Prevalence of oral and oropharyngeal human papillomavirus infection in Brazilian population studies: a systematic review^☆

ABSTRACT

INTRODUCTION:

Human papillomavirus has been associated with head and neck squamous cell carcinoma. However, there is no conclusive evidence on the prevalence of oral or pharyngeal infection by human papillomavirus in the Brazilian population.

OBJECTIVE:

To determine the rate of human papillomavirus infection in the Brazilian population.

METHODS:

Systematic review of published articles. Medline, The Cochrane Library, Embase, Lilacs (Latin American and Caribbean Health Sciences) and Scielo electronic databases were searched. The search included published articles up to December 2014 in Portuguese, Spanish and English. A wide search strategy was employed in order to avoid publication biases and to assess studies dealing only with oral and/or oropharyngeal human papillomavirus infections in the Brazilian population.

RESULTS:

The 42 selected articles enrolled 4066 patients. It was observed that oral or oropharyngeal human papillomavirus infections were identified in 738 patients (18.2%; IC 95 17.6-18.8), varying between 0.0% and 91.9%. The prevalences of oral or oropharyngeal human papillomavirus infections were respectively 6.2%, 44.6%, 44.4%, 27.4%, 38.5% and 11.9% for healthy people, those with benign oral lesions, pre-malignant lesions, oral or oropharyngeal squamous cell carcinoma, risk groups (patients with genital human papillomavirus lesions or infected partners) and immunocompromised patients. The risk of human papillomavirus infection was estimated for each subgroup and it was evident that, when compared to the healthy population, the risk of human papillomavirus infection was approximately 1.5-9.0 times higher, especially in patients with an immunodeficiency, oral lesions and squamous cell carcinoma. The rates of the most well-known oncogenic types (human papillomavirus 16 and/or 18) also show this increased risk.

CONCLUSIONS:

Globally, the Brazilian healthy population has a very low oral human papillomavirus infection rate. Other groups, such as at-risk patients or their partners, immunocompromised patients, people with oral lesions and patients with oral cavity or oropharyngeal squamous cell carcinoma have a high risk of human papillomavirus infection.

Keywords:
Human papillomavirus; Oropharynx; Mouth; Brazil; Prevalence

RESUMO

Introdução:

O papilomavírus humano (HPV) tem sido associado ao carcinoma de células escamosas (CCE) de cabeça e pescoço. No entanto, não existem evidências conclusivas sobre a prevalência de infecção oral ou faríngea pelo HPV na população brasileira.

Objetivo:

Determinar a taxa de infecção pelo HPV na população brasileira.

Método:

Revisão sistemática de artigos publicados. Foram feitas buscas nos seguintes bancos de dados eletrônicos: Medline, The Cochrane Library, Embase, Lilacs (Latin American and Caribbean Health Sciences) e Scielo. A busca considerou artigos publicados até dezembro de 2014, em português, espanhol e inglês. Foi utilizada uma ampla estratégia de busca com o intuito de evitar viés de publicação e também para que fossem avaliados estudos que tratassem apenas de infecções orais e/ou orofaríngeas pelo HPV na população brasileira.

Resultados:

Os 42 artigos selecionados incluíram 4.066 pacientes. Observou-se que infecções orais ou orofaríngeas pelo HPV foram identificadas em 738 pacientes (18,2%; IC95 17,6-18,8), variando entre 0,0-91,9%. As prevalências de infecções orais ou orofaríngeas pelo HPV foram, respectivamente, 6,2%, 44,6%, 44,4%, 27,4%, 38,5% e 11,9% em pacientes saudáveis, com lesões orais benignas, com lesões pré-malignas, com CCE oral ou orofaríngeo, grupos de risco (pacientes com lesões genitais pelo HPV ou parceiros infectados) e pacientes imunodeficientes. O risco de infecção pelo HPV foi estimado para cada subgrupo, quando ficou evidente que, em comparação com a população saudável, o risco de infecção por HPV foi aproximadamente 1,5-9,0 vezes mais alto, especialmente em pacientes com imunodeficiência, lesões orais e CCE. Os percentuais dos tipos oncogênicos mais conhecidos (HPV 16 e/ou 18) também mostram esse aumento no risco.

Conclusões:

A população brasileira saudável apresenta taxa de infecção oral pelo HPV muito baixa. Outros grupos, por exemplo, pacientes de risco ou seus parceiros, pacientes imunodeficientes, indivíduos portadores de lesões orais e pacientes com CCE de cavidade oral ou orofaringe apresentam maior risco de infecção pelo HPV.

Palavras-chave:
Papilomavírus humano; Orofaringe; Boca; Brasil; Prevalência

Introduction

Human papillomavirus (HPV) is one of the most common causes of sexually transmitted infections. HPV is classified as high-risk (or oncogenic), which is associated with malignancies, or low-risk (or non-oncogenic), which is related to benign diseases.¹ The relationship between HPV infections, especially types 16 and 18, and anogenital cancer is well established. In the last decade, relationships between HPV and head and neck squamous cell carcinoma (HNSCC) have been established, especially in younger patients without the classic risk factors (tobacco and alcohol abuse).²

The incidence of HNSCC is increasing worldwide, including in Brazil, and the role of HPV infection in its carcinogenesis might explain the trend.³ A previously published meta-analysis conducted in the 1990s with 4680 samples identified an HPV infection prevalence of 10.0% in normal mucosa, which was significantly less than for leukoplakia (22.2%) and oral SCC (46.5%).⁴ However, there is no conclusive evidence regarding the prevalence of oral or pharyngeal HPV infections in the Brazilian population. Existing studies resort to various methods, either in sampling or in the detection of HPV, eventually producing discrepant results.⁵

Therefore, the aim of the present study was to determine the rate of HPV infection in the Brazilian population based on a systematic review of published articles.

Methods

Ethics

The present study was not submitted to IRB because it was a systematic review exclusively with published articles.

Search strategy and inclusion criteria

Two authors performed searches of MEDLINE, The Cochrane Library, Embase, LILACS, and SciELO electronic databases. The search included published articles up to December of 2014 in Portuguese, Spanish, and English. A wide search strategy was employed in order to avoid publication biases and to assess studies dealing only with oral and/or oropharyngeal HPV infections in the Brazilian population. The following Medical Subject Headings and keywords were used: "human papillomavirus" and "Brazil" and "mouth" OR "human papillomavirus" and "Brazil" and "oropharynx". Reference lists of previously obtained articles were also analyzed manually so that other relevant studies could be identified for inclusion in the present study.

Exclusion criteria

Articles that were not published in Portuguese, Spanish, or English, or where the full text could not be obtained, were excluded from the search. Articles that had no data or insufficient data regarding HPV statuses were also excluded. Articles from the same institution by the same set of authors were screened for study time-period overlaps, and if repetitive information was presented, duplicated data were excluded and data from the most complete data set were analyzed. Other exclusion criteria were: articles that included only patients who tested positive for oral or oropharyngeal HPV; articles based on a pediatric population, animals, or cell lines; review articles, case reports, or case series studies; HPV in sites other than the mouth and/or oropharynx; articles that did not study HPV; and studies with populations other than Brazilians or multicentric studies in which it was not possible to separate the Brazilian population's HPV status.

