Manuscript accepted on :February 18, 2010
Published online on: --
Parvinder kour, Mohan lal, Rakesh Panjaliya, Vikas Dogra and Subash Gupta
Human Genetic Research cum Counseling Centre, Department of Zoology, University of Jammu, Jammu - 180 006 India.
Abstract
A total of 120 women were analyzed to find the role of risk factors (non cytogenetic) in cervical carcinogenesis. Each woman under investigation had a clinical history, gynecological examination and pap smear. A cervical biopsy was also taken for histopathology. The frequency of cervical cancer was found to be about 6.6% in the present study. The study revealed high parity and early marriage as predominant non cytogenetic factors in cervical carcinogenesis.
Keywords
Cervical carcinoma; Pap smear; parity; risk factors
Download this article as:Copy the following to cite this article: Kour P, lal M, Panjaliya R, Dogra V, Gupta S. Study of the Risk Factors Associated with Cervical Cancer. Biomed Pharmacol J 2010;3(1) |
Copy the following to cite this URL: Kour P, lal M, Panjaliya R, Dogra V, Gupta S. Study of the Risk Factors Associated with Cervical Cancer. Biomed Pharmacol J 2010;3(1). Available from: http://biomedpharmajournal.org/?p=1350 |
Introduction
Cervical carcinoma is one of the most common gynecologic malignancy world wide and a leading cause of death from genital malignancies. Approximately 5, 00,000 new cases of this cancer are diagnosed worldwide each year with the survival rate of only 40 % [1]. In the developing countries cervical carcinoma is ranked second with a relative frequency of 15% of all cancers in women, whereas in the developed countries this cancer is ranked fifth with a relative frequency of 4.4 % [2]. About 1/5 to 1/6 of the total incidence of cervical carcinoma in the world occurs in India [3]. In India, 365.71 million females above the age of 15 are at the risk of developing cervical cancer. It is estimated that about 132,082 women die due to cervical cancer every year, accounting for 26.7% of the world wide incidence. One woman in India die due to cervical cancer every 7 minutes accounting for more than 200 deaths every day The cumulative risk of the incidence of cervical cancer in women in India (age 0-64 yrs) is 2.4% compared to 1.3% for the world[ 4].
Epidemiological studies have shown the high risk Human PapillomaVirus (HPV) to be the most important risk factor and are present in 99.7% of the invasive cervical cancer worldwide [5]. Young age, early marriage, multiple sexual partners, poor genital hygiene, history of abortions, high parity, tobacco and oral contraceptive use, cigarette smoking, race, low socio economic status have also been identified as significant risk factors for the development of CaCx [6].
Material and Methods
The present study was conducted in the Department of Gynecology and Obstetrics SMGS Hospital, Government Medical College, Jammu and Human Genetic Research cum Counselling Centre, University of Jammu. Cases were selected from patients having complains of excessive vaginal discharge, post- coital bleeding, post- menopausal bleeding, history of pain in lower abdomen etc. and on per speculum examination with suspected cervical lesion or unhealthy cervix. The patients underwent gynecological examination & biopsy was taken. The histological study of the samples as well as pap smear test was performed by the Department of Pathology, Government Medical College, Jammu.
A structured questionnaire was used to obtain information on occupation, past medical history, smoking and sexual and reproductive factors including age at marriage, age at first issue and parity.
The different clinical lesions were defined as follows:
Erosion Cervix
On examination, there is a bright red area surrounding and extending beyond the external os on the ectocervix, with a clearly demarcated outer edge.
Hypertrophied Cervix
The size of the cervix is enlarged.
Suspicious and Unhealthy cervix
If abnormal growth, ulcer, or vasculature is present, the cervix is clinically diagnosed as unhealthy.
Observations
The cytological findings and histopathological study in the cervical smear of 120 women screened were as follows:
S.No. | Smears | Percentage |
1 | Normal Smears | 70 (58.33 %) |
2 | Epithelial cellular changes | 30 (25.0 %) |
a) Atrophy with inflammation | 15 (12.5 %) | |
b) Reactive cellular changes
Associated with inflammation |
23 (19.16 %) | |
3 | Epithelial cellular abnormalities | 12 (10 %) |
a) Squamous intraepithelial
lesions of cervix (SIL) |
4 (3.33 %) | |
b) Carcinoma cervix | 8 (6.66 %) |
The 10 cases of carcinoma cervix comprised of 3 cases at Stage IB, 4 cases at Stage IIA, and 1 case at Stage IV. All the SIL cases were Low grade SIL.
