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Clinics of Oncology
Research Article ISSN: 2640-1037 Volume 6
Prevalence of Hpv Infection in the Lekoumou and Niari Departments (Congo Brazzaville)
Ngatali CFS1
*, Bolenga Liboko AF2
, Nkoua Mbon JB3
, Doukaga Moussavou R4
and Moukassa D5
1
Department of oncology and Internal Medicine, Loandjili General Hospital, Congo
2
Pathology anatomy laboratory, Loandjili General Hospital,Pointe Noire, Congo
3
Department of oncology, CHU Brazzaville, Congo
4
Department of gynecology TiƩ-TiƩ Basic Hospital, Congo
5
General Hospital of Edith Lucie Bongo, Congo
*
Corresponding author:
Dr. Ngatali Christian,
Faculty of Health Sciences Brazzaville and
Loandjili General Hospital,
E-mail: christianngatali2003@yahoo.fr
Received: 03 Jan 2022
Accepted: 14 Jan 2022
Published: 21 Jan 2022
J Short Name: COO
Copyright:
Ā©2022 Ngatali CFS. This is an open access article distrib-
uted under the terms of the Creative Commons Attribution
License, which permits unrestricted use, distribution, and
build upon your work non-commercially.
Citation:
Ngatali CFS, Prevalence of Hpv Infection in the Lekou-
mou and Niari Departments (Congo Brazzaville).
Clin Onco. 2022; 6(1): 1-9
Keywords:
Prevalence; Human papillomavirus (HPV);
Lekoumou; Niari Congo Brazzaville
1. Abstract
1.1. Objective: to determine the prevalence of HPV infection in
women in Lekoumou and Niari departments.
1.2. Patients and Methods: We carried out a descriptive and
cross-sectional study over a period of 7 months from January to
July 2019 in the department of Lekoumou. 100 women ranging in
age from 16 to 73 years old. The variables studied were as follows:
age, marital status, level of education, risk factors for the onset of
HPV infection, age at first sexual intercourse, number of sexual
partners, parity, gesture. The multivariate analysis was done be-
tween age, number of level of instruction, parity, age of first sexual
intercourse and number of sexual Partners. The statistical analysis
and the data processing were carried out by the Excel 2016 soft-
ware and the graph pad prism version 5 software. The statistical
test used was the chi-square test.
1.3. Results: During this study we collected 100 women. The
mean age of the patients was 34.6 Ā± 11.9 with ranges ranging from
16 to 73 years. The most represented age groups were that of 20-29
years (31%) and that of 30-39 years (29%). The most represented
level of education was the college level in 53% of cases follow-up
of the level of primary education in 25% of cases . Almost Ā¾ of
our study population were married women (74%), single people
represented only 22% of the study population. The mean age at
first intercourse was 16.4 Ā± 2.3 with extremes ranging from 12
to 25 years. Almost all of the women (97%) had had their first
sexual intercourse before the age of 20. The average number of
sexual partners was 5.3 Ā± 3.2 with extremes ranging from 1 to 15
partners, 53% of women had at least 5 sexual partners. The mean
number of pregnancies was 4.9 Ā± 2.8 with extremes ranging from
0 to 13 pregnancies. Almost half of the women (49%) have carried
between 4-7 pregnancies. The mean number of deliveries (parity)
was 3.6 Ā± 2.4 with extremes ranging from 0 to 12 deliveries. 36%
of our study population had between 4 and 7 deliveries. Bivariate
analysis failed to find a statistically significant difference between
age and number of sexual partners, between age of first intercourse
and level of education and parity.
1.4. Conclusion: Cervical cancer is a public health problem. Prev-
alence of infection of HPV is relatively high in our context of low
incomes countries. It is important to know this prevalence in order
to assure prevention of cervical cancer.
2. Introduction
Human papillomavirus (HPV) is a virus belonging to a large het-
erogeneous family of small viruses called Papillomaviridae [1].
HPV infection is sexually transmitted (STI) and is ranked 3rd STI
worldwide. To date more than 230 types of human and animal pap-
illomavirus have been identified, 204 genotypes fully sequenced
[2]. About fifteen HPV are oncogenic and responsible for cancer-
ous pathology of the cervix [2]. The latter is a major public health
problem. Indeed, cervical cancer is the 4th most common cancer
in women in the world [3] and the leading cause of cancer death
in women in Africa. Today, thanks to perfect epidemiological and
molecular knowledge of HPV types and variants in developed
clinicsofoncology.com 1
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Volume 6 Issue 1 -2022 Review Article
countries, the incidence of cervical cancer continues to decrease,
unlike in developing countries, especially in Africa. sub-Saharan
region where the incidence is increasing exponentially mainly be-
cause of the poor organization of screening and prevention policies
[4]. In Congo, cervical cancer is the second most common cancer
in women in terms of incidence and the second in terms of mor-
tality [5]. Some epidemiological and molecular studies related to
HPV and CCU have been carried out in certain departments of the
country Ebatetou E.A. [6] and Boumba A. [7] showed the direct
involvement of HPV 16, 18, 33 and 31 in the development of pre-
cancerous lesions of the cervix, respectively. In the departments
of Niari and LĆ©koumou, as well as all the other departments of the
Congo, no studies have been carried out. It is in this context that
we set ourselves the objective of determining the prevalence of
HPV infection in the departments of LĆ©koumou and Niari.
