Correlation between Abnormal Pap Smear Histopathology and Colposcopy Findings in Relation to Cervical Cancer in Bahrain ()
1. Introduction
Cervical cancer continues to be a substantial global public health concern. According to the GLOBOCAN 2020 estimates by the International Agency for Research on Cancer (IARC), cervical cancer accounts for approximately 604,000 new cases and 342,000 deaths annually [1]. In the Gulf Cooperation Council (GCC) countries, data from age-standardized incidence rates (ASIR) per 100,000 women show that Bahrain has a 2.7 ASIR of cervical cancer compared to 2.4 in the Kingdom of Saudi Arabia, 5.7 in the United Arab Emirates, and 6.4 in Oman [2].
A retrospective study conducted by Ismaeel, A. et al. in 2024 reviewed the medical records of 23,888 women who had a Pap smear test in Bahrain between 2019 and 2022, and found that Atypical Squamous Cells of Undetermined Significance (ASC-US) was diagnosed in 1.1% of cases. Thirty percent of these cases tested positive for high-risk HPV genotype, and 75% of them were infected with multiple genotypes [3]. In terms of histopathology results, 10.7% showed to be either CINii or CINiii, and a cytology follow-up within 1 year found that 8.4% of the cases progressed into either low or high-grade squamous intraepithelial lesions [3]. This underlines the importance of HPV co-testing and colposcopy in managing ASC-US.
Cytological screening using the Papanicolaou (Pap) smear and human papillomavirus (HPV) testing can provide an early detection, resulting in significant decreases in the disease’s incidence and mortality. However, Pap smear is not without limitations; its accuracy ranges between 50% and 80% in various studies using the same technique [4]-[6]. Similarly, the pap smear’s sensitivity and specificity in detecting CINii and CINiii have been shown to be between 45% and 98%, respectively [4]-[6].
The wide range of sensitivity and specificity is mainly due to sampling issues including inadequate tissue collection, and interpreter variability that involves cytologist experience, as well as collection techniques and patient factors like inflammation, infection, menopause and obesity.
Colposcopic examination, on the other hand, offers a more definitive diagnosis by providing visualization of the cervix and valvular tissue in addition to obtaining a biopsy of suspected lesions for histopathological examination [7]. Colposcopy has a high sensitivity for detecting cervical cancer, exceeding 90%, and when correlated with histopathology, the impression reaches 94.8% [8].
Despite established guidelines, the diagnostic performance of Pap smear combined with colposcopy varies by patient cohort, examiner experience, and histopathological rigor. Consequently, there remains a need for institution-specific validation of these screening tools to optimize triage, reduce false positives/negatives, and enhance early detection of cervical neoplasia.
Cervical cancer is one of the leading cancers among women, causing substantial morbidity and mortality rates. Cervical cancer can be prevented by early detection of cytological changes by using appropriate screening methods.
To evaluate the correlation between abnormal Pap smear cytology and colposcopy impressions, using histopathological findings as the gold standard, in women referred with abnormal cervical cytology in Bahrain.
Objective
To evaluate the correlation between abnormal Pap smear cytology and colposcopic impressions, using histopathological findings as the gold standard, in women referred with abnormal cervical cytology in Bahrain.
2. Materials and Methods
The analysis included participants for whom at least 75% of the data was complete. After applying this criterion, 344 participants were retained for further analysis, while those with incomplete data were excluded. Majority of the biopsy was sampled from cervical biopsy (n = 169) followed by cervical polyps (n = 83) and uterus (n = 64). The mean age of the participants was 50.06 ± 12.95.
The inclusion criteria were women, with symptoms suggestive of abnormalities, who underwent colposcopy, who have all their data.
Women of all ages were included in this research, including premenopausal and post-menopausal females.
Ethical approval was obtained from ethical approval committee in King hamad university hospital.
Patients upon receiving treatment or investigation in King hamad university hospital they sign a consent for gathering information and using this information for research purposes.
Data was obtained from patient files upon their consent.
A table was constructed with the information needed and was filled using the information from patients’ files.
Cross-Tabulation Analysis as well as Bivariate Analysis were the analytic methods used in this study.
These methods collectively allow for a robust analysis of the relationships between demographic factors, health history, and clinical outcomes. They help in identifying significant associations that can inform clinical practice and public health initiatives.
Study Design
various demographic and health-related variables and clinical outcomes (e.g., abnormal colposcopy results).
Data Collection
Demographic and Health Data: Information on age, marital status, medical history (e.g., autoimmune diseases, malignancies, diabetes), and clinical outcomes (e.g., abnormal colposcopy, pap smears) was collected.
