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Syphilis epidemiology in Norway, 1992-2008: resurgence among men who have sex with men
© Jakopanec et al; licensee BioMed Central Ltd. 2010
Received: 29 December 2009
Accepted: 29 April 2010
Published: 29 April 2010
In recent years, the number of syphilis cases has stabilised in many countries of Western Europe, however several countries have reported increases among men who have sex with men (MSM). The aim of this article was to describe the epidemiology of early syphilis in Norway in 1992-2008.
Cases of early syphilis and congenital syphilis reported to the Norwegian Surveillance System for Communicable Diseases (MSIS) 1992-2008 were described by route of transmission, gender, age, birthplace, stage of disease, HIV co-infection, source partner and place of infection.
The incidence of reported syphilis ranged from 0.05 (1992) to 1.50 (2002) per 100 000 person-years. Of 562 cases reported to MSIS during the study period, 62% were men infected by another man. The proportion of those, infected homosexually increased from 0 (1992-1994) to 77% (2008). Most of them were Norwegians (83%). The proportion of HIV co-infection among homosexually infected increased over time and reached 39% in 2008. The majority reported being infected by a casual partner (73%) and in the municipality of Oslo (72%). Of 152 heterosexually infected men 64% were Norwegians; 51% were infected by casual contacts and 20% by commercial sex workers; 73% were infected abroad. Among 56 women, 57% were Norwegians, 57% were infected by a steady partner and 40% were infected abroad. Almost half (46%) were diagnosed in the early latent stage. Four cases had congenital syphilis, two of whom were adopted from abroad.
Syphilis is rare in Norway, but MSM represent almost two thirds of cases. The increase of HIV co-infected cases among MSM may enhance transmission of both infections. We recommend sexually active MSM to be tested for syphilis 2-4 times a year. Due to its variable clinical course, syphilis might be difficult to recognise at an early stage among women in a low-prevalence population. We estimate current practice of prenatal screening in Norway as sufficient.
Following increases in the early 2000s in Western European countries, the number of reported syphilis cases has recently stabilised; however many countries reported a high proportion of homosexually acquired syphilis (France, Denmark, Ireland, Germany, UK, Sweden, Netherlands) . Increases among men who have sex with men (MSM) have been reported worldwide  and a significant proportion of them have been found to be co-infected with HIV [3, 4].
Infectious stages of syphilis are primary, denoted by a painless ulcer in about one third of patients, and secondary, with diverse symptoms. Patients in the latent stage are seemingly unaffected, but about 25% may experience relapses to secondary syphilis during the early latent stage (i.e. less than a year since infection) [4, 5]. Vertical transmission may result in congenital syphilis, difficult to recognise in seemingly asymptomatic newborns . Untreated, syphilis may result in death and serious disability [4, 5], however effective penicillin-based treatment is inexpensive. Testing and treatment are free of charge in Norway.
Serological tests for syphilis lack sensitivity and though some may be helpful in assessing the stage of infection, they are unreliable . In determining the stage, particularly in asymptomatic patients, clinicians thus rely on previously documented syphilis tests, anamnesis (i.e. most likely time of exposure, data from contact tracing, known previous treatment) and clinical evaluation. Uncertain stage in asymptomatic patients with unknown duration of infection is an important limitation of early syphilis (i.e. primary, secondary and early latent syphilis) surveillance.
Using data from the Norwegian Surveillance System for Communicable Diseases (MSIS), we describe the epidemiology of early syphilis in Norway from 1992-2008.
Under the Infectious Disease Control Act, syphilis is a mandatory notifiable disease, therefore all clinicians and laboratories in Norway must notify all cases of newly diagnosed syphilis anonymously to the MSIS, based at the Norwegian Institute of Public Health (NIPH). Contact tracing and notification, mandatory by the same act, is the responsibility of the clinicians. Previously mandatory screening of pregnant women in Norway became optional in 1995; however, virtually all pregnant women are still tested. If a patient has a positive syphilis test, screening for other sexually transmitted infections (STIs) is recommended.