3. Patients and Methods
We conducted a descriptive and cross-sectional study over a period
of 7 months from January to July 2019 in the departments of Lek-
oumou and Niari. The analyzes were carried out in the Laboratory
of Medical and Morphological Analysis of the General Hospital
of Loandjili (HGL) and the Laboratory of Virology, Microbiology
and Quality / Eco-toxicology and Biodiversity (LVMQ / ETB) of
the Faculty of Sciences and Techniques du Maroc (FSTM). Our
study involved a population of 100 women ranging in age from 16
to 73 years old. All of these women voluntarily benefited from a
cervico-uterine sample. Sexually active patients aged 16 and over
who have given informed consent for adults and parental consent
for minors were included. We did not include patients who had
undergone total hysterectomy as well as those who were menstru-
ating. We carried out a simple random draw to constitute the size
of our sample.
3.1. Sampling method
Each patient was placed in a gynecological position. After placing
a sterile disposable speculum, two samples were taken:
ā€¢ The first sample was taken using an Ayre spatula from the exo
and endocervix. The collected cells were spread evenly and in a
thin layer on a glass slide, then fixed with a cytological fixative
spray (Spray name). Each blade was numbered.
ā€¢ The 2nd sample was taken using a cytobrush from the exo and
endocervix. The detachable head of the cytobrush was immersed
in a vial containing a 10% buffered formaldehyde solution. Each
bottle was numbered.
3.2. Storage and transport of samples
After collection at the Sibiti base hospital, Komono and MayƩyƩ
CSIs, the samples were transported to the Pointe-Noire LGH. Stor-
age was at -20 Ā° C.
The transport to Morocco was done in dry ice by plane, in the
hold, according to the WHO recommendations for the transport
of biological samples. In Morocco, the samples were immediately
returned to -20 Ā° C in order to maintain the cold chain.
3.3. Molecular analysis
The molecular analysis took place in 4 steps:
ā€¢ DNA extraction
ā€¢ The evaluation of the DNA extract
ā€¢ The detection of HPV viral DNA
ā€¢ HPV genotyping
3.4. DNA extraction
The DNA extraction took place in 5 phases
ā€¢ First phase: sample pretreatment
The cells were collected in a 1.5 mL eppendorf tube, to which were
added 250 Ī¼L of phosphate buffered saline (PBS). We carried out
two successive washes with PBS, by centrifugation at 12,000 rpm
for 15 min at 4 Ā° C.
ā€¢ Second phase: enzymatic digestion
ā€¢ Third phase: purification with phenol chloroform
ā€¢ Fourth phase: precipitation
ā€¢ Fifth phase: washing and rehydration
3.5. Evaluation of the DNA extract
4-2-1-Qualitative evaluation of the DNA extract by Ī²-globin PCR
All PCR amplifications were done in a GeneAmp Ā® PCR thermal
cycler
3.6. Detection of HPV viral DNA
4-3-1-Revelation
3.7. HPV genotyping by specific PCR
3-4-1-Analysis of specific PCR products
The variables studied were as follows:
- age,
- marital status,
- the level of education,
- the age of first sexual intercourse,
- the number of sexual partners,
- parity,
-the frequency of HPV infection
Bivariate analysis was done between age, education level, age at
first intercourse, number of sexual partners, marital status and par-
ity.
4. Statistical Analysis
All the results of this study were statistically analyzed from the
Chi-square test or Fisher's exact test using Epi-InfoTM software
version 7.1.1.14, USA (http://www.epiinfo.com). For all tests, the
association between two variables was considered statistically sig-
clinicsofoncology.com 3
Volume 6 Issue 1 -2022 Review Article
nificant when p <0.05.
5. Results
During this study we collected 100 women. The mean age of the
patients was 34.6 Ā± 11.9 years with ranges ranging from 16 to 73
years. The most represented age groups were that of 20-29 years
(31%) and that of 30-39 years (29%) (Table 1). The most repre-
sented level of education was the college level in 53% of cases
monitoring of the level of primary education in 25% of cases
(Figure 1). Almost Ā¾ of our study population were married wom-
en (74%). Singles represented only 22% of the study population
(Figure 2). The mean age at first intercourse was 16.4 Ā± 2.3 with
extremes ranging from 12 to 25 years Almost all of the women
(97%) constituting our study population had had their first sex-
ual intercourse before age 20 (Figure 3). The average number of
sexual partners was 5.3 Ā± 3.2 with extremes ranging from 1 to 15
partners, 53% of the women had at least 5 sexual partners (Table
2). The mean number of deliveries was 3.6 Ā± 2.4 with extremes
ranging from 0 to 12 deliveries. 36% of our study population had
between 4 and 7 deliveries (Figure 4). Out of 100 cases of women
studied, HPV viral DNA was identified in 29 cases, for an overall
prevalence of infection of 29%. (Table 3). HPV infection was ob-
served in 58.3% in women aged 50 and over while only 12.5% ā€‹ā€‹
of
cases in women under 20 were infected (Figure 5). No difference
significant was observed. p = 0.15; chi2 = 2.073 between the level
of instruction and the infection with HPV (Figure 6). Although
50% of the widows of our population are infected by HPV, we did
not observe a significant difference between the carrying of the
infection and marital status. P = 0.91; chi2 = 0.013. (Figure 7).
There was no association between age at first intercourse and HPV
infection (Figure 8). No significant difference was observed (p =
0.47). Chi2 = 0.522 between the number of sexual partners and
HPV infection in (Figure 9). There was no association between the
distribution of HPV infection by number of deliveries. The differ-
ence was not significant with a p = 0.16. Chi2 = 1.985 (Figure 10).
Table 1 : Distribution of patients according to Age
Age Group Number Percentage
<20 8 8%
20-29 31 31%
30-39 29 29%
40-49 20 20%
ā‰„ 50 12 12%
Total 100 100%
1- Sociodemographic characteristics ; Age
Partners Number Percentage
1 to 2 19 19%
2 to 4 28 28%
ā‰„ to 5 53 53%
Total 100 100%
Table 2 : Distribution of patient according to sexual partners
Sexual partners
Table 3 : Distribution of patients according to prevalence of infection of HPV.