Data extraction

All data were extracted by two independent authors using a data recording form developed for this purpose, which included the following: city and state, population characteristics, dates when the sample was obtained, the type of material collected (paraffin-embedded, fresh tissue, and/or brushing mucosa) and subsite (mouth and/or oropharynx), age, smoking status, alcohol intake, gender, technology used for HPV detection (polymerase chain reaction [PCR], in situ hybridization, and/or immunohistochemistry [IHC]), and general and specific HPV status (HPV 16 and/or HPV 18). Any discrepancies were addressed following discussion and consensus between the two authors.

Data analysis

The articles were initially organized in the following groups to facilitate the analysis: (1) oral or oropharyngeal HPV infection in healthy patients; (2) oral or oropharyngeal HPV infection in patients with benign or premalignant lesions; (3) HPV infections in the oral cavity and/or oropharyngeal squamous cell carcinoma (SCC); (4) oral or oropharyngeal HPV infection where patients or patients' partners had genital HPV infections; (5) oral or oropharyngeal HPV infection in immunodeficient patients.

For the statistical analysis, the HPV status data were categorized into the following groups: healthy patients, immunodeficient patients, high-risk patients (those with genital HPV infections or infected partners), patients with benign lesions, with premalignant lesions (dysplasia, leukoplakia or erythroplakia), and with squamous cell carcinoma (oral cavity or oropharyngeal SCC). Microsoft Excel (Microsoft Corp^(r) - Redmond, WA, United States) was used to tabulate data and to perform weighted average, frequency, and 95% confidence interval (95% CI) calculations. SPSS^(r) version 17.0 (SPSS^(r) Inc - Illinois, United States) was used for logistic regressions to assess the risk of HPV infection in each group, calculating odds ratios (OR) and 95% CIs. In all of these analyses, the probability of making an a or type I error was considered as less than 5% (p < 0.05).

Results

Using the established search strategy and inclusion criteria, 84 abstracts were identified (Fig. 1). Exclusion criteria included: studies with subsites other than the mouth or oropharynx (13), articles without HPV studies (seven), studies of pediatric populations (five), casuistic studies (four), unobtainable data (four), non-human samples (three), case reports or series of cases studies (three), review articles (two), and studies of non-Brazilian populations (one). Based on the criteria, 42 articles^{5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45and46} were included in the systematic review (Table 1), and it was noted that the great majority of the studies were conducted in the last decade, with oral samples.

Figure 1 -
Flowchart of article selection.

Table 1 -
Demographic data of populations and samples collected in the included studies.

Article	Brazilian city, state	Population characteristics	Sample date	Collected material	Subsite
Oral/oropharyngeal HPV infection in healthy patients
Sacramento (2006)6	São José do Rio Preto, SP	50 healthy patients	2006	Fresh tissue	Oropharynx
Esquenazi (2010)7	Rio de Janeiro, RJ	100 healthy university students	2006–2007	Brushing	Mouth
Horewicz (2010)8	Campinas, SP	104 patients with gingival disorders and healthy mucosa	2006–2009	Paraffin-embedded tissue	Mouth
Tristão (2012)9	Araras, SP	125 healthy patients	2007–2012	Brushing	Mouth
Kreimer (2013)10	São Paulo, SP	499 healthy men	2007–2013	Brushing	Mouth
Cavenaghi (2013)5	Votuporanga, SP	124 healthy patients	2011	Brushing	Mouth and oropharynx
Araujo (2014)11	Belém, PA	166 healthy patients	2014	Brushing	Mouth and oropharynx
Machado (2014)12	Campo Grande, MS	514 healthy men	2014	Brushing	Mouth
Oral/oropharyngeal HPV infection in patients with benign or premalignant lesions
Betiol (2012)13	Araras, SP	16 healthy patients and 8 cases of leukoplakia	2010–2012	Brushing	Mouth
Fonseca-Silva (2012)14	Montes Claros, MG	24 normal mucosa samples and 48 oral dysplasia lesions	Institutional archive	Paraffin-embedded tissue	Mouth
HPV infection in oral cavity and/or oropharyngeal squamous cell carcinoma patients
Comparative studies (healthy people versus SCC patients)
Cortezzi (2004)15	São José do Rio Preto and São Paulo, SP	16 SCC and 142 healthy patients	2004	Fresh tissue (SCC) Brushing (healthy)	Mouth and oropharynx
Silva (2007)16	São Paulo, SP	50 SCC and 10 healthy volunteers	2007	Fresh tissue	Mouth
Mazon (2011)17	Araraquara, SP	18 benign lesions, 18 premalignant lesions, and 19 SCC	Institutional archive	Paraffin-embedded tissue	Mouth
Comparative studies (benign lesions versus SCC patients)
Soares (2002)18	Araraquara, SP	20 cases of benign oral lesions and 10 SCC	1992–1998	Paraffin-embedded tissue	Mouth
Soares (2003)19	Araraquara, SP	30 benign lesions and 27 SCC	Institutional archive	Paraffin-embedded tissue	Mouth
Fregonesi (2003)20	Araraquara, SP	19 benign lesions, 10 premalignant lesions and 17 SCC	Institutional archive	Paraffin-embedded tissue	Mouth
Acay (2008)21	São Paulo, SP	40 leukoplakia and 10 SCC	Institutional archive	Paraffin-embedded tissue	Mouth
Lira (2010)22	Ribeirão Preto-SP	16 non-malignant oral lesions and 20 in situSCC and 50 SCC	2009	Paraffin-embedded tissue	Mouth
Fregonezi (2012)23	Ribeirão Preto, SP	19 benign oral lesions, 16 premalignant oral lesions and 17 SCC	1992–2005	Paraffin-embedded tissue
Populational studies
Miguel (1998)24	São Paulo, SP	28 SCC	1995–1996	Fresh tissue	Mouth and oropharynx
Soares (2007)25	Natal, RN	75 SCC	2000–2003	Paraffin-embedded tissue	Mouth
Oliveira (2008)26	Ribeirão Preto, SP	87 SCC	Institutional archive	Paraffin-embedded tissue	Mouth
Simonato (2008)27	Araçatuba, SP	29 SCC	1991–2005	Paraffin-embedded tissue	Mouth
Soares (2008)28	Natal, RN	33 SCC	1996–2004	Paraffin-embedded tissue	Mouth
Oliveira (2009)29	Natal, RN	88 SCC	1996–2004	Paraffin-embedded tissue	Mouth
Pereira (2011)30	Natal, RN	27 SCC	Institutional archive	Paraffin-embedded tissue	Mouth
Spindula-Filho (2011)31	Goiânia, GO	39 SCC and 8 verrucous carcinoma	2010	Paraffin-embedded tissue	Mouth
Cordeiro-Silva (2012)32	Vitória, ES and Goiânia, GO	45 SCC	2012	Paraffin and fresh tissue	Mouth and oropharynx
Kaminagakura (2012)33	São Paulo, SP	114 SCC	1970–2006	Paraffin-embedded tissue	Mouth
Marques-Silva (2012)34	Montes Claros, MG	40 SCC	1996–2007	Paraffin-embedded tissue	Mouth and oropharynx
Cantarutti (2014)35	Brasilia, DF	26 SCC	2005–2011	Paraffin-embedded tissue	Mouth and oropharynx
Lopez (2014)36	Goiânia, GO; Rio de Janeiro, RJ; São Paulo, SP; Ribeirão Preto, SP	222 SCC	1998–2008	Paraffin-embedded and fresh tissue	Mouth and oropharynx
Oral/oropharyngeal HPV infection in patients with genital HPV infection
Comparative studies (healthy people versus patients with genital HPV infection)
Gonçalves (2006)37	Campinas, SP	70 women with genital HPV infection and 70 healthy women	2001–2002	Saliva	Mouth
Marques (2013)38	Brasilia, DF	43 women with NIC lesions and 21 partners	2011	Brushing	Mouth and oropharynx
Ribeiro (2014)39	Recife, PE	31 married couples: men with penis squamous cell carcinoma or precursor lesions and their partners	2006–2007	Brushing	Mouth
Vidotti (2014)40	São Luis, MA	105 women with genital lesions clinically suspected for HPV infection	2011–2012	Brushing	Mouth
Populational studies
Castro (2009)41	Maceió, AL	30 women with genital HPV infection	2005–2006	Brushing	Mouth
Xavier (2009)42	São Paulo, SP	30 men with anogenital HPV infection	2009	Brushing and fresh tissue	Mouth
Peixoto (2011)43	Salvador, BA	100 women with genital lesions confirmed for HPV infection	2011	Brushing	Mouth
Zonta (2012)44	São Paulo, SP	27 women from prison with pre-malignant or malignant lesions of the uterine cervix	2012	Brushing	Mouth
Oral/oropharyngeal HPV infection in immunodeficient patients (all comparative studies with healthy patients)
Araujo (2011)45	Curitiba, PR	60 patients with Fanconi's anemia and severe anaplastic anemia and 16 healthy control	2011	Brushing	Mouth
Lima (2014)46	São Paulo, SP	100 women with HIV and 100 healthy women	2013	Brushing	Mouth

