Evidence map›Paper›PMID 39270211›Full record

ArticleJMIR medical informatics2024

Early Diagnosis of Hereditary Angioedema in Japan Based on a US Medical Dataset: Algorithm Development and Validation.

Kouhei Yamashita, Yuji Nomoto, Tomoya Hirose, Akira Yutani, Akira Okada, Nayu Watanabe, Ken Suzuki, Munenori Senzaki, Tomohiro Kuroda

Abstract read
In one paragraph

Article in JMIR medical informatics, 2024. 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

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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. Review
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

9 authors.

Kouhei YamashitaDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID https://orcid.org/0000-0003-4247-3407
Yuji NomotoDepartment of Palliative Care Medicine, Niigata City General Hospital, Niigata, Japan.ORCID https://orcid.org/0009-0002-9123-1121
Tomoya HiroseDepartment of Traumatology and Acute Critical Medicine, Graduate School of Medicine, Osaka University, Osaka, Japan.ORCID https://orcid.org/0000-0001-5959-4569
Akira YutaniDivision of Medical Information Technology and Administration Planning, Kyoto University Hospital, Kyoto, Japan.ORCID https://orcid.org/0000-0002-1430-8693
Akira OkadaHealthcare and Life Science, IBM Consulting, IBM Japan, Ltd, Tokyo, Japan.ORCID https://orcid.org/0009-0006-2166-2398
Nayu WatanabeHealthcare and Life Science, IBM Consulting, IBM Japan, Ltd, Tokyo, Japan.ORCID https://orcid.org/0009-0006-7404-0728
Ken SuzukiHealthcare and Life Science, IBM Consulting, IBM Japan, Ltd, Tokyo, Japan.ORCID https://orcid.org/0009-0009-9783-4573
Munenori SenzakiHealthcare and Life Science, IBM Consulting, IBM Japan, Ltd, Tokyo, Japan.ORCID https://orcid.org/0009-0004-2140-8256
Tomohiro KurodaDivision of Medical Information Technology and Administration Planning, Kyoto University Hospital, Kyoto, Japan.ORCID https://orcid.org/0000-0003-1472-7203

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHereditary angioedema (HAE), a rare genetic disease, induces acute attacks of swelling in various regions of the body. Its prevalence is estimated to be 1 in 50,000 people, with no reported bias among different ethnic groups. However, considering the estimated prevalence, the number of patients in Japan diagnosed with HAE remains approximately 1 in 250,000, which means that only 20% of potential HAE cases are identified.

objectiveThis study aimed to develop an artificial intelligence (AI) model that can detect patients with suspected HAE using medical history data (medical claims, prescriptions, and electronic medical records [EMRs]) in the United States. We also aimed to validate the detection performance of the model for HAE cases using the Japanese dataset.

methodsThe HAE patient and control groups were identified using the US claims and EMR datasets. We analyzed the characteristics of the diagnostic history of patients with HAE and developed an AI model to predict the probability of HAE based on a generalized linear model and bootstrap method. The model was then applied to the EMR data of the Kyoto University Hospital to verify its applicability to the Japanese dataset.

resultsPrecision and sensitivity were measured to validate the model performance. Using the comprehensive US dataset, the precision score was 2% in the initial model development step. Our model can screen out suspected patients, where 1 in 50 of these patients have HAE. In addition, in the validation step with Japanese EMR data, the precision score was 23.6%, which exceeded our expectations. We achieved a sensitivity score of 61.5% for the US dataset and 37.6% for the validation exercise using data from a single Japanese hospital. Overall, our model could predict patients with typical HAE symptoms.

conclusionsThis study indicates that our AI model can detect HAE in patients with typical symptoms and is effective in Japanese data. However, further prospective clinical studies are required to investigate whether this model can be used to diagnose HAE.

Indexed as

AIalgorithmalgorithmsangioedemaartificial intelligencebig dataearly detectionearly warningedemaEHREHRsElectronic health recordelectronic health recordselectronic medical recordelectronic medical recordsEMREMRsHAEhealth recordhealth recordsmachine learningMLpatient recordpersonal health recordPHRpractical modelpractical modelspredictionpredictive analyticspredictive modelpredictive modelspredictive systemrare diseasesreal world dataRWDscreening

Identifiers

PMID39270211
PMCPMC11437219

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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.