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Clinical and uterine cervix characteristics of women with Mycoplasma and Ureaplasma in genital discharge

SUMMARY

OBJECTIVE:

The objective of this study was to assess the clinical and uterine cervix characteristics of patients displaying vaginal discharge with positive results for Mycoplasma sp. and/or Ureaplasma spp.

METHODS:

An analytical cross-sectional study involving women aged 18–45 years was conducted. Microbiological assessments included Ureaplasma and Mycoplasma cultures, as well as human papillomavirus hybrid capture using ecto and endocervix swabs. All tests were two-tailed, and significance was set at p<0.05.

RESULTS:

Among 324 women, Ureaplasma prevalence was 17.9%, and Mycoplasma prevalence was 3.1%. The Ureaplasma-positive group exhibited a higher frequency of urinary tract infections (39.1 vs. 19%, p=0.002) and human papillomavirus (39.7 vs. 12.8%, p≤0.001) compared with controls. The Mycoplasma-positive group showed a higher frequency of non-contraceptive use compared with controls (66.2 vs. 30.0%, p=0.036). Abnormal colposcopic findings were more prevalent in the Mycoplasma/Ureaplasma-positive group than in controls (positive: 65% vs. control: 35%, p=0.001). Pap smear findings did not differ between the groups.

CONCLUSION:

Ureaplasma spp. was associated with urinary tract infections and human papillomavirus, while the presence of Mycoplasma sp. was linked to reduced contraceptive use. When analyzing both pathogens together, a higher frequency of abnormal colposcopic findings was observed, with no difference in cytological findings in the positive group.

KEYWORDS:
Mycoplasma ; Uterine cervicitis; HPV; Cervix

INTRODUCTION

The prevalence of vaginal colonization by Mycoplasma sp. and Ureaplasma spp. among women tends to increase post-puberty, correlating with the number of sexual partners over their lifetime. While some authors characterize these microorganisms as commensal residents, they are also linked to various pathological conditions, including premature birth, vaginal discharge, urethritis, pelvic inflammatory disease, and infertility11 Albig J, Micevska M, Jovchevski S, Georgiveska J, Cekovska S, Stankov A. Incidence and prevalence of vaginal infections in women of reproductive age in North Macedonia. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2023;44(2):73-80. https://doi.org/10.2478/prilozi-2023-0027
https://doi.org/10.2478/prilozi-2023-002...

2 Park JH, Kim N, Shin S, Roh EY, Yoon JH, Park H. Prevalence and correlated factors of sexually transmitted infections among women attending a Korean sexual assault center. J Forensic Leg Med. 2020;71:101935. https://doi.org/10.1016/j.jflm.2020.101935
https://doi.org/10.1016/j.jflm.2020.1019...
-33 Leli C, Mencacci A, Latino MA, Clerici P, Rassu M, Perito S, et al. Prevalence of cervical colonization by Ureaplasma parvum, Ureaplasma urealyticum, Mycoplasma hominis and Mycoplasma genitalium in childbearing age women by a commercially available multiplex real-time PCR: an Italian observational multicentre study. J Microbiol Immunol Infect. 2018;51(2):220-5. https://doi.org/10.1016/j.jmii.2017.05.004
https://doi.org/10.1016/j.jmii.2017.05.0...
.

Exposure of the cervicovaginal epithelium to Mycoplasma sp. and Ureaplasma spp. may give rise to a persistent intracellular infection, potentially leading to tissue damage mediated by inflammatory cytokines. Although the relationship between human papillomavirus (HPV) and these microorganisms is not conclusively established, the nature of the infection they cause allows for both direct interaction with HPV during co-infection of a single cell and indirect interaction through cytokine responses44 Audirac-Chalifour A, Torres-Poveda K, Bahena-Román M, Téllez-Sosa J, Martínez-Barnetche J, Cortina-Ceballos B, et al. Cervical microbiome and cytokine profile at various stages of cervical cancer: a pilot study. PLoS One. 2016;11(4):e0153274. https://doi.org/10.1371/journal.pone.0153274
https://doi.org/10.1371/journal.pone.015...
.

