Evidence mapPaperPMID 42074122Full record

ReviewInternational journal of molecular sciences2026

Rethinking Risk Prediction in Preeclampsia: From Biomarkers to Mechanistic Phenotypes and Longitudinal Models.

Salvador Espino-Y-Sosa, Elsa Romelia Moreno-Verduzco, Irma Eloisa Monroy-Muñoz, Juan Mario Solis-Paredes, Javier Pérez Durán, Lourdes Rojas Zepeda, Johnatan Torres-Torres

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 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

7 authors.

Salvador Espino-Y-SosaDepartment of Bioinformatics, Instituto Nacional de Perinatologia Isidro Espinosa de los Reyes, Mexico City 11000, Mexico.ORCID 0000-0001-7276-8463
Elsa Romelia Moreno-VerduzcoDepartment of Reproductive and Perinatal Health Research, Instituto Nacional de Perinatologia Isidro Espinosa de los Reyes, Mexico City 11000, Mexico.ORCID 0000-0002-8733-1800
Irma Eloisa Monroy-MuñozDepartment of Reproductive and Perinatal Health Research, Instituto Nacional de Perinatologia Isidro Espinosa de los Reyes, Mexico City 11000, Mexico.ORCID 0000-0001-8737-8935
Juan Mario Solis-ParedesDepartment of Bioinformatics, Instituto Nacional de Perinatologia Isidro Espinosa de los Reyes, Mexico City 11000, Mexico.ORCID 0000-0003-4529-8296
Javier Pérez DuránDepartment of Reproductive and Perinatal Health Research, Instituto Nacional de Perinatologia Isidro Espinosa de los Reyes, Mexico City 11000, Mexico.ORCID 0000-0003-3302-7720
Lourdes Rojas ZepedaMaternal-Fetal Deparment, Instituto Materno Infantil del Estado de Mexico, Toluca 50170, Mexico.
Johnatan Torres-TorresDepartment of Reproductive and Perinatal Health Research, Instituto Nacional de Perinatologia Isidro Espinosa de los Reyes, Mexico City 11000, Mexico.ORCID 0000-0002-9524-4133

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preeclampsia remains a major cause of maternal and perinatal morbidity and mortality worldwide, yet progress in biomarker discovery and predictive modeling has translated only modestly into clinically meaningful risk stratification. Over the past two decades, numerous biomarkers and predictors reflecting placental-angiogenic dysfunction, maternal cardiovascular maladaptation, and inflammatory-metabolic stress have been proposed, alongside increasingly sophisticated statistical and machine learning approaches. However, many predictive strategies continue to treat preeclampsia as a single disease entity and rely on static thresholds applied at isolated gestational time points. Accumulating biological and clinical evidence instead suggests that preeclampsia represents a heterogeneous syndrome composed of partially overlapping mechanistic phenotypes whose relative contributions vary across pregnancy and across individuals. In this narrative review, we argue that further progress in prediction is likely to depend less on the identification of additional biomarkers and more on how biological heterogeneity and temporal dynamics are integrated into predictive frameworks. We synthesize current evidence supporting multimarker approaches, phenotype-informed frameworks, and longitudinal risk trajectories that conceptualize prediction as a dynamic process rather than a binary classification task. We also examine the complementary roles of classical statistical models and machine learning, emphasizing that calibration, external validation, interpretability, transportability, and clinical usability are essential, alongside discrimination, for successful clinical implementation. Finally, we outline key research priorities for the next generation of predictive studies, including mechanistically grounded phenotyping, dynamic risk updating across gestation, rigorous evaluation across diverse populations, and explicit linkage of risk stratification to preventive interventions and clinical decision-making. Together, these directions support a shift toward an integrative, longitudinal, and clinically anchored approach to preeclampsia prediction.

Indexed as

BiomarkersPre-EclampsiaFemaleHumansMachine LearningPhenotypePrediction AlgorithmsPredictive Learning ModelsPregnancyRisk AssessmentBiomarkersbiomarkersmachine learningpreeclampsiapregnancy complicationsrisk assessment

Identifiers

PMID42074122
PMCPMC13115805

What Socratic 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 Socratic graph.