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Protective effect of oral contraceptive against Helicobacter pylori infection in US adult females: NHANES 1999–2000

Published online by Cambridge University Press:  26 April 2021

P. FongOpen the ORCID record for P. Fong[Opens in a new window] and
Q. T. Wang
P. Fong*
Affiliation:
School of Health Sciences and Sports, Macao Polytechnic Institute, Macao, China
Q. T. Wang
Affiliation:
Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China
*
Author for correspondence: P. Fong, E-mail: pedrofong@ipm.edu.mo
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Abstract

Recently, the antibacterial properties of oestrogen and progestogen were discovered. The aim of this study was to find the cross-sectional association between oral contraceptive use and Helicobacter pylori seroprevalence. Data were obtained from the US National Health and Nutrition Examination Survey (NHANES). The H. pylori immunoglobulin G (IgG) enzyme-linked immunosorbent assays were used to categorise participants as seropositive or seronegative. The study population included 799 female participants who had information on H. pylori seroprevalence and all other covariates and had not been taking any medications (except oral contraceptives). The bivariate Rao–Scott chi-square test indicated a significant association between H. pylori seroprevalence and contraceptive use (P < 0.01). The variables of race, education, poverty income ratio, smoking, and blood lead and cadmium levels were also significantly associated with H. pylori seroprevalence (P < 0.01). Multiple logistic regression analysis of the age-adjusted model revealed that contraceptive users are 65% less likely of being H. pylori seropositive as compared to non-contraceptive users (odds ratio (OR): 0.35, 95% confidence interval (CI): 0.18–0.68). This association is stronger with the final multivariate model (OR: 0.46, 95% CI: 0.23–0.89). Conclusions: This finding reveals the potential protective effect of oral contraceptives against H. pylori infection and serves as a foundation study for further investigations.

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Original Paper
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Epidemiology & Infection , Volume 149 , 2021, e120
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This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Copyright © The Author(s), 2021. Published by Cambridge University Press

Introduction

Recent studies found that the overall global prevalence of Helicobacter pylori infection is about 50% [Reference Zamani1]. H. pylori has been a WHO-ratified class I carcinogen since 1994 and it can increase the risk of causing various types of diseases, such as gastric ulcer, gastritis, gastric adenocarcinoma, and lymphoma [Reference Suerbaum and Michetti2]. H. pylori may also decrease the acidity in the human stomach, reducing the absorption of some essential minerals and vitamins, such as iron and vitamin B12 [Reference Carmel, Perez-Perez and Blaser3]. Many studies have attempted to find a novel effective treatment to eradicate H. pylori, especially the antibiotic-resistant strains [Reference Guevara and Cogdill4]. Many studies have also investigated dietary compounds that may inhibit the growth of H. pylori. For example, lactoferrin in cow's milk [Reference Wang5], sulforaphane in broccoli [Reference Fahey6] and octyl gallate [Reference Wolf7] as a food additive have shown their potentials in inhibiting the growth of H. pylori. However, reducing the global prevalence rate of H. pylori is still very challenging.

Many marketed drugs have shown to have therapeutic effects that have not been identified previously, including antibacterial effects. For instance, statin is a type of cholesterol-lowering drug that has demonstrated its antibacterial properties. Recently, rosuvastatin was shown to have significant antibacterial effects on both Gram-negative and Gram-positive species [Reference Al-Kuraishy, Al-Gareeb and Al-Buhadily8]. Thus, there is a possibility that some marketed drugs have anti-H. pylori properties that have not been identified. A recent study suggested that oestrogen can stimulate the production of antimicrobial peptides in the urothelial cells of women [Reference Lüthje9]. Another study found that mice feeding with oestrogen supplementation (17β-Oestradiol) suppressed H. pylori-induced gastric pathology [Reference Ohtani10]. Apart from oestrogen, another steroid hormone called progestogen was also found to have H. pylori bacteriolytic effects, which was stronger than that of oestradiol [Reference Hosoda11]. Oral contraceptives generally contain oestrogen and/or progestogen. This means they may affect the growth of H. pylori in the human gastric environment. This study aimed to study the effects of oral contraceptives on H. pylori prevalence using the US National Health and Nutrition Examination Survey (NHANES) dataset [Reference Johnson12].

