Keywords
Gonorrhoea, chlamydia, MSM, STI screening, PrEP, antimicrobial resistance
This article is included in the Pathogens gateway.
This article is included in the Antimicrobial Resistance collection.
Gonorrhoea, chlamydia, MSM, STI screening, PrEP, antimicrobial resistance
The various edits kindly suggested by the reviewers have been made. In particular we have included the concept of reverse causality in the discussion. We have also added the Callander et al., 2018, and Unemo et al. 2017, references as suggested.
To read any peer review reports and author responses for this article, follow the "read" links in the Open Peer Review table.
There have been large increases in antimicrobial resistance in a number of sexual transmitted infections (STI) in the recent past. There are serious concerns that both Neisseria gonorrhoeae (Ng) and Mycoplasma genitalium may become untreatable in the not too distant future1,2. For both these bacteria as well as macrolide resistance in Treponema pallidum, AMR has frequently first emerged in populations with a combination of high antimicrobial consumption and dense sexual networks3,4. HIV preexposure prophylaxis (PrEP) cohorts have dense sexual networks and the intense screening STI typically practiced translates into high antimicrobial exposures5,6. Three-monthly, 3-site Ng/Chlamydia trachomatis (Ct) screening for example translates into macrolide exposures of around 4400 standard units/1000 population/year, which is many times higher than levels associated with the induction of macrolide resistance in a range of bacteria including T. pallidum and Ng7,8. These findings have led a number of authors to review the evidence to support Ng/Ct screening in men who have sex with men (MSM) PrEP populations.
The US Preventive Task Force, concluded that there is insufficient evidence to advocate for or against screening for Ng in men, including MSM9. In a systematic review conducted to inform these guidelines, the authors found no randomised, controlled trials or controlled observational studies that assessed the utility of NG screening in men10. In a systematic review of observational studies, we found no evidence that even the most intense Ng/Ct screening such as screening 100% of PrEP cohorts every 3 months was associated with a decline in the prevalence of these infections11. Others have argued that this lack of an effect was because the PrEP recipients were having sex with (and being reinfected by) people who were not being screened12. This generates the hypothesis that we test in this paper that populations where a high proportion of MSM are screened for Ng/Ct will have a lower prevalence of these infections than populations with less screening. We test this hypothesis in European countries because the intensity of STI screening varies widely here and data for screening and prevalence estimates were available.
STI screening intensity. Country level STI screening prevalence were obtained from the European MSM Internet Survey (EMIS), which was an internet-based survey of over 160 000 MSM from 38 countries living in Europe13. The survey was conducted between June and August 2010. In the section where participants were asked about STI testing in the past 12 months, they were asked 3 questions that are relevant to Ng/Ct screening: Did you provide a urine sample for STI screening? Was urethral swab inserted into your penis for STI screening? Was a swab inserted into your anus for STI screening? EMIS combined the results from the first two questions into one variable reporting the proportion of respondents reporting ‘urethral STI screening’ – via either urine or urethral swab. The third question provided the proportion with ‘anal STI screening’. Typically, these urethral and anal samples are tested for Ng/Ct.
Ng/Ct prevalence/incidence.
1. National Ng and Ct incidence estimates for men in 2010 were taken from European Centre for Disease Prevention and Control (ECDC) figures14. These incidence estimates are based on national surveillance systems. The ECDC does not provide incidence estimates separately for MSM and thus we used the estimates for all men. MSM do however constitute a high proportion of diagnoses in all men14.
2. Systematic review of Ng/Ct prevalence in MSM
Ng/Ct prevalence estimates for MSM were taken from a published literature review of pharyngeal and anorectal Ng and Ct prevalence estimates in MSM (and other populations)15. All studies listed in PubMed reporting prevalence of extragenital Ng and Ct in MSM up to 1 December 2015 were included. A total of 53 studies were included from countries around the world. Of these 18 were from 6 European countries (Table 1). For the four European countries with more than one study we selected the study reporting prevalence estimates from 2010 or as soon after this year as possible. All selected studies were prevalence estimates established by Nucleic Acid Amplification Testing of MSM clients attending STI clinics.
