Evidence map›Paper›PMID 22729840›Full record

ArticleInternational journal of cancer2013

Persistence of newly detected human papillomavirus type 31 infection, stratified by variant lineage.

Long Fu Xi, Mark Schiffman, Laura A Koutsky, Zhonghu He, Rachel L Winer, Ayaka Hulbert, Shu-Kuang Lee, Yang Ke, Nancy B Kiviat

Abstract read
In one paragraph

Article in International journal of cancer, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Trial
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  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Human papillomavirus variants among Inuit women in northern Quebec, Canada.International journal of circumpolar health · 2015
    Article
  11. Article
  12. Human papillomavirus genomics: past, present and future.Current problems in dermatology · 2014
    Article
  13. Review
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 at 3 institutions in 2 countries.

Long Fu XiDepartment of Pathology, School of Medicine, School of Public Health, University of Washington, Seattle, WA 98104, USA. longfu@u.washington.edu
Mark Schiffman
Laura A Koutsky
Zhonghu He
Rachel L Winer
Ayaka Hulbert
Shu-Kuang Lee
Yang Ke
Nancy B Kiviat
University of Washington · USPeking University · CNDivision of Cancer Epidemiology and Genetics

Funding

Intratypic variation of oncogenic HPV types as a risk factor for cervical neoplasR01CA133569 · NCI · UNIVERSITY OF WASHINGTON · PI XI, LONG FU · 2009 to 2012
$1.7M
NCI NIH HHS CA133569NCI NIH HHS R01 CA133569
6 · The paper itself

Abstract

Variants of human papillomavirus (HPV) type 31 have been shown to be related both to risk of cervical lesions and racial composition of a population. It is largely undetermined whether variants differ in their likelihood of persistence. Study subjects were women who participated in the ASCUS-LSIL Triage Study and who had a newly detected HPV31 infection during a two-year follow-up with six-month intervals. HPV31 isolates were characterized by sequencing and assigned to one of three variant lineages. Loss of the newly detected HPV31 infection was detected in 76 (47.5%) of the 160 women (32/67 with A variants, 16/27 with B variants and 28/66 with C variants). The adjusted hazard ratio associating loss of the infection was 1.2 (95% CI, 0.7-2.1) for women with A variants and 2.1 (95% CI, 1.2-3.5) for women with B variants when compared with those with C variants. Infections with A and C variants were detected in 50 and 41 Caucasian women and in 15 and 23 African-American women, respectively. The likelihood of clearance of the infection was significantly lower in African-American women with C variants than in African-American women with A variants (p = 0.05). There was no difference in the likelihood of clearance between A and C variants among Caucasian women. Our data indicated that infections with B variants were more likely to resolve than those with C variants. The difference in clearance of A vs. C variants in African-Americans, but not in Caucasians, suggests a possibility of the race-related influence in retaining the variant-specific infection.

Indexed as

Viral LoadAdultBlack or African AmericanDisease ProgressionDNA, ViralFemaleGenetic VariationHuman papillomavirus 31HumansPapillomavirus InfectionsWhite PeopleYoung AdultDNA, Viral

Identifiers

PMID22729840
PMCPMC3465533
OpenAlexW1986909895

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.