Several studies indicate that the presence of Mycoplasma bacteria heightens the risk of more severe cervical lesions, such as low- and high-grade intraepithelial lesions55 Klein C, Samwel K, Kahesa C, Mwaiselage J, West JT, Wood C, et al. Mycoplasma co-infection is associated with cervical cancer risk. Cancers (Basel). 2020;12(5):1093. https://doi.org/10.3390/cancers12051093
https://doi.org/10.3390/cancers12051093...
. In addition, women with abnormal cervical cytologies exhibit a 17.6 times greater risk for co-infection with Mycoplasma hominis and Ureaplasma urealyticum66 Adamopoulou M, Avgoustidis D, Voyiatjaki C, Beloukas A, Yapijakis C, Tsiambas E, et al. Impact of combined mycoplasmataceae and HPV co-infection on females with cervical intraepithelial neoplasia and carcinoma. J BUON. 2021;26(4):1313-9. PMID: 34564986.

However, studies assessing the relationship between Ureaplasma/Mycoplasma and cervical cell changes are controversial. In 2018, a study examined the association between M. hominis infection and abnormal cervical cells but found no correlation between bacterial infections and abnormal cervical cytology77 Effiana M, Irsan A, Natalia D, Rahmayanti S, Indarti J, Rachmadi L, et al. Infections of Chlamydia trachomatis and Mycoplasma hominis as risk factors for abnormal cervical cells. Makara J Health Res. 2018;22(1):53-7. https://doi.org/10.7454/msk.v22i1.7965
https://doi.org/10.7454/msk.v22i1.7965...
. Another study investigated the relationship between Mycoplasma, Ureaplasma, and HPV infections in sex workers, also failing to identify a correlation between M. hominis, U. urealyticum, and HPV infection88 Feriyawati L, Anggraini DR, Nasution TA. Co-infection of Human Papillomavirus with Mycoplasma Hominis/Ureaplasma Urealyticum among female sex workers in Medan, Indonesia. Open Access Maced J Med Sci. 2019;7(20):3425-8. https://doi.org/10.3889/oamjms.2019.438
https://doi.org/10.3889/oamjms.2019.438...
.

Contrary to these findings, it has been observed that high-risk HPV (hr-HPV) infection is a necessary cause of cervical cancer. However, other common microbes in the lower genital tract may enhance hr-HPV infection and cervical cytopathy99 Lv P, Zhao F, Xu X, Xu J, Wang Q, Zhao Z. Correlation between common lower genital tract microbes and high-risk human papillomavirus infection. Can J Infect Dis Med Microbiol. 2019;2019:9678104. https://doi.org/10.1155/2019/9678104
https://doi.org/10.1155/2019/9678104...
. The association of co-infection between HPV and sexually transmitted infections was compared using cervical samples from women with cervical dysplasia. Significant correlations were found between HPV, sexually transmitted infections, abnormal cervical cytology, HPV status, types of sexually transmitted infections, and the presence of Ureaplasma spp. and M. hominis1010 Alotaibi HJ, Almajhdi FN, Alsaleh AN, Obeid DA, Khayat HH, Muammer TA, et al. Association of sexually transmitted infections and human papillomavirus co-infection with abnormal cervical cytology among women in Saudi Arabia. Saudi J Biol Sci. 2020;27(6):1587-95. https://doi.org/10.1016/j.sjbs.2020.03.021
https://doi.org/10.1016/j.sjbs.2020.03.0...
.

To clarify the importance of Mycoplasma/Ureaplasma infection in the uterine cervix, this study aimed to describe the gynecological clinical data and uterine cervix alterations in patients presenting with vaginal discharge and positive results for Mycoplasma sp. and Ureaplasma spp.

