Evidence map›Paper›PMID 42185983›Full record

ArticleBMC neurology2026

Evaluating the performance of ChatGPT in responding to myotonic dystrophy type 1 patient inquiries: a specialist physician-based study.

Gülşah Çelik, Hanife Hale Hekim, Meral Bilgilisoy Filiz, Naciye Füsun Toraman

Abstract read
In one paragraph

Article in BMC neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Gülşah ÇelikDepartment of Physical Medicine and Rehabilitation, Faculty of Medicine, Kastamonu University, Kastamonu, Turkey. gulsahberberr@gmail.com.ORCID http://orcid.org/0009-0002-1170-4110
Hanife Hale HekimDepartment of Physical Medicine and Rehabilitation, Antalya Training and Research Hospital, University of Health Sciences, Antalya, Turkey.ORCID http://orcid.org/0000-0001-6555-2111
Meral Bilgilisoy FilizDepartment of Physical Medicine and Rehabilitation, Antalya Training and Research Hospital, University of Health Sciences, Antalya, Turkey.ORCID http://orcid.org/0000-0002-3064-2878
Naciye Füsun ToramanDepartment of Physical Medicine and Rehabilitation, Antalya Training and Research Hospital, University of Health Sciences, Antalya, Turkey.ORCID http://orcid.org/0000-0002-8141-4525

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdvancements in artificial intelligence have led to the widespread use of large language models such as ChatGPT in healthcare communication. Myotonic dystrophy type 1, a chronic and multisystemic neuromuscular disorder, poses significant challenges for patients in understanding disease progression, symptom management, and future planning. Given the scarcity of specialized resources for rare diseases, AI-based tools may offer valuable support by delivering accessible and relevant information. This study aimed to evaluate ChatGPT-4o's performance in addressing patient-centered questions about myotonic dystrophy type 1.

methodsThis descriptive methodological study utilized ten frequently asked patient-style questions concerning myotonic dystrophy type 1, posed to ChatGPT-4o in Turkish using a standardized zero-shot prompting approach. A total of 53 specialist physicians in Physical Medicine and Rehabilitation and Neurology assessed the responses using a structured rubric across five domains: accuracy, currency, comprehensiveness, usefulness, and understandability. Each response was scored from 1 to 5.

resultsChatGPT-4o achieved high specialist physicians' satisfaction across all domains, with over 80% of responses rated ≥ 4. Accuracy received the highest score (85.7%), followed by usefulness and comprehensiveness (above 82%). Currency and understandability were rated slightly lower (81.9% and 81.5%, respectively).

conclusionChatGPT-4o generated responses that were generally accurate, relevant, and understandable, demonstrating promise as an accessible resource for rare disease contexts such as myotonic dystrophy type 1. It also showed strong potential as a supportive informational tool for specialist physicians. Ongoing model refinement and integration with up-to-date clinical data are essential to optimize its performance and ensure its safe, equitable use in healthcare communication.

Indexed as

Myotonic DystrophyPhysiciansAdultFemaleGenerative Artificial IntelligenceHumansLarge Language ModelsMaleArtificial intelligenceChatGPTExpert opinionLarge language modelsMyotonic dystrophy

Identifiers

PMID42185983
PMCPMC13383381

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.