Evidence map›Paper›PMID 21173647›Full record

ArticleObstetrics and gynecology2011

Early elevations of the complement activation fragment C3a and adverse pregnancy outcomes.

Anne M Lynch, Ronald S Gibbs, James R Murphy, Patricia C Giclas, Jane E Salmon, V Michael Holers

Open access · greenAbstract read
In one paragraph

Article in Obstetrics and gynecology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

68 citing papers in PubMed, 133 citations in OpenAlex.

  1. Complement factor B activation in patients with preeclampsia.Journal of reproductive immunology · 2015
    Trial
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  9. Sialidases derived frombioRxiv : the preprint server for biology · 2025
    Article
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  11. Article
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  15. Article
  16. Review
  17. Article
  18. Preeclampsia and Obesity-The Preventive Role of Exercise.International journal of environmental research and public health · 2023
    Review
  19. A review of the alternative pathway of complement and its relation to HELLP syndrome: is it time to consider HELLP syndrome a disease of the alternative pathway.The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians · 2022
    Review
  20. Observational

8 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Anne M LynchFrom the Department of Obstetrics and Gynecology, University of Colorado, School of Medicine, Aurora, Colorado.
Ronald S Gibbs
James R Murphy
Patricia C Giclas
Jane E Salmon
V Michael Holers
National Jewish Health · US

Funding

Predictors of Pregnancy Outcome In SLE and APSR01AR049772 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI SALMON, JANE E · 2003 to 2012
$12.6M
Mechanisms of aPL antibody-induced pregnancy lossR01AR038889 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI SALMON, JANE E · 1989 to 2010
$2.3M
Complement as a Mediator of Recurrent MiscarriagesR01AI055007 · NIAID · HOSPITAL FOR SPECIAL SURGERY · PI SALMON, JANE E · 2004 to 2008
$1.7M
Complement Activation and Pregnancy LossK23HD049684 · NICHD · UNIVERSITY OF COLORADO DENVER · PI LYNCH, ANNE M. · 2006 to 2009
$500k
Mechanisms of aPL antibody-induced pregnancy lossR55AR038889 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI SALMON, JANE E · 2005 to 2005
$100k
NIAID NIH HHS R01 AI055007NIAID NIH HHS R01 AI 55007NIAMS NIH HHS AR38889NIAMS NIH HHS AR49772NIAMS NIH HHS R01 AR038889NIAMS NIH HHS R01 AR049772NIAMS NIH HHS R55 AR038889NICHD NIH HHS K23 HD049684
6 · The paper itself

Abstract

objectiveTo estimate whether elevations of complement C3a early in pregnancy are predictive of the subsequent development of adverse pregnancy outcomes.

methodsA plasma sample was obtained from each enrolled pregnant woman before 20 weeks of gestation. The cohort (n=1,002) was evaluated for the development of adverse pregnancy outcomes defined as hypertensive diseases of pregnancy (gestational hypertension or preeclampsia), preterm birth (before 37 weeks of gestation), premature rupture of the membranes, pregnancy loss (during the embryonic and fetal period), intrauterine growth restriction, and the composite outcome of any adverse outcome.

resultsOne or more adverse pregnancy outcomes occurred in 211 (21%) of the cohort. The mean levels (ng/mL) of C3a in early pregnancy were significantly (P=<.001) higher among women with one or more adverse outcomes (858±435) compared with women with an uncomplicated pregnancy (741±407). Adjusted for parity and prepregnancy body mass index, women with levels of C3a in the upper quartile in early pregnancy were three times more likely to have an adverse outcome later in pregnancy compared with women in the lowest quartile (95% confidence interval, 1.8-4.8; P<.001). The link between early elevated C3a levels and adverse pregnancy outcomes was driven primarily by individual significant (P<.05) associations of C3a with hypertensive diseases of pregnancy, preterm birth, and premature rupture of the membranes.

conclusionElevated C3a as early as the first trimester of pregnancy is an independent predictive factor for adverse pregnancy outcomes, suggesting that complement-related inflammatory events in pregnancy contribute to the subsequent development of poor outcomes at later stages of pregnancy. LEVEL OF EVIDENCE: II.

Indexed as

AdultBiomarkersComplement C3aFemaleHumansLogistic ModelsPredictive Value of TestsPregnancyPregnancy ComplicationsPregnancy OutcomeProspective StudiesBiomarkersComplement C3a

Identifiers

PMID21173647
PMCPMC5267353
OpenAlexW2316383122

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.