Male Circumcision Reduces Penile HPV Incidence and Persistence: A Randomized Controlled Trial in Kenya.


Journal

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
ISSN: 1538-7755
Titre abrégé: Cancer Epidemiol Biomarkers Prev
Pays: United States
ID NLM: 9200608

Informations de publication

Date de publication:
06 2021
Historique:
received: 28 08 2020
revised: 24 01 2021
accepted: 22 03 2021
pubmed: 12 5 2021
medline: 27 1 2022
entrez: 11 5 2021
Statut: ppublish

Résumé

Male circumcision reduces the risk of human immunodeficiency virus infection in men. We assessed the effect of male circumcision on the incidence and natural history of human papillomavirus (HPV) in a randomized clinical trial in Kisumu, Kenya. Sexually active, 18- to 24-year-old men provided penile exfoliated cells for HPV DNA testing every 6 months for 2 years. HPV DNA was detected via GP5+/6+ PCR in glans/coronal sulcus and in shaft samples. HPV incidence and persistence were assessed by intent-to-treat analyses. A total of 2,193 men participated (1,096 randomized to circumcision; 1,097 controls). HPV prevalence was 50% at baseline for both groups and dropped to 23.7% at 24 months in the circumcision group, and 41.0% in control group. Incident infection of any HPV type over 24 months was lower among men in the circumcision group than in the control group [HR = 0.61; 95% confidence interval (CI), 0.52-0.72]. Clearance rate of any HPV infection over 24 months was higher in the circumcision group than in the control group (HR = 1.87; 95% CI, 1.49-2.34). Lower HPV point-prevalence, lower HPV incidence, and higher HPV clearance in the circumcision group were observed in glans but not in shaft samples. Male circumcision reduced the risk of HPV acquisition and reinfection, and increased HPV clearance in the glans. Providing voluntary, safe, and affordable male circumcision should help reduce HPV infections in men, and consequently, HPV-associated disease in their partners.

Sections du résumé

BACKGROUND
Male circumcision reduces the risk of human immunodeficiency virus infection in men. We assessed the effect of male circumcision on the incidence and natural history of human papillomavirus (HPV) in a randomized clinical trial in Kisumu, Kenya.
METHODS
Sexually active, 18- to 24-year-old men provided penile exfoliated cells for HPV DNA testing every 6 months for 2 years. HPV DNA was detected via GP5+/6+ PCR in glans/coronal sulcus and in shaft samples. HPV incidence and persistence were assessed by intent-to-treat analyses.
RESULTS
A total of 2,193 men participated (1,096 randomized to circumcision; 1,097 controls). HPV prevalence was 50% at baseline for both groups and dropped to 23.7% at 24 months in the circumcision group, and 41.0% in control group. Incident infection of any HPV type over 24 months was lower among men in the circumcision group than in the control group [HR = 0.61; 95% confidence interval (CI), 0.52-0.72]. Clearance rate of any HPV infection over 24 months was higher in the circumcision group than in the control group (HR = 1.87; 95% CI, 1.49-2.34). Lower HPV point-prevalence, lower HPV incidence, and higher HPV clearance in the circumcision group were observed in glans but not in shaft samples.
CONCLUSION
Male circumcision reduced the risk of HPV acquisition and reinfection, and increased HPV clearance in the glans.
IMPACT
Providing voluntary, safe, and affordable male circumcision should help reduce HPV infections in men, and consequently, HPV-associated disease in their partners.

Identifiants

pubmed: 33972367
pii: 1055-9965.EPI-20-1272
doi: 10.1158/1055-9965.EPI-20-1272
pmc: PMC8172477
mid: NIHMS1689643
doi:

Substances chimiques

DNA, Viral 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1139-1148

Subventions

Organisme : NIAID NIH HHS
ID : P30 AI050410
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI082151
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA114773
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI050440
Pays : United States
Organisme : CIHR
Pays : Canada

Commentaires et corrections

Type : CommentIn

Informations de copyright

©2021 American Association for Cancer Research.

Références

AIDS. 2006 Jul 13;20(11):1491-5
pubmed: 16847403
N Engl J Med. 2002 Apr 11;346(15):1105-12
pubmed: 11948269
J Infect Dis. 2011 Nov;204(9):1375-90
pubmed: 21965090
Lancet. 2007 Feb 24;369(9562):657-66
pubmed: 17321311
J Infect Dis. 2018 Sep 8;218(8):1219-1227
pubmed: 29800222
BMC Infect Dis. 2011 Jan 12;11:13
pubmed: 21226933
J Infect Dis. 2015 Mar 1;211(5):811-20
pubmed: 25261492
J Infect Dis. 2009 Jan 1;199(1):14-9
pubmed: 19086814
Sex Transm Dis. 2012 Feb;39(2):104-13
pubmed: 22249298
J Clin Microbiol. 2002 Mar;40(3):779-87
pubmed: 11880393
Cochrane Database Syst Rev. 2018 May 09;5:CD009069
pubmed: 29740819
Int J Cancer. 2010 Jan 15;126(2):572-7
pubmed: 19626601
Lancet. 2011 Jan 15;377(9761):209-18
pubmed: 21216000
Int J Cancer. 2011 Dec 15;129(12):2970-5
pubmed: 21462185
Cancer Causes Control. 2009 May;20(4):449-57
pubmed: 19082746
N Engl J Med. 2009 Mar 26;360(13):1298-309
pubmed: 19321868
Int J Cancer. 2009 May 15;124(10):2375-83
pubmed: 19189402
J Infect Dis. 2010 May 15;201(10):1455-62
pubmed: 20370483
Lancet. 2006 Apr 15;367(9518):1247-55
pubmed: 16631880
Lancet Glob Health. 2016 Jul;4(7):e453-63
pubmed: 27340003
J Infect Dis. 2009 Aug 1;200(3):370-8
pubmed: 19545209
Int J Cancer. 2007 Aug 1;121(3):621-32
pubmed: 17405118
J Infect Dis. 2017 Mar 1;215(5):772-780
pubmed: 28011913
J Infect Dis. 2011 Dec 1;204(11):1723-9
pubmed: 21984739
Lancet. 2007 Feb 24;369(9562):643-56
pubmed: 17321310
J Infect Dis. 2008 Mar 15;197(6):787-94
pubmed: 18284369
Sex Transm Dis. 2007 Nov;34(11):928-34
pubmed: 17621251
BMC Infect Dis. 2014 Feb 10;14:75
pubmed: 24517172

Auteurs

Jennifer S Smith (JS)

Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina. JenniferS@unc.edu.
Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina.

Danielle M Backes (DM)

Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina.

Michael G Hudgens (MG)

Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina.

Wenwen Mei (W)

Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina.

Hrishikesh Chakraborty (H)

Department of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina.

Eliane Rohner (E)

Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina.
Institute of Social and Preventive Medicine, University of Bern, Switzerland.

Stephen Moses (S)

Department of Community Health Sciences, University of Manitoba, Winnipeg, Canada.

Kawango Agot (K)

Impact Research and Development Organization, Kisumu, Kenya.

Chris J L M Meijer (CJLM)

Department of Pathology, Amsterdam UMC, location VUmc, Amsterdam, the Netherlands.

Robert C Bailey (RC)

Division of Epidemiology and Biostatistics, School of Public Health, University of Illinois at Chicago, Illinois.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH