Open Access
Adriana C Vidal1*, Jennifer S Smith2, Fidel Valea3, Rex Bentley4, Maggie Gradison5, Kimberly S H Yarnall5, Anne Ford6,
Francine Overcash1, Kathy Grant4, Susan K Murphy3 and Cathrine Hoyo1
1Department of Obstetrics and Gynecology, Division of Clinical and Epidemiologic Research, Program of Cancer Detection, Prevention and Control, Duke University School of Medicine, Durham, NC 27710, USA
2Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
3Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Duke University School of Medicine, Durham, NC 27710, USA
4Department of Pathology, Duke University School of Medicine, Durham, NC 27710, USA
5Department of Community and Family Medicine, Duke University School of Medicine, Durham, NC 27710, USA
6Department of Obstetrics and Gynecology, Division of Duke Women’s Health, Duke University School of Medicine, Durham, NC 27710, USA
Corresponding Author : Adriana C. Vidal
Department of Obstetrics and Gynecology
Division of Clinical Epidemiology
Duke University School of Medicine
P.O. Box 104006, Durham, NC 27710, USA
Tel: (919) 681-9391
E-mail: [email protected]
Received March 11, 2014; Accepted April 24, 2014; Published April 26, 2014
Citation: Vidal AC, Smith JS, Valea F, Bentley R, Gradison M, et al. (2014) HPV Genotypes and Cervical Intraepithelial Neoplasiain a Multiethnic Cohort in the Southeastern United States. J Vaccines Vaccin 5:224. doi:
Copyright: © 2014 Vidal AC et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Background: For poorly understood reasons, invasive cervical cancer (ICC) incidence and mortality rates are higher in women of African descent. Oncogenic human papillomavirus (HPV) genotypes distribution may vary between European American (EA) and African American (AA) women, and may contribute to differences in ICC incidence.

Methods: Five-hundred and seventy-two women were enrolled at the time of colposcopic evaluation following an abnormal liquid-based cytology screen. HPV infections were detected using HPV-linear array, and chi-squared tests and linear regression models were used to compare HPV genotypes across racial/ethnic groups by CIN status.

Results: Of the 572 participants, 494 (86%) had detectable HPV; 245 (43%) had no CINlesion, 239 (42%) had CIN1, and 88 (15%) had CIN2/3. Seventy-three percent of all women were infected with multiple HPV genotypes. After adjusting for race, age, parity, oral contraception use and current smoking, AAs were two times less likely to harbor HVP16/18 (OR=0.52, 95%CI 0.27-0.98, p=0.04) when all women were considered. This association remained unchanged when only women with CIN2/3 lesions were examined (OR=0.22, 95%CI 0.05-0.95, p=0.04). The most frequent high risk (HR)-HPV genotypes detected among EAs were 16, 18, 56, 39 and 66, while HPV genotypes 33, 35, 45, 58 and 68 were the most frequent ones detected in AAs.

Conclusions: Our data suggest that while HPV 16/18 are the most common genotypes among EA women with CIN, AAAAs harbor different genotypes.

Impact: If results from this study are replicated in larger cohorts, they may improve risk stratification in ICC screening.


Human papillomavirus; Cervical intraepithelial neoplasia; Invasive cervical cancer; Race/Ethnicity; South eastern united states


In 2009, there were an estimated 34,788 new cases of human papillomavirus (HPV)-associated cancers in the United States overall, of which 61% were among women (21,342) and 39% among men (13,446) [1]. Invasive cancer of the uterine cervix (ICC) accounted for an estimated 12,340 cases in 2013 and continues to be the most common HPV-associated cancer in women (53.4%), followed by cancer of the anus (16%), vulva (15%), oropharynx (12%), and vagina (3%) [1]. However, the incidence of ICC is not evenly distributed among racial/ethnic groups with African American and Hispanics affected disproportionally higher than European American women [2]. Liquid-based cytology screening rates, whether self-reported or estimated from insurance claims data, are comparable among African Americans and Hispanics compared to European Americans and fail to explain the racial/ethnic disparity [3-5].

Although African Americans and Hispanics have lower incidence rates for the more common cancer sites, they have the highest incidence of ICC of any ethnic group in the U.S. Currently, low grade squamous intraepithelial lesions (LSIL) and atypical squamous cells of undetermined significance (ASCUS) cases are dichotomized into ‘high-risk’ HPV positive or negative groups. Although the general consensus is that HR-HPV genotypes 16 and 18 causes 70% of ICC cases and 50% of CIN2-3, HPV- genotype distribution of high-risk HPV types may vary by age [6], race/ethnicity [7-9], which is also linked to socioeconomic status [10], and geographic region [11-15]. Thus far, two studies in the United States have described CIN2+ lesions in ethnically diverse populations [7,10] however neither study described the HPV distribution in the spectrum of all women with abnormal cytology-based findings, reporting for colposcopy. In this report, we describe HPV genotypes associated with CIN1-3 in a multiethnic cohort of women visiting colposcopy clinics following a cervical abnormality.


Study participants were recruited from one of 10 Duke University and Duke Primary Care (DPC) clinics in Durham County, North Carolina, during 2010-2012. All clinics used the same study protocol and the Duke University Pathology Laboratory for cytology and histological evaluation. All study participants were initially screened for cervical abnormalities with the Thin-Prep liquid-based cytology test (Cytyc®). Inclusion criteria were, a visit to one of 10 colposcopy clinic following an abnormal Pap test, of at least low grade squamous intra-epithelial lesion (LSIL), age 18 years or older, and English or Spanish speaking. Women who did not intend to receive follow-up care in one of the 10 DPC clinics or moved out of the area for other reasons were excluded. Of the 1,657 women with cytological abnormalities approached in the colposcopy clinic, 1,303 were enrolled, a response rate of 79%. These analyses are restricted to the first 572 in whom data on race/ethnic, HPV infection and CIN status were available. Participants with detected HPV genotypes were comparable to those of the entire cohort not included in this analysis with respect to age (p=0.83), HPV infection (p=0.87), yearly income (p=0.36), marital status (p=0.44), cigarette smoking (p=0.62) and prior HPV vaccination (p=0.57). This study was approved by Duke University School of Medicine Institutional Review Board.

Data collection

A standardized questionnaire that was either self- or interviewer-administered solicited information and included CIN and ICC progression risk factor data: age, race, marital status, parity, yearly income, cigarette smoking, oral contraceptive use, dietary, and sexual habits. Age and yearly income were treated as continuous variables; race/ethnicity was categorized as African American, European American, Hispanic and other; marital status into never married, married, widowed, living with partner, divorced/separated, and other; parity into nulliparity, one, two, three, and four or more births; HPV-DNA status, current smoking, oral contraceptive useand previous HPV vaccination into yes or no categories. Additional information on pathological findings, as well as lesion morphology (size and location), was abstracted from the medical records.


At the enrollment visit, the colposcopist co-investigator or designee obtained a cervical specimen using a plastic spatula and cytobrush and suspended it in the Thin Prep specimen vial containing a proprietary fluid with at least 50% methanol (Cytyc®, Marlborough, MA, USA) and provided this to the study interviewer at the end of the clinic visit. Colposcopy-directed biopsies were also obtained from the lesions and were placed on glass slides. All specimens were tested for adequacy using the 2002 ASCCP guidelines. The specimens were stored at 4°C prior to HPV testing.

Ascertainment of CIN

To ascertain the presence of CIN, the hemotoxylin and eosin stained slides of individuals with cytological abnormalities were read by the study pathologist laboratory.

HPV genotyping

Testing for 37 HPV DNA subtypes was performed by Dr. Gravitt’s laboratory at Johns Hopkins

University, as previously described [16]. Briefly, HPV genotyping was performed using HPV Linear Array (Roche Diagnostics) [16,17]; HPV genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68 were considered high-risk or oncogenic genotypes, whereas HPV6, 11, 26, 40, 42, 53, 55, 61, 62, 69, 70, 72, 73, 81, 82, 83 and 84 were considered low-risk (LR) HPV types [18,19]. If there were no detectable beta-globin levels in the sample, it was considered HPV negative.

Statistical Analysis

Women were classified as having either single or multiple infections. Of the first 691 women for whom HPV genotyping has been completed, 572 also had covariate data including race/ethnicity and age. Pearson’s Chi-squared and Fisher’s exact tests were used to compare women with no evidence of CIN and those with CIN (CIN1, CIN2 and CIN3). We computed the proportion of single and multiple HPV infections, and grouped them according to potential oncogenicity based on the Bethesda criteria [20], by CIN lesion. Analyses were repeated in European Americans and in African Americans and the prevalence of oncogenic HPV types, by race/ethnicity was estimated. Associations between HPV16/18 and race/ethnicity, adjusted for potential confounding by age, race, parity, oral contraceptive use, current smoking and HPV vaccine status were examined using logistic regression models. Statistical analyses were conducted using SAS 9.2 (SAS Institute, Cary, NC).


Of 572 participants, 494 (72%) were HPV-positive; 245 (43%) had no visible CIN, 239 (42%) had CIN1, and 88 (15%) had CIN2/3 (Table 1). Lower income women were more likely to have histological evidence of CIN regardless of grade, than higher income women (p<0.0001). Most women with CIN1 (70%) and CIN2 (61%) were younger (aged 20-29 years), whereas those with CIN3 were 30 years or older (p<0.0001). Those with CIN were more likely to be infected with at least one of the 31 HPV genotypes detected, which included low risk types (p=0.06), and to be unmarried (p= 0.001). Only 73 (13%) study participants reported being vaccinated against HPV, and most (63%) completed the vaccine doses between the ages of 18-29 years old (p=0.08). Most (92%) women with CIN reported having their sexual intercourse at age 16 years or younger. Seventy-three percent of women with CIN reported being current cigarette smokers, compared to 15% of women without visible CIN lesions (p=0.25).

Numbers do not necessarily reflect totals due to missing values (i.e. some participants did not fully complete the standardized questionnaire administered to assess risk exposures). HPV infection was found in 83% of women without CIN, and 88% and 94% in those with CIN1 and CIN2+, respectively. Most (73%) women harbored multiple HPV genotypes (Table 2). In women with no CIN, the most common HPV genotypes in single infections were 16, 35, 51 and 52, whereas in multiple infections 51, 52, 56, 59 and 66 were most commonly found. In CIN1, HPV genotypes 16, 31, 39, 51, 52, and 66 were the most frequent, whereas in CIN2/3 HPV 16, 18 (the latter found in multiple but not in single infections), 33, 35, 51 (in single infections) and 39 and 52 (in multiple infections) were the most common. In CIN3 lesions, the prevalence of HPV genotype 16 was 36%, followed by 31 (13%), 33 (9%), 35 (9%), 51 (9%) and 52 (9%) in single infections, and HPV 16, 52, 39, 18, 35, 45, 59 and 66 in multiple infections (Table 2).

Figure 1, shows the distribution of oncogenic HPV genotypes by race/ethnicity among all participants who reported to the colposcopy clinic, regardless of CIN status. African Americans were two times less likely to harbor high-risk HPV genotypes 16/18 compared to European Americans (p=0.004), whereas high-risk HPV 35 (p=0.01) and 58 (p=0.04) were the most common genotypes found in African Americans. HPV 45 (p=0.33), 33 (p=0.11), and 68 (p=0.15) were also more prevalent in African Americans compared to European Americans, however the differences were not statistically significant. Adjusting for age, race, parity, oral contraceptive use and current smoking, did not materially change these associations (OR=0.22 95%CI 0.05-0.95, p=0.04) (Table 3). Conversely, AA women with no evidence of CIN lesions were more likely to be infected with high-risk HPV types 45, 33, 58, 35, 68 (OR= 3.45 95%CI 1.23-9.68, p=0.01); an association that persisted in AA women with CIN-1 (OR= 4.78 95%CI 1.75-13.03, p=0.002), but not in those with CIN2/3 lesions (OR= 1.22 95%CI 0.32-4.61, p=0.76) (Table 3). Further restricting the analysis to those for which adequacy was assessed did not alter our findings. This pattern of differences persisted after the exclusion of 73 women who reported being vaccinated against HPV (Table 3); median age at vaccination was 21 years. It is worth noting that even after three to five years (2010-2012: recruitment period) that HPV vaccination was implemented in the USA (2007), the vaccination rate in this study group was still low.


Our key finding was that among women undergoing colposcopic evaluation following cytological abnormalities at enrollment, infection with HPV 16 and 18 that are included in bivalent and quadrivalent vaccine regimens, were the most commonly found in EA women. African American women were two times less likely to be infected with HPV 16 and 18. This race/ethnic difference persisted when comparisons were restricted to women with histologically confirmed CIN-1 and CIN2/3. Racial/ethnic differences have been recently reported among women with advanced lesions (CIN2 or worse) [7,10]. To our knowledge, this is the first evidence for racial/ethnic differences in the prevalence of HPV 16 and 18 infections among a large group of women with cytological abnormalities, before treatment decisions are made. We also found that genotypes most prevalent in AA women were HPV 45, 33, 58, 35 and 68. While most women harbor at least one HPV type co-infections were also common. Therefore, while the singular importance of HR-HPV 45, 33, 58, 35 and 68, as well as co-infections with multiple HPV types is still unclear, together these findings suggest that in cases where triage decisions are made based on infection with oncogenic HPV types 16 and 18, AAs may not receive follow-up care with comparable frequency, if they harbor other genotypes.