METHODS

An analytical cross-sectional study was conducted following the guidelines outlined in the STROBE statement1111 Elm E, Altman DG, Egger M, Pocock SJ, Gøtzsche PC, Vandenbroucke JP, et al. The strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies. J Clin Epidemiol. 2008;61(4):344-9. https://doi.org/10.1016/j.jclinepi.2007.11.008
https://doi.org/10.1016/j.jclinepi.2007....
. The study took place between 2022 and 2025 in a private health service located in a region of northeastern Brazil with a Human Development Index (HDI) of 0.63.

The inclusion criteria encompassed women aged 18–45 years, with an active sexual life and complaints of non-physiological vaginal discharge. Exclusion criteria comprised menopausal status, genital bleeding during examination, immunosuppression, pregnancy, incomplete medical records, and hysterectomy.

Clinical data were collected by reviewing patient medical records and documented on a study-specific form. Variables included age, menarche age, number of sexual partners, obstetric history, parity, abortions, contraceptive method, urinary tract infections (UTIs), HPV status, characteristics of vaginal discharge (odor and itching), and cultures for Ureaplasma spp. and Mycoplasma sp. Reports related to colposcopic, cytological, and microbiological examinations were also consulted.

Colposcopic findings were categorized as normal, abnormal, or miscellaneous. Cytological findings were classified as unsatisfactory, normal (including normal smears and inflammation/cytolysis), and abnormal (ASC-US, ASC-H, ACG, LIEBG, and LIEAG).

The sample selection involved individuals classified as "Positive for Ureaplasma" and/or "Positive for Mycoplasma" constituting the case group, and those labeled "Negative for Ureaplasma" and "Negative for Mycoplasma" forming the control group. In addition, the presence of Candida sp., Gardnerella, and HPV was also investigated.

Diagnosis of Ureaplasma and Mycoplasma was obtained through microbiological culture using semi-liquid medium A/3 and A/7 specific to these microorganisms. The Sabouraud-Agar culture was utilized for diagnosing fungi and hybrid capture for HPV. The presence of Gardnerella was indicated by the identification of clue cells in the Pap smear and the presence of an odor. Patients with dysuria or hematuria underwent a urine culture and antibiogram to evaluate urinary infection.

Numerical and categorical data from the collected information were tabulated and statistically analyzed using the SPSS (Statistical Package for the Social Sciences) program version 14.0 (SPSS Inc., Chicago, IL, USA). An inductive/inferential analysis was conducted to describe the population and compare the groups. The Student's t-test was employed for quantitative variables with a normal distribution, the Mann-Whitney test was used for non-normally distributed quantitative variables, and the chi-square test was used for variables with n>5, with Fisher's exact test applied when n<5 for qualitative variables. All tests were two-tailed, with a significance level set at 5% (p<0.05) and a confidence interval of 95%.

Ethics

The study adhered to the ethical and legal standards outlined in Resolution 466/12 of the National Health Council and received approval from the research ethics committee of the Fundação Bahiana para Desenvolvimento das Ciências, under CAAE number 6333520.5.0000.5544. Furthermore, the study was conducted by the Declaration of Helsinki and its subsequent revisions.

RESULTS

Initially, 404 patients were enrolled, with 80 subsequently excluded based on pre-established exclusion criteria. Ultimately, 324 women of reproductive age were selected, among whom 58 tested positive for Ureaplasma spp., 10 tested positive for Mycoplasma sp., and 256 had negative cultures for these microorganisms.

The prevalence rates were 3.1% (10/324) for Mycoplasma sp. and 17.9% (58/324) for Ureaplasma spp. Coital activity was more common among individuals aged 10–20 years (81.01%). Most reported having one to five sexual partners, with 67.1% having never been pregnant and 81.8% having no history of abortion. The majority (65.1%) used some form of contraceptive method. Notably, white discharge without odor or itching was prevalent in the sample (56.8%).

In the bivariate analysis, only the presence of HPV was associated with Ureaplasma infection, even after adjusting for confounding variables (OR: 17.42, 95%CI: 3.08–161.2, p=0.004). Regarding Mycoplasma infection, only the use of contraceptives proved to be a protective factor (OR: 0.23, 95%CI: 0.005–0.86, p=0.038). Among the patients studied, 211 (65.1%) were using a contraceptive method. The most used method was hormonal contraceptives (56.4%), in both its oral and injectable versions, followed by the variable of patients not using contraceptive methods (34.9%). The male condom was used for 52 (24.6%) of the patients' partners.

