Evidence map›Paper›PMID 42378311›Full record

ArticlePLoS genetics2026

Genetic survey of biomarkers at early and mid-pregnancy identifies pregnancy-specialized immune regulation.

Merve Cakir, Michela Traglia, Stacey Alexeeff, Jennifer L Ames, Paul Ashwood, Luke P Grosvenor, Erica P Gunderson, Danielle H J Kim, Jane W Liang, Yinge Qian and 5 more

Abstract read
In one paragraph

Article in PLoS genetics, 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

5 · Who and what money

Authors and funding

15 authors.

Merve CakirInstitute for Human Genetics, Department of Psychiatry and Behavioral Sciences, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, California, United States of America.ORCID https://orcid.org/0000-0003-1803-5693
Michela TragliaGladstone Institute of Data Science and Biotechnology, San Francisco, California, United States of America.
Stacey AlexeeffDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.ORCID https://orcid.org/0000-0001-8988-6976
Jennifer L AmesDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.ORCID https://orcid.org/0000-0003-0906-9162
Paul AshwoodDepartment of Medical Microbiology and Immunology, University of California Davis, Davis, California, United States of America.
Luke P GrosvenorDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.
Erica P GundersonDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.
Danielle H J KimDivision of Rheumatology/Allergy/Clinical Immunology, Department of Internal Medicine, University of California at Davis, Davis, California, United States of America.
Jane W LiangDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.ORCID https://orcid.org/0000-0002-2302-3809
Yinge QianDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.
Elizabeth SahagunDivision of Rheumatology/Allergy/Clinical Immunology, Department of Internal Medicine, University of California at Davis, Davis, California, United States of America.
Robert YolkenDepartment of Medicine, Johns Hopkins University, Baltimore, Maryland, United States of America.
Judy Van de WaterMIND Institute, University of California Davis, Davis, California, United States of America.
Lisa A CroenDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.ORCID https://orcid.org/0000-0001-7849-9428
Lauren A WeissInstitute for Human Genetics, Department of Psychiatry and Behavioral Sciences, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, California, United States of America.ORCID https://orcid.org/0000-0002-5700-135X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Much remains unknown about the genetics of immune system changes during pregnancy. We used SNP data in a pregnancy cohort to genetically investigate 47 immune biomarkers at two timepoints, along with change between timepoints (Δ). We identified 19 biomarkers with significant SNP-based heritability and 34 with genome-wide significant signals, demonstrating genetic regulation. The same biomarkers measured in early- and mid-pregnancy shared about half of significant associations across timepoints, with enrichment for immune pathways. In contrast, Δ showed enrichment in transcription factors and developmental processes. About half of suggestive associations overlapped with non-pregnancy associations. However, these data leave a substantial fraction of potentially timepoint-specific and pregnancy-unique findings. Nearby genes were enriched for high expression in decidual cells at the maternal-fetal interface, reinforcing the novelty of our results. We additionally explored the relationship between immune genetic associations and prior GWAS of pregnancy complications. Overall, we present the first two-timepoint genetic study of immune profile in pregnancy.

Indexed as

BiomarkersFemaleGenome-Wide Association StudyHumansPolymorphism, Single NucleotidePregnancyPregnancy ComplicationsBiomarkers

Identifiers

PMID42378311
PMCPMC13340790

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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.