HPV Number Percentage
Negative 71 71
Positive 29 29
Total 100 100
2-Prevalence of infection of HPV
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Volume 6 Issue 1 -2022 Review Article
Level of instruction
Figure 1: Distribution of patients according to level of instruction
Marital Status
Figure 2: Distribution of patient according to marital status
Age of first intercourse
Figure 3; Distribution of patient according to age of first intercourse
clinicsofoncology.com 5
Volume 6 Issue 1 -2022 Review Article
parity
Figure 4: Distribution of patient according to parity
3-Risk factors of infection of HPV
3-1-Age
Figure 5: Distribution of patients according to infection of HPV and Age
3-2-Level of instruction
Figure 6: Distribution of patients according to infection of HPV and level of instruction
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Volume 6 Issue 1 -2022 Review Article
3-3-Marital status
Figure 7: Distribution of patients according to infection of HPV and marital status
3-4-Age of first intercourse
Figure 8: Distribution of patients according to infection of HPV and Age of first intercourse
3-5-Number of sexual partners
Figure 9 : Distribution of patients according of infection of HPV and number of sexual partners
clinicsofoncology.com 7
Volume 6 Issue 1 -2022 Review Article
3-6-Parity
Figure 10 : Distribution of patients according to infection of HPV and parity
6. Discussion
6.1. Analysis of the methodology
6.2. Type and period of the study
The descriptive and transversal nature of this study ensures an op-
timal quality of the results, because the collection of information
was contemporaneous with the events described. The homogene-
ity of our study sample allowed us to make a simple analysis of
the results obtained, representative of the general population of
the study area.
6.3. Study population
The selection criteria were established in order to avoid bias in the
interpretation of the results. We performed cervico-uterine smears
(CDU) in women aged 16 years or older. For adolescents aged 16
to 18, informed consent from a parent or guardian was required to
be part of the study, while those over 18 had to consent themselves.
Quite similar criteria were also used by Xavier CastellsaguƩ in
2006 [8], in a study on the detection of the HPV genotype in rural
areas in Mozambique. The mean age of women in our study popu-
lation was lower than that observed in the Louie study population
in 2009 [9] which was estimated to be 33.9 years.
6.4. Sampling strategy
The constitution of the sample consisted in making a simple ran-
dom selection of women from the entire rural area of ā€‹ā€‹
the Kouilou
department, representing our sampling territory. The purpose of
this random selection was to obtain a number of cases representa-
tive of the general population, in order to ensure statistical signifi-
cance of the results. In total, we selected 100 cases for our cytolog-
ical and molecular studies of HPVs. Elsewhere, but close to us in
Kinshasa, in the Democratic Republic of Congo (DRC), Ali-Risasi
in 2008 [10] using the same methodology, had recruited 272 cases
to carry out this type of molecular study of HPV identification in
the area. urban.
6.5. Sampling method
Like the other teams, including Ali-Risasi in 2008 [10], we used
liquid phase cervico-uterine smear samples. It consisted of rotating
the cytobrush 3 times for each sample and this allowed us to have a
homogeneous study sample, collected under the same conditions.
The density of the cells obtained was perfect in all the samples,
between 1.8 and 2. Currently, the liquid phase smear with the
marketing of transport and preservation media has improved the
conventional smear. The advantage of the liquid phase smear with
cytobrush sample is that it allows both cytomorphological and mo-
lecular study to be done without having to use a second sample.
6.6. Choice of study methodology
According to Mougin in 2001 [11], epidemiological studies car-
ried out around the world have shown that HPV research should
take place well upstream of screening for dysplastic lesions and
the revelation of cervical cancer. Indeed, the detection of HPV in-
fections makes it possible to better identify populations at risk,
with the aim of carrying out better surveillance, and therefore good
prevention against this scourge. Currently, in the absence of a sero-
logical test, molecular biology techniques remain the only reliable
tools for detecting viral DNA in a biological sample.
The genotyping technique was motivated by the objective and pur-
pose of our study: that of studying the genomic variability of HPV
16 strains in our study population. Despite many existing genotyp-
ing techniques, only sequencing can achieve this goal by studying
mutations directly on a fragment of the sequenced gene. Indeed,
sequencing remains the genotyping technique par excellence today
and is used in several studies around the world,
clinicsofoncology.com 8
Volume 6 Issue 1 -2022 Review Article
6.7. Prevalence of HPV infection
In a sample of 100 women, our study found a prevalence of HPV
infection of 29%, of which 18% were HPV type 16 (HPV-HR).
In Africa, the work carried out on the genotyping of HPV strains
has found very high frequencies; indeed, CastellsaguƩ et al [8] in
Mozambique found a prevalence of 36% in 2001 with respective-
ly frequencies for subtypes 16, 18 and 45 of 15%, 13% and 8%,
Didelot-Rousseau et al [12] in Burkina-Faso found frequencies of
HPV infection of 62.7% including 36.4% of high-risk subtypes
(7.8% for HPV 16 and 6.4% for HPV 18) and a meta-analysis pub-
lished by Clifford et al [13] noted a frequency of HPV infections
in sub-Saharan Africa of 25.6% including 68.6% of HR HPV (8%
for HPV 16, 4 % for HPV 18 and 6% for HPV 45) in women with
normal cytology.