Several global studies have reported variability in the prevalence of HPV genotypes associated with cervical lesions by geographic region and race/ethnicity, with obvious potential implications for vaccine development [11-13]. Few studies, however, have examined the prevalence in the United States in women predominantly with CIN1 and ASCUS, where triage decisions are made. The current findings are consistent with a recent report demonstrating that HPV-16/18 infections are not common in high-grade cervical lesions among African American and Hispanic women who were not previously immunized against HPV [7,10]. In fact, this patient population is more likely to harbor HPV genotypes other than 16/18. Niccolai et al. [10] examined and adjusted their analyses for poverty factors and found that higher degree ofpoverty is a strong predictor of lower HPV-16 and 18 infections. Our present data showing that other high-risk HPV genotypes, besides 16/18, may be associated with CIN in African Americans raise the possibility that racial/ethnic disparity in ICC incidence could stem, in part from lack of adequate follow-up among AA when HPV genotypes other than 16 and 18 are detected. Moreover, the current bi- (16/18) and quadravalent (6/11/16/18) HPV vaccines do not completely cover all of the high-risk HPV genotypes. The nonavalent vaccine currently in Phase III clinical trials (V503-001- Clinical identifier: NCT00543543) include HPV genotypes 6, 11, 16, 18, 31, 33, 45, 52, and 58, however it does not include high-risk HPV 35 and 68, which were found more frequently in African American women in this study. Future HPV vaccine development efforts may consider including HPV genotypes 35 and 68 to cover populations that, as shown in our study, harbor more frequently high-risk HPV types other than 16 and 18.

Reasons why African American women are less likely to be infected with HPV 16 and 18 are not known. One possibility is that women of European descent are more susceptible to persistent infection with HR-HPV 16/18 genotypes. Alternatively, African American women may have lower exposure to HR-HPV 16/18 genotypes, or maybe more resistant to infection with 16/18, and possible be carriers of other HR-HPV genotypes that would increase susceptibility to developing high-grade lesions and subsequently ICC. Another possibility could be a differential ability to clear the HPV infection among racial/ethnic groups and/or the presence of different variants of HPV 16 and 18 [21]. We also cannot exclude the possibility that our findings were by chance alone. Nonetheless, both our findings and those of others [7] suggest that the distribution of HPV genotypes in high-grade CIN lesions in African American women in the US is similar to that found in Africa and South America, but differ from those observed in European American women [15]. Larger US studies are needed to confirm and explain this racial/ethnic difference.

Seventy-three percent of all women infected with HPV harbored multiple HPV genotypes, supporting previous evidence [12-14] that the risk for CIN2+ is higher in women with multiple HPV infections [4]. Even though these findings are consistent with those of others [5,9], it is not yet known how co-infections may lead to worse cervical disease prognosis. Current knowledge suggests that each cervical lesion is caused by a single HPV genotype [22]. It is possible that a combination of factors including a compromised immune system overloaded with multiple infections could increase the field of injury, leading to chronic inflammation and subsequent lesion progression. Alternatively, a genetic predisposition or an epigenetic alteration [23,24] may prompt susceptibility to multiple infections.

Approximately 90% of cervical HPV infections are cleared within two years by the host immune system [25,26]. However, persistent infection with high-risk HPV genotypes predicts progression from HPV infection to high-grade cervical intraepithelial lesions (CIN2/3) and to ICC [27]. It is possible that multiple infections with oncogenic HPV genotypes may influence the risk of CIN2+, however co-infections were equally common in African Americans and European Americans.

These findings should be interpreted in the context of the study limitations. The study participants did not include a large sample size of Hispanic women large enough for analyses therefore, the distribution of HPV genotypes in this ethnic group could not be determined. Future studies that include Latino women are required to elucidate the relative importance of high-risk HPV genotypes in this ethnic group. The study was not powered to histologically confirmed CIN2 and CIN3 lesions and hence CIN2 and CIN3 were combined, which while increasing the statistical power, makes discerning aspects of CIN2 not related to ICC difficult. However, CIN2/3 is the point of treatment in the US and the two CIN categories are sometimes difficult to distinguish. Two prior studies with a much larger sample size of CIN2/3 cases reported similar racial differences [7,10]. Despite these limitations, our findings support the idea that there maybe race/ethnic differences in the distribution of HPV subtypes, with implications for both screening and progression to ICC.

We have examined HPV genotypes in all women with abnormal cytological findings, including CIN1/2 and 3 in an ethnically diverse US population and found high risk HPV genotypes that vary by race/ethnicity, even before triage decisions are made. While small sample limits inference, the findings support the contention that there are racial/ethnic differences in the distribution of oncogenic HPV genotypes among women with and without CIN that require exploration in relation to progression to ICC. Larger studies are needed to confirm this evidence and to help guide cervical cancer risk stratification guidelines.


This paper was supported in part by grants from the National Institutes of HealtR01CA142983, and R01CA142983-02S1. We are grateful to Zhiqing Huang, Carole Grenier, Brittany Price, Yvette Lacobie, Aileen Deeds, Francine Overcash, Erin Erginer, Cara Davis, Allison Barratt, Amy Cantor, Paul Whitaker and Alex Reaves for excellent technical support.


Tables at a glance

Table 1  Table 2  Table 3

Figures at a glance

Figure 1


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