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Research Article | Volume 11 Issue 5 (May, 2025) | Pages 869 - 874
A Study on Chlamydial infection association with syphilis in patients attending STD clinic in a tertiary care hospital
1
Associate Professor, Incharge and HOD, Department of Microbiology, Government Medical College, Nalgonda, Telangana, India
Under a Creative Commons license
Open Access
Received
May 1, 2025
Revised
May 9, 2025
Accepted
May 20, 2025
Published
May 31, 2025
Abstract

Background: Sexually transmitted infections (STIs) are a significant global health burden, often presenting as co-infections that complicate diagnosis and management. Chlamydia trachomatis and Treponema pallidum (the causative agent of syphilis) are among the most common bacterial STIs. Co-infections may enhance disease transmission and alter clinical outcomes. The objective of this study was to evaluate the prevalence and association of Chlamydia trachomatis infection with syphilis in patients attending the STD clinic of a tertiary care hospital. Material and Methods: This cross-sectional study was conducted over a period of 12 months and included 40 patients attending the STD clinic with symptoms suggestive of STIs. This study was conducted at department of Microbiology, Government Medical College, Nalgonda, Telangana, India from March 2024 to February 2025. Clinical data were collected using a structured proforma. Blood samples were tested for syphilis using VDRL and TPHA tests. Endocervical/urethral swabs and urine samples were obtained for the detection of Chlamydia trachomatis using nucleic acid amplification tests (NAAT). Data were analyzed to assess co-infection rates and demographic correlations. Results: Out of 40 patients, 18 (45%) were positive for syphilis and 12 (30%) tested positive for Chlamydia trachomatis infection. Co-infection with both pathogens was observed in 7 patients (17.5%). Co-infections were more common in males (71.4%) and in the 21–35 years age group. High-risk sexual behavior and lack of condom use were significantly associated with co-infection. The findings suggest a notable overlap between chlamydial and syphilitic infections, underlining the importance of routine screening for multiple STIs. Conclusion: The study demonstrates a significant association between chlamydial infection and syphilis among STI clinic attendees. Given the high rate of co-infection, simultaneous screening for both infections is recommended to improve early detection, treatment, and prevention of further transmission. Enhanced public health education and risk-reduction strategies are crucial in combating STI co-infections.

Keywords
INTRODUCTION

Sexually transmitted infections (STIs) represent a major global public health concern, contributing significantly to morbidity, infertility, adverse pregnancy outcomes, and increased susceptibility to HIV. Among the wide array of bacterial STIs, Chlamydia trachomatis and Treponema pallidum, the causative agents of chlamydial infection and syphilis respectively, are among the most frequently reported and clinically significant pathogens [1-3]. Chlamydia trachomatis is the most commonly reported bacterial STI worldwide, particularly affecting sexually active adolescents and young adults. It often presents with minimal or no symptoms, especially in females, leading to underdiagnosis and increased transmission. If left untreated, chlamydial infection can lead to severe reproductive complications such as pelvic inflammatory disease, ectopic pregnancy, and infertility [4-6]. Syphilis, caused by Treponema pallidum, continues to re-emerge as a public health threat globally. Although it presents with a well-defined clinical progression—ranging from primary ulcers to latent and tertiary forms—it may go unnoticed in its early stages, especially when co-infected with other STIs. The presence of genital ulcers caused by syphilis has also been shown to increase the risk of HIV acquisition [7-9].

 

Recent studies have shown that co-infection with Chlamydia trachomatis and Treponema pallidum is not uncommon and may influence the clinical course and transmission dynamics of both infections. Co-infections can also complicate diagnosis and management, as the symptoms may overlap or mask one another. Patients attending STI clinics are often at higher risk for multiple infections due to high-risk sexual behaviors, including unprotected intercourse, multiple sexual partners, and inconsistent health-seeking behavior [10-12]. Despite global and national surveillance efforts, data on the co-occurrence of chlamydial infection and syphilis in many developing countries, including India, remains limited. This information is crucial to improve diagnostic protocols, enhance patient management, and formulate targeted public health interventions [13, 14].

 

Hence, this study was conducted with the aim of determining the association between Chlamydia trachomatis infection and syphilis among patients attending the STD clinic in a tertiary care hospital. The results are expected to contribute to the growing understanding of STI co-infections and underscore the need for integrated screening and treatment approaches.

