Evidence map›Paper›PMID 25976733›Full record

ArticleInternational journal of cancer2015

Short-term natural history of high-risk human papillomavirus infection in mid-adult women sampled monthly.

Tsung-chieh Jane Fu, Long Fu Xi, Ayaka Hulbert, James P Hughes, Qinghua Feng, Stephen M Schwartz, Stephen E Hawes, Laura A Koutsky, Rachel L Winer

Abstract read
In one paragraph

Article in International journal of cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Serum Concentrations of Emerging Vitamin D Biomarkers and Detection of Prevalent High-Risk HPV Infection in Mid-adult Women.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Human Papillomavirus: The Equal Opportunity Pathogen.The Journal of infectious diseases · 2017
    Article
  10. Review
  11. Article
  12. 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

9 authors.

Tsung-chieh Jane FuDepartment of Epidemiology, University of Washington, Seattle, WA.
Long Fu XiDepartment of Pathology, University of Washington, Seattle, WA.
Ayaka HulbertFred Hutchinson Cancer Research Center, Seattle, WA.
James P HughesDepartment of Biostatistics, University of Washington, Seattle, WA.
Qinghua FengFIDALAB, Seattle, WA.
Stephen M SchwartzDepartment of Epidemiology, University of Washington, Seattle, WA.
Stephen E HawesDepartment of Epidemiology, University of Washington, Seattle, WA.
Laura A KoutskyDepartment of Epidemiology, University of Washington, Seattle, WA.
Rachel L WinerDepartment of Epidemiology, University of Washington, Seattle, WA.

Funding

Natural History of HPV Infections in Mid-adult WomenP01AI083224 · NIAID · UNIVERSITY OF WASHINGTON · PI WINER, RACHEL L. · 2010 to 2010
$1.1M
NIAID NIH HHS P01 AI083224NIAID NIH HHS P01 AI083224-01A1
6 · The paper itself

Abstract

Characterizing short-term HPV detection patterns and viral load may inform HPV natural history in mid-adult women. From 2011-2012, we recruited women aged 30-50 years. Women submitted monthly self-collected vaginal samples for high-risk HPV DNA testing for 6 months. Positive samples were tested for type-specific HPV DNA load by real-time PCR. HPV type-adjusted linear and Poisson regression assessed factors associated with (i) viral load at initial HPV detection and (ii) repeat type-specific HPV detection. One-hundred thirty-nine women (36% of 387 women with ≥4 samples) contributed 243 type-specific HR HPV infections during the study; 54% of infections were prevalent and 46% were incident. Incident (vs. prevalent) detection and past pregnancy were associated with lower viral load, whereas current smoking was associated with higher viral load. In multivariate analysis, current smoking was associated with a 40% (95% CI: 5-87%) increase in the proportion of samples that were repeatedly positive for the same HPV type, whereas incident (vs. prevalent) detection status and past pregnancy were each associated with a reduction in the proportion of samples repeatedly positive (55%, 95% CI: 38-67% and 26%, 95% CI: 10-39%, respectively). In a separate multivariate model, each log10 increase in viral load was associated with a 10% (95% CI: 4-16%) increase in the proportion of samples repeatedly positive. Factors associated with repeat HPV detection were similar to those observed in longer-term studies, suggesting that short-term repeat detection may relate to long-term persistence. The negative associations between incident HPV detection and both viral load and repeat detection suggest that reactivation or intermittent persistence was more common than new acquisition.

Indexed as

AdultDNA, ViralEarly DiagnosisFemaleHumansLongitudinal StudiesMiddle AgedPapillomaviridaePapillomavirus InfectionsRisk FactorsSmokingVaginal SmearsViral LoadDNA, Viralhuman papillomavirusnatural historyviral loadwomen

Identifiers

PMID25976733
PMCPMC4591913

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.