Brazil is a large country with a population of approximately 200,000,000. The articles analyzed came from all over the country, with concentrations in state capitals and more developed regions (for example, the Southeast Region, which had 61.9% of the studies, especially São Paulo State) as shown in Fig. 2.

Figure 2 -
Article distribution according to Brazilian city and state.

Demographic data

Eight articles (19%) studied oral or oropharyngeal HPV infection in healthy patients, two (4.8%) exclusively analyzed HPV status of patients with benign or premalignant oral lesions, 22 (52.4%) analyzed SCC patients (comparative or population studies), eight (19%) specifically studied oral or oropharyngeal HPV infections in patients with genital HPV infections or lesions or with infected partners, and two (4.8%) studied immunodeficient patients (Fanconi's anemia and HIV patients).

Thirty-four articles (80.9%) included demographic data, which are displayed inTable 2. It was observed that the weighted average for age was higher in the SCC group (59 years old) than the others (30-36 years old). Tobacco use and alcohol intake were similarly higher in these patients.

Table 2 -
Clinical characteristics of patients of the included studies (when obtained from original article).

Article	Age	Smoking status (%)	Alcohol intake (%)	Men/women
Oral/oropharyngeal HPV infection in healthy patients
Sacramento (2006)6	Mean of 25 y	14.3%	71.4%	21/29
Esquenazi (2010)7	Mean of 23 y	3.0%	3.0%	40/60
Horewicz (2010)8	Mean of 38 y	3.8%	–	28/76
Tristão (2012)9	Predominantly between 18 and 21 y	–	–	37/88
Kreimer (2013)10	47% under 30 y 83% under 44 y	40.0%	74.0%	499/0
Cavenaghi (2013)5	Mean of 51 y	75.0%	37.1%	77/47
Araujo (2014)11	Mean of 36 y	6.6%	23.5%	63/103
Machado (2014)12	Mean of 23 y	–	–	0/514
Weighted average	30 years	318/1043 (30.5%)	493/939 (52.5%)	–
Oral/oropharyngeal HPV infection in patients with benign or premalignant lesions
Fonseca-Silva (2012)14	Means: 32 y (control); 54 y (dysplasia)	56.9%	61.1%	39/33
HPV infection in oral cavity and/or oropharyngeal squamous cell carcinoma patients
Comparative studies (healthy people versus SCC patients)
Cortezzi (2004)15	Mean of 61 y	–	–	106/52
Silva (2007)16	Over 40 y	100.0%	–	–
Comparative studies (benign lesions versus SCC patients)
Lira (2010)22	Mean of 57 y	80.2%	66.3%	71/15
Population studies
Miguel (1998)24	Mean of 61 y	90.5%	–	42/3
Soares (2007)25	Mean of 65 y	–	–	49/26
Oliveira (2008)26	Mean of 59 y	81.6%	–	73/14
Simonato (2008)27	79.3% under 60 y	89.7%	62.1%	27/2
Soares (2008)28	Mean of 65 y	–	–	–
Oliveira (2009)29	59% over 60 y	–	–	57/31
Pereira (2011)30	Mean of 63 y	–	–	19/8
Spindula-Filho (2011)31	55.3% over 65 y	72.3%	61.7%	34/13
Cordeiro-Silva (2012)32	44.5% over 58 y	80.0%	68.9%	35/10
Kaminagakura (2012)33	Mean of 51 y	84.0%	62.0%	81/33
Marques-Silva (2012)34	33.3% under 45 y	96.0%	93.3%	34/6
Cantarutti (2014)35	Mean of 56 y	92.0%	65.0%	16/10
Lopez (2014)36	45% under 55 y	93.7%	95.6%	–
Weighted average	59 years	703/801 (87.8%)	458/609 (75.2%)	–
Oral/oropharyngeal HPV infection in patients with genital HPV infection
Comparative studies (healthy people versus patients with genital HPV infection)
Gonçalves (2006)37	Mean of 30 y	29.3%	–	0/140
Marques (2013)38	Mean of 45 y	–	–	21/43
Ribeiro (2014)39	Mean of 32 y	27.4%	–	31/31
Vidotti (2014)40	41.9% under 30 y	7.6%	33.3%	0/105
Population studies
Castro (2009)41	Mean of 28 y	30.0%	0.0%	0/30
Xavier (2009)42	Mean of 29 y	–	–	30/0
Peixoto (2011)43	Mean of 30 y	15.0%	88.1%	0/100
Zonta (2012)44	74.1% under 35 y	66.7%	–	0/27
Weighted average	32 years	90/437 (20.6%)	123/235 (52.3%)	–
Oral/oropharyngeal HPV infection in immunodeficient patients (all comparative studies with healthy people)
Lima (2014)46	Mean of 36 y	31.0%	50.0%	0/200
Weighted average	36 years	62/200 (31.0%)	100/200 (50.0%)	–

Oral/oropharyngeal HPV status

The 42 articles included 4066 enrolled patients. It was observed that oral or oropharyngeal HPV infections were identified in 738 patients (18.2%; 95% CI 17.6%-18.8%), varying between 0.0% and 91.9%. HPV status was assessed using PCR in 90.5% of the studies and by in situ hybridization in the others.

