Evidence map›Paper›PMID 29549429›Full record

ArticleParasitology research2018

Integrated morphologic and molecular analysis of Trichomonas vaginalis, Mycoplasma hominis, and human papillomavirus using cytologic smear preparations.

I Nikas, A Hapfelmeier, M Mollenhauer, D Angermeier, M Bettstetter, R Götz, M Schmidmayr, V Seifert-Klauss, A Muckenhuber, U Schenck and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Parasitology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. 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

11 authors at 3 institutions in 2 countries.

I NikasInstitute of Pathology, Technische Universität München, Trogerstraße 18, 81675, Munich, Germany.
A HapfelmeierInstitute of Medical Informatics, Statistics and Epidemiology, Technische Universität München, Munich, Germany.
M MollenhauerInstitute of Pathology, Technische Universität München, Trogerstraße 18, 81675, Munich, Germany.
D AngermeierInstitute of Pathology, Technische Universität München, Trogerstraße 18, 81675, Munich, Germany.
M BettstetterMolekularpathologie Südbayern, Munich, Germany.
R GötzInstitute of Pathology, Technische Universität München, Trogerstraße 18, 81675, Munich, Germany.
M SchmidmayrFrauenklinik und Poliklinik, Technische Universität München, Munich, Germany.
V Seifert-KlaussFrauenklinik und Poliklinik, Technische Universität München, Munich, Germany.
A MuckenhuberInstitute of Pathology, Technische Universität München, Trogerstraße 18, 81675, Munich, Germany.
U SchenckInstitute of Pathology, Technische Universität München, Trogerstraße 18, 81675, Munich, Germany.
Gregor WeirichInstitute of Pathology, Technische Universität München, Trogerstraße 18, 81675, Munich, Germany. gregor.weirich@tum.de.ORCID http://orcid.org/0000-0003-1659-1581
Technical University of Munich · DETUM Klinikum · DEEuropean University Cyprus · CY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenic microbes may colonize the female genital tract via sexual transmission and cause health issues like inflammation or malignancy, summarized as sexually transmitted disease (STD). A major representative of such pathogens is Trichomonas vaginalis (T.v.), whose role in the etiology of cervical cancer remains elusive. Traditional morphologic screening of cervical smears is able to detect T.v., although its identification may be complicated by look-alikes such as degenerated granulocytes and basal cells. In addition, the parasite's endosymbiont Mycoplasma hominis (M.h.) cannot be detected in the Pap test. This investigation was aimed at designing a PCR-based method to detect specific pathogenic germs by using cervical cytology slides to overcome morphologic uncertainty and increase diagnostic accuracy. To test our molecular screening method on T.v., M.h., and HPV in archival smears, we elaborated a multiplex PCR approach based on microdissection. This assay was applied to a minute quantity of starting material which harbored or was suspected to harbor T.v.; the resulting isolated DNA was used for subsequent molecular analyses of T.v., M.h., and HPV. We clarified the diagnosis of genital T.v. infection in 88 and 1.8% of morphologically suspicious and T.v.-negative cases, respectively. We also revealed a tendency of M.h. co-infection in high-risk HPV cases. In conclusion, a microdissection-based approach to detect pathogenic microbes such as T.v., HPV, and M.h. is a molecular tool easy to implement and may help to better understand the interactivity of these germs with respect to pathogenesis.

Indexed as

AdolescentAdultCoinfectionDNA, BacterialDNA, ProtozoanDNA, ViralFemaleHumansMultiplex Polymerase Chain ReactionMycoplasma hominisMycoplasma InfectionsPapanicolaou TestPapillomaviridaePapillomavirus InfectionsTrichomonas vaginalisTrichomonas VaginitisDNA, BacterialDNA, ProtozoanDNA, ViralCervical cancerHigh-risk HPVMicrodissectionMultiplex PCRPap testScreening

Identifiers

PMID29549429
OpenAlexW2792332169

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.