Evidence map›Paper›PMID 38072839›Full record

ArticleParasitology research2023

Impact of chronic toxoplasmosis in pregnancy: association between maternal seropositivity for Toxoplasma gondii IgG antibodies and fetal growth restriction.

Victor Otero Martinez, Nathália Ribeiro Dos Santos, Homègnon Antonin Ferréol Bah, Erival Amorim Gomes Junior, Daisy Oliveira Costa, José Antonio Menezes-Filho

Abstract read
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In one paragraph

Article in Parasitology research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Seroprevalence ofPathogens (Basel, Switzerland) · 2026
    Article
  2. Article
  3. Seroprevalence ofMicroorganisms · 2024
    Article
  4. Article
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.

Victor Otero MartinezGraduate Program in Pharmacy, College of Pharmacy, Federal University of Bahia, Salvador, Bahia, Brazil. victor_otero1@hotmail.com.ORCID http://orcid.org/0000-0002-0537-1797
Nathália Ribeiro Dos SantosGraduate Program in Pharmacy, College of Pharmacy, Federal University of Bahia, Salvador, Bahia, Brazil.
Homègnon Antonin Ferréol BahLaboratory of Toxicology, College of Pharmacy, Federal University of Bahia, Salvador, Bahia, Brazil.
Erival Amorim Gomes JuniorLaboratory of Toxicology, College of Pharmacy, Federal University of Bahia, Salvador, Bahia, Brazil.
Daisy Oliveira CostaGraduate Program in Pharmacy, College of Pharmacy, Federal University of Bahia, Salvador, Bahia, Brazil.
José Antonio Menezes-FilhoGraduate Program in Pharmacy, College of Pharmacy, Federal University of Bahia, Salvador, Bahia, Brazil.
Universidade Federal da Bahia · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 421550/2018-0
6 · The paper itself

Abstract

Insults caused by acute infections during the gestational period on fetal development are known; however, new evidence suggests that chronic infectious diseases can also impact the maternal immune status and lead to negative consequences for the neonate. This study investigated the association between the prevalence of specific antibodies in pregnant women and alterations in fetal development at birth. A follow-up study evaluated women during the gestational period and their respective newborns at delivery time. The pregnant women were tested for the presence of antibodies to infectious agents: Toxoplasma gondii (T. gondii), cytomegalovirus (CMV), syphilis, human immunodeficiency virus (HIV), hepatitis B and C. Semi-structured questionnaires were administered to the pregnant women at the time of recruitment after obtaining informed consent. Detailed information about the newborns was extracted from medical records. The seroprevalence of chronic T. gondii infection, as determined by the presence of IgG antibodies against the protozoan, was found to be 56.2%, while the overall prevalence of CMV IgG antibodies was 96.3%. Non-primiparous pregnant women from socio-economic classes, less affluent groups, and skilled working-class individuals had higher chances of testing positive for specific T. gondii IgG antibodies. Newborns classified as small for gestational age represented 12.9% of the total. Those born to mothers seropositive for anti-T. gondii IgG antibodies were 9.4 times more likely to be born small for gestational age (p = 0.035). The results suggest that chronic T. gondii infection may contribute to higher rates of newborns with growth restriction. These findings add to a growing body of evidence regarding the impact of chronic infectious diseases on intrauterine fetal development.

Indexed as

Cytomegalovirus InfectionsHepatitis BToxoplasmaToxoplasmosisAntibodies, ProtozoanFemaleFetal Growth RetardationFollow-Up StudiesHumansImmunoglobulin GImmunoglobulin MInfant, NewbornPregnancyRisk FactorsSeroepidemiologic StudiesAntibodies, ProtozoanImmunoglobulin GImmunoglobulin MBirth cohortPregnancySerologySmall for gestational ageToxoplasmosis

Identifiers

PMID38072839
OpenAlexW4389573606

What OpenQuestion holds

Textmetadata
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.