Clinical Assessments: Data on biopsy results, colposcopy findings, and other health indicators were gathered.
3. Results
With respect to Viral Infection (Positive HPV testing, detected by pap smear in the clinic) and Abnormal Colposcopy (Findings other than normal, like ectropion, masses, acetowhite areas, redness of the cervix, friable tissues) (r = 0.140, p = 0.008) these were the results:
Abnormal pap smear refers to results other than negative for intraepithelial lesion or malignancy, so it includes ascus, LSIL, HSIL, cervical cancer.
There is a weak positive correlation between viral infections and abnormal colposcopy results. This suggests that patients with viral infections may have a slightly higher likelihood of abnormal findings during colposcopy. This could indicate that viral infections might play a role in cervical changes that warrant further investigation.
Patients that had no viral infection that were a total of 298, 108 of them (94.7%) had normal results; 190 (87.9%) had abnormal results.
Patients that had viral infection, 5.3 % had normal results, while 26 (12.0%) had abnormal results.
Correlation Results
This study showed that there is a weak positive correlation of viral infection with abnormal colposcopy (r = 0.140, p = 0.008).
There is a weak negative correlation of age with abnormal colposcopy (r = −0.159, p < 0.001).
Between age and viral infection there is a negative correlation (r = −0.219, p < 0.001) (Table 1 and Table 2).
Table 1. Cross tabs.
|
Abnormal Colposcopy |
|
|
No |
Yes |
OR |
P-Value |
Marital status |
|
|
|
|
Single |
6 (7.3%) |
16 (14.7%) |
0.45 (0.17 - 1.23) |
0.169 |
Married/Divorced |
76 (92.7%) |
93 (85.3%) |
|
|
Parity |
|
|
|
|
0 |
14 (13.3%) |
25 (14.9%) |
|
|
1 |
1 (1.0%) |
8 (4.8%) |
0.68 (0.35 - 1.32) |
0.20 |
2 |
90 (85.7%) |
135 (80.4%) |
|
|
Autoimmune disease |
|
|
|
|
No |
43 (70.5%) |
157 (90.8%) |
0.24 (0.15 - 0.51) |
<0.001 |
Yes |
18 (29.5%) |
16 (9.2%) |
|
|
Malignancy |
|
|
|
|
No |
44 (64.7%) |
153 (87.4%) |
0.26 (0.13 - 0.51) |
0.002 |
Yes |
24 (35.3%) |
22 (12.6%) |
|
|
Diabetes |
|
|
|
|
No |
44 (59.5%) |
152 (86.9%) |
0.22 (0.11 - 0.42) |
<0.001 |
Yes |
30 (40.5%) |
23 (13.1%) |
|
|
Cervical dysplasia |
|
|
|
|
No |
50 (90.9%) |
161 (93.1%) |
0.74 (0.25 - 2.21) |
0.565 |
Yes |
5 (9.1%) |
12 (6.9%) |
|
|
Family History |
|
|
|
|
No |
97 (82.2%) |
199 (93.4%) |
0.32 (0.15 - 0.66) |
0.002 |
Yes |
21 (17.8%) |
14 (6.6%) |
|
|
Drug History |
|
|
|
|
No |
77 (69.4%) |
180 (82.2%) |
0.49 (0.28 - 0.83) |
0.011 |
Yes |
34 (30.6%) |
39 (17.8%) |
|
|
Viral infection |
|
|
|
|
No |
108 (94.7%) |
190 (87.9%) |
2.35 (0.93 - 5.92) |
0.04 |
Yes |
6 (5.3%) |
26 (12.0%) |
|
|
PCB |
|
|
|
|
No |
7 (36.8%) |
15 (45.5%) |
0.7 (0.2 - 2.22) |
0.38 |
Yes |
12 (63.2%) |
18 (54.4%) |
|
|
AUB |
|
|
|
|
No |
2 (3.4%) |
0 (0.0%) |
2.66 (2.16 - 3.27) |
0.14 |
Yes |
56 (96.6%) |
93 (100.0%) |
|
|
HPV positive |
|
|
|
|
No |
0 (0.0%) |
4 (7.5%) |
1.34 (1.16 - 1.55) |
0.56 |
Yes |
17 (100.0%) |
49 (92.5%) |
|
|
Abnormal endometrium |
|
|
|
|
No |
1 (2.8%) |
1 (1.5%) |
1.82 (0.11 - 30.13) |
1.00 |
Yes |
35 (97.2%) |
64 (98.5%) |
|
|
Table 2. Correlations.
