19%, 39%) of the 121 adults with results from ASD-related genetic testing recorded. Conclusions: Genetic testing can offer clinical and research insights. Yet it is underutilized in this population of adults with ASD. Nearly half of the adults in our sample lacked documentation of genetic testing. Thus, the percentage of adults with confirmed ASD who had any recommended genetic testing may be even lower than reported. Adults with ASD may benefit from having their genetic testing history reviewed in the clinic and the latest genetic testing performed.

Identifiers

PMID39228695
PMCPMC11370500

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.