General HPV, HPV 16, HPV 18, and HPV 16/18 prevalences are displayed in Table 3. It was observed that higher rates of HPV infection occurred in patients with oral lesions and in people in high-risk groups (patients with genital lesions or infected partners). It was also noted that the healthy population had a very low HPV infection rate (6.2%; 95% CI 5.7-6.7%).

Table 3 -
HPV status in each subgroup.

Article	Total	HPV+	HPV 16	HPV 18	HPV 16/18
Oral/oropharyngeal HPV infection in healthy patients
Cortezzi (2004)15	142	15 (10.6%)	13 (9.1%)	–	13 (9.1%)
Gonçalves (2006)37	70	3 (4.3%)	–	–	–
Sacramento (2006)6	50	7 (14.0%)	1 (2.0%)	1 (2.0%)	2 (4.0%)
Silva (2007)16	10	1 (10.0%)	–	–	–
Esquenazi (2010)7	100	0 (0.0%)	–	–	–
Horewicz (2010)8	104	0 (0.0%)	0 (0.0%)	–	–
Araujo (2011)45	16	1 (6.2%)	0 (0.0%)	0 (0.0%)	0 (0.0%)
Betiol (2012)13	16	3 (18.8%)	0 (0.0%)	3 (18.8%)	3 (18.8%)
Fonseca-Silva (2012)14	24	7 (29.2%)	5 (20.8%)	2 (8.3%)	7 (29.2%)
Tristão (2012)9	125	29 (23.2%)	–	–	–
Kreimer (2013)10	499	10 (2.0%)	3 (0.6%)	0 (0.0%)	3 (0.6%)
Cavenaghi (2013)5	124	3 (2.4%)	–	–	–
Araujo (2014)11	166	40 (24.1%)	0 (0.0%)	5 (3.0%)	5 (3.0%)
Lima (2014)46	100	2 (2.0%)	–	–	–
Machado (2014)12	514	7 (1.3%)	0 (0.0%)	0 (0.0%)	0 (0.0%)
Total	2060	128/2060 (6.2%) (95% CI 5.7%–6.7%)	22/1551 (1.4%) (95% CI 1.2%–1.6%)	11/1285 (0.9%) (95% CI 0.8%–1.0%)	33/1551 (2.1%) (95% CI 1.9%–2.3%)
Oral/oropharyngeal HPV infection in patients with benign lesions
Soares (2003)19	30	6 (20.0%)	–	–	2 (6.7%)
Fregonesi (2003)	19	6 (31.6%)	–	–	4 (21.0%)
Lira (2010)22	16	16 (100.0%)	–	–	–
Mazon (2011)17	18	6 (33.0%)	0 (0.0%)	0 (0.0%)	0 (0.0%)
Fregonezi (2012)23	18	11 (61.1%)	0 (0.0%)	7 (39.0%)	7 (39.0%)
Total	101	45/101 (44.6%) (95% CI 43.7–45.4)	0/36 (0.0%) (95% CI NA)	7/36 (19.4%) (95% CI 17.8–21.1)	13/85 (15.3%) (95% CI 14.7–15.9)
Oral/oropharyngeal HPV infection in patients with premalignant lesions
Soares (2002)18	20	2 (10.0%)	–	–	–
Fregonesi (2003)20	10	6 (60.0%)	–	–	4 (40.0%)
Acay (2008)	40	9 (22.5%)	–	–	5 (12.5%)
Mazon (2011)17	18	4 (22.0%)	0 (0.0%)	4 (22.0%)	4 (22.0%)
Betiol (2012)13	8	8 (100.0%)	0 (0.0%)	5 (62.5%)	5 (62.5%)
Fonseca-Silva (2012)14	48	34 (70.8%)	31 (64.6%)	3 (6.2%)	34 (70.8%)
Fregonezi (2012)23	16	8 (50.0%)	0 (0.0%)	4 (25.0%)	4 (25.0%)
Total	160	71/160 (44.4%) (95% CI 42.7%–46.1%)	31/90 (34.4%) (95% CI 31.2%–37.7%)	16/90 (17.8%) (95% CI 17.6%–38.6%)	51/140 (36.4%) (95% CI 34.4%–38.6%)
Oral/oropharyngeal HPV infection in patients with oral or oropharyngeal SCC
Miguel (1998)24	28	4 (14.3%)	–	–	–
Soares (2002)18	10	0 (0.0%)	–	–	–
Soares (2003)19	27	13 (48.1%)	–	–	10 (37.0%)
Fregonesi (2003)20	17	6 (35.3%)	–	–	5 (29.0%)
Cortezzi (2004)15	16	4 (25.0%)	4 (25.0%)	–	–
Silva (2007)16	50	37 (74.0%)	–	–	–
Soares (2007)25	75	18 (24.0%)	1 (1.3%)	14 (18.7%)	15 (20.0%)
Acay (2008)21	10	3 (30.0%)	–	–	2 (20.0%)
Oliveira (2008)26	87	17 (19.5%)	4 (4.6%)	3 (3.4%)	7 (8.0%)
Simonato (2008)27	29	5 (17.2%)	–	–	–
Soares (2008)28	33	11 (33.3%)	2 (6.1%)	9 (27.3%)	11 (33.3%)
Oliveira (2009)29	88	26 (29.5%)	1 (3.8%)	21 (80.8%)	22 (25.0%)
Lira (2010)22	70	63 (90.0%)	11 (13.9%)	17 (21.5%)	28 (40.0%)
Mazon (2011)17	19	11 (58.0%)	1 (5.3%)	10 (53.0%)	11 (58.0%)
Pereira (2011)30	27	9 (33.3%)	1 (3.7%)	9 (33.3%)	9 (33.3%)
Spindula-Filho (2011)31	47	0 (0.0%)	–	–	–
Cordeiro-Silva (2012)32	45	3 (6.0%)	–	–	–
Fregonezi (2012)23	17	5 (29.4%)	0 (0.0%)	2 (11.8%)	2 (11.8%)
Kaminagakura (2012)33	114	22 (19.2%)	22 (19.2%)	–	22 (19.2%)
Marques-Silva (2012)34	40	30 (75.0%)	10 (25.0%)	23 (57.5%)	30 (75.0%)
Cantarutti (2014)35	26	0 (0.0%)	–	–	–
Lopez (2014)36	222	14 (6.3%)	8 (3.6%)	–	8 (3.6%)
Total	1097	301/1097 (27.4%) (95% CI 26.6%–28.3%)	65/808 (8.0%) (95% CI 7.6%–8.5%)	108/456 (23.7%) (95% CI 23.0%–24.4%)	182/846 (21.5%) (95% CI 20.9%–22.1%)
Oral/oropharyngeal HPV infection in patients with genital lesions, HPV infection, or partners of this population.
Gonçalves, 200637	70	26 (37.1%)	–	–	–
Castro, 200941	30	0 (0.0%)	–	–	–
Xavier, 200942	30	1 (3.3%)	–	–	–
Peixoto, 201143	100	81 (81.0%)	–	–	–
Zonta, 201244	27	23 (85.2%)	2 (7.4%)	1 (3.7%)	3 (11.1%)
Marques, 201338	64	2 (3.1%)	–	–	–
Ribeiro, 201439	62	30 (48.4%)	–	–	–
Vidotti, 201440	105	25 (23.8%)	–	–	–
Total	488	188/488 (38.5%) (95% CI 36.2%–40.9%)	2/23 (7.4%) (95% CI NA)	1/23 (3.7%) (95% CI NA)	3/23 (11.1%) (95% CI NA)
Oral/oropharyngeal HPV infection in immunodeficient patients
Araujo, 201145	60	20 (33.3%)	8 (13.3%)	2 (3.3%)	10 (16.7%)
Lima, 201446	100	11 (11.0%)	–	–	–
Total	160	31/160 (19.4%) (95% CI 18.4%–20.4%)	8/60 (13.3%) (95% CI NA)	2/60 (3.3%) (95% CI NA)	10/60 (16.7%) (95% CI NA)

