Evidence map›Paper›PMID 39701359›Full record

Trial reportFertility and sterility2025

Preconception Chlamydia trachomatis seropositivity and fecundability, live birth, and adverse pregnancy outcomes.

Yajnaseni Chakraborti, Stefanie N Hinkle, Jørgen Skov Jensen, Catherine L Haggerty, Toni Darville, Sunni L Mumford, Enrique F Schisterman, Robert M Silver, Brandie DePaoli Taylor

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Fertility and sterility, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. PreconceptionmedRxiv : the preprint server for health sciences · 2026
    Article
  2. Current Evidence of Maternal Infection With Chlamydia trachomatis and Preeclampsia Risk.American journal of reproductive immunology (New York, N.Y. : 1989) · 2025
    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

9 authors.

Yajnaseni ChakrabortiDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Stefanie N HinkleDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Obstetrics and Gynecology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Jørgen Skov JensenResearch Unit for Reproductive Microbiology, Statens Serum Institut, Copenhagen, Denmark.
Catherine L HaggertyDepartment of Epidemiology, School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Toni DarvilleDepartment of Pediatrics, University of North Carolina Chapel Hill, Chapel Hill, North Carolina.
Sunni L MumfordDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Obstetrics and Gynecology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Enrique F SchistermanDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Obstetrics and Gynecology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Robert M SilverDepartment of Obstetrics and Gynecology, School of Medicine, University of Utah, Salt Lake City, Utah.
Brandie DePaoli TaylorDepartment of Obstetrics and Gynecology, University of Texas Medical Branch, Galveston, Texas; Academic Research, Advocate Aurora Research Institute, Milwaukee, Wisconsin. Electronic address: brandie.taylor@aah.org.

Funding

Immune activating syncytiotrophoblast microvesicles and danger associated molecular patterns in preeclampsia riskR01AI141501 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SHARMA, SURENDRA · 2019 to 2023
$2.8M
Early Double Low-Dose Aspirin to Reduce Preeclampsia and Miscarriage: a Global Approach RCTR01HD112308 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI Kurt T Barnhart, Enrique F. Schisterman · 2023 to 2026
$2.7M
Evaluating the intersection between sexually transmitted infections, inflammation and reproductive successR01AI143653 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI TAYLOR, BRANDIE DEPAOLI · 2020 to 2023
$1.9M
NIAID NIH HHS R01 AI141501NIAID NIH HHS R01 AI143653NICHD NIH HHS R01 HD112308
6 · The paper itself

Abstract

objectiveTo study the impact of preconception Chlamydia trachomatis seropositivity on fecundability, live birth, and pregnancy loss and to assess the effect of low-dose aspirin therapy (81 mg/day) on live birth and pregnancy loss.

designPreconception cohort study conducted using data and specimens from the Effects of Aspirin in Gestation and Reproduction study-a randomized placebo-controlled trial. SUBJECTS: A total of 1,228 individuals with proven fecundity and a history of 1-2 pregnancy losses. EXPOSURE: Preconception C. trachomatis seropositivity determined using an enzyme-linked immunoabsorbent assay-based synthetic peptide assay at baseline.

main outcome measuresTime-to pregnancy (fecundability) was defined as number of menstrual cycles to beta human chorionic gonadrotropin-detected pregnancy; live birth status was determined from medical record abstraction; pregnancy loss was defined as any loss post positive beta human chorionic gonadrotropin test.

resultsAfter adjusting for confounders (baseline demographic and reproductive history variables), C. trachomatis seropositivity (n = 134/1228, 11%) was associated with a reduced live birth likelihood (relative risk [RR]: 0.77, 95% confidence interval [CI]: 0.59, 0.99) and an increased risk of pregnancy loss (RR: 1.16, 95% CI: 1.04, 1.29), but was not associated with fecundability (fecundability odds ratio: 0.92, 95% CI: 0.71, 1.20). Among a subset of C. trachomatis seropositive individuals with chronic inflammation indicated by increased C-reactive protein levels ≥1.95 but ≤10 mg/L (n = 50/134, 37.3%), low-dose aspirin therapy improved live birth rates (RR: 1.68, 95% CI: 0.96, 2.92) and reduced the risk of pregnancy loss (RR: 0.83, 95% CI: 0.65, 1.10). However, the sample size reduced precision.

conclusionPrior exposure to C. trachomatis among women with a history of pregnancy loss may impact risk of pregnancy loss. Our results indicate the need for future studies exploring mechanisms by which C. trachomatis may influence long-term reproductive function, because this may identify treatments to improve outcomes among those with a history of infection.

Indexed as

Chlamydia InfectionsChlamydia trachomatisFertilityLive BirthAbortion, SpontaneousAdultAspirinFemaleHumansPreconception CarePregnancyPregnancy OutcomeRisk FactorsTime-to-PregnancyYoung AdultAspirinChlamydiafecunditypregnancypregnancy loss

Identifiers

PMID39701359
PMCPMC12158647

What Socratic holds

Textmetadata
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.