Human papillomavirus genotypes among women with or without HIV infection: an epidemiological study of Moroccan women from the Souss area
https://doi.org/10.1186/s13027-015-0040-y
© Belglaiaa et al. 2015
Received: 13 July 2015
Accepted: 21 October 2015
Published: 8 December 2015
Abstract
Background
Data on Human PapillomaVirus (HPV) infection are scarce in Morocco. The objective of the study was to determine the prevalence of HPV and cervical cytology abnormalities in women from the Souss area, Morocco.
Methods
Two hundred and thirty two women who attended the Hassan II hospital (Agadir, Morocco) were recruited in this study. Socio-economic data, sexual activity, reproductive life, history of Pap smear, smoking and HIV status were recorded. Cervical samples were taken using an Ayre spatula. Cytology was reported using the Bethesda system. HPVs were first detected by MY09/11 consensus PCR and then genotyped with INNO-LiPA® assay. Data were analyzed using the logistic regression model.
Results
The median age of women was 42 years (18–76 years). HIV prevalence was 36.2 %. Any HPV type prevalence was 23.7 % in the study population, lower in HIV-negative women (13.3 %) than in HIV-positive women (39.3 %). HPV16 was the most prevalent type (6.5 %), followed by HPV53 and HPV74 (3.4 % each). Most women had normal cervical smears (82 %), the remaining were diagnosed with LGSIL (13 %) and HGSIL (5 %). HPV was detected in 17.4 % of normal smears, 43.4 % of LGSIL and 75 % of HGSIL. HIV status was the most powerful predictor of high risk (hr) and probable hr (phr) HPV infection (odds ratio 4.16, 95 % confidence interval 1.87–9.24, p = 0.0005) followed by abnormal cytology (OR 3.98, 95 % CI 1.39–11.40, p = 0.01), independently of socio-demographic and behavioral risk factors.
Conclusions
In a Moroccan hospital based-population of the Souss area, HPV infections are frequently detected. In addition, high prevalence of hr and phrHPVs and precancerous lesions among HIV-positive women is likely associated with an increased risk of cervical cancer. This highlights the need for HPV and cervical cancer prevention campaigns in Morocco.
Keywords
Background
Human papillomavirus (HPV) infection is the most common sexually transmitted infection (STI) worldwide and the necessary causative agent of precancerous and cancerous lesions of the cervix. The role of high risk HPV (hrHPV) in the development of virtually all cervical cancers (CC) has been well established for more than 20 years [1–3]. CC is the second most common cancer in Moroccan women, after breast cancer. Current estimates indicate that the age-standardized incidence of CC among women in Morocco is 14.3 new cases per 100 000 women/year corresponding to 2258 new cases /year, and the death rate due to this disease is 7 per 100 000 corresponding to 1076 cases/year [4].
To date, more than 200 HPV genotypes have been identified. About 40 of them infect the genital tract, of which 12 were classified as carcinogenic, one as “probably carcinogenic” and 12 as “possibly carcinogenic” to humans [5]. HPV types 16 and 18 are responsible for about 70 % of CC worldwide [6] and 60–70 % of high grade lesions, depending on the geographical area [7]. However, HPV infection of the uterine cervix does not always induce cellular abnormalities [8], indicating that other factors play a role in the development of cervical neoplasia. Human immunodeficiency virus (HIV) infection, another STI with extensive public health impact [9], shares many common behavioural risk factors with HPV infection. HPV and HIV coinfection increases the risk of neoplasia of the lower genital tract [10]. Women with HIV infection commonly harbor a broader range of HPV genotypes, often with multiple concurrent HPV infections, compared to HIV-negative women [11, 12]. HIV influences the natural history of HPV by increasing virulence and the likelihood of persistent infection, and also by hastening the time-course of HPV disease [13, 14].
In late 2013, it was estimated that there were 31 000 persons living with HIV in Morocco, with 50 % of the cases having been registered between 2006–2013. The Souss-Massa-Draa region of Morocco is one of the 5 areas with a high HIV burden accounting for 70 % of notified cases [15]. In the Souss area, women who attend public health-care clinics are most of the time not screened and not treated for HPV-associated lesions. Moreover, there is no epidemiological data available on HPV infection in this region and, as such, the prevalence of HPV infection remains unknown. Therefore, in the present study, we evaluated the prevalence and distribution of HPV genotypes, as well as cervical cytology results, in a hospital based-population of women from the Souss area according to demographic and lifestyle factors and HIV status which may influence HPV infection.
Patients and methods
Study population and sample collection
Data on cytology and HPV detection were obtained from 232 women 18 years and older who attended the Hassan II Hospital of Agadir between June 2014 and February 2015. Patients consulted physicians for gynecological care or for different clinical symptoms such as vaginal discharge, vaginal bleeding, vulva itching, lower abdominal and pelvic pain, infertility, menorrhagia, or other symptoms suggestive of gynecological disorders. Women who were virgin, pregnant or had a history of hysterectomy were excluded from the study. More than 80 % of the study population have been diagnosed with or without HIV infection in a free and anonymous screening centre (CIDAG) and HIV status was noted in medical records.
Women received counselling regarding HPV infection and cervical cancer screening. They underwent a pelvic examination and cervical samples were obtained using an extended tip “Ayre” spatula. After the conventional cervical smear was spread onto a glass slide, the tip of the spatula was broken off and placed in a container containing 3 mL of universal transport medium specimen (UTM™) and stored at -20 °C until HPV testing. Furthermore, interviews were conducted to record epidemiological data concerning socio-economic data (level of educational, employment), sexual activity (age at first intercourse, number of sexual partners, contraceptive use and duration), reproductive life (age at first pregnancy, number of births and miscarriages, menopause), past history of Pap smear tests, gynecological lesions and smoking.
Informed consent was obtained prior to enrollment of participants. The study was approved by the institutional board of the Hassan II Hospital of Agadir and conducted in accordance with good clinical practices to benefit the patient.
Cytology data
The smears were processed for Papanicolaou staining and analyzed according to the Bethesda classification as Negative for Intraepithelial Lesion or Malignancy (NILM) or epithelial cell abnormalities, LGSIL (Low Grade Squamous Intraepithelial Lesion) and HGSIL (High Grade Squamous Intraepithelial Lesion).
DNA extraction from cervical samples
DNA extraction from cervical smears was performed using QIAamp DNA Mini Kit (Qiagen, Courtaboeuf, France). Aliquots of 3 mL of samples were centrifugated at 4000 rpm for 10 min, the supernatant was removed and the pellet was resuspended in 400 μL TE buffer (10 mM Tris–HCl, 1 mM EDTA, pH8). Then, 400 μL of AL buffer (Qiagen) and 40 μL proteinase K (Qiagen) were added and the mix was digested overnight at 56 °C. All lysates were processed according to the manufacturer’s instructions; DNA was eluted in 80 μL of elution buffer and stored at -20 °C until use.
The quality of extracted DNA was controlled by PCR amplification of the β-globin gene using the primers PC04 (5′-CAA-CTT-CAT-CCA-CGT-TCA-CC-3′) and GH20 (5′-GAA-GAG-CCA-AGG-ACA-GGT-AC-3′), which gives a fragment of 265 bp.
Human Papillomavirus DNA detection and genotyping
HPV DNA was detected by a standard polymerase chain reaction (PCR) protocol with consensus primer pair MY09/MY11 (5′-CGT-CCM-ARR-GGA-WAC-TGA-TC-3′ and 5′-GCM-CAG-GGW-CAT-AAY-AAT-GG-3′), allowing the production of 450-bp fragments in the HPV L1 open reading frame and the detection of more than 40 low- and high-risk genital HPV types [16]. Identification of HPV genotype(s) in samples positive for HPV DNA by MY09/11 PCR was done using the INNO-LiPA HPV Genotyping Extra® (Fujirebio, Courtaboeuf, France).
HPV genotyping was centrally performed at the Department of Cellular and Molecular Biology at the University Hospital of Besançon (France) according to the manufacturer’s instructions. The genotyping test allows the detection of 28 HPV genotypes: 18 high risk (hr) HPV and probable hr (phr) types (HPV-16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73 and 82), 7 low-risk (lr) (HPV-6, 11, 40, 43, 44, 54 and 70) and 3 HPV types not classified (HPV-69, 71 and 74). HPV amplimers which did not hybridize to any specific probe were considered as uncharacterized (HPVX) [17].
Statistical analysis
Quantitative and qualitative variables were described as number and percentages. The distribution of HPV genotypes was summarized using frequency distribution and stratified by cytology results (NILM, LGSIL, and HGSIL). Univariate and multivariate logistic regression models were used to identify risk factors associated successively with HPV infection (any HPV and/or hr and phrHPV) and abnormal cytology. Odds ratios (ORs) and 95 % confidence intervals (CI) were used to quantify the association between risk factors and positivity for any HPV and/or hr and phrHPV genotypes or abnormal cytology. A p-value <0.05 was considered statistically significant. Statistical analyses were performed using SAS version 9.4 (SAS Institute Inc., Cary, North California, USA).
Results
Patient characteristics
Sociodemographic, behavioral, and clinical characteristics of Moroccan women participating in the study (n = 232)
Characteristic | n (%) |
|---|---|
Age (years) | |
<45 | 149 (64.2) |
≥45 | 83 (35.8) |
Educational level | |
Illiterate | 155 (66.8) |
Primary school | 38 (16.4) |
Secondary and high school | 39 (16.8) |
Employment | |
No | 195 (84.0) |
Yes | 37 (16.0) |
Marital status | |
Married | 130 (56.0) |
Single + divorced + widowed | 102 (44.0) |
HIV status | |
Negative | 105 (45.3) |
Positive | 84 (36.2) |
Unknown | 43 (18.5) |
Age at first intercourse (years) | |
≥20 | 100 (43.1) |
17–19 | 66 (28.4) |
≤16 | 66 (28.4) |
Age at first pregnancy (years) | |
≤ 18 | 97 (41.8) |
> 18 | 135 (58.2) |
Number of live births | |
0–1 | 83 (35.8) |
2–3 | 96 (41.4) |
≥4 | 53 (22.8) |
Number of miscarriage | |
0 | 149 (64.2) |
≥1 | 83 (35.8) |
Lifetime sexual partners | |
Single | 154 (66.4) |
Multiple | 78 (33.6) |
History of contraception use | |
No | 57 (24.6) |
Yes | 175 (75.4) |
Oral contraceptive use | |
No | 77 (33.2) |
Yes (alone or in combination) | 155 (66.8) |
Intra-uterine device use | |
No | 221 (95.2) |
Yes (alone or in combination) | 11 (4.8) |
Condom use | |
No | 192 (82.8) |
Yes (alone or in combination) | 40 (17.2) |
Duration of oral contraceptive use (years) | |
< 5 | 114 (49.1) |
≥ 5 | 118 (50.9) |
Smoking exposure | |
No | 208 (89.7) |
Yes | 24 (10.3) |
Past history of gynecological lesionsa | |
No | 202 (87.1) |
Yes | 30 (12.9) |
Menopause | |
No | 190 (81.9) |
Yes | 42 (18.1) |
Number of Pap smears | |
Never | 189 (81.5) |
≥1 | 43 (18.5) |
Pap smearb | |
NILM | 190 (81.9) |
LGSIL | 30 (12.9) |
HGSIL | 12 (5.2) |
As regards the results of the Pap smears, 190 (81.9 %, 95 % CI [76.9 – 86.9]) were NILM, 30 (12.9 %, 95 % CI [8.6 – 17.2]) were LGSIL and 12 (5.2 %, 95 % CI [2.3 – 8.1]) were HGSIL. In this series, no cervical cancer was detected.
HPV detection and genotyping
HPV DNA was detected in 23.7 % (55/232) of the cases but 3 samples (1.3 %) could not be genotyped because they did not match any of the specific probes of the assay (HPVX); thus specific HPV genotypes were available for 52 cases. Eighteen women (34.6 %) were infected by a single HPV genotype and 34 (65.4 %) by multiple HPV genotypes. Among women with multiple genotypes, there were 15 women with dual infection (44.1 %), 9 women with triple infection (26.5 %), 4 women with 4 genotypes (11.7 %) and 6 women with 5 or more genotypes (17.6 %). Multiple infections were only half as frequent in HGSIL (33.3 %, 3/9) as in LGSIL (69.2 %, 9/13) and NILM smears (66.6 %, 22/33).
Distribution of specific Human Papillomavirus (HPV) genotypes in all infections (single or multiple) tested in 55 Moroccan women from the Souss area, Morocco
HPV genotypes | Total n (%) | NILM n (%) | LGSIL n (%) | HGSIL n (%) |
|---|---|---|---|---|
hrHPV | ||||
16 | 15 (6.5) | 4 (2.1) | 7 (23.3) | 4 (33.3) |
18 | 7 (3.0) | 2 (1.1) | 2 (6.7) | 3 (25.0) |
31 | 6 (2.6) | 4 (2.1) | 2 (6.7) | - |
33 | 6 (2.6) | 1 (0.5) | 4 (13.3) | 1 (8.3) |
35 | 2 (0.9) | 2 (1.1) | - | - |
39 | 4 (1.7) | 2 (1.1) | 2 (6.7) | - |
45 | 2 (0.9) | 2 (1.1) | - | - |
51 | 5 (2.2) | 5 (2.6) | - | - |
52 | 7 (3.0) | 5 (2.6) | 2 (6.7) | - |
56 | 6 (2.6) | 4 (2.1) | 1 (3.3) | 1 (8.3) |
58 | 5 (2.2) | 4 (2.1) | - | 1 (8.3) |
68 | 1 (0.4) | 1 (0.5) | - | - |
82 | 3 (1.3) | 2 (1.1) | 1 (3.3) | - |
phr HPV | ||||
26 | 3 (1.3) | 2 (1.1) | - | 1 (8.3) |
53 | 8 (3.4) | 5 (2.6) | 3 (10.0) | - |
66 | 5 (2.2) | 4 (2.1) | 1 (3.3) | - |
lrHPV | ||||
6 | 5 (2.2) | 3 (1.6) | 2 (6.7) | - |
11 | 1 (0.4) | - | 1 (3.3) | - |
44 | 3 (1.3) | 3 (1.6) | - | - |
54 | 7 (3.0) | 7 (3.7) | - | - |
70 | 4 (1.7) | 2 (1.1) | 2 (6.7) | - |
Additional HPV | ||||
69/71 | 5 (2.2) | 2 (1.1) | 3 (10.0) | - |
74 | 8 (3.4) | 7 (3.7) | 1 (3.3) | - |
HPVX | 9 (3.9) | 8 (4.2) | - | 1 (8.3) |
Association between infection by any HPV and by hr and phrHPV types and cytology results among Moroccan women from the Souss area, Morocco
Cytology | n (%) | HPV+ n (%) | OR [95 % CI] | p-value | hr and phra n (%) | OR [95 % CI] | p-value |
|---|---|---|---|---|---|---|---|
NILM | 190 (81.9) | 33 (17.4) | 1.00 | 27 (14.2) | 1.00 | ||
LGSIL | 30 (12.9) | 13 (43.3) | 4.25 [1.76–10.26] | 0.001 | 12 (40.0) | 4.02 [1.74–9.28] | 0.001 |
HGSIL | 12 (5.2) | 9 (75.0) | 13.97 [3.24–60.26] | <0.001 | 9 (75.0) | 18.10 [4.60–71.16] | <.0001 |
Distribution of HPV genotypes among the 33 HIV+/HPV+ Moroccan women from the Souss area, Morocco. The prevalence of HPV genotypes was calculated by dividing the number of women harboring specific HPV genotype as a single infection (black bars) or multiple infections (grey bars) by the number of HIV+/HPV+ women