The risk of HPV infection was estimated for each subgroup (Table 4). It was evident that, when compared to the healthy population, the risk of HPV infection was approximately 1.5- to 9.0-fold higher, especially in patients with an immunodeficiency, oral lesions, and SCC. The rates of the most well-known oncogenic types (HPV 16 and/or 18) also show this increased risk.

Table 4 -
Risk of HPV infection in each subgroup.

Group	OR (95% CI)	p a
Any HPV infection
Healthy patients	Reference	–
Immunodeficient patients	5.797 (3.696–9.091)	<0.0001
Risk group	3.888 (3.369–4.487)	<0.0001
Benign lesions	2.686 (2.312–3.121)	<0.0001
Premalignant lesions	2.094 (1.904–2.304)	<0.0001
Oral or oropharyngeal SCC	3.097 (2.700–3.553)	<0.0001
HPV 16 infection
Healthy patients	Reference	–
Immunodeficient patients	9.400 (4.021–21.977)	<0.0001
Risk group	2.476 (1.167–5.255)	0.018
Benign lesions	N/C	–
Premalignant lesions	2.467 (2.121–2.870)	<0.0001
Oral or oropharyngeal SCC	1.725 (1.180–1.522)	0.005
HPV 18 infection
Healthy patients	Reference	–
Immunodeficient patients	3.894 (0.844–17.960)	0.081
Risk group	2.254 (0.793–6.402)	0.127
Benign lesions	3.044 (2.169–4.271)	<0.0001
Premalignant lesions	2.242 (1.839–2.740)	<0.0001
Oral or oropharyngeal SCC	2.051 (1.807–2.327)	<0.0001
HPV 16/18 infection
Healthy patients	Reference	–
Immunodeficient patients	7.833 (3.689–16.633)	<0.0001
Risk group	2.476 (1.324–4.629)	0.005
Benign lesions	2.040 (1.624–2.562)	<0.0001
Premalignant lesions	2.278 (2.017–2.573)	<0.0001
Oral or oropharyngeal SCC	1.477 (1.043–2.092)	0.028

• N/C, not calculated because there was no valid case for analysis.^aLogistic regression.

Discussion

This studied summarized, for the first time, the prevalence of oral and oropharyngeal infections in the Brazilian population. This systematic review was conducted with a large series of oral and oropharyngeal HPV statuses in different populations, and data were stratified into groups of patients in order to acquire clinically relevant information toward the management of each specific group. However, some points require discussion.

Oral/oropharyngeal HPV infection

The prevalence of oral HPV has been estimated to be in the range 2.4-7.5% among young adults in the United States.⁴⁷ A recent study⁴⁸ investigated the prevalence of oral HPV infections in the general US population (5579 men and women aged between 14 and 69 years) in 2009 and 2010. The overall prevalence of oral HPV infections for any HPV type was 6.9% (95% CI 5.7%-8.3%), the prevalence of high-risk HPV types was 3.7% (95% CI 3.0%-4.6%), and that of HPV 16 was 1.0% (95% CI 0.7%-1.3%). The present study identified a rate of 6.2% for any HPV infection and 1.4% for HPV 16 infection among 2060 healthy patients, which is similar to large series around the world.

Considering other groups analyzed in the present study, other studies also identified an increased prevalence of oral HPV infection. A study conducted in Zagreb, Croatia, established a rate of 17.7% for HPV positivity in oral lesions, with a significantly higher presence in benign proliferative mucosal lesions (18.6%). High-risk HPV types were predominantly found in potentially malignant oral disorders (HPV 16 in 4.3%) with a rate for any HPV infection of 15.5%.⁴⁹ A meta-analysis conducted with dysplasia specimens from the oral cavity and oropharynx identified an overall prevalence of HPV 16/18 of 24.5% (95% CI 16.4%-36.7%).⁵⁰ Another study identified a prevalence of 6.9% for oral HPV infection in HIV patients.⁵¹ Studies of this relationship in other immunodeficient patients are scarce. Oral HPV infections were found in almost 10.2% to 75% of patients with genital HPV lesions or infected partners worldwide.^52and53

Genomic DNA of oncogenic HPV, especially type 16, has been detected in approximately 25% of HNSCC cases worldwide.⁵⁴ In a large-scale meta-analysis, Kreimer et al. ⁵⁵ reported an overall HPV prevalence of 25.9% in HNSCC (23.5% for oral cavity SCC and 35.6% for oropharyngeal SCC). In a recent French multi-institutional study, St Guily et al. ⁵⁶ reported an overall prevalence of 46.5% for oropharyngeal SCC and 10.5% for oral cavity SCC. The present review established a similar rate of 27.4% for HPV infections in patients with SCC of the oral cavity or oropharynx and of 8.0% specifically for HPV 16 infection. For HPV 18 infection, a rate of 23.7% was observed among SCC patients in the present review, possibly the first report in this field with a large sample. Other series,⁵⁵ however, reported an unexpected extreme rarity of HPV 18 in the oropharynx that was confirmed in other large studies, and the authors discussed how this was a difficult fact to explain.

O'Rorke et al.⁵⁷ performed a meta-analysis with 42 articles studying the survival rate of HNSCC patients. They concluded that patients with HPV-positive HNSCC had a 54% better overall survival rate compared to HPV-negative patients (HR 0.46, 95% CI 0.37-0.57) and that both progression-free survival and disease-free survival were significantly improved in HPV-positive HNSCCs. This was not the aim of the present review, but it demonstrates the current relevance of the study of this topic.