In our study, the HPV-HR consisted exclusively of type 16. This
rate remains within the limit of most studies carried out in Africa
on the general population which is 54.6% according to Munoz et
al in 2003 [14] and 52 , 9% according to Didellot-Rousseau et al
in 2006 [12]. In Congo, the only molecular studies on HPV have
been carried out by Boumba [7], he focused on the genotyping
of oncogenic HPV in circulation in Congo-Brazzaville, with the
result of a prevalence of HPV 16 of 62.12% in an urban population
of the city of Pointe-Noire. We note that this prevalence is close
to that which we observed, thus confirming the high prevalence
of HPV 16, a high risk oncogenic virus in the rural population of
Kouilou. We were thus able to conclude that the HPV 16 virus in
these two areas (urban in the study by Boumba , rural in ours) is
present at high rates.
6.8. Analysis of HPV infection and associated risk factors
Several studies have shown that certain factors such as sexual be-
havior, parity, pregnancy, age, marital status, level of education
are the risk factors most involved in the development of precan-
cerous and cancerous lesions of the cervix. uterus. In our study,
the statistical analysis between the majority of these risk factors
(in particular parity, age, marital status and level of education) and
HPV infection (viral DNA positivity) n 'showed no significant dif-
ference. This result, although contrary to most studies around the
world, does not call into question the association between these
risk factors and the carriage of HPV infection. Indeed, these risk
factors are reported in the literature as risk factors associated with
HPV infection and these complications [15]. The non-significance
of certain risk factors in our study could be explained on the one
hand by the fact that certain risk factors require a very large sam-
ple to be significant and on the other hand by the fact that some
of these factors are markers of sexual activity more than cervical
HPV lesions according to Mougin in 2001 [16] and Woodnam in
2001 [17]. Only the age of the first sexual intercourse (less than
20 years) is statistically significant for all the risk factors studied,
these observations have been noted in several studies in the world,
those of Castellsague [8] and Munoz [14] for example.
7. Conclusion
Cervical cancer is a public health problem apart from HPV in-
fection which is the risk factor there are some co-factors such as
parity, age at first intercourse. The prevalence of HPV infection
is relatively high in the LĆ©koumou and Niari regions. This high
prevalence may justify primary and secondary prevention against
cervical cancer in our resource-constrained setting.
8. Conflict of Interest
Where were no conflict of interest during this study.
References:
1. Bernard HU, Burk RD, Chen Z, Van Doorslaer K, Hausen H, De
Villiers EM, et al. Classification of papillomaviruses (PVs) based
on 189 PV types and proposal of taxonomic amendments. Virology.
2010; 401(1): 70-79.
2. De Villiers EM. Cross-roads in the classification of papillomaviruses.
Virology. 2013; 445: 2-10.
3. Bzhalava D, Eklund C, Dillner J. International standardization and
classification of human papillomavirus types. Virology. 2015; 476:
341-344.
4. Monsonego J. Papillomavirus and cervical cancer. Medicine/
Science. 1996; 12: 733-744.
5. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Je-
mal A, et al. Global Cancer Statistics 2020: GLOBOCAN Estimates
of Incidence and Mortality Worldwide for 36 Cancers in 185 Coun-
tries. CA Cancer J. Clin. 2021; 71: 209-249.
6. Ebatetou-Ataboho E, Alidjinou EK, SanƩ F, Moukassa D, Dewilde
A. Cervical samples dried on filter paper and dried vaginal tam-
pons can be useful to investigate the circulation of high-risk HPV in
Congo. J Clin Virol. 2013; 57(2): 161-164.
7. Boumba AL, Hilali L, Mouallif M, Moukassa D, Ennaji MM. Speci-
fic genotypes of human papillomavirus in 125 high-grade squamous
lesions and invasive cervical cancer cases from Congolese women.
BioMed Central Public Health. 2014; 14(1): 1320.
8. CastellsaguƩ X, MenƩndez C, Loscertales M, Kornegay R, Santos
F, GĆ³mez-olivĆ© FX, et al. Human papillomavirus genotypes in ru-
ral Mozambique For personal use. Only reproduce with permission
from The Lancet Publishing Group. 2001; 358: 1429-1430.
9. Louie KS, De Sanjose S, Mayaud P. Epidemiologie and prevention
of human papillomavirus and cervical cancer in sub-saharan Africa :
a comprehensive review. Trop Med Int Health. 2009; 10(14): 1287-
1302.
10. Ali-Risasi C, Praet M, Van Renterghem L, Zinga-Ilunga B, Sengeyi
D, Lokomba V, et al. Genotypic profile of the human papillomavirus
encountered in the Kinshasa environment: vaccine interest. Tropical
medicine. 2008; 68: 617-620.
11. Mougin C, Dalstein V, Pretet J, Gay C, Schaal P, Riethmuller D.
Epidemiology of HPV cervical infections: recent knowledge. Presse
Medicale 2001; 30(20): 1017-1023.
clinicsofoncology.com 9
Volume 6 Issue 1 -2022 Review Article
12. Didelot-Rousseau MN, Nagot N, Costes-Martineau V, VallĆØs X,
Ouedraogo A, Konate I, et al. Human papillomavirus genotype dis-
tribution and cervical squamous intraepithelial lesions among high-
risk women with and without HIV-1 infection in Burkina Faso. Vac-
cine 2006; 355-362.
13. Clifford G, Franceschi S, Diaz M, Munoz N, Villa LL. Chapter 3:
HPV type-distribution in women with and without cervical neoplas-
tic diseases. Vaccine 2006; 24(S3): S26-34.
14. Munoz N, Castellsague X, Berrington A, Gissmann L. Chapter 1:
HPV in the etiology of human cancer. Vaccine 2006; 24(S3): S1-10.
15. De Vuyst H, Alemany L, Lacey C, Chibwesha CJ, Sahasrabuddhe V,
Banura C, et al. The Burden of Human Papillomavirus Infections and
Related Diseases in Sub-Saharan Africa. Vaccine 2013; 31: F32-46.
