Evidence map›Paper›PMID 41262830›Full record

ReviewCureus2025

Exploring the Diagnostic Capability of Artificial Intelligence in Dermatology for Darker Skin Tones: A Narrative Review.

Teniola Dowie

Abstract readReview
In one paragraph

Review in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. An Introduction to AI for Clinicians: Tutorial.Interactive journal of medical research · 2026
    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

1 author.

Teniola DowieAccident and Emergency, Northern Care Alliance Trust, Manchester, GBR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the use of artificial intelligence (AI) as a diagnostic tool increases in the field of dermatology, there has been a growing need to diversify datasets to improve its diagnostic capability in darker skin tones. Currently, AI is not as effective as a diagnostic tool in darker skin tones (Fitzpatrick IV-VI) as it has been in lighter skin-toned (Fitzpatrick I-III) populations. This narrative review will provide a summary of the recent data and advancements made within the area. Medline and PubMed databases were searched with the following search terms: dermato* AND (skin tone or race or skin colour or ethnicity or race or Fitzpatrick) AND (ai or artificial intelligence). Texts were filtered for full text and English language from 2020 to 2025. Results including patients under 18 years of age were excluded, which resulted in 52 papers. After scanning through titles and abstracts, a total of eight papers remained that were relevant to the review. AI models have demonstrated lower accuracy in recognising cutaneous pathology in darker skin tones in the majority of studies. When looking at the results after training the models with diverse datasets, there was an overall improvement in the accuracy of AI to recognise pathology in Fitzpatrick skin tone IV-VI. Several studies also showed that there is some benefit to training AI with artificially pigmented images to improve its accuracy. AI has significant potential to enhance dermatology by improving diagnostic accuracy, reducing variability, and improving efficiency. Expanding datasets further appears to be of benefit in improving accuracy in darker skin tones. Further studies with larger sample sizes are needed to analyse other reasons the algorithms have lower accuracy in darker skin tones and how this could be mitigated.

Indexed as

artificial intelligence in medicinecutaneous oncologydark skindermatopathologydiverse populationsmedical dermatology

Identifiers

PMID41262830
PMCPMC12624499

What OpenQuestion holds

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Registered trials

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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.