Demographics

Demographically, patients with HPV-related HNSCCs are more likely to be male, white, non-smokers, non-drinkers, younger in age, and have a higher socioeconomic status.^{57 58 59and60} Changes in sexual behavior, including a higher number of lifetime sex partners, an increase in oral sex practices, same sex-contact, and earlier age of sexual activity have all been implicated in HPV-related HNSCC.^57and61 Many of the studies included in this review did not present findings by potentially important covariates (age, gender, tobacco use, alcohol use, etc.), as was observed in other studies. ^55and62 Moreover, only eight studies (38.1%) employed a cancer-free control group, which is difficult and can sometimes cause an overestimation of the odds ratio of HPV risk infection between HNSCC groups. The same trend was observed by Herrero et al. ⁶²

The variations in oral HPV prevalence among different studies may be due to differences in study populations, sampling and testing methods, and possibly the time periods studied.⁴⁷

Sample analysis

In the absence of a standardized detection technique, considerable variations in the prevalence of HPV infections have been recorded in the literature.⁵⁴ This was not observed in the present review because the great majority of the studies employed GP 5+/6+ or MY09/11 primers in polymerase chain reaction (PCR) or HPV type-specific in situ hybridization.

Geographic distribution

The prevalence of HPV was assessed in a study with 1688 healthy men (median age of 31 years) in the U.S., Mexico, and Brazil. The prevalence of all HPV types was 4.0% (95% CI 3.1%-5.0%).¹⁰ The most prevalent high-risk HPV type was HPV 16 in all three countries; however, HPV55 was more common in Mexico compared to the U.S. or Brazil. The geographic heterogeneity might be partly explained by regional differences in the distribution of risk factors other than HPV infection in HNSCC patients.⁵⁵

The study by Gillison et al.⁴⁸ estimated an HPV infection rate of 6.9% in the general U.S. population in a sample obtained in 2009 and 2010. This rate was slightly higher than that observed in a systematic review that included data from 1997 to 2009 (4.5%; 95% CI 3.9-5.1).⁶³

These results suggest that the prevalence of HPV may vary depending on distinct population characteristics and the time period studied, which might explain the wide range of HPV prevalence among different studies included in this systematic review.

Limitations

There are a few limitations in this study that should be noted. The most important was in the data collection; because this work was a systematic review of published articles, some data could not be obtained, especially regarding demographics. Additionally, as seen in Fig. 2, the whole Brazilian population was not included, because of the lack of studies in some regions. Another important point is that because aggregate patient data were used, it is possible that there was heterogeneity in these studies and inconsistencies in the datasets that were unknown due to the summarization of the data. Moreover, the majority of the studies were small and used nonprobability samples, and it is difficult to differentiate studies that enrolled consecutive patients from studies that used alternative inclusion criteria, such as institutional archives of paraffin-embedded tissues. Nevertheless, these nonprobability samples did not represent the Brazilian population as a whole; however, the present study is the first one to consolidate the data of oral and oropharyngeal HPV infection in Brazil. HPV prevalence appeared to be inversely proportional to the study sample size, and the poor quality of some of the cancer specimens may also have affected the prevalence estimates. All of these points were also mentioned as limitations in other systematic review series.⁵⁵

Conclusion

In summary, the healthy Brazilian population has a very low oral/oropharyngeal HPV infection rate. Other groups, such as at-risk patients or their partners, immunodeficient patients, people with oral lesions and, especially, patients with oral cavity or oropharyngeal SCC, have high risks of HPV infection. Because aggregate patient data results varied, a large-scale study considering the whole country, including a more diverse population, must be conducted to confirm the findings of this review.

