|Year : 2017 | Volume
| Issue : 1 | Page : 60-64
Proton pump inhibitors are associated with a reduced likelihood for sexually transmitted diseases in women in the emergency department
Johnathan Michael Sheele1, Nathan Morris2, Donald Byars3, Frank Counselman3
1 Department of Emergency Medicine, University Hospitals Cleveland Medical Center & Case Western Reserve University, Cleveland, OH 44106, USA
2 Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, OH 44106, USA
3 Department of Emergency Medicine, Eastern Virginia Medical School, Emergency Physicians of Tidewater, Norfolk, VA, USA
|Date of Web Publication||30-Mar-2017|
Dr. Johnathan Michael Sheele
Department of Emergency Medicine, University Hospitals Cleveland Medical Center & Case Western Reserve University, Cleveland, OH 44106
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: Proton pump inhibitors (PPIs) have been shown in cell culture to kill Trichomonas vaginalis (TV) at lower half maximal inhibitory concentration values than metronidazole (Flagyl), the most common medication used to treat the infection. However, there have been no previous clinical investigations to determine if PPIs are associated with reduced risk for TV. Materials and Methods: We examined the records of female patients who received testing in the emergency department for TV, Neisseria gonorrhoea (GC), and Chlamydia trachomatis (CT) between 2010 and 2014 at two academic medical centers to determine if PPI and histamine type 2 receptor antagonist (H2RA) drugs were associated with TV and GC/CT infections. Results: We found that H2RAs were associated with an increased likelihood for TV (odds ratio [OR]: 2.0, P< 0.0001) and GC and/or CT infections (OR: 1.49, P< 0.0001). PPIs were associated with a reduced likelihood for TV (OR: 0.75, P< 0.0001) and GC and/or CT infections (OR: 0.57, P< 0.0001). In patients infected with GC and/or CT, the likelihood of coinfection with TV was reduced in those taking a PPI (OR: 0.64, P = 0.054) and increased in those taking an H2RA (OR: 1.62, P = 0.003). Conclusions: PPIs are associated with a reduced risk for TV and GC/CT infection.
Keywords: Chlamydia trachomatis, histamine type-2 receptor antagonist, Neisseria gonorrhoea, proton pump inhibitor, sexually transmitted disease, Trichomonas vaginalis
|How to cite this article:|
Sheele JM, Morris N, Byars D, Counselman F. Proton pump inhibitors are associated with a reduced likelihood for sexually transmitted diseases in women in the emergency department. Indian J Sex Transm Dis 2017;38:60-4
|How to cite this URL:|
Sheele JM, Morris N, Byars D, Counselman F. Proton pump inhibitors are associated with a reduced likelihood for sexually transmitted diseases in women in the emergency department. Indian J Sex Transm Dis [serial online] 2017 [cited 2019 Nov 19];38:60-4. Available from: http://www.ijstd.org/text.asp?2017/38/1/60/203438
| Introduction|| |
Trichomonas vaginalis (TV) are motile, flagellated, protozoan parasites that inhabit the genital tracts of men and women., Trichomoniasis is the most common curable sexually transmitted disease (STD) in women, causing 7.4 million infections in the United States and 170 million infections worldwide: more infections than chlamydia, syphilis, and gonorrhea combined.,,,, Up to 30%–50% of women and 70%–75% of men have asymptomatic TV infections. TV is one of the United States Centers for Disease Control and Prevention's top five neglected parasitic diseases in the United States.