Risk factors
Univariate model for identification of factors associated with any HPV, hr and phrHPV genotypes and the presence of abnormal Pap smear
Characteristic | HPV+ | hr and phrHPVa | Abnormal Pap** | ||||||
|---|---|---|---|---|---|---|---|---|---|
n (%) | OR (95 % CI) | p-value | n (%) | OR (95 % CI) | p-value | n (%) | OR (95 % CI) | p-value | |
Age (years) | |||||||||
≥ 45 | 18 (21.7) | 1.00 | 17 (20.5) | 1.00 | 19 (22.9) | 1.00 | |||
<45 | 37 (24.8) | 1.19 [0.63–2.26] | 0.59 | 31 (20.8) | 1.02 [0.53–1.98] | 0.95 | 23 (15.4) | 0.43 [0.22–0.85] | 0.01 |
Educational level | |||||||||
Secondary and high school | 9 (23.1) | 1.00 | 7 (17.9) | 1.00 | 2 (5.1) | 1.00 | |||
Primary school | 6 (15.8) | 0.60 [0.19–1.91] | 0.39 | 4 (10.5) | 0.52 [0.14–1.95] | 0.33 | 7 (18.4) | 8.35 [0.97–71.65] | 0.05 |
Illiterate | 40 (25.8) | 1.12 [0.49–2.57] | 0.79 | 37 (23.9) | 1.39 [0.57–3.41] | 0.47 | 33 (21.3) | 10.00 [1.32–75.68] | 0.02 |
Employment | |||||||||
Yes | 8 (21.6) | 1.00 | 8 (21.6) | 1.00 | 1 (2.7) | 1.00 | |||
No | 47 (24.1) | 1.15 [0.49–2.69] | 0.75 | 40 (20.5) | 0.94 [0.40–2.20] | 0.88 | 41 (21) | 9.58 [1.27–72.00] | 0.03 |
Marital status | |||||||||
Married | 26 (20.0) | 1.00 | 21 (16.1) | 1.00 | 18 (13.8) | 1.00 | |||
Single + divorced + widowed | 29 (28.4) | 1.59 [0.87–2.92] | 0.14 | 27 (26.5) | 1.87 [0.98–3.55] | 0.05 | 24 (23.5) | 1.51 [0.77–2.96] | 0.22 |
HIV status | |||||||||
Negative | 14 (13.3) | 1.00 | 13 (12.4) | 1.00 | 12 (11.4) | 1.00 | |||
Positive | 33 (39.3) | 4.21 [2.06–8.58] | <0.0001 | 29 (34.5) | 3.73 [1.79–7.78] | 0.0004 | 22 (26.2) | 2.75 [1.27–5.96] | 0.01 |
Age at first intercourse (years) | |||||||||
≥20 | 23 (23.0) | 1.00 | 20 (20) | 1.00 | 14 (14) | 1.00 | |||
17–19 | 14 (21.2) | 1.15 [0.50–2.64] | 0.73 | 12 (18.2) | 1.65 [0.72–3.82] | 0.24 | 12 (18.2) | 1.60 [0.63–4.09] | 0.32 |
≤16 | 18 (27.3) | 1.61 [0.73–3.56] | 0.24 | 16 (24.2) | 1.15 [0.48–2.77] | 0.76 | 16 (24.2) | 2.31 [0.94–5.66] | 0.06 |
Age at first pregnancy (years) | |||||||||
> 18 | 28 (20.7) | 1.00 | 24 (17.7) | 1.00 | 22 (16.3) | 1.00 | |||
≤ 18 | 32 (32.9) | 1.47 [0.8–2.71] | 0.21 | 24 (24.7) | 1.52 [0.80–2.98] | 0.20 | 20 (20.6) | 1.19 [0.60–2.32] | 0.62 |
Number of live births | |||||||||
0–1 | 22 (26.5) | 1.00 | 18 (21.7) | 1.00 | 14 (63.6) | 1.00 | |||
2–3 | 23 (23.9) | 0.87 [0.44–1.72] | 0.69 | 21 (21.9) | 1.01 [0.50–2.06] | 0.97 | 21 (21.9) | 1.38 [0.65–2.92] | 0.40 |
≥4 | 10 (18.8) | 0.65 [0.28–0.50] | 0.30 | 9 (17) | 0.74 [0.30–1.79] | 0.50 | 7 (13.2) | 0.75 [0.28–2.00] | 0.56 |
Number of miscarriage | |||||||||
0 | 33 (22.1) | 1.00 | 27 (18.1) | 1.00 | 19 (12.7) | 1.00 | |||
≥1 | 22 (26.5) | 1.27 [0.68–2.36] | 0.45 | 21 (25.3) | 1.53 [0.80–2.92] | 0.20 | 23 (27.7) | 2.06 [1.05–4.06] | 0.03 |