Upon a positive syphilis test, all 22 local laboratories in Norway send their notification to both NIPH and the clinician involved. Both of these notification forms carry the same unique non-identifying number for an individual patient. Having received notification from the laboratory, clinicians fill out the corresponding clinical report on the stage of the disease, patient's demographic data, symptoms, co-existing STIs, risk behaviour (including most likely transmission route and time of exposure) and their source partner, and send it to the NIPH. There, only one co-existing STI can be entered into the MSIS database. If the patient is reported to have an HIV infection, HIV is always entered.
At NIPH, only newly recognised cases with early syphilis, defined as laboratory confirmed, primary, secondary or early latent syphilis (less than a year since infection) are entered into the MSIS database. The reports on a single patient from laboratories and clinicians are merged using the unique non-identifying number. Every reported case is individually evaluated at NIPH and clinicians can be contacted if the stage of syphilis is unclear or if they failed to report on a case, notified by laboratory only.
Selected characteristics of sexually infected cases with early syphilis reported to the Norwegian surveillance system for communicable diseases, absolute numbers, (N = 558), 1992-2008.
n = 56 (%)
n = 152 (%)
n = 350 (%)
Median age in years
≥ 45 years
Reason for being in Norway
First generation immigrant/adopted
Other, including permanent residents
Indications for testing
Routine testing of an immigrant
No specific reason/other
Median duration of symptoms in days***
Stage of early syphilis
Other reported STI****
Commercial sex worker
Place of infection
- In Russia
- In Oslo
General practitioner, private specialist
The data on all cases of early or congenital syphilis were obtained from MSIS. The size of population used for calculating incidence rate for each year was obtained from Statistics Norway  and was about 4.5 million. We used Stata 9.2 software (STATA Corp., TX, USA) for the analysis. Simple linear regression analysis was used to estimate trends over time. Given that the data between subsequent years may be correlated and the variability between the years may not be constant over time, the regression coefficients and their 95% confidence intervals (CI) were calculated using the Newey-West procedure. Bivariate comparisons between groups were performed using Pearson's chi squared test. Due to different mode of transmission, cases of congenital syphilis were described separately.
From 1992 to 2008, 562 cases of syphilis diagnosed in Norway were reported to MSIS, including four congenital cases.
Men, infected homosexually
Men, homosexually infected with syphilis, who were also HIV positive, were more likely to be residents of Oslo (p = 0.001), being diagnosed with syphilis later in the course of disease (primary vs. secondary or early latent, p = 0.006) and in a hospital (p < 0.001) than HIV negative, but they did not differ by age, birthplace, indications for syphilis testing, source partner and place of infection.
Men, infected heterosexually
During the study period, 152 men were infected heterosexually. No obvious time trend was observed (p for trend = 0.158). More than half (57%) were older than 34 years. Most (64%) were Norwegian, with a notable proportion reporting a birthplace in Asia (16%). The majority (80%) reported symptoms and their infection was mostly discovered in the primary stage. Two men were HIV positive. Casual contacts and commercial sex workers (CSW) were the source of infection in 71%. Most acquired their infection abroad (73%) (Table 1); predominantly in Russia (13%), Pakistan (10%), Brazil (7%) and Thailand (6%). Most Norwegians were infected abroad, mainly in other countries of Europe (36%), Asia (18%) and South and Mid America (16%). Immigrants were mainly infected during travels back to their continent of birth.
Among 56 women reported to be infected with syphilis from 1992-2008, 68% were younger than 35 years. Most of the cases were Norwegian (57%) and 55% acquired their infection in Norway. However, out of 31 infected in Norway, 14 reported their male partner had been infected abroad. Contact tracing was the predominant cause for testing in women (30%), followed by symptoms (27%) and pregnancy (23%). Almost half (46%) of all cases were discovered in the early latent stage of disease. STI co-infections were rare (Table 1). Women reported a steady partner as the source of infection in 57%.
Children with congenital syphilis
The age of the four patients with congenital syphilis at the time of diagnosis ranged from one to five years, one of them was a boy. Two of these children were adopted from abroad. The biological mother of one child was born in Norway, but acquired her infection abroad, while the mother of the other child was infected in Norway and tested positive with her second pregnancy in 2003, when the affected child was five years old.
Syphilis is a rare disease in Norway. However, since 1999, there has been a resurgence among MSM, disproportionately affecting HIV positive men. The epidemic among MSM is mainly concentrated in the capital Oslo. Up to 73% of heterosexual men and 41% of women reported being infected abroad. Compared to men, women seem to be more frequently diagnosed as late as the early latent stage and are diagnosed predominantly by contact tracing. Men infected heterosexually reported being infected by casual partner or a CSW in 71% of cases, as opposed to women, who appear to be mostly infected by their steady partners.
One of the strengths of our study is a probable high coverage of diagnosed patients in MSIS [9, 10] due to double notifications from both laboratories and clinicians and a long tradition of reporting among the latter. A large set of variables on each patient is available; allowing for demographic and behavioural insight.
Our study is subject to several limitations. Due to the clinical course of this disease, some infected may stay undiagnosed. Others, discovered by routine testing and possibly asymptomatic, need to be evaluated by a clinician for stage. We cannot completely exclude, however, that some patients, reported as "early latent syphilis" may have been infected longer than a year. This would particularly affect data on women in our study. Contrary to this, every year, about hundred cases are only lab-reported. Clinicians are aware we only include new cases of early syphilis in the database, as we publish this information in a yearly national MSIS report . Contrary to our experience with gonorrhoea with high reporting from both laboratories and clinicians , clinicians may opt out from sending in their part of the reporting form for syphilis, if the person has been infected for more than a year or has been known to have a positive test from before. If the stage is unknown or in cases, only reported by the laboratories, internal evaluation at NIPH includes the testing sites (asylum centres), the immigrant status and unknown date of exposure of most of these cases, to determine the likelihood of late syphilis, however it may happen there are some missed early cases among them. Clinicians may also be contacted by NIPH to verify information. Furthermore, behaviour data is subject to response and recall bias. Data in a few variables are frequently missing, including co-infection data. We believe, however, that reporting is reliable on HIV co-infection. Capacity for entering several co-infections at a time should be improved in MSIS. The fact that hardly any cases were reported as homosexually acquired until 1999 cannot be explained by changes in the notification system or improved sexual behaviour reporting as in comparison, 10-42 cases of homosexually acquired gonorrhoea per year were reported in the same time period and in the same surveillance system .
Among European countries with various systems of syphilis surveillance, the highest incidence rates for early syphilis in 2007 (per 100 000 person-years) were reported from: the UK (4.4, primary and secondary stages only), Czech Republic (4.0), Sweden (2.6, less than two yeas since infection), Germany (2.5) [1, 13]. At NIPH, no total counts of reported syphilis cases are kept, but late latent probably represent a majority (more than 50%). In the period from 2002-2007, late cases represented 50-73% of all reported cases in Czech Republic, 35-51% in Germany and 24-50% in Slovenia .
Compared to infected women in our study, heterosexual men were older, more likely to be diagnosed in a primary stage and to report symptoms, and less likely to be diagnosed through contact tracing. Similar findings were reported from a London-based study . Men are more likely than women to report having been infected abroad, which resembles the situation in Sweden, however women in Sweden acquired their infection abroad more frequently and had a higher median age (33 years) than women in Norway . A prevalence of HIV co-infection among heterosexuals, much higher than in our study (from 6-13%), has been reported from London and France [14, 15]. Compared to London with 12% of heterosexual men reporting being clients of CSW , a higher proportion of men in Norway used commercial sex services, however they did so mostly abroad.