References

• ¹
  Sanders AE, Slade GD, Patton LL. National prevalence of oral HPV infection and related risk factors in the U.S. adult population. Oral Dis. 2012;18:430-41.
• ²
  Matos LL, Manfro G, Santos RV, Stabenow E, Mello ES, Alves VA, et al. Tumor thickness as a predictive factor of lymph node metastasis and disease recurrence in T1N0 and T2N0 squamous cell carcinoma of the oral tongue. Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118:209-17.
• ³
  Pinto FR, de Matos LL, Palermo FC, Kulcsar MA, Cavalheiro BG, de Mello ES, et al. Tumor thickness as an independent risk factor of early recurrence in oral cavity squamous cell carcinoma. Eur Arch Otorhinolaryngol. 2014;271:1747-54.
• ⁴
  Miller CS, Johnstone BM. Human papillomavirus as a risk factor for oral squamous cell carcinoma: a meta-analysis, 1982-1997. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2001;91:622-35.
• ⁵
  Cavenaghi VB, Ghosn EJ, Cruz N, Rossi LM, da Silva L, Costa HO, et al. Determination of HPV prevalence in oral/oropharyngeal mucosa samples in a rural district of Sao Paulo. Braz J Otorhi- nolaryngol. 2013;79:599-602.
• ⁶
  Sacramento PR, Babeto E, Colombo J, Cabral Ruback MJ, Bonilha JL, Fernandes AM, et al. The prevalence of human papillomavirus in the oropharynx in healthy individuals in a Brazilian population. J Med Virol. 2006;78:614-8.
• ⁷
  Esquenazi D, Bussoloti Filho I, Carvalho Mda G, Barros FS. The frequency of human papillomavirus findings in normal oral mucosa of healthy people by PCR. Braz J Otorhinolaryngol. 2010;76:78-84.
• ⁸
  Horewicz VV, Feres M, Rapp GE, Yasuda V, Cury PR. Human papillomavirus-16 prevalence in gingival tissue and its asso- ciation with periodontal destruction: a case-control study. J Periodontol. 2010;81:562-8.
• ⁹
  Tristao W, Ribeiro RM, Oliveira CA, Betiol JC, Bettini Jde S. Epidemiological study of HPV in oral mucosa through PCR. Braz J Otorhinolaryngol. 2012;78:66-70.
• ¹⁰
  Kreimer AR, Pierce Campbell CM, Lin HY, Fulp W, Papenfuss MR, Abrahamsen M, et al. Incidence and clearance of oral human papillomavirus infection in men: the HIM cohort study. Lancet. 2013;382:877-87.
• ¹¹
  Araujo MV, Pinheiro HH, Pinheiro Jde J, Quaresma JA, Fuzii HT, Medeiros RC. Prevalence of human papillomavirus (HPV) in Belem, Para State, Brazil, in the oral cavity of individuals without clinically diagnosable injuries. Cad Saude Publica. 2014;30:1115-9.
• ¹²
  Machado AP, Gatto de Almeida F, Bonin CM, Martins Prata TT, Sobrinho Avilla L, Junqueira Padovani CT, et al. Presence of highly oncogenic human papillomavirus in the oral mucosa of asymptomatic men. Braz J Infect Dis. 2014;18:266-70.
• ¹³
  Betiol JC, Kignel S, Tristao W, Arruda AC, Santos SK, Barbieri R, et al. HPV 18 prevalence in oral mucosa diagnosed with verrucous leukoplakia: cytological and molecular analysis. J Clin Pathol. 2012;65:769-70.
• ¹⁴
  Fonseca-Silva T, Farias LC, Cardoso CM, Souza LR, Carvalho Fraga CA, Oliveira MV, et al. Analysis of p16(CDKN2A) methylation and HPV-16 infection in oral mucosal dysplasia. Pathobiology. 2012;79:94-100.
• ¹⁵
  Cortezzi SS, Provazzi PJ, Sobrinho JS, Mann-Prado JC, Reis PM, de Freitas SE, et al. Analysis of human papillomavirus prevalence and TP53 polymorphism in head and neck squamous cell carcinomas. Cancer Genet Cytogenet. 2004;150:44-9.
• ¹⁶
  Silva CE, da Silva ID, Cerri A, Weckx LL. Prevalence of human papillomavirus in squamous cell carcinoma of the tongue. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007;104:497-500.
• ¹⁷
  Mazon RC, Rovigatti Gerbelli T, Benatti Neto C, de Oliveira MR, Antonio Donadi E, Guimaraes Goncalves MA, et al. Abnormal cell-cycle expression of the proteins p27, mdm2 and cathepsin B in oral squamous-cell carcinoma infected with human papillomavirus. Acta Histochem. 2011;113:109-16.
• ¹⁸
  Soares CP, Malavazi I, dos Reis RI, Neves KA, Zuanon JA, Benatti Neto C, et al. Presence of human papillomavirus in malignant oral lesions. Rev Soc Bras Med Trop. 2002;35:439-44.
• ¹⁹
  Soares CP, Benatti Neto C, Fregonezi PA, Teresa DB, Santos RT, Longatto Filho A, et al. Computer-assisted analysis of p53 and PCNA expression in oral lesions infected with human papillomavirus. Anal Quant Cytol Histol. 2003;25:19-24.
• ²⁰
  Fregonesi PA, Teresa DB, Duarte RA, Neto CB, de Oliveira MR. Soares CP. p16(INK4A) immunohistochemical overexpression in premalignant and malignant oral lesions infected with human papillomavirus. J Histochem Cytochem. 2003;51:1291-7.
• ²¹
  Acay R, Rezende N, Fontes A, Aburad A, Nunes F, Sousa S. Human papillomavirus as a risk factor in oral carcinogenesis: a study using in situ hybridization with signal amplification. Oral Microbiol Immunol. 2008;23:271-4.
• ²²
  Lira RC, Miranda FA, Guimaraes MC, Simoes RT, Donadi EA, Soares CP, et al. BUBR1 expression in benign oral lesions and squamous cell carcinomas: correlation with human papillomavirus. Oncol Rep. 2010;23:1027-36.
• ²³
  Fregonezi PA, Silva TG, Simoes RT, Moreau P, Carosella ED, Klay CP, et al. Expression of nonclassical molecule human leukocyte antigen-G in oral lesions. Am J Otolaryngol. 2012;33:193-8.
• ²⁴
  Miguel RE, Villa LL, Cordeiro AC, Prado JC, Sobrinho JS, Kowalski LP. Low prevalence of human papillomavirus in a geographic region with a high incidence of head and neck cancer. Am J Surg. 1998;176:428-9.
• ²⁵
  Soares RC, Oliveira MC, Souza LB, Costa AL, Medeiros SR, Pinto LP. Human papillomavirus in oral squamous cells carcinoma in a population of 75 Brazilian patients. Am J Otolaryngol. 2007;28:397-400.
• ²⁶
  Oliveira LR, Ribeiro-Silva A, Ramalho LN, Simoes AL, Zucoloto S. HPV infection in Brazilian oral squamous cell carcinomapatients and its correlation with clinicopathological outcomes. Mol Med Rep. 2008;1:123-9.
• ²⁷
  Simonato LE, Garcia JF, Sundefeld ML, Mattar NJ, Veronese LA, Miyahara GI. Detection of HPV in mouth floor squamous cell carcinoma and its correlation with clinicopathologic variables, risk factors and survival. J Oral Pathol Med. 2008;37:593-8.
• ²⁸
  Soares RC, Oliveira MC, de Souza LB, Costa Ade L, Pinto LP. Detection of HPV DNA and immunohistochemical expression of cell cycle proteins in oral carcinoma in a population of Brazilian patients. J Appl Oral Sci. 2008;16:340-4.
• ²⁹
  Oliveira MC, Soares RC, Pinto LP, Souza LB, Medeiros SR, Costa Ade L. High-risk human papillomavirus (HPV) is not associated with p53 and bcl-2 expression in oral squamous cell carcinomas. Auris Nasus Larynx. 2009;36:450-6.
• ³⁰
  Pereira KM, Soares RC, Oliveira MC, Pinto LP, Costa Ade L. Immunohistochemical staining of Langerhans cells in HPV- positive and HPV-negative cases of oral squamous cells carcinoma. J Appl Oral Sci. 2011;19:378-83.
• ³¹
  Spindula-Filho JV, da Cruz AD, Oton-Leite AF, Batista AC, Leles CR, de Cassia Goncalves Alencar R, et al. Oral squamous cell carcinoma versus oral verrucous carcinoma: an approach to cellular proliferation and negative relation to human papillomavirus (HPV). Tumour Biol. 2011;32:409-16.
• ³²
