Evidence map›Paper›PMID 41660256›Full record

ArticleiScience2026

Machine learning identifies proteomic risk factors across 23 diseases.

Lingqi Meng, Mengzhen Li, Xiangtai Kong, Tonghua Zhang, María Bueno Álvez, Xinmeng Liao, Hasan Türkez, Ozlem Altay, Cheng Zhang, Mathias Uhlén and 1 more

Abstract read
In one paragraph

Article in iScience, 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. 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

11 authors.

Lingqi MengScience for Life Laboratory, KTH Royal Institute of Technology, 17165 Stockholm, Sweden.
Mengzhen LiScience for Life Laboratory, KTH Royal Institute of Technology, 17165 Stockholm, Sweden.
Xiangtai KongScience for Life Laboratory, KTH Royal Institute of Technology, 17165 Stockholm, Sweden.
Tonghua ZhangScience for Life Laboratory, KTH Royal Institute of Technology, 17165 Stockholm, Sweden.
María Bueno ÁlvezScience for Life Laboratory, KTH Royal Institute of Technology, 17165 Stockholm, Sweden.
Xinmeng LiaoScience for Life Laboratory, KTH Royal Institute of Technology, 17165 Stockholm, Sweden.
Hasan TürkezDepartment of Medical Biology, Faculty of Medicine, Atatürk University, Erzurum, Turkey.
Ozlem AltayScience for Life Laboratory, KTH Royal Institute of Technology, 17165 Stockholm, Sweden.
Cheng ZhangScience for Life Laboratory, KTH Royal Institute of Technology, 17165 Stockholm, Sweden.
Mathias UhlénScience for Life Laboratory, KTH Royal Institute of Technology, 17165 Stockholm, Sweden.
Adil MardinogluScience for Life Laboratory, KTH Royal Institute of Technology, 17165 Stockholm, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Achieving minimally invasive and rapid detection is a crucial goal in modern medicine. The comprehensive characterization of the blood proteome holds great promise in advancing our understanding of disease etiology, facilitating early diagnosis, risk stratification, and improved monitoring across various diseases and their subtypes. In this study, we collected plasma proteomes from over 3000 patients, representing 23 distinct diseases, encompassing a total of 1462 proteins. Based on histological knowledge, we developed a two-stage hierarchical multi-disease classifier and applied it to perform multi-disease classification on the collected proteomic data. Our results demonstrate that this empirically guided two-stage hierarchical multi-disease classifier outperforms traditional machine learning algorithms in terms of prediction performance, showing better balance and more meaningful feature selections. This finding highlights the positive role that domain expertise can play in machine learning-based disease detection, and underscores the potential of plasma proteomics for multi-disease screening.

Indexed as

machine learningmedicineproteomics

Identifiers

PMID41660256
PMCPMC12874149

What OpenQuestion holds

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LicenceCC BY
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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.