TV can cause pelvic inflammatory disease, increase the risk of human immunodeficiency virus transmission, and can cause complications during pregnancy including premature rupture of membranes, premature labor, and low birth weight babies.,, Trichomoniasis is characterized by vaginitis, vaginal pruritus, vulvitis, dysuria, dyspareunia, and a malodorous frothy yellow or green mucopurulent vaginal discharge.,
Proton pump inhibitors (PPIs) are among the most commonly prescribed medications in the United States. There are several United States Food and Drug Administration (FDA)-approved PPIs including omeprazole (Prilosec); lansoprazole (Prevacid); rabeprazole (Aciphex); pantoprazole (Protonix); esomeprazole (Nexium); and dexlansoprazole (Kapidex). All PPIs are structurally similar weak bases that accumulate as prodrugs in acidic environments where they undergo acid-catalyzed conversion to the active drug. PPIs are used to treat several conditions, including gastroesophageal reflux disease, nonsteroidal-induced gastrointestinal lesions, Zollinger–Ellison syndrome, dyspepsia, and for the elimination of Helicobacter pylori. PPIs are well tolerated with few significant side effects. The investigators are unaware of any study that have evaluated whether PPIs affect vaginal pH, accumulate in vaginal secretions, or if there are any functional H +/K + ATPase in the genital tract of women.,
PPIs are benzimidazole derivatives and are structurally similar to other drugs such as benzimidazole 2-methylcarbamates (BC), albendazole (ABZ), and mebendazole (MBZ), all of which kill the human protozoan parasites Giardia lamblia, Entamoeba histolytica, and TV in cell culture.,,, ABZ and MBZ kill TV by affecting β-tubulin polymerization and alteration of the TV cytoskeleton, microtubules, and microribbons. Quantitative structure-activity relationship (SAR) analyses studies based on comparative molecular field analysis, molecular similarity indices in comparative analysis studies, and SAR studies based on structure-activity-similarity maps found that PPIs should be expected to have trichomonicidal activity based on previous results with BC, ABZ, and MBZ.In vitro studies have shown that PPIs, and in particular pantoprazole, kill TV 1.9–3.1 times better than the drug metronidazole, the medication most commonly used to treat TV., The TV 50% inhibitory concentration (IC50) (μM) is 0.0756 for pantoprazole, 1.5905 for ABZ, and 0.2360 for metronidazole.
TV is incapable of de novo synthesis of purine and pyrimidine rings; it relies on uridine nucleoside ribohydrolase (UNH) to cleave a bond between uracil and ribose in the uridine salvage pathway. Pantoprazole was found to inhibit UNH in an in vitro assay with an IC50 of 14.5 μM; however, it is unclear if this is the mechanism responsible for PPI toxicity against TV.
Tritrichomonas foetus (TF), a sexually transmitted parasitic disease, which causes trichomoniasis in cattle, is the most similar nonhuman trichomonad to TV., The PPI omeprazole was found to kill metronidazole-resistant TF at 22 μg/mL (63 μM) in cell culture. The authors suggest that omeprazole works by inhibition of pyruvate decarboxylase (PDC), which is an enzyme responsible for ethanol production. PDC was inhibited by omeprazole with an IC50 of 16 μg/mL.
The investigators are unaware of previous clinical investigations to determine if PPI use is associated with a reduced risk for TV infection in humans. Neisseria More Details gonorrhoea (GC) and Chlamydia trachomatis (CT) – two STDs diagnosed in the emergency department (ED) in women also at risk for TV – are not known to be affected by PPIs and were used as controls. Histamine type 2 receptor antagonists (H2RAs) were used as additional controls because they have similar clinical indications as PPIs but have no known effect on GC, CT, or TV.
| Materials and Methods|| |
We received the Institutional Review Board approval from University Hospitals (UH) (IRB #08-14-12) and exemption from Eastern Virginia Medical School (EVMS) (IRB #15·06·NH·0123) to conduct this chart review study. The chart review data were abstracted from each institution's respective electronic medical records: UHCare for UH and Epic for Sentara Healthcare, which is affiliated with EVMS. The data were for women aged 18–40 years who received testing for TV, GC, and CT in the emergency department between 2010 and 2014. The data were provided to study investigators without protected health information in a de-identified, aggregate manner.
Subjects were considered infected with TV if they had TV reported on their wet prep or they had a positive APTIMA nucleic acid amplification test (NAAT) for TV. Subjects were considered positive for GC/CT if a NAAT was positive for either or both GC and CT. Subjects were considered to be taking a PPI (omeprazole, lansoprazole, rabeprazole, pantoprazole, esomeprazole, or dexlansoprazole) and/or H2RA (cimetidine, famotidine, nizatidine, or ranitidine) if it was listed on their chart during the medical encounter when testing for STDs was conducted.