Number of sexual partners | |||||||||
Single | 33 (21.4) | 1.00 | 26 (16.8) | 1.00 | 27 (17.5) | 1.00 | |||
multiple | 22 (28.2) | 1.44 [0.77–2.69] | 0.25 | 21 (26.9) | 1.93 [1.01–3.70] | 0.04 | 15 (19.2) | 0.86 [0.42–1.77] | 0.68 |
History of contraception use | |||||||||
No | 11 (19.3) | 1.00 | 10 (17.5) | 1.00 | 9 (15.8) | 1.00 | |||
Yes | 44 (25.1) | 0.40 [0.67–2.95] | 0.37 | 38 (21.7) | 1.30 [0.60–2.82] | 0.50 | 33 (18.8) | 1.05 [0.48–2.30] | 0.89 |
Oral contraceptive use | |||||||||
No | 16 (20.7) | 1.00 | 14 (18.2) | 1.00 | 13 (16.8) | 1.00 | |||
Yes (alone or in combination) | 39 (25.1) | 1.28 [0.66–2.48] | 0.46 | 34 (21.9) | 1.26 [0.63–2.53] | 0.51 | 29 (18.7) | 0.87 [0.43–1.75] | 0.70 |
Condom use | |||||||||
No | 44 (22.9) | 1.00 | 38 (19.8) | 1.00 | 0.46 | 35 (18.2) | 1.00 | ||
Yes (alone or in combination) | 11 (27.5) | 1.28 [0.59–2.76] | 0.54 | 10 (25) | 1.35 [0.61–3.00] | 7 (17.5) | 1.16 [0.49–2.74] | 0.73 | |
Smoking exposure | |||||||||
No | 46 (22.1) | 1.00 | 39 (18.7) | 1.00 | 36 (17.3) | 1.00 | |||
Yes | 9 (37.5) | 2.11 [0.87–5.14] | 0.1 | 9 (37.5) | 2.60 [1.06–6.37] | 0.03 | 6 (25) | 0.89 [0.29–2.77] | 0.84 |
History of gynecological lesions | |||||||||
No | 49 (24.2) | 1.00 | 43 (21.3) | 1.00 | 36 (17.8) | 1.00 | |||
Yes | 6 (20.0) | 1.28 [0.50–3.31] | 0.61 | 5 (16.7) | 1.35 [0.49–3.74] | 0.56 | 6 (20) | 1.12 [0.4–3.12] | 0.82 |
Menopause | |||||||||
No | 47 (24.7) | 1.00 | 40 (21) | 1.00 | 33 (17.3) | 1.00 | |||
Yes | 8 (19.0) | 1.40 [0.60–3.23] | 0.43 | 8 (19) | 1.13 [0.49–2.64] | 0.77 | 9 (21.4) | 0.55 [0.25–1.20] | 0.13 |
Number of Pap smears | |||||||||
never | 48 (25.4) | 1.00 | 41 (21.7) | 1.00 | 37 (19.5) | 1.00 | |||
≥1 | 7 (16.3) | 0.57 [0.24–1.37] | 0.21 | 7 (16.3) | 0.70 [0.29–1.69] | 0.43 | 5 (11.6) | 0.54 [0.20–1.47] | 0.22 |
Multivariate analysisa of the characteristics associated with hr and phrHPV types
Characteristics | OR (95 % CI) | p-value |
|---|---|---|
Educational level | ||
Secondary and high school | 1.00 | |
Primary school | 0.51 [0.12–2.05] | 0.34 |
Illiterate | 1.35 [0.49–3.68] | 0.56 |
Marital status | ||
Married | 1.00 | |
Single or divorced or widowed | 1.17 [0.50–2.73] | 0.72 |
HIV status | ||
Negative | 1.00 | |
Positive | 4.16 [1.87–9.24] | 0.0005 |
Age at first pregnancy (years) | ||
> 18 | 1.00 | |
≤ 18 | 1.41 [0.66–3.03] | 0.38 |
Number of miscarriages | ||
0 | 1.00 | |
≥1 | 0.96 [0.45–2.07] | 0.92 |
Number of sexual partners | ||
Single | 1.00 | |
Multiple | 0.71 [0.30–1.70] | 0.44 |
Smoking exposure | ||
No | 1.00 | |
Yes | 2.04 [0.65–6.42] | 0.22 |
Multivariate analysis*of the characteristics associated with an abnormal cytology (Low Grade and High-Grade Squamous Intraepithelial Lesion)