  Cordeiro-Silva MF, Stur E, Agostini LP, de Podesta JR, de Oliveira JC, Soares MS, et al. Promoter hypermethylation in primary squamous cell carcinoma of the oral cavity and oropharynx: a study of a Brazilian cohort. Mol Biol Rep. 2012;39:10111-9.
• ³³
  Kaminagakura E, Villa LL, Andreoli MA, Sobrinho JS, Vartanian JG, Soares FA, et al. High-risk human papillomavirus in oral squamous cell carcinoma of young patients. Int J Cancer. 2012;130:1726-32.
• ³⁴
  Marques-Silva L, Farias LC, Fraga CA, de Oliveira MV, Cardos CM, Fonseca-Silva T, et al. HPV-16/18 detection does not affect the prognosis of head and neck squamous cell carcinoma in younger and older patients. Oncol Lett. 2012;3:945-9.
• ³⁵
  Cantarutti AL, Fernandes LP, Saldanha MV, Marques AE, Vianna LM, de Melo NS, et al. Evaluation of immunohistochemical expression of p16 and presence of human papillomavirus in oral and oropharyngeal carcinoma. J Craniofac Surg. 2014;25:210-4.
• ³⁶
  Lopez RV, Levi JE, Eluf-Neto J, Koifman RJ, Koifman S, Curado MP, et al. Human papillomavirus (HPV) 16 and the prognosis of head and neck cancer in a geographical region with a low prevalence of HPV infection. Cancer Causes Control. 2014;25:461-71.
• ³⁷
  Goncalves AK, Giraldo P, Barros-Mazon S, Gondo ML, Amaral RL, Jacyntho C. Secretory immunoglobulin A in saliva of women with oral and genital HPV infection. Eur J Obstet Gynecol Reprod Biol. 2006;124:227-31.
• ³⁸
  Marques AE, Fernandes LP, Cantarutti AL, Oyama CN, Figueiredo PT, Guerra EN. Assessing oral brushing technique as a source to collect DNA and its use in detecting human papillomavirus. Pathol Res Pract. 2013;209:291-5.
• ³⁹
  Ribeiro CMB, Ferrer I, Santos de Farias AB, Fonseca DD, Morais Silva IH, Monteiro Gueiros LA, et al. Oral and genital HPV genotypic concordance between sexual partners. Clin Oral Investig. 2014;18:261-8.
• ⁴⁰
  Vidotti LR, Vidal FC, Monteiro SC, Nunes JD, Salgado JV, Brito LM, et al. Association between oral DNA-HPV and genital DNA- HPV. J Oral Pathol Med. 2014;43:289-92.
• ⁴¹
  Castro TM, Bussoloti Filho I, Nascimento VX, Xavier SD. HPV detection in the oral and genital mucosa of women with positive histopathological exam for genital HPV, by means of the PCR. Braz J Otorhinolaryngol. 2009;75:167-71.
• ⁴²
  Xavier SD, Bussoloti Filho I, de Carvalho JM, Castro TM, Framil VM, Syrjanen KJ. Prevalence of human papillomavirus (HPV) DNA in oral mucosa of men with anogenital HPV infection. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009;108:732-7.
• ⁴³
  Peixoto AP, Campos GS, Queiroz LB, Sardi SI. Asymptomatic oral human papillomavirus (HPV) infection in women with a histopathologic diagnosis of genital HPV. J Oral Sci. 2011;53:451-9.
• ⁴⁴
  Zonta MA, Monteiro J, Santos G Jr, Pignatari AC. Oral infection by the human papilloma virus in women with cervical lesions at a prison in Sao Paulo, Brazil. Braz J Otorhinolaryngol. 2012;78:66-72.
• ⁴⁵
  Araujo MR, Rubira-Bullen IR, Santos CF, Dionisio TJ, Bonfim CM, De Marco L, et al. High prevalence of oral human papillomavirus infection in Fanconi&apos;s anemia patients. Oral Dis. 2011;17:572-6.
• ⁴⁶
  Lima MD, Braz-Silva PH, Pereira SM, Riera C, Coelho AC, Gallottini M. Oral and cervical HPV infection in HIV-positive and HIV-negative women attending a sexual health clinic in Sao Paulo, Brazil. Int J Gynaecol Obstet. 2014;126:33-6.
• ⁴⁷
  Chung CH, Bagheri A, D&apos;Souza G. Epidemiology of oral human papillomavirus infection. Oral Oncol. 2014;50:364-9.
• ⁴⁸
  Gillison ML, Broutian T, Pickard RK, Tong ZY, Xiao W, Kahle L, et al. Prevalence of oral HPV infection in the United States, 2009-2010. JAMA. 2012;307:693-703.
• ⁴⁹
  Mravak-Stipetic M, Sabol I, Kranjcic J, Knezevic M, Grce M. Human papillomavirus in the lesions of the oral mucosa according to topography. PLoS ONE. 2013;8:e69736.
• ⁵⁰
  Jayaprakash V, Reid M, Hatton E, Merzianu M, Rigual N, Marshall J, et al. Human papillomavirus types 16 and 18 in epithelial dysplasia of oral cavity and oropharynx: a meta-analysis, 1985-2010. Oral Oncol. 2011;47:1048-54.
• ⁵¹
  Anaya-Saavedra G, Flores-Moreno B, Garcia-Carranca A, Irigoyen-Camacho E, Guido-Jimenez M, Ramirez-Amador V. HPV oral lesions in HIV-infected patients: the impact of long-term HAART. J Oral Pathol Med. 2013;42:443-9.
• ⁵²
  Vogt SL, Gravitt PE, Martinson NA, Hoffmann J, D&apos;Souza G. Concordant oral-genital HPV infection in South Africa couples: evidence for transmission. Front Oncol. 2013;3:303.
• ⁵³
  Ragin C, Edwards R, Larkins-Pettigrew M, Taioli E, Eckstein S, Thurman N, et al. Oral HPV infection and sexuality: a cross- sectional study in women. Int J Mol Sci. 2011;12:3928-40.
• ⁵⁴
  Melkane AE, Auperin A, Saulnier P, Lacroix L, Vielh P, Casiraghi O, et al. Human papillomavirus prevalence and prognostic implication in oropharyngeal squamous cell carcinomas. Head Neck. 2014;36:257-65.
• ⁵⁵
  Kreimer AR, Clifford GM, Boyle P, Franceschi S. Human papillomavirus types in head and neck squamous cell carcinomas worldwide: a systematic review. Cancer Epidemiol Biomarkers Prev. 2005;14:467-75.
• ⁵⁶
  St Guily JL, Jacquard AC, Pretet JL, Haesebaert J, Beby-Defaux A, Clavel C, et al. Human papillomavirus genotype distribution in oropharynx and oral cavity cancer in France - the EDiTH VI study. J Clin Virol. 2011;51:100-4.
• ⁵⁷
  Rorke MA, Ellison MV, Murray LJ, Moran M, James J, Anderson LA. Human papillomavirus related head and neck cancer survival: a systematic review and meta-analysis. Oral Oncol. 2012;48:1191-201.
• ⁵⁸
  Chaturvedi AK, Engels EA, Anderson WF, Gillison ML. Incidence trends for human papillomavirus-related and -unrelated oral squamous cell carcinomas in the United States. J Clin Oncol. 2008;26:612-9.
• ⁵⁹
  Ang KK, Harris J, Wheeler R, Weber R, Rosenthal DI, Nguyen- Tan PF, et al. Human papillomavirus and survival of patients with oropharyngeal cancer. N Engl J Med. 2010;363:24-35.
• ⁶⁰
  D&apos;Souza G, Kreimer AR, Viscidi R, Pawlita M, Fakhry C, Koch WM, et al. Case-control study of human papillomavirus and oropharyngeal cancer. N Engl J Med. 2007;356:1944-56.
• ⁶¹
  Heck JE, Berthiller J, Vaccarella S, Winn DM, Smith EM, Shan&apos;gina O, et al. Sexual behaviours and the risk of head and neck cancers: a pooled analysis in the International Head and Neck Cancer Epidemiology (INHANCE) consortium. Int J Epidemiol. 2010;39:166-81.
• ⁶²
  Herrero R, Castellsague X, Pawlita M, Lissowska J, Kee F, Balaram P, et al. Human papillomavirus and oral cancer: the International Agency for Research on Cancer multicenter study. J Natl Cancer Inst. 2003;95:1772-83.
• ⁶³
  Kreimer AR, Bhatia RK, Messeguer AL, Gonzalez P, Herrero R, Giuliano AR. Oral human papillomavirus in healthy individuals: a systematic review of the literature. Sex Transm Dis. 2010;37:386-91.

• ☆
  Please cite this article as: de Matos LL, Miranda GA, Cernea CR. Prevalence of oral and oropharyngeal human papillomavirus infection in Brazilian population studies: a systematic review. Braz J Otorhinolaryngol. 2015;81:554-67.

Publication Dates

• Publication in this collection
  Sep-Oct 2015

History

• Received
  30 Mar 2015
• Accepted
  22 Apr 2015