Similar to many other European countries , the epidemics among MSM in Scandinavia are mainly concentrated in men above 30 in metropolitan areas [13, 17]. A high, but stable proportion of syphilis and HIV co-infections among MSM in several countries has been ascribed to serosorting, practice of oral sex and compromised immune system [14, 17, 18]. While information on co-infection is not always available, others have also reported a simultaneous increase of HIV and syphilis among MSM from 2000-2005 [19, 20]. HIV positive MSM were also less likely to be in the primary stage of syphilis when diagnosed as reported from London Enhanced Syphilis Surveillance programme (2001-2004) .
The increase of pharyngeal, frequently asymptomatic STIs among MSM has been associated with the practice of unprotected oral sex, which is perceived as low risk for HIV transmission [12, 18, 21]. This might explain the differences in syphilis stage at the time of diagnosis between homosexually and heterosexually infected men, as initial painless lesion ("chancre"), appearing in the oropharynx (as well as the rectum) may pass unnoticed among MSM. Differences in syphilis stage between serodiscordant homosexual men may be explained by potentially asymptomatic disease among the HIV positive  and a possible overlap of the primary and secondary stage . Genital ulcers, including syphilitic chancre, can facilitate HIV acquisition and transmission , which may, together with frequent partner exchange, explain a simultaneous increase of both infections among MSM.
Compared to official population data, foreign-born people are over-represented among syphilis cases in Norway . The reason could be opportunistic testing of immigrants originating from countries with higher syphilis prevalence. Occasional increases of syphilis cases, linked to CSW, refugees/asylum seekers, immigrants from the eastern Europe, especially Russia, or travelling to these regions, were reported by several countries (Czech Republic, Slovenia, Finland, UK) [24–26]. In Norway, only sporadic syphilis cases related to Russia with limited secondary transmission were noted . It needs to be emphasized, however, that sexual contact abroad is a key risk factor for heterosexually-acquired syphilis in Norway.
Whether or not a proportion of reported cases with late syphilis represents a public health problem we should further focus on in Norway, is debatable. As noted, the majority of these cases are immigrants from countries with high syphilis prevalence and were infected in countries of their origin many years ago. On the other hand, mild, unspecific and painless syphilis symptoms make it difficult to diagnose the disease early, especially in women or MSM, who may not notice initial lesions in difficult-to-visualise areas . The rarity of the disease in Norway makes it a diagnostic challenge. It is therefore important to focus diagnostic efforts on specific population groups such as MSM and immigrants and, to find women cases, to conduct thorough contact tracing.
An evaluation of the recommendations for yearly syphilis testing of HIV positive MSM in the Netherlands revealed up to third of infections were asymptomatic and only discovered by screening . Clinical care of HIV positive MSM, such as CD4 T cell count or HIV viral load, can conveniently include syphilis testing . We recommend that the epidemic of syphilis among MSM, concentrated in Oslo, be tackled by enhanced syphilis testing for sexually active MSM, whenever they present at the STI clinic or at a general practitioner, ideally 2-4 times a year .
The evidence for cost-effectiveness of prenatal screening policy in a very low-risk population (< 1%) seems to be contradictory  and universal screening does not prevent mothers from being infected later in the pregnancy. We estimate current recommendations and practice in Norway as sufficient.
In summary, syphilis in Norway is mainly transmitted among MSM in Oslo. Increasing co-infection with HIV in this group underlines the need for enhanced screening and prevention programmes. We recommend sexually active MSM to be tested 2-4 times a year. Among heterosexuals, coincidental import from other countries has been observed, but further spread in Norway was limited.
We thank Oliver Kacelnik from NIPH for language revision.
