Abstract

Dear Editor:
Studies in sexually transmitted disease (STD) and HIV clinics show that the cumulative prevalences (for all anatomic sites—pharynx, rectum, and urine) of Neisseria gonorrhea (GC) and Chlamydia trachomatis (CT) among men who have sex with men (MSM), regardless of symptoms, range from 6%–25% and 2%–12%, respectively. 1,2 The prevalence (for both organisms and all anatomic sites) in studies of predominantly asymptomatic samples of HIV-positive MSM (the most recently published of which reported a combined GC, CT, and syphilis prevalence of 14% among a sample composed entirely of asymptomatic, HIV-positive MSm3) has been 4%–11%. 4,5 Since GC and CT infections may be asymptomatic, the Centers for Disease Control and Prevention (CDC) recommends screening MSM for both organisms. 6
The majority of GC/CT prevalence studies among MSM have occurred at STD/HIV clinics among younger men, many of whom were symptomatic; furthermore, the 20- to 24-year-old age group has the highest prevalence of GC/CT infection in men. 7 Evidence suggests there is an increasing incidence of HIV among older MSM, 8,9 and because nonulcerative sexually transmitted infections (STIs) increase risk of HIV transmission 10,11 more data are needed from community-based, asymptomatic cohorts of older MSM to evaluate GC/CT screening strategies. To address this paucity of data, we performed a pilot study to evaluate the prevalence of rectal, urethral and pharyngeal GC/CT in the pharynx, rectum and urethra among 147 asymptomatic MSM in the Multicenter AIDS Cohort Study (MACS), a long-standing cohort of aging MSM, whose average age is 51 years.
Each DC MACS participant is seen semiannually at the Whitman Walker Clinic (WWC) for a detailed interview, a physical examination, and phlebotomy. The study questionnaires are available at
Comparisons between patients with “ever” versus “never” positive tests were performed using the χ 2 method and exact p values for all outcomes except age, which was compared using a t test. Prevalence estimates were calculated using the number of participant screening visits. Descriptive statistics and t test results were calculated using SAS version 9.1 (SAS Institute, Inc., Cary, NC), while χ 2 tests and 95% exact Casella-Blythe-Still confidence intervals were computed in StatXact version 4 (Cytel Inc., Cambridge, MA) to accommodate the small numbers of positive tests.
Of the 160 active Washington, D.C. MACS participants, 156 attended at least one visit from December 2006 to December 2007, and 147 (94%) of these were enrolled. Of the 9 not enrolled, 8 declined, and 1 was excluded because he had deferred the physical examination. There were 242 participant screening visits (65% screened twice). The participants were predominantly white and middle-aged (mean, 50.9 years) and all were asymptomatic; 45% were HIV positive (Table 1). Of 242 sets of specimens tested, 14 tested positive, yielding a GC/CT prevalence from all anatomic sites of 5.8% (Table 2). In the pharynx, 7 samples (2.9%) were positive for GC and 1 (0.4%) for CT. In the rectum, 2 samples were positive for GC (0.8%) and 4 for CT (1.7%). All urine samples tested were negative for both organisms. The average age of those with positive GC/CT results was 49.6 ± 8.3. Meeting sexual partners on the internet was the only statistically significant correlate of GC/CT infection (p < 0.01, Table 2).
Due to missing data, the percentages do not sum to 100.
MACS, Multicenter AIDS Cohort Study; SHARE, ; GC, Neisseria gonorrheae; CT, Chlamydia trachomatis; SD, standard deviation; STD, sexually transmitted disease.
GU, gonorrhea in urine; GP, gonorrhea in pharynx; GR, gonorrhea in rectum; CU, chlamydia in urine; CP, chlamydia in pharynx; CR, chlamydia in rectum; CI, confidence interval.
Among this sample of aging MACS participants, of whom 45% were HIV positive, we found the prevalence of asymptomatic GC/CT infection (5.8%) to be similar to that found among predominantly HIV-infected, asymptomatic MSM tested at STD/HIV clinics (4%–11% for both organisms and all anatomic sites). 3 –5 Our results were also similar to those found from urine and rectal GC/CT screening of asymptomatic participants from the Pittsburgh MACS site. 1 The lower prevalence of pharyngeal GC in our study compared to the 9.2% found by Kent et al. 2 in San Francisco is probably explained by the fact that the latter study included symptomatic patients. The lower GC/CT prevalence in our study compared to the approximately 11% found by Rieg et al. 3 in Los Angeles could be due to demographic differences between the study populations (the latter being 100% HIV positive, predominantly Hispanic, and younger). It is also important to note that the GC/CT prevalence from our sample of asymptomatic MSM in Washington, D.C. may not be representative of MSM countrywide because the prevalence of these organisms in the Northeast has been consistently lower than other regions of the United States, particularly the South and the Midwest. 13,14
Evidence suggests there is an increasing incidence of HIV among older MSM, but the role GC/CT infection plays in HIV transmission in this aging population remains unclear. Our results further suggest that older MSM continue to engage in high-risk sexual behavior; therefore, increased vigilance with GC/CT screening among older MSM is warranted. We are aware that the sample size is quite small, nevertheless our findings offer a thought provoking glimpse of what seems to be a percolating problem among older MSM, particularly those who are HIV positive who practice high-risk sex. We expected that the prevalence would be low since these men should have been intrinsically educated about preventing the spread of HIV and other STIs by participating in this cohort study, however it was not. Taken together with the recommended CDC testing guidelines, the intersection of the increasing U.S. incidence of HIV infection and STI infection rate shown here among older MSM should not be ignored.
Footnotes
Acknowledgments
Supported by The Whitman Walker Clinic and the Multicenter AIDS Cohort Study, which is funded by the National Institute of Allergy and Infectious Diseases, with additional supplemental funding from the National Cancer Institute and the National Heart, Lung and Blood Institute: UO1-AI-35042, 5-MO1-RR-00722 (GCRC), UO1-AI-35043, UO1-AI-37984, UO1-AI-35039, UO1-AI-35040, UO1-AI-37613, UO1-AI-35041. Website located at