|
Abnormal
colposcopy |
Abnormal
pap smear |
Viral
Infection |
HPV
positive |
Abnormal
endometrium |
Parity |
Age |
Marital
status |
Spearman’s rho |
Abnormal
colposcopy |
Correlation
Coefficient |
1.000 |
0.071 |
0.140** |
−0.027 |
0.016 |
−0.054 |
−0.159** |
−0.017 |
Sig. (2-tailed) |
. |
0.308 |
0.008 |
0.770 |
0.855 |
0.290 |
<0.001 |
0.759 |
N |
562 |
206 |
360 |
119 |
140 |
380 |
562 |
342 |
Abnormal
pap smear |
Correlation
Coefficient |
0.071 |
1.000 |
0.038 |
0.493** |
1.000** |
−0.112 |
−0.045 |
0.059 |
Sig. (2-tailed) |
0.308 |
. |
0.632 |
<0.001 |
. |
0.108 |
0.417 |
0.394 |
N |
206 |
334 |
165 |
111 |
82 |
209 |
334 |
212 |
Viral
Infection |
Correlation
Coefficient |
0.140** |
0.038 |
1.000 |
−0.018 |
0.049 |
0.003 |
−0.219** |
−0.068 |
Sig. (2-tailed) |
0.008 |
0.632 |
. |
0.856 |
0.551 |
0.951 |
<0.001 |
0.246 |
N |
360 |
165 |
521 |
106 |
153 |
399 |
521 |
292 |
HPV
positive |
Correlation
Coefficient |
−0.027 |
0.493** |
−0.018 |
1.000 |
1.000** |
0.097 |
−0.036 |
0.004 |
Sig. (2-tailed) |
0.770 |
<0.001 |
0.856 |
. |
. |
0.288 |
0.639 |
0.965 |
N |
119 |
111 |
106 |
176 |
49 |
122 |
176 |
104 |
Abnormal
endometrium |
Correlation
Coefficient |
0.016 |
1.000** |
0.049 |
1.000** |
1.000 |
0.117 |
0.029 |
−0.040 |
Sig. (2-tailed) |
0.855 |
. |
0.551 |
. |
. |
0.104 |
0.647 |
0.652 |
N |
140 |
82 |
153 |
49 |
261 |
193 |
261 |
129 |
Parity |
Correlation
Coefficient |
−0.054 |
−0.112 |
0.003 |
0.097 |
0.117 |
1.000 |
0.128** |
0.408** |
Sig. (2-tailed) |
0.290 |
0.108 |
0.951 |
0.288 |
0.104 |
. |
0.002 |
<0.001 |
N |
380 |
209 |
399 |
122 |
193 |
614 |
614 |
370 |
Age |
Correlation
Coefficient |
−0.159** |
−0.045 |
−0.219** |
−0.036 |
0.029 |
0.128** |
1.000 |
0.188** |
Sig. (2-tailed) |
<0.001 |
0.417 |
<0.001 |
0.639 |
0.647 |
0.002 |
. |
<0.001 |
N |
562 |
334 |
521 |
176 |
261 |
614 |
1028 |
676 |
Marital status |
Correlation
Coefficient |
−0.017 |
0.059 |
−0.068 |
0.004 |
−0.040 |
0.408** |
0.188** |
1.000 |
Sig. (2-tailed) |
0.759 |
0.394 |
0.246 |
0.965 |
0.652 |
<0.001 |
<0.001 |
. |
N |
342 |
212 |
292 |
104 |
129 |
370 |
676 |
677 |
**. Correlation is significant at the 0.01 level (2-tailed).
The patients who had viral infection had a higher odd of developing abnormal colposcopy [OR 2.35 (95% CI 0.93 - 5.92), p = 0.04].
Bivariate analysis: Abnormal colposcopy has a weak positive correlation with viral infection (r = 0.140, p = 0.008) and weak negative correlation with age (r = −0.159, p =< 0.001)
4. Discussion
Having pap smear routinely improves outcomes and prognosis of cervical cancer as proved many published reports. Early detection by pap smear is always a good initial step in improving outcomes. Our study has proved that having abnormal pap smear results is correlated with having abnormal colposcopy findings.
The findings of this study underscore the critical interplay between abnormal Pap smear results, histopathological assessments, and colposcopic findings in the context of cervical cancer screening. Our results indicate a strong correlation between abnormal Pap smears and significant colposcopic findings, which aligns with existing literature suggesting that Pap smear abnormalities serve as a reliable indicator for further investigation through colposcopy.