For the UH dataset, we determined the breakdown of how TV was diagnosed in our subjects. We found that 90% of subjects diagnosed with TV had only a wet prep performed while 10% of subjects were diagnosed by NAAT. TV was excluded as a diagnosis in our study subjects based on a negative wet prep only (i.e., no NAAT performed after a negative wet prep) in 82% of subjects. The breakdown of subjects diagnosed with TV at EVMS who had a wet prep and/or NAAT was not available to the investigators for analysis.
| Results|| |
There were 654,538 women aged 18–40 years in the Sentara Epic database and 48,372 in the UH database (total 702,910). After meeting appropriate inclusion and exclusion criteria, there were 87,550 subjects from EVMS and 30,901 subjects from UH that were used in the final data set for a total of 118,451 charts reviewed. A summary of the data is provided in [Table 1].
|Table 1: The number of subjects with TV and GC and/or CT (GC/CT) who are taking a PPI, H2RA, or neither class of drug|
Click here to view
[Table 2] shows the odds ratio (OR) for PPI use, H2RA use, and persons taking neither a PPI nor H2RA in relation to the results of the TV and GC/CT testing for both UHCare and the Sentara healthcare systems (EVMS)-Epic and the combined UHCare and Epic datasets. Using the combined UHCare and Epic databases, we found that PPI use, compared with no PPI or H2RA use, was associated with a reduced likelihood for both TV (OR: 0.75, 95% confidence interval [CI]: 0.65–0.86, P< 0.0001) and GC/CT (OR: 0.57, 95% CI: 0.50–0.64, P< 0.0001) infections. Using the combined UHCare and Epic databases, we also found that H2RA use, compared to no PPI or H2RA use, was associated with an increased likelihood for both TV (OR: 2.0, 95% CI: 1.77–2.36, P< 0.0001) and GC/CT (1.49, 95% CI: 1.30–1.71, P< 0.0001) infection. However, the associations between PPI and H2RA use and TV did not achieve statistical significance when only the UHCare data were analyzed but was highly statistically significant in the Epic dataset.
|Table 2: The Odds ratios for PPI and H2RA use and TV and GC and/or CT (GC/CT) infection in female patients 18-40 years of age in the ED|
Click here to view
[Table 3] shows the OR for TV and GC/CT use when PPI use (intervention) is compared to H2RA use (control) in the combined UHCare and Epic datasets (compared to [Table 2]] where PPI and H2RA use was compared to no PPI or H2RA use). We performed this analysis because PPIs and H2RAs treat many of the same clinical symptoms but have different mechanisms of action. We found a statistically significant association between PPI use and not being infected with TV (OR: 0.37, 95% CI: 0.30–0.45, P< 0.0001) and GC and/or CT (OR: 0.38, 95% CI: 0.31–0.46, P< 0.0001) compared with H2RA use.
|Table 3: The Odds ratio of PPI use, compared with H2RA use, for TV and G/CT infection|
Click here to view
We examined the association between TV infection in women who were also coinfected with GC and/or CT (i.e., +TV+GC-CT, +TV-GC+CT, or +TV+GC+CT) and whether they were taking PPIs or H2RAs. The results are summarized in [Table 4]. We found that PPI use, compared with no PPI or H2RA use, was associated with a reduced likelihood for TV infection in women who were coinfected with TV and GC/CT (i.e., +TV+GC-CT, +TV-GC+CT, or +TV+GC+CT) (OR: 0.64, 95% CI: 0.40–1.01, P = 0.05). We found that H2RA use, compared with no PPI or H2RA use, was associated with an increased likelihood for TV infection in women who were also coinfected with GC/CT (i.e., +TV+GC-CT, +TV-GC+CT, or +TV+GC+CT) (OR: 1.62, 95% CI: 1.17–2.25, P = 0.004). When controlling for GC/CT coinfection, we found that PPI use, compared with H2RA use, was associated with a reduced likelihood for TV infection in women who were coinfected with GC/CT (i.e., +TV+GC-CT, +TV-GC+CT, or +TV+GC+CT) (OR: 0.39 95% CI: 0.22–0.68, P = 0.001).
|Table 4: The Odds ratio for TV infection in those women infected with GC and/or CT who are taking PPIs, H2RAs, or neither drug|
Click here to view
| Discussion|| |
We report a reduced likelihood of TV and GC/CT infection in women in the ED taking a PPI and an increased likelihood of TV and GC/CT infection when taking an H2RA. The reduced likelihood of both TV and GC/CT infection in our subjects taking a PPI may be the result of an unidentified confounder; however, when we controlled for GC/CT infection, PPI use was still associated with a reduced likelihood of TV infection.
There are limitations to this chart review study including: we used retrospective data; we did not take into account medical compliance with PPIs and H2RAs; the medical record may not accurately reflect the medications that patients have been prescribed; the medical record may not reflect over-the-counter H2RA or PPI drugs taken intermittently for symptomatic relief of gastrointestinal distress; and we did not control for the different FDA-approved PPIs or doses. Most of the subjects in our UH dataset were identified as infected or uninfected with TV based on a wet prep, known to have only moderate sensitivity, and not a NAAT that has excellent sensitivity and specificity.