- ESSTI: Sexually Transmitted Infections in Europe. Surveillance Annual Report No. 3 2008 [EuropeanSurveillance of Sexually Transmitted Infections network]. Health Protection Agency; 3 [updated. 2008, [http://ec.europa.eu/health/ph_projects/2004/action2/action2_2004_08_en.htm] ; citedGoogle Scholar
- Karp G, Schlaeffer F, Jotkowitz A, Riesenberg K: Syphilis and HIV co-infection. Eur J Intern Med. 2009, 20: 9-13. 10.1016/j.ejim.2008.04.002.View ArticlePubMedGoogle Scholar
- Diaz A, Junquera ML, Esteban V, Martinez B, Pueyo I, Suarez J, Urena JM, Varela JA, Vall M, del RJ, Sanz I, Belda J, Boronat J, Gomez P, Gual F, Colomo C, Lopez de MJ, Balaguer J, Landa MC, Lezaun ME, Camara MC, Fernandez E, Bru FJ, Alastrue I, Ordonana JR, de AC, Azpiri MA, Gomez L, Trullen J, Diez M: HIV/STI co-infection among men who have sex with men in Spain. Euro Surveill. 2009, 14-Google Scholar
- Zetola NM, Engelman J, Jensen TP, Klausner JD: Syphilis in the United States: an update for clinicians with an emphasis on HIV coinfection. Mayo Clin Proc. 2007, 82: 1091-1102. 10.4065/82.9.1091.View ArticlePubMedGoogle Scholar
- American Public Health Association: Control of communicable diseases manual. 2004, Washington: The AssociationGoogle Scholar
- Shafii T, Radolf JD, Sanchez PJ, Schulz KF, Murphy FK: Congenital Syphilis. Sexually Transmitted Diseases. Edited by: Holmes KK, Sparling PF, Stamm EW, Piot P, Wasserheit JN, Corey L, et al. 2008, The McGraw-Hill Companies, Inc., 1577-1612.Google Scholar
- McMillan A, Young H: Qualitative and quantitative aspects of the serological diagnosis of early syphilis. Int J STD AIDS. 2008, 19: 620-624. 10.1258/ijsa.2008.008103.View ArticlePubMedGoogle Scholar
- Statistics Norway [Statistisk sentralbyrå]. [updated. 2009, [http://www.ssb.no] Nov 24; cited
- Aavitsland P, Nilsen Ø: A new anonymous case reporting system for sexually transmitted diseases in Norway. Norsk Epidemiologi. 1995, 5: 39-43.Google Scholar
- Lowndes CM, Fenton KA: Surveillance systems for STIs in the European Union: facing a changing epidemiology. Sex Transm Infect. 2004, 80: 264-271. 10.1136/sti.2004.010389.View ArticlePubMedPubMed CentralGoogle Scholar
- Nilsen O, Blystad H: Gonoré og syfilis i Norge 2008. 13-5-2009. Norwegian Institute of Public Health. MSIS-rapport. 4-3-2010.Google Scholar
- Jakopanec I, Borgen K, Aavitsland P: The epidemiology of gonorrhoea in Norway, 1993-2007: past victories, future challenges. BMC Infect Dis. 2009, 9: 33-10.1186/1471-2334-9-33.View ArticlePubMedPubMed CentralGoogle Scholar
- Velicko I, Arneborn M, Blaxhult A: Syphilis epidemiology in Sweden: re-emergence since 2000 primarily due to spread among men who have sex with men. Euro Surveill. 2008, 13-Google Scholar
- Righarts AA, Simms I, Wallace L, Solomou M, Fenton KA: Syphilis surveillance and epidemiology in the United Kingdom. Euro Surveill. 2004, 9: 21-25.PubMedGoogle Scholar
- Couturier E, Michel A, Janier M, Dupin N, Semaille C: Syphilis surveillance in France, 2000-2003. Euro Surveill. 2004, 9: 8-10.PubMedGoogle Scholar
- Nicoll A, Hamers FF: Are trends in HIV, gonorrhoea, and syphilis worsening in western Europe?. BMJ. 2002, 324: 1324-1327. 10.1136/bmj.324.7349.1324.View ArticlePubMedPubMed CentralGoogle Scholar