The NHANES is a US national programme of the Centers for Disease Control and Prevention (CDC) to study the health of Americans. The data of the NHANES were obtained by both physical examinations and interviews. The dataset has been used in many types of research, including drug repurposing (i.e. to find new medical indications for existing marketed drugs) [Reference Prakash13]. It has also been recognised as an essential part of a systematic framework that was used to study unidentified disease–drug associations [Reference Dong14]. Thus, NHANES is a reputable dataset for research purposes.

Methods

Study population

Data in this study was obtained from the 1999–2000 continuous cycle of the US NHANES dataset [Reference Johnson12]. It is a cross-sectional survey aimed at evaluating the health and nutritional status of Americans. The participants of this survey were US non-institutionalised civilians selected by the National Center for Health Statistics using a stratified and multistage probability design. The survey was approved by the US CDC, and all participants gave informed consent. The sample weights were based on the population estimated by the US Bureau of the Census [15]. The 1999–2000 cycle is the only continuous NHANES survey that contains data on H. pylori seropositivity. The number of participants with H. pylori data was 7493. After the exclusion of participants with no information on the laboratory and demographic covariates, the final sample size of this study was 799 participants (Fig. 1).

Fig. 1.

Flow chart of study populations.

H. pylori seroprevalence

H. pylori immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) was performed on the serum samples of the 7493 participants. The assays were manufactured by Wampole Laboratories (Cranbury, NJ) and were used to detect the amount of IgG antibodies to H. pylori [16]. The samples were collected, stored and tested in the University of Washington under the NHANES protocol [16]. The ELISA optical density (OD) values of all the participants were ranging from 0 to 5.73. Values of >1.1 and <0.9 were considered as seropositive and seronegative, respectively, whereas 0.9–1.1 were equivocal values [Reference Meier17]. The participants with equivocal OD values (N = 170) were excluded in this study to prevent misleading statistical outcomes, and the available samples were reduced to 7323.

Contraceptives and other drugs use assessment

The Dietary Supplements and Prescription Medication Section (DSQ) of the NHANES contains interview questions and answers regarding medication usage of the participants [18]. The questions include whether the participant had taken any medications in the past month, and if so, how long the participant had been taking the medications. The therapeutic drug class code of the medications was assigned based on the FDA's National Drug Code Directory [19]. The code for contraceptive drugs is 1040. The interviews, data collection and data processing methods were performed under the NHANES protocol [18]. Among the 15 643 participants involved in the interviews of the DSQ section, 149 had reported taking contraceptives in the past month and they were all female. As this study wants to ensure that contraceptives had enough exposure time to produce the effects on H. pylori, only the participants who had been taken the contraceptive for at least 90 days were involved in this study. Thus, the number of participants who took contraceptives was reduced to 131.

Medications, such as proton pump inhibitors and antacids, may affect H. pylori infection [Reference Laine20]. To exclude this potential bias, all the participants who had taken any medications (except contraceptives) in the past 90 days were excluded from this study. Among the 15 643 participants in the DSQ section, 6363 of them were not taking any medications. The total number of participants who had been taking contraceptives or no medications was 6494 (131 + 6363). Among them, only 4668 had H. pylori data.