Characteristics | OR [95 % CI] | p-value |
|---|---|---|
Age (years) | ||
<45 | 1.00 | |
≥ 45 | 0.30 [0.09–1.01] | 0.052 |
Educational level | ||
Secondary and high school | 1.00 | |
Primary school | 3.77 [0.44–32.36] | 0.23 |
Illiterate | 3.18 [0.30–33.71] | 0.34 |
Employment | ||
No | 1.00 | |
Yes | 5.86 [0.69–50.13] | 0.11 |
HIV status | ||
Negative | 1.00 | |
Positive | 3.98 [1.39–11.40] | 0.01 |
Age at first intercourse (years) | ||
≥20 | 1.00 | |
17–19 | 2.41 [0.64–9.08] | 0.19 |
≤16 | 2.43 [0.69–8.60] | 0.17 |
Number of miscarriages | ||
0 | 1.00 | |
≥1 | 2.84 [1.14–7.12] | 0.02 |
Menopause | ||
No | 1.00 | |
Yes | 1.33 [0.35–5.12] | 0.68 |
Number of Pap smears | ||
Never | 1.00 | |
≥1 | 0.74 [0.20–2.66] | 0.64 |
Discussion
In Morocco, cervical cancer (CC) is the second cause of cancer deaths in women after breast cancer, and represents a major public health problem. Here, we observed that more than 80 % of women had never been screened for CC, and the prevalence of HPV infection was high (23.7 %), with differences according to HIV status. Indeed, the rate of HPV was 13.3 % in HIV-negative women and 39.3 % in HIV-positive women. Three Moroccan studies in patients attending the Hospital in Rabat [18, 19] and Casablanca [20] reported results similar to ours. The overall prevalence of HPV was lower (6 %) in the study by Amrani et al., but the number of cytological intraepithelial lesions was low (2.5 % LGSIL and 0.7 % HGSIL) [21] compared to our series (12.9 % of LGSIL and 5.2 % of HGSIL). By contrast, the rate of HPV was high in two geographical areas with high incidence of CC (according to the Rabat and Casablanca Cancer Registries), reaching 32 % in a series of women living in Rabat [22] and 42.5 % in women with normal cytology native of north-central of Morocco [23]. We cannot exclude a bias in the latter studies that did not report HIV status of women. As in most developing countries, some cultural factors can be related to this high HPV prevalence, especially misconceptions and beliefs that prevent people from discussing diseases of the genital tract.
In our study, HPV16 was the most prevalent genotype among the overall HPV-positive population, followed by HPV53 and HPV74. This is in line with studies from around the world, where HPV16 was identified as the most common hrHPV [24–26]. HPV16 and HPV18 represented 3.3 % in NILM smears, 30 % in LGSIL and 58.3 % of HGSIL (Table 2). This finding is consistent with data published recently by the Morocco-ICO Information Centre on HPV and Cancers [4]. Bearing in mind that HPV16 and 18 are responsible for about 70 % of CC cases [3, 27, 28], we suggest the need for HPV screening and anti-HPV vaccination as a primary preventive measure among Moroccan women.
