Evidence map›Paper›PMID 37973775›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2024

Effect of Anti-TNF Biologic Exposure During Pregnancy on Villitis of Unknown Etiology Diagnoses in Patients with Autoimmune Disease.

Hannah M Scott, Ramila Mehta, Megan E Branda, Jennifer Hughes, Sunanda V Kane, Sylvie Girard, Andrew P Norgan, Regan N Theiler, Elizabeth Ann L Enninga

Open access · greenAbstract read
In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2024. 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
0.3field-weighted citation impact, top 36% of its field
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, 1 citations in OpenAlex.

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

9 authors at 3 institutions in 1 country.

Hannah M ScottDepartment of Obstetrics and Gynecology, Mayo Clinic, 200 First Ave. SW, Rochester, MN, 55905, USA.
Ramila MehtaDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Megan E BrandaDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Jennifer HughesICON PLC, Nashville, TN, USA.
Sunanda V KaneDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
Sylvie GirardDepartment of Obstetrics and Gynecology, Mayo Clinic, 200 First Ave. SW, Rochester, MN, 55905, USA.
Andrew P NorganDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Regan N TheilerDepartment of Obstetrics and Gynecology, Mayo Clinic, 200 First Ave. SW, Rochester, MN, 55905, USA.
Elizabeth Ann L EnningaDepartment of Obstetrics and Gynecology, Mayo Clinic, 200 First Ave. SW, Rochester, MN, 55905, USA. Enninga.elizabethann@mayo.edu.ORCID 0000-0003-3621-7335
Mayo Clinic · USMayo Clinic in Arizona · USMayo Clinic in Florida · US

Funding

Mayo Clinic Interdisciplinary Women's Health Research ProgramK12HD065987 · NICHD · MAYO CLINIC ROCHESTER · PI KANTARCI, KEJAL · 2010 to 2023
$6.7M
NICHD NIH HHS K12 HD065987
6 · The paper itself

Abstract

Tumor necrosis factor-α (TNF-α) antagonists are highly effective in controlling autoimmune diseases. This has led to speculation that they might also be useful in treating inflammatory placental conditions, such as chronic villitis of unknown etiology (VUE). VUE affects 10-15% of term placentas and is associated with recurrent fetal growth restriction (FGR) and pregnancy loss. We aimed to evaluate outcomes in patients with autoimmune diseases with and without anti-TNF-α biologic exposure during gestation. This retrospective cohort study compared pregnant women with autoimmune disease taking anti-TNF-α biologics (n = 89) to pregnant women with autoimmune disease but not taking a biologic (n = 53). We extracted data on all patients meeting our inclusion criteria over a 20-year period. Our primary outcome was the diagnosis of VUE by histology. Our secondary outcomes were maternal and neonatal complications such as preeclampsia, FGR, and neonatal intensive care admission. Kruskal-Wallis and chi-squared tests were performed as appropriate for statistical analysis. Maternal characteristics were comparable between groups, and there was no increase in adverse pregnancy outcomes based on anti-TNF-α treatment. Exposure to anti-TNF-α therapy had no significant effect on the incidence of VUE or other obstetric complications. Within the cohort exposed to anti-TNF-α biologics during pregnancy, the rate of VUE was 9.3%, which is comparable to the reported general population risk. Our data support the safety profile of biologic use in pregnancy.

Indexed as

Autoimmune DiseasesBiological ProductsChorioamnionitisPlacenta DiseasesChorionic VilliFemaleFetal Growth RetardationHumansInfant, NewbornPlacentaPregnancyPregnancy OutcomeRetrospective StudiesTumor Necrosis Factor InhibitorsBiological ProductsTumor Necrosis Factor InhibitorsAutoimmune diseaseBiologic therapyChronic villitisImmunotherapyPlacentaPregnancyTumor necrosis factor alpha/α

Identifiers

PMID37973775
PMCPMC10960686
OpenAlexW4388735412

What Socratic holds

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LicenceTDM
Read underepoch 390

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 Socratic graph.