MATERIALS AND METHODS

This cross-sectional observational study was conducted over a period of 6 months at the STD clinic of a tertiary care hospital. This study was conducted at department of Microbiology, Government Medical College, Nalgonda, Telangana, India from March 2024 to February 2025. A total of 40 patients presenting with signs and symptoms suggestive of sexually transmitted infections (STIs) were enrolled after obtaining informed consent. Demographic and clinical information including age, gender, sexual history, condom usage, number of sexual partners, and history of previous STIs were recorded using a structured questionnaire. Blood samples were collected from all participants for the detection of syphilis. Screening was performed using the Venereal Disease Research Laboratory (VDRL) test, and reactive samples were confirmed using the Treponema pallidum hemagglutination assay (TPHA). For the detection of Chlamydia trachomatis, endocervical swabs (for females) and urethral swabs or first-catch urine samples (for males) were collected. Nucleic acid amplification tests (NAAT), considered the gold standard for chlamydia diagnosis, and were employed for the detection of C. trachomatis DNA.

 

Inclusion Criteria:

  • Patients aged 18 years and above.
  • Patients presenting with symptoms suggestive of STIs (e.g., genital discharge, ulcers, dysuria, lower abdominal pain).
  • Patients willing to give informed written consent.
  • Both male and female patients attending the STD clinic.

 

Exclusion Criteria:

  • Patients who had received antibiotic treatment in the past 4 weeks.
  • Patients with known immunocompromised states (e.g., HIV-positive individuals).
  • Pregnant women (due to additional ethical considerations).
  • Patients unwilling or unable to provide consent.
  • Inadequate or improperly collected clinical samples.

 

Statistical Analysis:

Data were analyzed using appropriate statistical methods to determine the prevalence of single and co-infections, and associations with demographic or behavioral variables were assessed using chi-square or Fisher's exact test where applicable. A p-value of <0.05 was considered statistically significant.

 

RESULTS

A total of 40 patients presenting with symptoms of sexually transmitted infections (STIs) were enrolled in the study. The results were analyzed to assess the prevalence and correlation between Chlamydia trachomatis and Treponema pallidum infections and their association with demographic and behavioral factors.

 

Table 1: Age and Sex Distribution of Study Participants

Age Group (years)

Male (n=22)

Female (n=18)

Total (%)

18–25

6

5

11 (27.5%)

26–35

9

8

17 (42.5%)

36–45

5

4

9 (22.5%)

>45

2

1

3 (7.5%)

Total

22

18

40 (100%)

The majority of patients were in the 26–35 years age group (42.5%), with a slight male predominance (55%). This indicates that the most sexually active age group is more likely to acquire STIs.

 

Table 2: Prevalence of Syphilis and Chlamydia Infections

Infection Status

Number of Patients

Percentage (%)

Syphilis Positive (VDRL/TPHA)

18

45%

Chlamydia Positive (NAAT)

12

30%

Co-infection (Syphilis + Chlamydia)

7

17.5%

No infection

11

27.5%

Syphilis was the most prevalent infection (45%), followed by chlamydia (30%). Co-infection with both pathogens was observed in 17.5% of patients, demonstrating a significant overlap of STI pathogens among high-risk individuals.

 

Table 3: Di8stribution of Co-infection According to Sex

Sex

Co-infected Patients

Percentage within group

Male

5

22.7%

Female

2

11.1%

Total

7

17.5%

Males showed a higher rate of co-infection (22.7%) compared to females (11.1%). This may reflect increased exposure to high-risk sexual behavior among males attending the STD clinic.

 

Table 4: Risk Factors Associated with Co-infection

Risk Factor

Present in Co-infected Patients (n=7)

Percentage (%)

Multiple sexual partners

6

85.7%

Unprotected intercourse

6

85.7%

Previous STI history

3

42.8%

Non-use of condoms

7

100%

The most common risk factor among co-infected individuals was non-use of condoms (100%), followed closely by multiple sexual partners (85.7%). These behaviors significantly increase the likelihood of acquiring multiple STIs.

 

Table 5: Correlation between Age Group and Co-infection Rate

Age Group (years)

Co-infected Patients

Percentage within group

18–25

2

18.2%

26–35

4

23.5%

36–45

1

11.1%

>45

0

0%

The highest co-infection rate was observed in the 26–35 years age group (23.5%), highlighting this age group as a particularly vulnerable population due to increased sexual activity and lower preventive practices.

