Evidence map›Paper›PMID 31344101›Full record

Observational studyPloS one2019

A novel nested polymerase chain reaction targeting the testis-specific protein Y-encoded family of genes for high sensitivity of recent semen exposure detection: Comparison with four other assays of semen detection.

Katia Giguère, François A Leblond, Ella Goma-Matsétsé, Vibhuti Dave, Luc Béhanzin, Fernand A Guédou, Michel Alary

Open access · goldAbstract readComparative StudyObservational Study
In one paragraph

Observational study in PloS one, 2019. 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
–field-weighted citation impact, top 86% 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, 0 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

7 authors at 5 institutions in 2 countries.

Katia GiguèreCentre de recherche du CHU de Québec, Université Laval, Québec, Québec, Canada.ORCID 0000-0001-5043-426X
François A LeblondCentre de Recherche de l'Hôpital Maisonneuve Rosemont, Montréal, Québec, Canada.
Ella Goma-MatsétséDispensaire IST, Centre de santé communal de Cotonou 1, Cotonou, Bénin.
Vibhuti DaveCentre de Recherche de l'Hôpital Maisonneuve Rosemont, Montréal, Québec, Canada.
Luc BéhanzinCentre de recherche du CHU de Québec, Université Laval, Québec, Québec, Canada.
Fernand A GuédouCentre de recherche du CHU de Québec, Université Laval, Québec, Québec, Canada.
Michel AlaryCentre de recherche du CHU de Québec, Université Laval, Québec, Québec, Canada.
Centre hospitalier de l'Université Laval · CAHôpital Maisonneuve-Rosemont · CAInstitut National de Santé Publique du Québec · CAProgamme National Contre le Tuberculose · BJUniversité de Parakou · BJ

Funding

CIHR FDN-143218CIHR ROH-115205
6 · The paper itself

Abstract

objectivesBecause self-report of sexual behaviours is prone to biases, biomarkers of recent semen exposure are increasingly used to assess unprotected sex. We aimed to present a novel nested polymerase chain reaction (PCR) assay targeting testis-specific protein Y-encoded (TSPY) genes and to compare its performance in detecting recent semen exposure with that of four other assays.

methodsForty-five vaginal samples were selected at baseline of a prospective observational demonstration study of early antiretroviral treatment and pre-exposure prophylaxis among female sex workers in Benin. Semen exposure was assessed with: a rapid prostate-specific antigen (PSA) detection assay, a quantitative PCR targeting the sex-determining region (SRY) gene, a standard PCR targeting SRY, a standard PCR targeting TSPY, and a nested PCR targeting TSPY (n-TSPY). Because we had hypothesized that n-TSPY would be the most sensitive of the five assays while remaining specific, and as our results suggested that it was the case, sensitivity and specificity were calculated for each assay in comparison with n-TSPY.

resultsThe n-TSPY could detect male DNA at concentration 16 and 64 times lower compared to s-TSPY and s-SRY, respectively. Among the 45 vaginal samples, prevalences of semen exposure according to the different assays varied from 22.2% (95%CI: 11.2%-37.1%) to 70.5% (95%CI: 54.8%-83.2%), with the highest prevalence measured with n-TSPY. The n-TSPY products were of expected size and we observed no false-positive in female DNA controls. The assay that offered the second best performance in detecting semen exposure was the PSA rapid test, with a sensitivity of 61.3% and a specificity of 100% compared to n-TSPY.

conclusionsCompared to n-TSPY, all other PCR assays had poor performance to detect semen exposure. The n-TSPY is an accessible assay that may have great utility in assessing semen exposure in studies where many factors are expected to accelerate biomarkers' clearance.

Indexed as

Unsafe SexBeninBiomarkersBody FluidsCell Cycle ProteinsFeasibility StudiesFemaleHumansMaleMultigene FamilyOccupational ExposurePolymerase Chain ReactionPredictive Value of TestsSemenSemen AnalysisSensitivity and SpecificityBiomarkersCell Cycle ProteinsTSPY1 protein, human

Identifiers

PMID31344101
PMCPMC6657882
OpenAlexW2964285136

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.