Evidence map›Paper›PMID 31376187›Full record

ArticleThe Prostate2019

Trichomonas vaginalis infection and prostate-specific antigen concentration: Insights into prostate involvement and prostate disease risk.

Marvin E Langston, Ankita Bhalla, John F Alderete, Remington L Nevin, Ratna Pakpahan, Johannah Hansen, Debra Elliott, Angelo M De Marzo, Charlotte A Gaydos, William B Isaacs and 5 more

Open access · greenAbstract read
In one paragraph

Article in The Prostate, 2019. 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
1.5field-weighted citation impact, top 19% 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, 40 citations in OpenAlex.

  1. Pathogens (Basel, Switzerland) · 2023
    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

15 authors at 5 institutions in 1 country.

Marvin E LangstonDivision of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0002-4777-2425
Ankita BhallaDivision of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, Missouri.
John F AldereteSchool of Molecular Biosciences, College of Veterinary Medicine, Washington State University, Pullman, Washington.ORCID 0000-0002-6741-9426
Remington L NevinDepartment of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.ORCID 0000-0002-0534-1889
Ratna PakpahanDivision of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, Missouri.
Johannah HansenDivision of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, Missouri.
Debra ElliottDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Angelo M De MarzoDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0003-4847-5307
Charlotte A GaydosDivision of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
William B IsaacsDepartment of Urology, The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0001-6599-6775
William G NelsonDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Lori J SokollDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Jonathan M ZenilmanDivision of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Elizabeth A PlatzDepartment of Urology, The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0003-3676-8954
Siobhan SutcliffeDivision of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0002-4613-8107
Johns Hopkins University · USLangston University · USWashington University in St. Louis · USLos Angeles County Department of Public Health · USWashington State University · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI WILLIAM George NELSON · 1985 to 2026
$208.6M
Postdoctoral Training in Cancer Prevention and ControlT32CA190194 · NCI · WASHINGTON UNIVERSITY · PI GRAHAM A. COLDITZ, AIMEE S JAMES · 2014 to 2026
$4.7M
NCI NIH HHS P30 CA006973NCI NIH HHS T32190194NCI NIH HHS T32 CA190194
6 · The paper itself

Abstract

backgroundThe protist Trichomonas vaginalis causes a common, sexually transmitted infection and has been proposed to contribute to the development of chronic prostate conditions, including benign prostatic hyperplasia and prostate cancer. However, few studies have investigated the extent to which it involves the prostate in the current antimicrobial era. We addressed this question by investigating the relation between T. vaginalis antibody serostatus and serum prostate-specific antigen (PSA) concentration, a marker of prostate infection, inflammation, and/or cell damage, in young, male, US military members.

methodsWe measured T. vaginalis serum IgG antibodies and serum total PSA concentration in a random sample of 732 young, male US active duty military members. Associations between T. vaginalis serostatus and PSA were investigated by linear regression.

resultsOf the 732 participants, 341 (46.6%) had a low T. vaginalis seropositive score and 198 (27.0%) had a high score, with the remainder seronegative. No significant differences were observed in the distribution of PSA by T. vaginalis serostatus. However, slightly greater, nonsignificant differences were observed when men with high T. vaginalis seropositive scores were compared with seronegative men, and when higher PSA concentrations were examined (≥0.70 ng/mL). Specifically, 42.5% of men with high seropositive scores had a PSA concentration greater than or equal to 0.70 ng/mL compared with 33.2% of seronegative men (adjusted P = .125).

conclusionsOverall, our findings do not provide strong support for prostate involvement during T. vaginalis infection, although our suggestive positive findings for higher PSA concentrations do not rule out this possibility entirely. These suggestive findings may be relevant for prostate condition development because higher early- to mid-life PSA concentrations have been found to predict greater prostate cancer risk later in life.

Indexed as

AdultAntibodies, ProtozoanHumansImmunoglobulin GMaleMilitary PersonnelProstate-Specific AntigenProstatic DiseasesTrichomonas InfectionsTrichomonas vaginalisUnited StatesAntibodies, ProtozoanImmunoglobulin GProstate-Specific Antigeninflammationprostate cancer etiologysexually transmitted infectionT. vaginalis

Identifiers

PMID31376187
PMCPMC6715535
OpenAlexW2965394137

What OpenQuestion holds

Textmetadata
LicenceTDM
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.