Evidence map›Paper›PMID 42821002›Full record

ReviewHernia : the journal of hernias and abdominal wall surgery2026

Toward precision hernia surgery: integrating biomarkers, genomics, quantitative imaging, and artificial intelligence in abdominal wall repair.

Bruno Amantini Messias, Guilherme Costa E Silva, Pedro Henrique de Freitas Amaral, Diogo Parente Falcão, Sergio Roll, Jaques Waisberg

Abstract readReview
In one paragraph

Review in Hernia : the journal of hernias and abdominal wall surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Bruno Amantini MessiasServidor Publico Estadual Hospital (IAMSPE), 1800, Pedro de Toledo Street, São Paulo, 04039-000, Brazil. Bruno22med@hotmail.com.ORCID http://orcid.org/0000-0003-4426-5150
Guilherme Costa E SilvaSamaritano Hospital, 1486, Conselheiro Botero Street, São Pulo, 01232-010, Brazil.
Pedro Henrique de Freitas AmaralSanta Casa of São Paulo, 112, Cesario Mota Junior Street, São Paulo, 01221-020, Brazil.
Diogo Parente FalcãoSao Marcelino Champagnat Hospital, 1399, Presidente Affonso Camargo Avenue, Curitiba, 80050-370, Brazil.
Sergio RollSanta Casa of São Paulo, 112, Cesario Mota Junior Street, São Paulo, 01221-020, Brazil.
Jaques WaisbergServidor Publico Estadual Hospital (IAMSPE), 1800, Pedro de Toledo Street, São Paulo, 04039-000, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDespite technical advances, the expansion of minimally invasive approaches and the development of novel biomaterials, recurrence and complications following abdominal wall hernia (AWH) repair remain frequent. This variability likely reflects anatomical and technical factors and host biological heterogeneity. Precision herniology is emerging as a translational paradigm integrating biomarkers, genetics, quantitative imaging, and artificial intelligence to refine risk stratification and therapeutic planning.

methodsWe conducted a critical narrative review with translational scope. PubMed/MEDLINE, Scopus, Web of Science, and Embase were searched from January 2015 to June 2026. We prioritized adult studies across four axes: (i) biomarkers of collagen, extracellular matrix, and cellular mechanisms; (ii) genetics and susceptibility to AWH; (iii) immunonutritional markers; (iv) artificial intelligence (AI) and machine learning (ML) for predicting complexity and complications.

resultsThe literature reveals convergent, albeit heterogeneous, signals indicating that host biology may contribute to variability in hernia phenotype and surgical outcomes. Alterations in collagen turnover and in the MMP-TIMP axis, fibroblast heterogeneity, inflammatory signaling, polygenic architecture related to connective tissue integrity, immunonutritional markers associated with perioperative vulnerability, and quantitative imaging metrics analyzed by AI/ML models represent biologically plausible, clinically relevant domains.

conclusionAvailable data support the plausibility that host biological heterogeneity contributes to the formation, healing, prosthetic integration, and recurrence of AWH, thereby broadening the traditional paradigm centered predominantly on defect anatomy. The main value of this work is the critical integration of molecular and cellular biomarkers, genetics, quantitative imaging, and AI/ML into a unified conceptual framework for future precision herniology research.

Indexed as

Artificial IntelligenceHernia, AbdominalHerniorrhaphyPrecision MedicineAbdominal WallBiomarkersGenomicsHumansBiomarkersAbdominalExtracellular matrixFibroblastsHerniaInflammationMeshPrecision medicine

Identifiers

PMID42821002
PMCPMC13630981

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.