Evidence map›Paper›PMID 24848950›Full record

ArticlePloS one2014

Urinary estrogen metabolites and self-reported infertility in women infected with Schistosoma haematobium.

Júlio Santos, Maria João Gouveia, Nuno Vale, Maria de Lurdes Delgado, Ana Gonçalves, José M Teixeira da Silva, Cristiano Oliveira, Pedro Xavier, Paula Gomes, Lúcio L Santos and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
3.2field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 36 citations in OpenAlex.

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  18. Bladder cancer and urinary Schistosomiasis in Angola.Journal of nephrology research · 2015
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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

17 authors at 6 institutions in 4 countries.

Júlio SantosClínica da Sagrada Esperança, Luanda, Angola.
Maria João GouveiaCIQUP, Chemistry and Biochemistry Department, Faculty of Sciences, University of Porto, Porto, Portugal.
Nuno ValeCIQUP, Chemistry and Biochemistry Department, Faculty of Sciences, University of Porto, Porto, Portugal.
Maria de Lurdes DelgadoINSA, National Institute of Health, Porto, Portugal.
Ana GonçalvesCentre for Reproductive Genetics Prof. Alberto Barros, Porto, Portugal.
José M Teixeira da SilvaCentre for Reproductive Genetics Prof. Alberto Barros, Porto, Portugal.
Cristiano OliveiraCentre for Reproductive Genetics Prof. Alberto Barros, Porto, Portugal.
Pedro XavierCentre for Reproductive Genetics Prof. Alberto Barros, Porto, Portugal.
Paula GomesCIQUP, Chemistry and Biochemistry Department, Faculty of Sciences, University of Porto, Porto, Portugal.
Lúcio L SantosClínica da Sagrada Esperança, Luanda, Angola; Experimental Therapeutics and Pathology Research Group, Portuguese Institute of Oncology, Porto, Portugal.
Carlos LopesClínica da Sagrada Esperança, Luanda, Angola; Department of Pathology and Molecular Immunology, Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, Porto, Portugal.
Alberto BarrosCentre for Reproductive Genetics Prof. Alberto Barros, Porto, Portugal; Department of Genetics, Faculty of Medicine, University of Porto, Porto, Portugal.
Gabriel RinaldiDepartment of Microbiology, Immunology and Tropical Medicine, and Research Center for Neglected Diseases of Poverty, School of Medicine & Health Sciences, George Washington University, Washington, D.C., United States of America; Departamento de Genética, Facultad de Medicina, Universidad de la República, (UDELAR), Montevideo, Uruguay.
Paul J BrindleyDepartment of Microbiology, Immunology and Tropical Medicine, and Research Center for Neglected Diseases of Poverty, School of Medicine & Health Sciences, George Washington University, Washington, D.C., United States of America.
José M Correia da CostaINSA, National Institute of Health, Porto, Portugal; Center for the Study of Animal Science, CECA/ICETA, University of Porto, Porto, Portugal.
Mário SousaDepartment of Microscopy, Laboratory of Cell Biology, Institute of Biomedical Sciences Abel Salazar (ICBAS), Multidisciplinary Unit for Biomedical Research-UMIB, University of Porto, Porto, Portugal.
Mónica C BotelhoINSA, National Institute of Health, Porto, Portugal; Center for the Study of Animal Science, CECA/ICETA, University of Porto, Porto, Portugal.
Universidade do Porto · PTCentro de Genética Clínica · PTClínica Sagrada Esperança · AONational Institute of Health Dr. Ricardo Jorge · PTGeorge Washington University · USUniversidad de la República · UY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSchistosomiasis is a neglected tropical disease, endemic in 76 countries, that afflicts more than 240 million people. The impact of schistosomiasis on infertility may be underestimated according to recent literature. Extracts of Schistosoma haematobium include estrogen-like metabolites termed catechol-estrogens that down regulate estrogen receptors alpha and beta in estrogen responsive cells. In addition, schistosome derived catechol-estrogens induce genotoxicity that result in estrogen-DNA adducts. These catechol estrogens and the catechol-estrogen-DNA adducts can be isolated from sera of people infected with S. haematobium. The aim of this study was to study infertility in females infected with S. haematobium and its association with the presence of schistosome-derived catechol-estrogens. METHODOLOGY/PRINCIPAL

findingsA cross-sectional study was undertaken of female residents of a region in Bengo province, Angola, endemic for schistosomiasis haematobia. Ninety-three women and girls, aged from two (parents interviewed) to 94 years were interviewed on present and previous urinary, urogenital and gynecological symptoms and complaints. Urine was collected from the participants for egg-based parasitological assessment of schistosome infection, and for liquid chromatography diode array detection electron spray ionization mass spectrometry (LC/UV-DAD/ESI-MSn) to investigate estrogen metabolites in the urine. Novel estrogen-like metabolites, potentially of schistosome origin, were detected in the urine of participants who were positive for eggs of S. haematobium, but not detected in urines negative for S. haematobium eggs. The catechol-estrogens/ DNA adducts were significantly associated with schistosomiasis (OR 3.35; 95% CI 2.32-4.84; P≤0.001). In addition, presence of these metabolites was positively associated with infertility (OR 4.33; 95% CI 1.13-16.70; P≤0.05). CONCLUSIONS/SIGNIFICANCE: Estrogen metabolites occur widely in diverse metabolic pathways. In view of the statistically significant association between catechol-estrogens/ DNA adducts and self-reported infertility, we propose that an estrogen-DNA adduct mediated pathway in S. haematobium-induced ovarian hormonal deregulation could be involved. In addition, the catechol-estrogens/ DNA adducts described here represent potential biomarkers for schistosomiasis haematobia.

Indexed as

AdolescentAdultAgedAged, 80 and overAngolaAnimalsChildChild, PreschoolCross-Sectional StudiesDNA AdductsEstrogensFemaleHumansInfertility, FemaleMiddle AgedParasite Egg CountDNA AdductsEstrogens

Identifiers

PMID24848950
PMCPMC4029575
OpenAlexW2109119013

What OpenQuestion holds

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LicenceCC BY
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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.