16. Mougin C, Dalstein V, Pretet J, Gay C, Schaal P, Riethmuller D.
Epidemiology of HPV cervical infections: recent knowledge. Presse
Medicale. 2001; 30(20): 1017-1023.
17. Woodman CBJ, Collins S, Winter H. Natural history of cervical pa-
pillomavirus infection in young women: a longitudinal cohort study.
Lancet 2001; 357: 1831-1836.

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Prevalence of Hpv Infection in the Lekoumou and Niari Departments (Congo Brazzaville)

  • 1. Clinics of Oncology Research Article ISSN: 2640-1037 Volume 6 Prevalence of Hpv Infection in the Lekoumou and Niari Departments (Congo Brazzaville) Ngatali CFS1 *, Bolenga Liboko AF2 , Nkoua Mbon JB3 , Doukaga Moussavou R4 and Moukassa D5 1 Department of oncology and Internal Medicine, Loandjili General Hospital, Congo 2 Pathology anatomy laboratory, Loandjili General Hospital,Pointe Noire, Congo 3 Department of oncology, CHU Brazzaville, Congo 4 Department of gynecology TiĆ©-TiĆ© Basic Hospital, Congo 5 General Hospital of Edith Lucie Bongo, Congo * Corresponding author: Dr. Ngatali Christian, Faculty of Health Sciences Brazzaville and Loandjili General Hospital, E-mail: christianngatali2003@yahoo.fr Received: 03 Jan 2022 Accepted: 14 Jan 2022 Published: 21 Jan 2022 J Short Name: COO Copyright: Ā©2022 Ngatali CFS. This is an open access article distrib- uted under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and build upon your work non-commercially. Citation: Ngatali CFS, Prevalence of Hpv Infection in the Lekou- mou and Niari Departments (Congo Brazzaville). Clin Onco. 2022; 6(1): 1-9 Keywords: Prevalence; Human papillomavirus (HPV); Lekoumou; Niari Congo Brazzaville 1. Abstract 1.1. Objective: to determine the prevalence of HPV infection in women in Lekoumou and Niari departments. 1.2. Patients and Methods: We carried out a descriptive and cross-sectional study over a period of 7 months from January to July 2019 in the department of Lekoumou. 100 women ranging in age from 16 to 73 years old. The variables studied were as follows: age, marital status, level of education, risk factors for the onset of HPV infection, age at first sexual intercourse, number of sexual partners, parity, gesture. The multivariate analysis was done be- tween age, number of level of instruction, parity, age of first sexual intercourse and number of sexual Partners. The statistical analysis and the data processing were carried out by the Excel 2016 soft- ware and the graph pad prism version 5 software. The statistical test used was the chi-square test. 1.3. Results: During this study we collected 100 women. The mean age of the patients was 34.6 Ā± 11.9 with ranges ranging from 16 to 73 years. The most represented age groups were that of 20-29 years (31%) and that of 30-39 years (29%). The most represented level of education was the college level in 53% of cases follow-up of the level of primary education in 25% of cases . Almost Ā¾ of our study population were married women (74%), single people represented only 22% of the study population. The mean age at first intercourse was 16.4 Ā± 2.3 with extremes ranging from 12 to 25 years. Almost all of the women (97%) had had their first sexual intercourse before the age of 20. The average number of sexual partners was 5.3 Ā± 3.2 with extremes ranging from 1 to 15 partners, 53% of women had at least 5 sexual partners. The mean number of pregnancies was 4.9 Ā± 2.8 with extremes ranging from 0 to 13 pregnancies. Almost half of the women (49%) have carried between 4-7 pregnancies. The mean number of deliveries (parity) was 3.6 Ā± 2.4 with extremes ranging from 0 to 12 deliveries. 36% of our study population had between 4 and 7 deliveries. Bivariate analysis failed to find a statistically significant difference between age and number of sexual partners, between age of first intercourse and level of education and parity. 1.4. Conclusion: Cervical cancer is a public health problem. Prev- alence of infection of HPV is relatively high in our context of low incomes countries. It is important to know this prevalence in order to assure prevention of cervical cancer. 2. Introduction Human papillomavirus (HPV) is a virus belonging to a large het- erogeneous family of small viruses called Papillomaviridae [1]. HPV infection is sexually transmitted (STI) and is ranked 3rd STI worldwide. To date more than 230 types of human and animal pap- illomavirus have been identified, 204 genotypes fully sequenced [2]. About fifteen HPV are oncogenic and responsible for cancer- ous pathology of the cervix [2]. The latter is a major public health problem. Indeed, cervical cancer is the 4th most common cancer in women in the world [3] and the leading cause of cancer death in women in Africa. Today, thanks to perfect epidemiological and molecular knowledge of HPV types and variants in developed clinicsofoncology.com 1
  • 2. clinicsofoncology.com 2 Volume 6 Issue 1 -2022 Review Article countries, the incidence of cervical cancer continues to decrease, unlike in developing countries, especially in Africa. sub-Saharan region where the incidence is increasing exponentially mainly be- cause of the poor organization of screening and prevention policies [4]. In Congo, cervical cancer is the second most common cancer in women in terms of incidence and the second in terms of mor- tality [5]. Some epidemiological and molecular studies related to HPV and CCU have been carried out in certain departments of the country Ebatetou E.A. [6] and Boumba A. [7] showed the direct involvement of HPV 16, 18, 33 and 31 in the development of pre- cancerous lesions of the cervix, respectively. In the departments of Niari and LĆ©koumou, as well as all the other departments of the Congo, no studies have been carried out. It is in this context that we set ourselves the objective of determining the prevalence of HPV infection in the departments of LĆ©koumou and Niari. 