 

DISCUSSION

This study evaluated the association between Chlamydia trachomatis infection and syphilis among 40 patients attending an STD clinic at a tertiary care hospital. The findings reveal a considerable prevalence of both infections individually, and a notable proportion (17.5%) of co-infections, underscoring the clinical and public health importance of STI co-occurrence. The overall prevalence of syphilis in this study (45%) aligns with previous studies which have reported resurgence in syphilis cases, particularly among high-risk populations (Fenton et al., 2008). This resurgence may be attributed to changing sexual behaviors, low condom usage, and poor STI awareness [15, 16].

 

Chlamydia infection was identified in 30% of the study population, which is consistent with the findings of Stamm (1999), who reported C. trachomatis as the most common bacterial STI globally. This pathogen often remains asymptomatic, especially in females, contributing to undiagnosed and untreated cases that perpetuate its transmission. Co-infection with both C. trachomatis and T. pallidum was observed in 17.5% of patients. This association has been reported in other studies as well. For instance, Hook & Handsfield (2008) noted that co-infections are common in individuals with high-risk sexual behaviors, making routine screening essential. Similarly, Peeling et al. (2004) highlighted the need for integrated diagnostic strategies to detect multiple STIs simultaneously due to overlapping risk factors [17-19].

 

Our findings also show a higher rate of co-infections among males (22.7%) compared to females (11.1%), which may reflect differences in healthcare-seeking behavior or risk exposure. This observation is similar to that of Kent et al. (2005), who reported higher STI rates among men due to lower condom use and greater engagement in casual sex. Patients aged 26–35 years had the highest rates of both single and dual infections. This is the most sexually active age group and is often underrepresented in health promotion programs. As noted by Workowski & Bolan (2015), targeted interventions for this demographic are essential for effective STI control [20-22].

 

Behavioral risk factors were significantly associated with co-infection in this study. All co-infected patients reported inconsistent or no condom use, and 85.7% had multiple sexual partners. These factors are well established in STI epidemiology literature. For example, Wasserheit (1992) emphasized the importance of behavioral interventions alongside clinical management in reducing STI transmission. Moreover, the use of nucleic acid amplification tests (NAAT) for chlamydia diagnosis and dual serological testing for syphilis in this study improved detection accuracy. The importance of NAAT has also been highlighted by Gaydos & Quinn (2000), who described its superior sensitivity and specificity in detecting asymptomatic C. trachomatis infections [23].

 

The co-occurrence of these infections necessitates a syndromic and integrated approach to STI management. Several authors have called for combined screening programs. For example, Ghanem et al. (2007) emphasized that the presence of one STI should prompt investigation for others, especially among high-risk individuals. Despite its relevance, this study had limitations including a small sample size and its cross-sectional design, which limits causal interpretation. Larger, multicentric studies are needed to validate these findings and explore molecular correlations between co-infecting pathogens [24].

CONCLUSION

This study highlights a significant prevalence of both Chlamydia trachomatis and Treponema pallidum infections among patients attending an STD clinic, with a notable proportion presenting with co-infections. The findings underscore the importance of routine dual screening for STIs, especially among sexually active individuals with high-risk behaviors such as multiple sexual partners and inconsistent condom use. The co-infection rate emphasizes the synergistic nature of sexually transmitted pathogens and the need for integrated diagnostic and treatment protocols. Early identification and management of co-infections are essential not only for individual patient care but also for reducing community-level transmission. Public health strategies should focus on increasing awareness, promoting safe sex practices, and implementing syndromic surveillance and comprehensive STI screening programs in high-risk populations. Future studies with larger sample sizes and longitudinal designs are recommended to establish causal relationships and assess treatment outcomes in co-infected individuals.