Majority of the females in the present study belonged to age group of 50-69 yrs (Table 1). Incidence of CaCx was found to be common (56.6 %) in the females who were Para three & above, whereas (33.3 %)) who were Para two (Table 2). According to the area distribution of these patients, 81.6 %belonged to rural areas and only 10%belonged to urban area (Table 3). Incidence of CaCx was found to be higher in Hindus as compared to Muslims (Table 4).More than 55%of the females under study were married at the age of 21-25 (Table 5). When ages at first issue of these patients were taken into consideration about 55% of the patients belonged to age group 19-22 and 28.3% belonged to the age group 16-19 (Table 6). Histopathological reports showed 4 cases of Stage IIA, 3 cases of Stage IB & 1 case of Stage IVB (Table 7).
Table 1: Patients belonging to different age group.
S. No. | Age (in years) | Number of patients | Percentage frequency |
1. | 20-24 | 1 | 0.833% |
2 | 25-29 | 3 | 2.5% |
3 | 30-39 | 30 | 25.0% |
4 | 40-49 | 24 | 20.0% |
5 | 50-69 | 50 | 43.3% |
6 | 70-79 | 1 | 0.833% |
7 | 80-89 | 1 | 0.833% |
Table 2: Relation of cervical cytopathologies with parity.
S. No | Parity group | Number of cases |
1. | Nulliparous | 2 |
2. | Para 1 | 10 |
3. | Para 2 | 40 |
4. | Para 3 and above | 68 |
Table 3: Number of patients belonging to rural/urban background
S. No. | Area | Number of patients | Percentage |
1. | Rural | 98 | 81.6% |
2. | Urban | 12 | 10.8% |
Table 4: Number of patients belonging to different religions.
S.No. | Religion | Number of patients | Percentage |
1. | Hindu | 107 | 89% |
2. | Muslim | 3 | 2.5% |
3. | Sikhs | 10 | 8% |
Table 5: Relationship of cervical cytopathologies with age at Marriage.
S.No | Age at marriage | Number of patients | Percentage |
1. | 16-20 | 30 | 25% |
2. | 21-25 | 70 | 58.3% |
3. | 26-30 | 16 | 13.3% |
4. | 31-35 | 4 | 3.3% |
Table 6: Relationship of cervical cytopathologies with age at 1st Issue.
S.No. | Age at marriage | Number of patients | Percentage |
1. | 16-19 | 34 | 28.33% |
2. | 19-22 | 66 | 55% |
3. | 22-25 | 10 | 8.33% |
4. | 25-30 | 11 | 9.1% |
Discussion
Although oncogenic HPV infection has been established as a causative factor of the precursors of cancer cervix as well as their progression to higher grade and eventually to malignancy, there are some other predisposing factors which play a substantive roli in the causation and progression of these lesions. We have tried to delineate these risk factors in case of cervical dysplasia and malignancy observed during 8 months cytological screening in 120 women, at SMGS, Government Medical College, Jammu.
Different risk factors associated with the development of cervical carcinoma detected in the present study have been analyzed in detail. The findings are summarized in below:
Maximum numbers of the patients (43.3 %) were in the age group of 50-69 (Table 1). The present findings with respect to age were found consistent with the observations made by Spanos et al. [9], Parkin et al. [10], Miller [11] and Misra et al. [12].
Majority of the patients were multiparous (Table 2). Various workers like Wahi et al. [13], Brinton et al. [14], Aras and Pai [15] and Munoz et al. [16] also recorded a strong relationship of the risk of cervical carcinoma to the number of live births. Trauma to the cervix during delivery could be the possible explanations but alternative mechanisms that warrant exploration include increased susceptibility to infection through immunosuppression, hormonal influences and dietary deficiencies (Brinton et al. [14]).
Maximum number of the patients in this study belonged to the rural areas (81.6%) and 10% belonged to urban areas (Table 3). Our findings were consistent with the reports of Coker et al. [18], Gajalakshmi and Shanta [19] that the incidence of cervical cancer is higher among the patients living in the rural areas. Since the recognized risk factors like illiteracy, low socioeconomic status early menarche, poor genital hygiene is widely prevalent in the rural population (Dutta et al. [20])
The incidence of cervical malignancy was significantly lower in Muslims (Table 4). This was in accordance with the study done by Wahi et al. [21] and Gajalakshmi and Shanta [19] that circumcision as practiced by Muslim could account for the lower incidence of cervical carcinoma as compared to Hindu community.
