Evidence map›Paper›PMID 36580336›Full record

ArticleJAMA network open2022

Association of Developmental Language Disorder With Comorbid Developmental Conditions Using Algorithmic Phenotyping.

Rachana Nitin, Douglas M Shaw, Daniel B Rocha, Courtney E Walters, Christopher F Chabris, Stephen M Camarata, Reyna L Gordon, Jennifer E Below

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 3 pooled it
6.6field-weighted citation impact, top 3% 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.

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

11 citing papers in PubMed, 3 syntheses or guidelines pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Guideline
  4. Article
  5. Article
  6. Article
  7. Review
  8. Assessing childhood maltreatment exposure using the child behavior checklist.Frontiers in child and adolescent psychiatry · 2025
    Article
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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

8 authors at 4 institutions in 1 country.

Rachana NitinVanderbilt Brain Institute, Vanderbilt University, Nashville, Tennessee.
Douglas M ShawVanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, Tennessee.
Daniel B RochaPhenomic Analytics and Clinical Data Core, Geisinger, Danville, Pennsylvania.
Courtney E WaltersDepartment of Otolaryngology-Head & Neck Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.
Christopher F ChabrisGeisinger Health System, Lewisburg, Pennsylvania.
Stephen M CamarataDepartment of Hearing and Speech Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
Reyna L GordonVanderbilt Brain Institute, Vanderbilt University, Nashville, Tennessee.
Jennifer E BelowVanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, Tennessee.
Vanderbilt University Medical Center · USVanderbilt University · USGeisinger Health System · USNew York Hospital Queens · US

Funding

Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Lea K Davis · 2020 to 2026
$10.3M
Developmental stuttering: Population-based genetic discoveryR01DC017175 · NIDCD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BELOW, JENNIFER, KRAFT, SHELLY JO · 2018 to 2022
$3.5M
Neurobiological Markers of Rhythm: Risk and Resilience for Language AcquisitionR01DC016977 · NIDCD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GORDON, REYNA LEIGH · 2019 to 2023
$3.5M
Rhythm in Atypical Language Development: Mechanisms and Individual DifferencesR03DC014802 · NIDCD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GORDON, REYNA LEIGH · 2015 to 2017
$481k
Genetic Study of Developmental Stuttering.R03DC015329 · NIDCD · WAYNE STATE UNIVERSITY · PI KRAFT, SHELLY JO · 2016 to 2018
$465k
Mapping the Genetic and Neural Architecture of Human Rhythm and Communication TraitsK18DC017383 · NIDCD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GORDON, REYNA LEIGH · 2018 to 2019
$237k
NICHD NIH HHS P50 HD103537NIDCD NIH HHS K18 DC017383NIDCD NIH HHS R01 DC016977NIDCD NIH HHS R01 DC017175NIDCD NIH HHS R03 DC014802NIDCD NIH HHS R03 DC015329
6 · The paper itself

Abstract

Importance: Developmental language disorder (DLD) is a common (with up to 7% prevalence) yet underdiagnosed childhood disorder whose underlying biological profile and comorbidities are not fully understood, especially at the population level. Objective: To identify clinically relevant conditions that co-occur with DLD at the population level. Design, Setting, and Participants: This case-control study used an electronic health record (EHR)-based population-level approach to compare the prevalence of comorbid health phenotypes between DLD cases and matched controls. These cases were identified using the Automated Phenotyping Tool for Identifying Developmental Language Disorder algorithm of the Vanderbilt University Medical Center EHR, and a phenome enrichment analysis was used to identify comorbidities. An independent sample was selected from the Geisinger Health System EHR to test the replication of the phenome enrichment using the same phenotyping and analysis pipeline. Data from the Vanderbilt EHR were accessed between March 2019 and October 2020, while data from the Geisinger EHR were accessed between January and March 2022. Main Outcomes and Measures: Common and rare comorbidities of DLD at the population level were identified using EHRs and a phecode-based enrichment analysis. Results: Comorbidity analysis was conducted for 5273 DLD cases (mean [SD] age, 16.8 [7.2] years; 3748 males [71.1%]) and 26 353 matched controls (mean [SD] age, 14.6 [5.5] years; 18 729 males [71.1%]). Relevant phenotypes associated with DLD were found, including learning disorder, delayed milestones, disorders of the acoustic nerve, conduct disorders, attention-deficit/hyperactivity disorder, lack of coordination, and other motor deficits. Several other health phenotypes not previously associated with DLD were identified, such as dermatitis, conjunctivitis, and weight and nutrition, representing a new window into the clinical complexity of DLD. Conclusions and Relevance: This study found both rare and common comorbidities of DLD. Comorbidity profiles may be leveraged to identify risk of additional health challenges, beyond language impairment, among children with DLD.

Indexed as

Attention Deficit Disorder with HyperactivityLanguage Development DisordersLearning DisabilitiesCase-Control StudiesComorbidityHumansMale

Identifiers

PMID36580336
PMCPMC9857086
OpenAlexW4313325228

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.