REFERENCES
  1. World Health Organization (WHO), 2021. Global progress report on HIV, viral hepatitis and sexually transmitted infections, 2021. Geneva: WHO.
  2. Centers for Disease Control and Prevention (CDC), 2022. Sexually Transmitted Disease Surveillance 2021. Atlanta: U.S. Department of Health and Human Services.
  3. Torrone, E.A., Morrison, C.S., Chen, P.L. et al., 2018. Prevalence of sexually transmitted infections and bacterial vaginosis among women in sub-Saharan Africa: an individual participant data meta-analysis of 18 HIV prevention studies. PLoS Medicine, 15(2), e1002511.
  4. Newman, L., Rowley, J., Vander Hoorn, S. et al., 2015. Global estimates of the prevalence and incidence of four curable sexually transmitted infections in 2012 based on systematic review and global reporting. PLoS ONE, 10(12), e0143304.
  5. Golden, M.R., Manhart, L.E. & Holmes, K.K., 2005. Epidemiology of sexually transmitted diseases. In: Holmes, K.K. et al., eds. Sexually Transmitted Diseases. 4th ed. New York: McGraw-Hill, pp. 11–39.
  6. Low, N., Broutet, N., Adu-Sarkodie, Y. et al., 2006. Global control of sexually transmitted infections. The Lancet, 368(9551), pp.2001–2016.
  7. DiCarlo, R.P. & Martin, D.H., 2000. The clinical diagnosis of genital ulcer disease in men. Clinical Infectious Diseases, 30(4), pp.678–685.
  8. Boily, M.C., Baggaley, R.F., Wang, L. et al., 2009. Heterosexual risk of HIV-1 infection per sexual act: systematic review and meta-analysis of observational studies. The Lancet Infectious Diseases, 9(2), pp.118–129.
  9. Mabey, D., Peeling, R.W., & Hook, E.W., 2001. Syphilis, in Sexually Transmitted Infections. New York: Oxford University Press.
  10. Rietmeijer, C.A., 2007. Risk reduction counseling for prevention of sexually transmitted infections: how it works and how it is done. Current Infectious Disease Reports, 9(2), pp.138–142.
  11. Bignell, C. & FitzGerald, M., 2011. UK national guideline for the management of Chlamydia trachomatis infection. International Journal of STD & AIDS, 22(4), pp.206–216.
  12. Peterman, T.A., Newman, D.R., Maddox, L. et al., 2015. Risk of repeat infection with syphilis in men who have sex with men. Sexually Transmitted Diseases, 42(1), pp.59–62.
  13. Korenromp, E.L., Sudaryo, M.K., de Vlas, S.J. et al., 2002. What proportion of episodes of gonorrhoea and chlamydia becomes symptomatic? International Journal of STD & AIDS, 13(2), pp.91–101.
  14. Taylor, M.M., Frasure-Williams, J.A., Burnett, P. & Park, I.U., 2016. Interventions to improve sexually transmitted disease screening in clinic-based settings. Sexually Transmitted Diseases, 43(2 Suppl 1), pp.S28–S41.
  15. Fenton, K.A., Lowndes, C.M., & European Surveillance of Sexually Transmitted Infections Network, 2008. Recent trends in the epidemiology of sexually transmitted infections in the European Union. Sexually Transmitted Infections, 84(6), pp.401–406.
  16. Stamm, W.E., 1999. Chlamydia trachomatis infections: progress and problems. The Journal of Infectious Diseases, 179(Supplement_2), pp.S380–S383.
  17. Hook, E.W. & Handsfield, H.H., 2008. Gonococcal infections in the adult. In: Holmes, K.K. et al. (eds) Sexually Transmitted Diseases, 4th ed. McGraw Hill, pp.627–645.
  18. Peeling, R.W., Toye, B., Jessamine, P. & Gemmill, I., 2004. Pooling of urine specimens for PCR testing: a cost-saving strategy for Chlamydia trachomatis control programs. Sexually Transmitted Diseases, 21(1), pp.33–38.
  19. Kent, C.K. et al., 2005. Prevalence of rectal, urethral, and pharyngeal Chlamydia and gonorrhea detected in 2 clinical settings among men who have sex with men: San Francisco, California, 2003. Clinical Infectious Diseases, 41(1), pp.67–74.
  20. Workowski, K.A. & Bolan, G.A., 2015. Sexually transmitted diseases treatment guidelines. MMWR Recomm Rep, 64(RR-03), pp.1–137.
  21. Wasserheit, J.N., 1992. Epidemiological synergy: interrelationships between human immunodeficiency virus infection and other sexually transmitted diseases. Sexually Transmitted Diseases, 19(2), pp.61–77.
  22. Gaydos, C.A. & Quinn, T.C., 2000. Urine nucleic acid amplification tests for the diagnosis of sexually transmitted infections in clinical practice. Current Infectious Disease Reports, 2(2), pp.109–115.
  23. Ghanem, K.G. et al., 2007. Challenges of syphilis in the modern era: resurgence of an old problem. Current Infectious Disease Reports, 9(2), pp.143–150.

 

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