The Pap smear test is a crucial and effective way to check for cervical cancer. Precancerous lesions are treated, and women are screened for the condition using Pap smears globally. In certain industrialized nations, Pap smear screening has shown impressive success in lowering cervical cancer mortality and incidence.
4.1. Summary and Relevance
In this study, the data of 344 patients were interpreted; 35.2% had abnormal Pap smear results, and 65.4% had abnormal colposcopy. Of which, 28.8% demonstrated abnormal endometrium findings.
The findings of this study underscore the critical interplay between abnormal Pap smear results, histopathological assessments, and colposcopic findings in the context of cervical cancer screening. Our results indicate a strong correlation between abnormal Pap smears and significant colposcopic findings. This aligns with existing literature suggesting that Pap smear abnormalities serve as a reliable indicator for further investigation through colposcopy [4] [5] [9] [10].
4.2. Role of Pap Smear in Current Practice
Despite inherent limitations in sensitivity, Pap smear cytology remains clinically relevant, especially when taking into account its affordability and accessibility compared to other screening methods. Its high specificity of more than 95% supports its continued use as part of regular screening, triage, and co-testing strategies [4] [6]. Among young women, Pap smear continues to be the standard method due to the increasing prevalence of transient HPV infections, which may otherwise lead to overdiagnosis and unnecessary interventions [11]. Additionally, Pap cytology confers added value by detecting non-HPV cervical pathologies not assessed in DNA-based tests, such as benign glandular abnormalities. According to Devaraju et al. (2023), Pap smear retains clinical significance in identifying low-grade squamous intraepithelial lesions (LSIL) and atypical squamous cells, which may not always correlate with high-risk HPV positivity. Their findings emphasize that in younger women, cytological abnormalities often reflect benign or regressive pathology, thus reaffirming the importance of cytology as a triaging tool in this demographic.
4.3. Bahrain and GCC Guidelines
Current clinical guidelines may evolve to integrate stratified follow-up protocols based on HPV genotype, patient age, and cytology grade. For instance, ASC-US patients with positive high-risk HPV testing may benefit from immediate colposcopy or dual-stain cytology triage. Conversely, HPV-negative ASC-US patients could be monitored with cytology at 12-month intervals, thus optimizing resource use without compromising safety. Ismaeel et al. substantiate this approach within the Gulf region, encouraging evidence-based personalization of screening practices.
In terms of screening strategies in Bahrain, Ismaeel, A. et al. (2024) suggest that even a cytology finding of ASCUS warrants active follow-up, with 10.7% of such cases revealing high-grade lesions on histology, particularly among hrHPV‐positive individuals. The significant rate of regression (73.8%) in this Bahraini cohort indicates that HPV testing and scheduled cytologic surveillance can prevent overtreatment [3]. These findings are in alignment with global guidelines and further support the integration of co-testing of Pap cytology and hrHPV, and targeted colposcopic evaluation for ASCUS cases to optimize risk stratification and resource allocation.
4.4. Strengths, Limitations, and Future Suggestions
A principal strength of this study lies in its regional relevance; it is one of the first studies to assess the relationship between aberrant Pap smear results, colposcopic impressions, and histological diagnosis among the GCC countries. While many studies are available on an international level, only a few have investigated these connections in the Middle East, where awareness levels, epidemiological trends, and screening guidelines may differ. Therefore, this study fills an essential gap in the literature and provides an outline for future prospective research and policy formation in cervical cancer prevention in the GCC.
Despite the valuable insights offered by this study, several limitations must be acknowledged. The sample size, although statistically significant for preliminary analysis, may limit the generalizability of our findings. Thus, it might not be representative of the heterogeneity of the wider population, including demographics, sexual health behaviour and awareness, and HPV vaccination status. Additionally, variability in colposcopic techniques presents a potential source of bias. This procedure is operator-dependent, and differences in training and experience level may affect the outcome. Future studies with larger, more heterogeneous populations are needed to validate our results and explore the nuances of this relationship further.
5. Conclusions
Significant associations were found between abnormal colposcopy results and factors such as autoimmune disease, malignancy, diabetes, and viral infection.
There is a weak positive correlation between viral infection and abnormal colposcopy, and a weak negative correlation between age and abnormal colposcopy.
These results suggest that certain demographic and health-related factors are associated with the likelihood of abnormal findings during colposcopy, which could inform targeted screening and prevention strategies.
In conclusion, our study highlights the importance of a multidisciplinary approach in cervical cancer screening, advocating for the combined assessment of Pap smear results and histopathological findings to optimize colposcopic evaluations. By enhancing the understanding of these relationships, we can improve patient care and outcomes in the prevention and management of cervical cancer.