Country | Screening Prevalence in 2010 (%) | STI Incidence in men 2010 (cases/100 000/ year) | STI Prevalence in MSM attending STI clinics (%) | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
N. gonorrhoeae | C. trachomatis | Reference | |||||||||
Urethral | Anal | Ng | Ct | Urethral | Rectal | Pharyngeal | Urethral | Rectal | Pharyngeal | ||
Bulgaria | 39.2 | 10.0 | 2.7 | .5 | |||||||
Cyprus | 59.9 | 17.3 | .5 | ||||||||
Czech Rep. | 67.2 | 19.6 | 10.4 | ||||||||
Germany | 56.6 | 20.6 | 1.9 | 4.6 | 5.5 | 3.4 | 8 | 1.5 | doi.org/10.1136/ sextrans-2012-050929 | ||
Denmark | 71 | 40.0 | 13.2 | 383.7 | 2.6 | 2.6 | 0 | doi.org/10.1136/ sti.73.6.493 | |||
Estonia | 58.4 | 14.2 | 6.5 | 40.5 | |||||||
Greece | 41.4 | 11.8 | 4.6 | 1.4 | |||||||
Spain | 52 | 15.2 | 9.5 | doi.org/10.1177/095646 2413486455 | |||||||
Finland | 89 | 37.9 | 7.2 | 201 | |||||||
Ireland | 91 | 67.2 | 20.5 | 104.7 | 0 | 4.1 | 3.3 | 1.7 | 6.6 | .8 | |
Lithuania | 63.6 | 13.3 | 18.3 | 15.7 | |||||||
Luxembourg | 41.9 | 9.1 | 1.2 | 0 | |||||||
Latvia | 64 | 14.9 | 26 | 33.8 | |||||||
Malta | 85 | 70.6 | 20.9 | 37.5 | |||||||
Netherlands | 87 | 63.0 | 3.4 | 5.5 | 3.9 | 4.3 | 10.1 | 1.7 | doi.org/10.1177/095646 2414521165 | ||
Norway | 84 | 47.2 | 15 | 353.8 | |||||||
Poland | 37 | 8.9 | 1.5 | 2.2 | |||||||
Portugal | 68.9 | 9.5 | 1.5 | ||||||||
Romania | 45 | 6.5 | 4.1 | .7 | |||||||
Sweden | 92 | 59.0 | 13.3 | 333.3 | |||||||
Slovenia | 50 | 29.0 | 4.1 | ||||||||
Slovakia | 60 | 16.9 | 3.6 | ||||||||
United Kingdom | 94 | 69.7 | 42.2 | 4.7 | 9 | 5.2 | 5.3 | 6.5 | 2.2 | doi.org/10.1258/ ijsa.2012.011378 |
In all analyses the correlation between screening intensity and Ng/Ct prevalence/incidence was tested using Spearman’s correlation. The statistical analyses were performed in STATA 13.
The proportion of respondents in each of the 23 countries reporting anal STI screening varied widely from 6.5 to 70.6% to (median 17.3%, IQR 11.8–47.1; Table 1). Likewise, there were large variations in the proportion reporting genital STI screening (range 37.0 to 94.0%, median 63.6 IQR 50.0–85.0%). There was a strong correlation between the proportions reporting anal and genital STI screening (rho=0.81; p<0.0001).
For 19 countries with data, the incidence of Ng for men in 2010 ranged between 1.2 and 42.2 cases per 100 000 men per year (median 7.2, IQR 3.6–18.3). There was an even wider distribution in estimated Ct incidence for the 18 countries with data (range 0 to 383.7, median 24.8, IQR 1.3–201).
There was less variance in the prevalence estimates of Ng and Ct in MSM (Table 1). Rectal Ng: median 5.5%, IQR 4.6–7; pharyngeal Ng: median 5.4%, IQR 3.9–6.5; urethral Ng: median 1.9%, IQR 1–3.4. Rectal Ct: median 7.3%, IQR 6.5–10.0; pharyngeal Ct: median 1.3, IQR 0.8–1.7; urethral Ct: median 3, IQR 2.5–5.3; Table 1.
The intensity of both anal and genital screening was found to be positively associated with country level Ng incidence rates (rho 0.74; p=0.0004; rho=0.73; p=0.0004, respectively) and Ct incidence rates (rho 0.71; p=0.001; rho=0.78; p=0.0001, respectively; Figure 1).
Country designations: AT, Austria; BE, Belgium; CZ, Czech Republic; DE, Germany; DK, Denmark; EL, Greece; ES, Spain; FI, Finland; FR, France; HR, Croatia; HU, Hungary; IE, Ireland; IT, Italy; LU, Luxembourg; LV, Latvia; NL, the Netherlands; PT, Portugal; SE, Sweden; SI, Slovenia; SK, Slovakia; UK, United Kingdom.
No associations were found between anal or genital screening intensity and Ng or Ct prevalence in clinic populations (Table 2).
All P-values were greater than 0.1.
STI prevalence | Anal testing | Urethral testing |
---|---|---|
N. gonorrhoeae | ||
Pharyngeal | -0.70 | -0.70 |
Rectal | 0.40 | 0.40 |
Urethral | 0.40 | 0.40 |
C. trachomatis | ||
Pharyngeal | 0.50 | 0.50 |
Rectal | -0.20 | -0.20 |
Urethral | 0.30 | 0.30 |
The prevalence of Ng and Ct has been increasing in MSM populations in a number of countries16,17. Intensified screening in MSM would be one way to reduce the incidence and prevalence of these infections. In this analysis, we did not find evidence of a negative correlation between the intensity of STI screening in MSM and the incidence/prevalence of Ng/Ct. Instead, we found evidence of a positive association between the intensity of screening in MSM and the estimated incidence rate for men. This positive association may be explained by the fact the incidence estimates are influenced by the intensity of screening – countries with more intensive screening programmes would be expected to diagnose more asymptomatic Ng and Ct infections which lead to higher incidence estimates. This could also be considered a form of reverse causation: the higher prevalence of Ng/Ct is the cause rather than the effect of more intensive screening.