Analysis of co-infections revealed that the presence of Ureaplasma spp. occurred simultaneously with HPV infection in 39.7% (n=23) of cases, showing a significant difference (p=0.001) and a moderate strength of association (contingency coefficient=0.261). However, there is a higher likelihood of patients with non-physiological genital flow being negative for both infections, accounting for 87.2% (n=232) in our sample. Further examination of HPV positivity within groups revealed an uneven distribution (p=0.001), with a higher frequency of oncogenic HPV. In the Ureaplasma-positive group, the frequency of oncogenic HPV was 22.4% (n=13). Other infections did not show differences (Table 1).

Table 1
Description of data on the presence and absence of infections in the group of patients positive or negative for Ureaplasma sp.

Regarding co-infections involving HPV and Mycoplasma, it was noted that most cases tested negative for both HPV and Mycoplasma, comprising 83.1% (n=261) of the total cases. Among those cases that tested positive for Mycoplasma, 60% (n=6) were negative for HPV (OR=1.38). However, this association demonstrated a weak correlation (contingency coefficient=0.104) and lacked statistical significance between the groups (p=0.079). In the case of Fungi and Gardnerella, both exhibited higher percentages of negative cases in both groups, those with and without Mycoplasma. The analysis of the two infections revealed a greater occurrence of patients in the sample but did not indicate simultaneous infection with Mycoplasma (OR Fungi=1.14; OR Gardnerella=1.0). Nevertheless, no differences were identified in the studied groups for both fungi (p=0.235) and Gardnerella (p=0.403) (Table 2).

Table 2
Description of data on the presence and absence of infections in the group of patients positive or negative for Mycoplasma sp.

DISCUSSION

We observed a prevalence of 3.08% for Mycoplasma sp. and 17.9% for Ureaplasma spp. among women reporting non-physiological vaginal discharge. The higher prevalence of Ureaplasma compared with Mycoplasma aligns with previous studies where Ureaplasma spp. values ranged from 4.8 to 48.07%, while Mycoplasma sp. values varied between 0.8 and 23.4%1212 Xie L, Li Q, Dong X, Kong Q, Duan Y, Chen X, et al. Cervical cytopathological findings in Korean women with Chlamydia trachomatis, Mycoplasma hominis, and Ureaplasma urealyticum infections. Mol Clin Oncol. 2021;15(1):132.

13 Leli C, Mencacci A, Latino MA, Clerici P, Rassu M, Perito S, et al. Prevalence of cervical colonization by Ureaplasma parvum, Ureaplasma urealyticum, Mycoplasma hominis and Mycoplasma genitalium in childbearing age women by a commercially available multiplex real-time PCR: an Italian observational multicentre study. J Microbiol Immunol Infect. 2018;51(2):220-5. https://doi.org/10.1016/j.jmii.2017.05.004
https://doi.org/10.1016/j.jmii.2017.05.0...

14 Zdrodowska-Stefanow B, Kłosowska WM, Ostaszewska-Puchalska I, Bułhak-Kozioł V, Kotowicz B. Ureaplasma urealyticum and Mycoplasma hominis infection in women with urogenital diseases. Adv Med Sci. 2006;51:250-3. PMID: 17357319
-1515 Christofolini DM, Leuzzi L, Mafra FA, Rodart I, Kayaki EA, Bianco B, et al. Prevalence of cases of Mycoplasma hominis, Mycoplasma genitalium, Ureaplasma urealyticum and Chlamydia trachomatis in women with no gynecologic complaints. Reprod Med Biol. 2012;11(4):201-5. https://doi.org/10.1007/s12522-012-0132-y
https://doi.org/10.1007/s12522-012-0132-...
.

