Evidence map›Paper›PMID 25932915›Full record

ArticlePloS one2015

High Prevalence and Genotype Diversity of Anal HPV Infection among MSM in Northern Thailand.

Taweewat Supindham, Suwat Chariyalertsak, Utaiwan Utaipat, Toshiyuki Miura, Darin Ruanpeng, Nuntisa Chotirosniramit, Natthapol Kosashunhanan, Patcharaphan Sugandhavesa, Pongpun Saokhieo, Radchanok Songsupa and 2 more

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Trial
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  7. Increased CD4BMC infectious diseases · 2022
    Article
  8. Article
  9. Article
  10. Anal human papillomavirus prevalence and risk factors among men who have sex with men in Vietnam.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2021
    Article
  11. Article
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  15. Article
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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

12 authors.

Taweewat SupindhamResearch Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
Suwat ChariyalertsakResearch Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
Utaiwan UtaipatResearch Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
Toshiyuki MiuraDepartment of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Darin RuanpengResearch Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
Nuntisa ChotirosniramitResearch Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
Natthapol KosashunhananResearch Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
Patcharaphan SugandhavesaResearch Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
Pongpun SaokhieoResearch Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
Radchanok SongsupaResearch Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
Sumalee SiriaunkgulDepart of Pathology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Antika WongthaneeResearch Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHPV infection is common and may cause cancer among men who have sex with men (MSM). Anal HPV infection (HPV+) was found in 85% of HIV-positive (HIV+) and 59% of HIV-negative (HIV-) MSM in Bangkok, central Thailand. As little is known about HPV in this group in northern Thailand, we studied MSM subgroups comprised of gay men (GM), bisexual men (BM), and transgender women (TGW).

methodsFrom July 2012 through January 2013, 85 (42.5% of 200) GM, 30 (15%) BM, and 85 (42.5%) TGW who practiced receptive anal intercourse were recruited after informed consent, followed by self-assisted computer interview, HIV testing, and anal swabs for HPV genotyping.

resultsOf 197 adequate specimens, the overall prevalence of any HPV was 157 (80%). Prevalence was 89% (76/85) in GM, 48% (14/29) in BM, and 81% (67/83) in TGW. The most common high-risk types were HPV16 (27% of 197), HPV58 (23%), and HPV51 (18%). Prevalence of high-risk types was 74% in 85 GM, 35% in 29 BM, and 71% in 83 TGW. Prevalence of any HPV type, or high-risk type, was 100% and 94%, respectively, among 48 HIV+ MSM, 70% and 54% among 120 HIV- MSM. Of the 197 specimens, 36% (70) had HPV types 16 and/or 18 in the bivalent vaccine, compared to 48% (95) with ≥1 of types 16/18/06/11 in the quadrivalent, 56% (111) for 16/18/31/33/45/52/58 in the 7-valent, and 64% (126) for 16/18/31/33/45/52/58/06/11 in the 9-valent. HIV+, GM, and TGW were independently associated with HPV infection.

conclusionsWe found higher rates of both any HPV and high-risk types than previous studies. Among the heretofore unstudied TGW, their equivalent HPV rates were comparable to GM. Current and investigational HPV vaccines could substantially protect GM, BM, and TGW from the serious consequences of HPV infection especially among HIV + MSM.

Indexed as

Genetic VariationAdolescentAdultAnus DiseasesCoinfectionDemographyFemaleGenotypeHIV InfectionsHomosexuality, MaleHumansLogistic ModelsMaleMiddle AgedOdds RatioPapillomaviridaePapillomavirus Vaccines

Identifiers

PMID25932915
PMCPMC4416722

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Registered trials

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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.