3. Patients and Methods We conducted a descriptive and cross-sectional study over a period of 7 months from January to July 2019 in the departments of Lek- oumou and Niari. The analyzes were carried out in the Laboratory of Medical and Morphological Analysis of the General Hospital of Loandjili (HGL) and the Laboratory of Virology, Microbiology and Quality / Eco-toxicology and Biodiversity (LVMQ / ETB) of the Faculty of Sciences and Techniques du Maroc (FSTM). Our study involved a population of 100 women ranging in age from 16 to 73 years old. All of these women voluntarily benefited from a cervico-uterine sample. Sexually active patients aged 16 and over who have given informed consent for adults and parental consent for minors were included. We did not include patients who had undergone total hysterectomy as well as those who were menstru- ating. We carried out a simple random draw to constitute the size of our sample. 3.1. Sampling method Each patient was placed in a gynecological position. After placing a sterile disposable speculum, two samples were taken: ā€¢ The first sample was taken using an Ayre spatula from the exo and endocervix. The collected cells were spread evenly and in a thin layer on a glass slide, then fixed with a cytological fixative spray (Spray name). Each blade was numbered. ā€¢ The 2nd sample was taken using a cytobrush from the exo and endocervix. The detachable head of the cytobrush was immersed in a vial containing a 10% buffered formaldehyde solution. Each bottle was numbered. 3.2. Storage and transport of samples After collection at the Sibiti base hospital, Komono and MayĆ©yĆ© CSIs, the samples were transported to the Pointe-Noire LGH. Stor- age was at -20 Ā° C. The transport to Morocco was done in dry ice by plane, in the hold, according to the WHO recommendations for the transport of biological samples. In Morocco, the samples were immediately returned to -20 Ā° C in order to maintain the cold chain. 3.3. Molecular analysis The molecular analysis took place in 4 steps: ā€¢ DNA extraction ā€¢ The evaluation of the DNA extract ā€¢ The detection of HPV viral DNA ā€¢ HPV genotyping 3.4. DNA extraction The DNA extraction took place in 5 phases ā€¢ First phase: sample pretreatment The cells were collected in a 1.5 mL eppendorf tube, to which were added 250 Ī¼L of phosphate buffered saline (PBS). We carried out two successive washes with PBS, by centrifugation at 12,000 rpm for 15 min at 4 Ā° C. ā€¢ Second phase: enzymatic digestion ā€¢ Third phase: purification with phenol chloroform ā€¢ Fourth phase: precipitation ā€¢ Fifth phase: washing and rehydration 3.5. Evaluation of the DNA extract 4-2-1-Qualitative evaluation of the DNA extract by Ī²-globin PCR All PCR amplifications were done in a GeneAmp Ā® PCR thermal cycler 3.6. Detection of HPV viral DNA 4-3-1-Revelation 3.7. HPV genotyping by specific PCR 3-4-1-Analysis of specific PCR products The variables studied were as follows: - age, - marital status, - the level of education, - the age of first sexual intercourse, - the number of sexual partners, - parity, -the frequency of HPV infection Bivariate analysis was done between age, education level, age at first intercourse, number of sexual partners, marital status and par- ity. 4. Statistical Analysis All the results of this study were statistically analyzed from the Chi-square test or Fisher's exact test using Epi-InfoTM software version 7.1.1.14, USA (http://www.epiinfo.com). For all tests, the association between two variables was considered statistically sig-
  • 3. clinicsofoncology.com 3 Volume 6 Issue 1 -2022 Review Article nificant when p <0.05. 5. Results During this study we collected 100 women. The mean age of the patients was 34.6 Ā± 11.9 years with ranges ranging from 16 to 73 years. The most represented age groups were that of 20-29 years (31%) and that of 30-39 years (29%) (Table 1). The most repre- sented level of education was the college level in 53% of cases monitoring of the level of primary education in 25% of cases (Figure 1). Almost Ā¾ of our study population were married wom- en (74%). Singles represented only 22% of the study population (Figure 2). The mean age at first intercourse was 16.4 Ā± 2.3 with extremes ranging from 12 to 25 years Almost all of the women (97%) constituting our study population had had their first sex- ual intercourse before age 20 (Figure 3). The average number of sexual partners was 5.3 Ā± 3.2 with extremes ranging from 1 to 15 partners, 53% of the women had at least 5 sexual partners (Table 2). The mean number of deliveries was 3.6 Ā± 2.4 with extremes ranging from 0 to 12 deliveries. 36% of our study population had between 4 and 7 deliveries (Figure 4). Out of 100 cases of women studied, HPV viral DNA was identified in 29 cases, for an overall prevalence of infection of 29%. (Table 3). HPV infection was ob- served in 58.3% in women aged 50 and over while only 12.5% ā€‹ā€‹ of cases in women under 20 were infected (Figure 5). No difference significant was observed. p = 0.15; chi2 = 2.073 between the level of instruction and the infection with HPV (Figure 6). Although 50% of the widows of our population are infected by HPV, we did not observe a significant difference between the carrying of the infection and marital status. P = 0.91; chi2 = 0.013. (Figure 7). There was no association between age at first intercourse and HPV infection (Figure 8). No significant difference was observed (p = 0.47). Chi2 = 0.522 between the number of sexual partners and HPV infection in (Figure 9). There was no association between the distribution of HPV infection by number of deliveries. The differ- ence was not significant with a p = 0.16. Chi2 = 1.985 (Figure 10). Table 1 : Distribution of patients according to Age Age Group Number Percentage <20 8 8% 20-29 31 31% 30-39 29 29% 40-49 20 20% ā‰„ 50 12 12% Total 100 100% 1- Sociodemographic characteristics ; Age Partners Number Percentage 1 to 2 19 19% 2 to 4 28 28% ā‰„ to 5 53 53% Total 100 100% Table 2 : Distribution of patient according to sexual partners Sexual partners Table 3 : Distribution of patients according to prevalence of infection of HPV. HPV Number Percentage Negative 71 71 Positive 29 29 Total 100 100 2-Prevalence of infection of HPV