To deal with this bias and the fact that the ECDC Ng/Ct incidence estimates do not provide incidence estimates for MSM, we also evaluated the association between screening intensity and Ng/Ct prevalence in MSM attending STI clinics. Here we found no evidence of an association between screening intensity and prevalence.
These findings are open to a number of interpretations. Firstly, screening intensity may be negatively associated with Ng/Ct rates but we missed this association due to methodological issues. Our estimates of screening intensity were based on a single cross-sectional source. Although EMIS had a large sample size and the accuracy of its prevalence estimates for other variables has been validated in other studies13,18, these screening estimates may be inaccurate and may have changed over time. As noted above, the STI incidence estimates were for all men and were likely strongly influenced by practices such as screening intensity, access to health care and accuracy of national case reporting. The STI prevalence estimates in MSM were all taken from men attending STI clinics and thus are likely higher than general populations of MSM. The study design of each of the 6 studies contributing Ng and CT prevalence estimates differed somewhat further limiting the extent to which correlations could be assessed between screening intensity and prevalence across these studies. We could find no comparable data on the prevalence of Ng or Ct in general MSM populations.
Alternatively, screening intensity as measured may not be associated with reduced Ng/Ct rates in MSM. Randomized controlled trials of the efficacy of screening for Ct in women on the prevalence of Ct have produced equivocal results19–22. Although no RCTs have been conducted in MSM, a systematic review of observational studies revealed that Ng/Ct screening, even when conducted at 3-sites every 3-months, was not associated with reductions in the prevalence of Ng or Ct11. If we consider Ng, numerous aspects of the way it circulates in contemporaneous populations of MSM may explain why screening has little or no effect on prevalence. Symptomatic disease is thought to typically occur soon (2–21 days) after infection and if symptoms do not develop the infection (particularly in the pharynx and rectum) tends to persist in a low abundance, low infectious state for up to 6 months23. Highly exposed individuals develop a type-specific immunity, but this immunity is largely ineffective in low exposure individuals23,24. As a result, the vast majority of Ng infections are asymptomatic and self-limiting in MSM PrEP populations23,25. Similar considerations apply to Ct. In the case of Ct there is however better evidence that treatment of Ct results in “arrested immunity” and thereby paradoxically increases the probability of reinfection26,27. If screening results in ‘arrested immunity’ it may paradoxically increase Ng/Ct prevalence/symptomatic disease. The sexual networks of PrEP recipients are very dense (up to a mean of 18 partners per 3 months28) and this is responsible for generating the high prevalences of Ng and Ct5. Removing individuals piecemeal from this network for screening and treating has no effect on the underlying determinant of high prevalence. As a result, the probability of reinfection and prevalence remaining high.
Mathematical models of Ng and Ct transmission in European countries like Belgium have thus found that the sexual network of MSM was so dense that current levels of Ng screening were having little to no effects on Ng prevalence29. In contrast, a modelling study from the United States found that 6-monthly screening of an expanded number of PrEP recipients could avert 40% of Ng and Ct infections30. This study did not however model pharyngeal transmission of Ng (which plays a major role in transmission) and did not model the impact of immunity or Ng’s ability to adapt to antibiotic pressure. These omissions may explain the discrepancy between its prediction, and our and the earlier systematic review of observational studies11.
Based on the findings of this study and those reviewed here we conclude that we can still not exclude the possibility that intense screening (at least 3-site, 3-monthly) may have a small to moderate influence on Ng/Ct prevalence in MSM. Randomized controlled trials are urgently required to test this hypothesis. In the interim, given the mounting evidence that Ng/Ct screening does not have a large effect on prevalence but does result in high levels of antimicrobial exposure, consideration should be given to reducing the intensity or stopping Ng/Ct screening in MSM in a phased and controlled manner that allows a detailed evaluation of the risks and benefits of screening.
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Is the work clearly and accurately presented and does it cite the current literature?
Yes
Is the study design appropriate and is the work technically sound?
Partly
Are sufficient details of methods and analysis provided to allow replication by others?
Yes
If applicable, is the statistical analysis and its interpretation appropriate?
Partly
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Mathematical modelling of infectious diseases
Is the work clearly and accurately presented and does it cite the current literature?
Yes
Is the study design appropriate and is the work technically sound?
Yes
Are sufficient details of methods and analysis provided to allow replication by others?
Yes
If applicable, is the statistical analysis and its interpretation appropriate?
Yes
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Yes
Competing Interests: No competing interests were disclosed.
Is the work clearly and accurately presented and does it cite the current literature?
Yes
Is the study design appropriate and is the work technically sound?
Yes
Are sufficient details of methods and analysis provided to allow replication by others?
Yes
If applicable, is the statistical analysis and its interpretation appropriate?
Yes
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Yes
References
1. European Centre for Disease Prevention and Control: Sexually transmitted infections in Europe 1990–2010. ECDC. 2012. Publisher Full Text | Reference SourceCompeting Interests: No competing interests were disclosed.
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Version 1 06 Feb 19 |
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