Contrary to this pattern, some studies reported a higher prevalence of Mycoplasma than Ureaplasma. For instance, Cardillo found 35.89% for Mycoplasma spp. and 25.54% for U. urealyticum1515 Christofolini DM, Leuzzi L, Mafra FA, Rodart I, Kayaki EA, Bianco B, et al. Prevalence of cases of Mycoplasma hominis, Mycoplasma genitalium, Ureaplasma urealyticum and Chlamydia trachomatis in women with no gynecologic complaints. Reprod Med Biol. 2012;11(4):201-5. https://doi.org/10.1007/s12522-012-0132-y
https://doi.org/10.1007/s12522-012-0132-...
, and Christofolini et al.1616 Rar VA, Maksimova TG, Trukhina AV, Rempel' EG, Klimashevskaia NI, Riabova EN, et al. [Level of colonization by Ureaplasma urealyticum of definite biovars in a group of women with different clinical symptoms]. Zh Mikrobiol Epidemiol Immunobiol. 2004;(4):(4):12-7. PMID: 15481912 found 11.3% for M. hominis and 0.94% for U. urealyticum. Such discrepancies in frequency among studies may result from variations in the populations studied and the techniques used to detect microorganisms1212 Xie L, Li Q, Dong X, Kong Q, Duan Y, Chen X, et al. Cervical cytopathological findings in Korean women with Chlamydia trachomatis, Mycoplasma hominis, and Ureaplasma urealyticum infections. Mol Clin Oncol. 2021;15(1):132.,1717 Moridi K, Hemmaty M, Azimian A, Fallah MH, Khaneghahi Abyaneh H, Ghazvini K. Epidemiology of genital infections caused by Mycoplasma hominis, M. genitalium and Ureaplasma urealyticum in Iran; a systematic review and meta-analysis study (2000-2019). BMC Public Health. 2020;20(1):1020. https://doi.org/10.1186/s12889-020-08962-5
https://doi.org/10.1186/s12889-020-08962...
.

Furthermore, we identified an association between Ureaplasma infection and UTIs, consistent with a 2020 meta-analysis by Moridi et al.1717 Moridi K, Hemmaty M, Azimian A, Fallah MH, Khaneghahi Abyaneh H, Ghazvini K. Epidemiology of genital infections caused by Mycoplasma hominis, M. genitalium and Ureaplasma urealyticum in Iran; a systematic review and meta-analysis study (2000-2019). BMC Public Health. 2020;20(1):1020. https://doi.org/10.1186/s12889-020-08962-5
https://doi.org/10.1186/s12889-020-08962...
evaluating the prevalence of M. hominis, Mycoplasma genitalium, and U. urealyticum among Iranian couples. They reported a U. urealyticum prevalence of 17.53% and an M. hominis prevalence of 9.68%, noting higher infection rates in women with symptoms of genito-UTI compared with men with UTI (7.67% vs. 5.88 and 21.04% vs. 12.13%, respectively).