  • 4. clinicsofoncology.com 4 Volume 6 Issue 1 -2022 Review Article Level of instruction Figure 1: Distribution of patients according to level of instruction Marital Status Figure 2: Distribution of patient according to marital status Age of first intercourse Figure 3; Distribution of patient according to age of first intercourse
  • 5. clinicsofoncology.com 5 Volume 6 Issue 1 -2022 Review Article parity Figure 4: Distribution of patient according to parity 3-Risk factors of infection of HPV 3-1-Age Figure 5: Distribution of patients according to infection of HPV and Age 3-2-Level of instruction Figure 6: Distribution of patients according to infection of HPV and level of instruction
  • 6. clinicsofoncology.com 6 Volume 6 Issue 1 -2022 Review Article 3-3-Marital status Figure 7: Distribution of patients according to infection of HPV and marital status 3-4-Age of first intercourse Figure 8: Distribution of patients according to infection of HPV and Age of first intercourse 3-5-Number of sexual partners Figure 9 : Distribution of patients according of infection of HPV and number of sexual partners
  • 7. clinicsofoncology.com 7 Volume 6 Issue 1 -2022 Review Article 3-6-Parity Figure 10 : Distribution of patients according to infection of HPV and parity 6. Discussion 6.1. Analysis of the methodology 6.2. Type and period of the study The descriptive and transversal nature of this study ensures an op- timal quality of the results, because the collection of information was contemporaneous with the events described. The homogene- ity of our study sample allowed us to make a simple analysis of the results obtained, representative of the general population of the study area. 6.3. Study population The selection criteria were established in order to avoid bias in the interpretation of the results. We performed cervico-uterine smears (CDU) in women aged 16 years or older. For adolescents aged 16 to 18, informed consent from a parent or guardian was required to be part of the study, while those over 18 had to consent themselves. Quite similar criteria were also used by Xavier CastellsaguĆ© in 2006 [8], in a study on the detection of the HPV genotype in rural areas in Mozambique. The mean age of women in our study popu- lation was lower than that observed in the Louie study population in 2009 [9] which was estimated to be 33.9 years. 6.4. Sampling strategy The constitution of the sample consisted in making a simple ran- dom selection of women from the entire rural area of ā€‹ā€‹ the Kouilou department, representing our sampling territory. The purpose of this random selection was to obtain a number of cases representa- tive of the general population, in order to ensure statistical signifi- cance of the results. In total, we selected 100 cases for our cytolog- ical and molecular studies of HPVs. Elsewhere, but close to us in Kinshasa, in the Democratic Republic of Congo (DRC), Ali-Risasi in 2008 [10] using the same methodology, had recruited 272 cases to carry out this type of molecular study of HPV identification in the area. urban. 6.5. Sampling method Like the other teams, including Ali-Risasi in 2008 [10], we used liquid phase cervico-uterine smear samples. It consisted of rotating the cytobrush 3 times for each sample and this allowed us to have a homogeneous study sample, collected under the same conditions. The density of the cells obtained was perfect in all the samples, between 1.8 and 2. Currently, the liquid phase smear with the marketing of transport and preservation media has improved the conventional smear. The advantage of the liquid phase smear with cytobrush sample is that it allows both cytomorphological and mo- lecular study to be done without having to use a second sample. 6.6. Choice of study methodology According to Mougin in 2001 [11], epidemiological studies car- ried out around the world have shown that HPV research should take place well upstream of screening for dysplastic lesions and the revelation of cervical cancer. Indeed, the detection of HPV in- fections makes it possible to better identify populations at risk, with the aim of carrying out better surveillance, and therefore good prevention against this scourge. Currently, in the absence of a sero- logical test, molecular biology techniques remain the only reliable tools for detecting viral DNA in a biological sample. The genotyping technique was motivated by the objective and pur- pose of our study: that of studying the genomic variability of HPV 16 strains in our study population. Despite many existing genotyp- ing techniques, only sequencing can achieve this goal by studying mutations directly on a fragment of the sequenced gene. Indeed, sequencing remains the genotyping technique par excellence today and is used in several studies around the world,
  • 8. clinicsofoncology.com 8 Volume 6 Issue 1 -2022 Review Article 6.7. Prevalence of HPV infection In a sample of 100 women, our study found a prevalence of HPV infection of 29%, of which 18% were HPV type 16 (HPV-HR). In Africa, the work carried out on the genotyping of HPV strains has found very high frequencies; indeed, CastellsaguĆ© et al [8] in Mozambique found a prevalence of 36% in 2001 with respective- ly frequencies for subtypes 16, 18 and 45 of 15%, 13% and 8%, Didelot-Rousseau et al [12] in Burkina-Faso found frequencies of HPV infection of 62.7% including 36.4% of high-risk subtypes (7.8% for HPV 16 and 6.4% for HPV 18) and a meta-analysis pub- lished by Clifford et al [13] noted a frequency of HPV infections in sub-Saharan Africa of 25.6% including 68.6% of HR HPV (8% for HPV 16, 4 % for HPV 18 and 6% for HPV 45) in women with normal cytology. In our study, the HPV-HR consisted exclusively of type 16. This rate remains within the limit of most studies carried out in Africa on the general population which is 54.6% according to Munoz et al in 2003 [14] and 52 , 9% according to Didellot-Rousseau et al in 2006 [12]. In Congo, the only molecular studies on HPV have been carried out by Boumba [7], he focused on the genotyping of oncogenic HPV in circulation in Congo-Brazzaville, with the result of a prevalence of HPV 16 of 62.12% in an urban population of the city of Pointe-Noire. We note that this prevalence is close to that which we observed, thus confirming the high prevalence of HPV 16, a high risk oncogenic virus in the rural population of Kouilou. We were thus able to conclude that the HPV 16 virus in these two areas (urban in the study by Boumba , rural in ours) is present at high rates. 