- Cowan S: Syphilis in Denmark-Outbreak among MSM in Copenhagen, 2003-2004. Euro Surveill. 2004, 9: 25-27.PubMedGoogle Scholar
- Marcus U, Bremer V, Hamouda O, Kramer MH, Freiwald M, Jessen H, Rausch M, Reinhardt B, Rothaar A, Schmidt W, Zimmer Y: Understanding recent increases in the incidence of sexually transmitted infections in men having sex with men: changes in risk behavior from risk avoidance to risk reduction. Sex Transm Dis. 2006, 33: 11-17. 10.1097/01.olq.0000187224.10428.31.View ArticlePubMedGoogle Scholar
- Branger J, Meer van der JT, van Ketel RJ, Jurriaans S, Prins JM: High incidence of asymptomatic syphilis in HIV-infected MSM justifies routine screening. Sex Transm Dis. 2009, 36: 84-85. 10.1097/OLQ.0b013e318186debb.View ArticlePubMedGoogle Scholar
- Sullivan PS, Hamouda O, Delpech V, Geduld JE, Prejean J, Semaille C, Kaldor J, Folch C, Op de CE, Marcus U, Hughes G, Archibald CP, Cazein F, McDonald A, Casabona J, van SA, Fenton KA: Reemergence of the HIV epidemic among men who have sex with men in North America, Western Europe, and Australia, 1996-2005. Ann Epidemiol. 2009, 19: 423-431. 10.1016/j.annepidem.2009.03.004.View ArticlePubMedGoogle Scholar
- Emerson CR, Lynch A, Fox R, Smyth B, Gray S, Dinsmore WW, Maw RD: The syphilis outbreak in Northern Ireland. Int J STD AIDS. 2007, 18: 413-417. 10.1258/095646207781024874.View ArticlePubMedGoogle Scholar
- Lukehart SA: Biology of Treponemes. Sexually Transmitted Diseases. Edited by: Holmes KK, Sparling PF, Stamm EW, Piot P, Wasserheit JN, Corey L, et al. 2008, The McGraw-Hill Companies, Inc., 647-659.Google Scholar
- Innvandring og innvandrere 2008. Daugstad, G. 2009, . Oslo-Kongsvinger, Statistics Norway. Statistical Analyses. 24-11-2009Google Scholar
- Hiltunen-Back E, Haikala O, Koskela P, Vaalasti A, Reunala T: Epidemics due to imported syphilis in Finland. Sex Transm Dis. 2002, 29: 746-751. 10.1097/00007435-200212000-00002.View ArticlePubMedGoogle Scholar
- Sherrard J, Luzzi G, Edwards A: Imported syphilis and other sexually transmitted infections among UK travellers to Russia and Poland. Genitourin Med. 1997, 73: 75-PubMedPubMed CentralGoogle Scholar
- Uuskula A, Puur A, Toompere K, DeHovitz J: Trends in the epidemiology of bacterial sexually transmitted infections in eastern Europe, 1995-2005. Sex Transm Infect. 2010, 86: 6-14. 10.1136/sti.2009.037044.View ArticlePubMedGoogle Scholar
- Aavitsland P: Gonorrhea and syphilis from Russia to Norway. EpiNorth. 2000, 1: 13-16.Google Scholar
- Klausner JD: Frequency of syphilis testing in HIV-infected patients: more and more often. Sex Transm Dis. 2009, 36: 86-87. 10.1097/OLQ.0b013e3181960bb7.View ArticlePubMedGoogle Scholar
- Zetola NM, Klausner JD: Syphilis and HIV infection: an update. Clin Infect Dis. 2007, 44: 1222-1228. 10.1086/513427.View ArticlePubMedGoogle Scholar
- Schmid GP, Stoner BP, Hawkes S, Broutet N: The need and plan for global elimination of congenital syphilis. Sex Transm Dis. 2007, 34: S5-10. 10.1097/01.olq.0000261456.09797.1b.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/10/105/prepub
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