We noted that low risk HPV types were found in 8 % of women with NILM smears and 16.7 % of women with LGSIL but not in women with HGSIL. This confirms that lrHPV rarely cause CIN3 or cancer [29–31].
Interestingly, in the present study, multiple HPV infections were observed in 65.4 % of HPV-positive specimens, but only in 33.3 % of HGSIL cases. Meftah el khair et al. reported 34 % of multiple infections in CC from Moroccan women [32]. Co-infection with multiple HPV genotypes has been described in many molecular epidemiologic studies [33–35] and confers an increased risk of high-grade lesions and invasive cervical cancer [36]. This has recently been confirmed in a study including 5,871 sexually active women aged 18-25 years from Costa Rica, in which Chaturvedi et al. reported that women with multiple infections were at significantly increased risk of CIN2+ and HGSIL+ as compared with those with single infections [34]. The present findings provide evidence that women with multiple infections should be closely monitored to prevent progression to CC especially in the context of co-infection with HIV.
Reported data on smoking and sexual behavior may be biased because the women may give what is believed to be the desired or socially acceptable answers. This would result in the absence of association between known risk factors with HPV infection in our population.
By contrast, a significant association was found between HIV infection and hr and phrHPV as well as between HIV infection and abnormal cytology. An important clinical consequence of our results is that HIV appears to be the strongest risk factor for HPV infection, independently of the usual socio-demographic and behavioural risk factors.
In the Souss area, the burden of HIV/AIDS is high. In female sex-workers, the prevalence of HIV is above 5 % in Agadir [15]. In recent years, HIV-infected women were referred from the infectious diseases department of the Hassan II Hospital in Agadir to the pathology department of the same Hospital for CC screening at no cost. To the best of our knowledge, there are no previously published studies from Morocco that have investigated the prevalence of HPV genotypes in the population of HIV-positive women, and the relationship between HPV, HIV and cervical cytology. The prevalence of HPV infection in HIV+ women with normal smears (32.2 %) is quite similar to that published in the meta-analysis of Clifford et al. reporting a 36.3 % HPV prevalence among 3230 HIV-infected women with no cytological abnormalities [11]. Moreover, multiple infections were found in 75.7 % of HIV-positive women. This is in agreement with the study of Stuardo et al. who reported 78.4 % of multiple infections in HIV-infected Spanish women [37] and consistent with data from other studies showing that HIV-infected women not only have a higher prevalence of HPV infection, but are also infected by a wider variety of HPV types than HIV-negative [11, 38, 39]. This has been attributed to lower clearance of HPV [10, 40] or continued sexual exposure to novel HPV types allowing different viral types to settle in the cervical epithelium. Multiple infections could also be due to the reduced systemic and local immunity in HIV-positive women [41].
This study has limitations. The limited number of women included in the study may explain the absence of significant relationship between HPV infection and classical risk factors such as sexual habits. Furthermore, the study population is not representative of the general population of the Souss area. However, this pilot study on a hospital based-population in Agadir is groundwork and a great opportunity to define a more complete research in the future.
In summary, the high prevalence of HPV infection and the diverse distribution of HPV genotypes among Moroccan women from the Souss area emphasizes the need to implement CC screening programs and HPV vaccination for primary prevention [42].
Declarations
Acknowledgements
The authors would like to thank the staff of the pathology department of Hassan II Hospital for technical support and data collection. We are indebted to E. Chezy for excellent technical assistance with INNO-LiPA® Genotyping assay. We are grateful to F. Ecarnot (EA3920, University Hospital Besancon, France) for critical revision of this manuscript. Financial support for this work was provided by the University of Franche-Comte, Ligue Contre le Cancer (CCIR-GE) and Doctoral School “Environnements-Santé”, Besançon, France. Mrs E. Belglaiaa is a recipient of a predoctoral scholarship from the Moroccan Ministry of Higher Education and Scientific Research, and was also granted two scholarships from the Association Française des Femmes Diplômées des Université (AFFDU), Dole and Besançon, France.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Authors’ Affiliations
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