6.8. Analysis of HPV infection and associated risk factors Several studies have shown that certain factors such as sexual be- havior, parity, pregnancy, age, marital status, level of education are the risk factors most involved in the development of precan- cerous and cancerous lesions of the cervix. uterus. In our study, the statistical analysis between the majority of these risk factors (in particular parity, age, marital status and level of education) and HPV infection (viral DNA positivity) n 'showed no significant dif- ference. This result, although contrary to most studies around the world, does not call into question the association between these risk factors and the carriage of HPV infection. Indeed, these risk factors are reported in the literature as risk factors associated with HPV infection and these complications [15]. The non-significance of certain risk factors in our study could be explained on the one hand by the fact that certain risk factors require a very large sam- ple to be significant and on the other hand by the fact that some of these factors are markers of sexual activity more than cervical HPV lesions according to Mougin in 2001 [16] and Woodnam in 2001 [17]. Only the age of the first sexual intercourse (less than 20 years) is statistically significant for all the risk factors studied, these observations have been noted in several studies in the world, those of Castellsague [8] and Munoz [14] for example. 7. Conclusion Cervical cancer is a public health problem apart from HPV in- fection which is the risk factor there are some co-factors such as parity, age at first intercourse. The prevalence of HPV infection is relatively high in the LĆ©koumou and Niari regions. This high prevalence may justify primary and secondary prevention against cervical cancer in our resource-constrained setting. 8. Conflict of Interest Where were no conflict of interest during this study. References: 1. Bernard HU, Burk RD, Chen Z, Van Doorslaer K, Hausen H, De Villiers EM, et al. Classification of papillomaviruses (PVs) based on 189 PV types and proposal of taxonomic amendments. Virology. 2010; 401(1): 70-79. 2. De Villiers EM. Cross-roads in the classification of papillomaviruses. Virology. 2013; 445: 2-10. 3. Bzhalava D, Eklund C, Dillner J. International standardization and classification of human papillomavirus types. Virology. 2015; 476: 341-344. 4. Monsonego J. Papillomavirus and cervical cancer. Medicine/ Science. 1996; 12: 733-744. 5. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Je- mal A, et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Coun- tries. CA Cancer J. Clin. 2021; 71: 209-249. 6. Ebatetou-Ataboho E, Alidjinou EK, SanĆ© F, Moukassa D, Dewilde A. Cervical samples dried on filter paper and dried vaginal tam- pons can be useful to investigate the circulation of high-risk HPV in Congo. J Clin Virol. 2013; 57(2): 161-164. 7. Boumba AL, Hilali L, Mouallif M, Moukassa D, Ennaji MM. Speci- fic genotypes of human papillomavirus in 125 high-grade squamous lesions and invasive cervical cancer cases from Congolese women. BioMed Central Public Health. 2014; 14(1): 1320. 8. CastellsaguĆ© X, MenĆ©ndez C, Loscertales M, Kornegay R, Santos F, GĆ³mez-olivĆ© FX, et al. Human papillomavirus genotypes in ru- ral Mozambique For personal use. Only reproduce with permission from The Lancet Publishing Group. 2001; 358: 1429-1430. 9. Louie KS, De Sanjose S, Mayaud P. Epidemiologie and prevention of human papillomavirus and cervical cancer in sub-saharan Africa : a comprehensive review. Trop Med Int Health. 2009; 10(14): 1287- 1302. 10. Ali-Risasi C, Praet M, Van Renterghem L, Zinga-Ilunga B, Sengeyi D, Lokomba V, et al. Genotypic profile of the human papillomavirus encountered in the Kinshasa environment: vaccine interest. Tropical medicine. 2008; 68: 617-620. 11. Mougin C, Dalstein V, Pretet J, Gay C, Schaal P, Riethmuller D. Epidemiology of HPV cervical infections: recent knowledge. Presse Medicale 2001; 30(20): 1017-1023.
  • 9. clinicsofoncology.com 9 Volume 6 Issue 1 -2022 Review Article 12. Didelot-Rousseau MN, Nagot N, Costes-Martineau V, VallĆØs X, Ouedraogo A, Konate I, et al. Human papillomavirus genotype dis- tribution and cervical squamous intraepithelial lesions among high- risk women with and without HIV-1 infection in Burkina Faso. Vac- cine 2006; 355-362. 13. Clifford G, Franceschi S, Diaz M, Munoz N, Villa LL. Chapter 3: HPV type-distribution in women with and without cervical neoplas- tic diseases. Vaccine 2006; 24(S3): S26-34. 14. Munoz N, Castellsague X, Berrington A, Gissmann L. Chapter 1: HPV in the etiology of human cancer. Vaccine 2006; 24(S3): S1-10. 15. De Vuyst H, Alemany L, Lacey C, Chibwesha CJ, Sahasrabuddhe V, Banura C, et al. The Burden of Human Papillomavirus Infections and Related Diseases in Sub-Saharan Africa. Vaccine 2013; 31: F32-46. 16. Mougin C, Dalstein V, Pretet J, Gay C, Schaal P, Riethmuller D. Epidemiology of HPV cervical infections: recent knowledge. Presse Medicale. 2001; 30(20): 1017-1023. 17. Woodman CBJ, Collins S, Winter H. Natural history of cervical pa- pillomavirus infection in young women: a longitudinal cohort study. Lancet 2001; 357: 1831-1836.