Recent studies propose a potential interference of M. hominis, U. urealyticum, and Ureaplasma parvum with HPV infection, leading to virus persistence. Some studies found a positive relationship between U. urealyticum and HPV, while others reported an overall correlation between Ureaplasma spp. and M. hominis with HPV91010 Alotaibi HJ, Almajhdi FN, Alsaleh AN, Obeid DA, Khayat HH, Muammer TA, et al. Association of sexually transmitted infections and human papillomavirus co-infection with abnormal cervical cytology among women in Saudi Arabia. Saudi J Biol Sci. 2020;27(6):1587-95. https://doi.org/10.1016/j.sjbs.2020.03.021
https://doi.org/10.1016/j.sjbs.2020.03.0...
,1212 Xie L, Li Q, Dong X, Kong Q, Duan Y, Chen X, et al. Cervical cytopathological findings in Korean women with Chlamydia trachomatis, Mycoplasma hominis, and Ureaplasma urealyticum infections. Mol Clin Oncol. 2021;15(1):132.,1414 Zdrodowska-Stefanow B, Kłosowska WM, Ostaszewska-Puchalska I, Bułhak-Kozioł V, Kotowicz B. Ureaplasma urealyticum and Mycoplasma hominis infection in women with urogenital diseases. Adv Med Sci. 2006;51:250-3. PMID: 17357319,1818 Kletzel HH, Rotem R, Barg M, Michaeli J, Reichman O. Ureaplasma urealyticum: the role as a pathogen in women's health, a systematic review. Curr Infect Dis Rep. 2018;20(9):33. https://doi.org/10.1007/s11908-018-0640-y
https://doi.org/10.1007/s11908-018-0640-...
. Our study aligns with these findings, showing a significant relationship between Ureaplasma spp. and the presence of HPV. However, contradicting these results, a 2018 Indonesian study concluded no connection between Ureaplasma and Mycoplasma sp. and HPV88 Feriyawati L, Anggraini DR, Nasution TA. Co-infection of Human Papillomavirus with Mycoplasma Hominis/Ureaplasma Urealyticum among female sex workers in Medan, Indonesia. Open Access Maced J Med Sci. 2019;7(20):3425-8. https://doi.org/10.3889/oamjms.2019.438
https://doi.org/10.3889/oamjms.2019.438...
.

Additionally, a study by Zdrodowska-Stefanow et al.1414 Zdrodowska-Stefanow B, Kłosowska WM, Ostaszewska-Puchalska I, Bułhak-Kozioł V, Kotowicz B. Ureaplasma urealyticum and Mycoplasma hominis infection in women with urogenital diseases. Adv Med Sci. 2006;51:250-3. PMID: 17357319 demonstrated that the risk of HPV infection doubled when a woman was infected with any of the four species of Mycoplasma. In cases of concomitant U. urealyticum infection, the risk of HPV infection was 4.7 times higher. In contrast, another study from 2018 concluded that Ureaplasma spp. and Mycoplasma sp. were not linked to HPV1212 Xie L, Li Q, Dong X, Kong Q, Duan Y, Chen X, et al. Cervical cytopathological findings in Korean women with Chlamydia trachomatis, Mycoplasma hominis, and Ureaplasma urealyticum infections. Mol Clin Oncol. 2021;15(1):132.. The complexity of these relationships underscores the need for further research and genotyping of Ureaplasma spp. species1414 Zdrodowska-Stefanow B, Kłosowska WM, Ostaszewska-Puchalska I, Bułhak-Kozioł V, Kotowicz B. Ureaplasma urealyticum and Mycoplasma hominis infection in women with urogenital diseases. Adv Med Sci. 2006;51:250-3. PMID: 17357319.

Regarding colposcopic findings, we noted a higher prevalence of abnormal results in positive patients, contrasting with a study reporting inconclusive colposcopy outcomes in patients with U. urealyticum and M. hominis1515 Christofolini DM, Leuzzi L, Mafra FA, Rodart I, Kayaki EA, Bianco B, et al. Prevalence of cases of Mycoplasma hominis, Mycoplasma genitalium, Ureaplasma urealyticum and Chlamydia trachomatis in women with no gynecologic complaints. Reprod Med Biol. 2012;11(4):201-5. https://doi.org/10.1007/s12522-012-0132-y
https://doi.org/10.1007/s12522-012-0132-...
. However, concerning cytological findings in our study, no significant association was observed. This aligns with the study by Effiana et al., which found no relationship between M. hominis and altered Pap smear results77 Effiana M, Irsan A, Natalia D, Rahmayanti S, Indarti J, Rachmadi L, et al. Infections of Chlamydia trachomatis and Mycoplasma hominis as risk factors for abnormal cervical cells. Makara J Health Res. 2018;22(1):53-7. https://doi.org/10.7454/msk.v22i1.7965
https://doi.org/10.7454/msk.v22i1.7965...
. Yet, earlier studies demonstrated that U. urealyticum, U. parvum, and M. hominis may increase the risk of cytological changes in the uterine cervix88 Feriyawati L, Anggraini DR, Nasution TA. Co-infection of Human Papillomavirus with Mycoplasma Hominis/Ureaplasma Urealyticum among female sex workers in Medan, Indonesia. Open Access Maced J Med Sci. 2019;7(20):3425-8. https://doi.org/10.3889/oamjms.2019.438
https://doi.org/10.3889/oamjms.2019.438...
,99 Lv P, Zhao F, Xu X, Xu J, Wang Q, Zhao Z. Correlation between common lower genital tract microbes and high-risk human papillomavirus infection. Can J Infect Dis Med Microbiol. 2019;2019:9678104. https://doi.org/10.1155/2019/9678104
https://doi.org/10.1155/2019/9678104...
,1010 Alotaibi HJ, Almajhdi FN, Alsaleh AN, Obeid DA, Khayat HH, Muammer TA, et al. Association of sexually transmitted infections and human papillomavirus co-infection with abnormal cervical cytology among women in Saudi Arabia. Saudi J Biol Sci. 2020;27(6):1587-95. https://doi.org/10.1016/j.sjbs.2020.03.021
https://doi.org/10.1016/j.sjbs.2020.03.0...
.