Only 3.4% of subjects in our dataset were taking a PPI, and 1.4% was taking an H2RA. The increased cost of PPIs over H2RAs may be a confounder because the demographic most at risk for STD infection are young, socioeconomically disadvantaged women who may not be able to afford the relatively more expensive PPIs.
We did not observe a statistically significant reduced likelihood of TV infection in those subjects taking a PPI when only the smaller UHCare dataset was used. A statistically significant effect was only seen when evaluating the Epic and the combined Epic + UHCare datasets. It is possible that this difference in effect is the result of an unidentified confounding variable, which could include differences in the socioeconomic status of subjects at the different institutions, sample size, race (as it relates to potential drug pharmacokinetics), methods used for diagnosing TV, and the accuracy of the ED electronic medical record to reflect the drugs patients are actually taking.
The investigators are unaware of any previous investigation into whether PPIs are found in the genital secretions of women although it may be theoretically possible based on the known pharmacokinetics of the drugs. The results of this study support the need for further investigation into the pharmacokinetics of PPIs in the genital tract of women including a more rigorous evaluation to whether PPIs have any in vivo antitrichomonal effects.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Coleman JS, Gaydos CA, Witter F. Trichomonas vaginalis
vaginitis in obstetrics and gynecology practice: New concepts and controversies. Obstet Gynecol Surv 2013;68:43-50.
Nielsen TJ, Pradhan P, Brittingham A, Wilson WA. Glycogen accumulation and degradation by the trichomonads Trichomonas vaginalis
and Trichomonas tenax
. J Eukaryot Microbiol 2012;59:359-66.
Centers for Disease Control and Prevention. Sexually transmitted diseases treatment guidelines. Morb Mortal Wkly Rep 2010;59:58-61.
Weinstock H, Berman S, Cates W Jr. Sexually transmitted diseases among American youth: Incidence and prevalence estimates, 2000. Perspect Sex Reprod Health 2004;36:6-10.
Cudmore SL, Delgaty KL, Hayward-McClelland SF, Petrin DP, Garber GE. Treatment of infections caused by metronidazole-resistant Trichomonas vaginalis
. Clin Microbiol Rev 2004;17:783-93.
Schwebke JR, Burgess D. Trichomoniasis. Clin Microbiol Rev 2004;17:794-803.
Draper D, Jones W, Heine RP, Beutz M, French JI, McGregor JA. Trichomonas vaginalis
weakens human amniochorion in an in vitro
model of premature membrane rupture. Infect Dis Obstet Gynecol 1995;2:267-74.
Shi S, Klotz U. Proton pump inhibitors: An update of their clinical use and pharmacokinetics. Eur J Clin Pharmacol 2008;64:935-51.
Pérez-Villanueva J, Romo-Mancillas A, Hernández-Campos A, Yépez-Mulia L, Hernández-Luis F, Castillo R. Antiprotozoal activity of proton-pump inhibitors. Bioorg Med Chem Lett 2011;21:7351-4.
Sears SD, O'Hare J.In vitro
susceptibility of Trichomonas vaginalis
to 50 antimicrobial agents. Antimicrob Agents Chemother 1988;32:144-6.
Cedillo-Rivera R, Muñoz O. In-vitro
susceptibility of Giardia lamblia
to albendazole, mebendazole and other chemotherapeutic agents. J Med Microbiol 1992;37:221-4.
Chavez B, Cedillo-Rivera R, Martinez-Palomo A. Giardia lamblia
: Ultrastructural study of the in vitro
effect of benzimidazoles. J Protozool 1992;39:510-5.
Shea TA, Burburan PJ, Matubia VN, Ramcharan SS, Rosario I Jr., Parkin DW, et al.
Identification of proton-pump inhibitor drugs that inhibit Trichomonas vaginalis
uridine nucleoside ribohydrolase. Bioorg Med Chem Lett 2014;24:1080-4.
Sutak R, Tachezy J, Kulda J, Hrdý I. Pyruvate decarboxylase, the target for omeprazole in metronidazole-resistant and iron-restricted Tritrichomonas foetus
. Antimicrob Agents Chemother 2004;48:2185-9.
[Table 1], [Table 2], [Table 3], [Table 4]