The frequency of this malignancy was higher in women who were married between 21-25 years (Table 5). These findings were consistent with findings proposed by Misra et al. [12].
55% of women had first issue at the age of 19-22 yrs (Table 6). This was in accordance with the study conducted by Dutta et al. [20] Thompson [22] and Varghese [23] that young age at first pregnancy is also a risk factor for CaCx.
Acknowledgement
Authors are extremely thankful to the J&K State Council for Science and Technology, Department of Science and Technology, J & K State for providing financial support to conduct the research work.
References
- WHO/ICO Information Centre on HPV and Cervical Cancer (HPV Information Centre). Summary report on HPV and Cervical Cancer statistics in India. 2007.
- Green J, Berrington G, Sweetland S, Beral V, Chilvers, Crossley B, Deacon J, Hermon C. Risk factors for adenocarcinoma and squamous cell carcinoma of the cervix in women aged 20-44 years: the UK National Case- Control study of Cervical Cancer. British Journal of Cancer 2003; 89:2078-2086.
- Spanos WJ, King A, Keeney E, Wagner R and Slater JM. Age as a prognostic factor in carcinoma of the cervix. Gynecol Oncol., 1989; 35: 66-68.
- Parkin DM, Pisani P, Ferlay J. Estimates of the worldwide incidence of eighteen major cancers in 1985. Int. J. Cancer 1993; 54: 594–606.
- Miller AB. 1992. Cervical Cancer Screening Programmes: Managerial Guidelines. WHO, Geneva.
- Misra JS, Srivastava S, Singh U, Srivastava AN. Risk factors and strategies for control of carcinoma cervix in India: Hospital based cytological screening experience of 35 years. Indian Journal of Cancer 2009; 46: 155-159.
- Wahi PN, Mali S, Luthra UK. Factors influencing cancer of the uterine cervix in North India. Cancer 1968; 23: 1221-1226.
- Brinton LA, Reeves WC, Brenes MM, Herrero R, Brinton R, Gaitan E, Tenorio, Garcia M , Rawls WE. Parity as a risk factor for cervical cancer. American Journal of Epidemiology 1989; 130: 486-496.
- Aras R, Pai NP. High fertility: risk factor for carcinoma cervix. The Journal of Family Welfare 1991; 41: 48-51.
- Munoz N, Franceshi S, Bosetti C, Moreno V, Smith JS, Shah KV, Meijer CJ, Bosch F. Role of parity and Human papillomavirus in cervical cancer: the IARC multicentric case control study. Lancet 2002; 359: 1093-1101.
- Coker AL, Fang S, Eggleston KS. Socioeconomic status and cervical cancer survival among older women: Findings from the SEER- Medicine linked data cohorts. 2006.
- Gajalakshmi CK, Shanta V. Association between cervical and penile cancer in Madras, India. Gynecologic Oncology 2006; 102: 278-284.
- Dutta PK, Upadhya A, Dutta N, Urmil AC, Thergoakar MP, Ganguly SS. A case control study of cervix cancer patients attending Command Hospital, Pune. Ind. J. Cancer 1990; 27: 101-8.
- Wahi PN, Luthra UK, Mali S, Mitra AB. Religion and cervical carcinoma in Agra. Indian Journal of Cancer 1972; 9: 210-25.
- Thompson JD. Cancer of cervix. In: Te Linde RW, Rock JA, Thompson JD, editors. Te Linde’s Operative Gynecology. Philadelphia: J B Lippincott Company 1992, 1162-3.
- Varghese PR. Protective effect of a traditional practice against cervix Cancer in Kerala. J. Hum. Ecol. 2004; 15: 187-190.
- Atkin NB, Baker MC, Fox MF. Chromosome changes in 43 carcinomas of the cervix uteri. Cancer Genet. Cytogenetic. 1990, 44: 229–241.
- Skyldberg B, Fujioka K, Hellstrom AC et al. Human papillomavirus infection, centrosome aberration and genetic instability in cervical lesions. Mod. Pathol 2001; 14: 279-284.
- Hidalgo A, Schewe C, Petreson BL et al. Human papillomavirus status and chromosomal imbalances in primary cervical carcinomas and tumor cell lines. Eur. J. Cancer 2000; 36: 542-548.