The influence of the vaginal microbiome on the development of neoplastic lesions in the uterine cervix has been documented in previous studies. While some reported the relevance of Mycoplasma sp. and Ureaplasma spp. in the context of cervical cancer88 Feriyawati L, Anggraini DR, Nasution TA. Co-infection of Human Papillomavirus with Mycoplasma Hominis/Ureaplasma Urealyticum among female sex workers in Medan, Indonesia. Open Access Maced J Med Sci. 2019;7(20):3425-8. https://doi.org/10.3889/oamjms.2019.438
https://doi.org/10.3889/oamjms.2019.438...
,1414 Zdrodowska-Stefanow B, Kłosowska WM, Ostaszewska-Puchalska I, Bułhak-Kozioł V, Kotowicz B. Ureaplasma urealyticum and Mycoplasma hominis infection in women with urogenital diseases. Adv Med Sci. 2006;51:250-3. PMID: 17357319,1616 Rar VA, Maksimova TG, Trukhina AV, Rempel' EG, Klimashevskaia NI, Riabova EN, et al. [Level of colonization by Ureaplasma urealyticum of definite biovars in a group of women with different clinical symptoms]. Zh Mikrobiol Epidemiol Immunobiol. 2004;(4):(4):12-7. PMID: 15481912, others did not find a clear relationship with the onset and progression of CIN88 Feriyawati L, Anggraini DR, Nasution TA. Co-infection of Human Papillomavirus with Mycoplasma Hominis/Ureaplasma Urealyticum among female sex workers in Medan, Indonesia. Open Access Maced J Med Sci. 2019;7(20):3425-8. https://doi.org/10.3889/oamjms.2019.438
https://doi.org/10.3889/oamjms.2019.438...
,1717 Moridi K, Hemmaty M, Azimian A, Fallah MH, Khaneghahi Abyaneh H, Ghazvini K. Epidemiology of genital infections caused by Mycoplasma hominis, M. genitalium and Ureaplasma urealyticum in Iran; a systematic review and meta-analysis study (2000-2019). BMC Public Health. 2020;20(1):1020. https://doi.org/10.1186/s12889-020-08962-5
https://doi.org/10.1186/s12889-020-08962...
. The varied findings emphasize the intricacies of these interactions and the need for future investigation in this field.

CONCLUSION

Ureaplasma spp. was more prevalent and associated with UTI and HPV, whereas Mycoplasma sp. was linked to reduced contraceptive use. In addition, abnormal colposcopic findings were more prevalent in patients positive for Ureaplasma spp. and/or Mycoplasma sp.

However, more robust studies are needed to explore the interrelationship of Ureaplasma and Mycoplasma with HPV and preneoplastic lesions.

  • Funding: none.

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Publication Dates

  • Publication in this collection
    19 July 2024
  • Date of issue
    2024

History

  • Received
    08 Jan 2024
  • Accepted
    02 Mar 2024
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