Covariate assessment

Literature suggested that H. pylori infection was associated with age [Reference Graham21], race [Reference Graham21], education [Reference Moreira22], poverty [Reference Graham21], body mass index (BMI) [Reference Suki23], smoking [Reference Ogihara24], alcohol [Reference Zhang25], caffeine [Reference Monno26], vitamin C [Reference Simon, Hudes and Perez-Perez27], sources of drinking water (well or municipal) [Reference Rolle-Kampczyk28], home water treatment devices [Reference Krueger and Wade29] and the amounts of lead and cadmium in blood [Reference Krueger and Wade29]. The 1999–2000 cycle of the NHANES contains the data on these factors, and they are considered as covariates in this study. Age, race, education and poverty were categorised as listed in Table 1. The youngest participant who had been taking contraceptives was 20 years old in the NHANES dataset. BMI status was categorised into underweight (<18.5 kg/m2), normal or healthy weight (18.5–24.9 kg/m2), overweight (25.0–29.9 kg/m2) and obese (>30.0 kg/m2) according to the CDC reference values [30]. Smoking status was classified into current, previous and never smoked. Participants who had smoked at least 100 cigarettes in their entire life but not currently smoking were considered previous smokers. Alcohol users were categorised into weekly, monthly and yearly drinkers, as well as not reported, based on the interview answers in the NHANES dataset [31]. Caffeine intake (mg), vitamin C (mg), amounts of lead and cadmium in blood (μg/dl) were categorised into their approximate-weighted quartiles. The participants were asked whether home water treatment devices had been used. Water treatment devices include aerators, ceramic or charcoal filters, water softeners, reverse osmosis and Brita or other pitcher water filter [32]. The source of drinking water was categorised into water company (municipal) or public/private well according to the Housing Characteristics section of the NHANES dataset [32].

Table 1.

Weighted characteristics of 799 participants by H. pylori seroprevalence, NHANES 1999–2000

H. pylori, Helicobacter pylori; NHANES, US National Health and Nutrition Examination Survey; BMI, body mass index.

a Rao–Scott χ 2 statistics.

Among the 4668 participants who had H. pylori and medications data available, only 799 of them had all of the above information on covariates (Fig. 1). The final sample size was 799.

Statistical analysis

Data were analysed using R Studio (R version 3.6.3) to evaluate the associations between the categorical variables: H. pylori seroprevalence, contraceptives use and the covariates. The 2-year medical examined sample weights [15] of the NHANES 1999–2000 cycle were used to account for the reference population. Bivariate associations between H. pylori seroprevalence and all other variables were assessed using the Rao and Scott [Reference Rao and Scott33] χ 2 test. Multiple logistic regression analysis was conducted using the R package ‘survey’ (https://cran.r-project.org/web/packages/survey/index.html) to estimate the odds ratio (OR) and 95% confidence interval (CI) of H. pylori seroprevalence and contraceptive use. Covariates were adjusted to develop models using forward stepwise modelling, starting with age then poverty, race, education, BMI, smoking, source of drinking water, home water treatment device, amounts of lead and cadmium in blood, vitamin C, alcohol and caffeine.

Results

In all, 24% of the weighted samples were H. pylori seropositive, and 17.5% of patients had been taking contraceptive drugs for >90 days (Table 1). Among the contraceptive drug users, 12.8% were seropositive and 87.2% were seronegative. For the non-contraceptive drug users, 27.1% and 72.9% were seropositive and seronegative, respectively (Table 1). The seropositive percentage of non-contraceptive users and contraceptive users were 27.1% and 12.8%, respectively, thus their rate ratio was 0.472 (P < 0.01). This indicates that the contraceptive users were 52.8% less likely to be H. pylori seropositive than those of the non-contraceptive users.

The majority of the participants involved in this study were between 20 and 34 years old (Table 1). The percentage of participants who were 50 years old or above was the lowest among all age groups (17.5%), of which 24.8% and 75.2% of them were contraceptive users and non-contraceptive users, respectively. In all, 67% of the participants were non-Hispanic Whites and >80% were at least high school graduates. Most participants had a normal or healthy weight (39.8%) or were overweight (30.3%), and only 2.5% of participants were underweight. Most of them never smoked (62%) and 25.1% of them did not drink regularly (yearly drinker). A significant proportion (31.2%) of an unknown amount of alcohol intake was observed. With regard to water-related covariates, most participants did not have a water treatment device (71.1%), and only 13% of participants had well water as their source of tap water.

The statistical bivariate test indicated a significant association between age and H. pylori seroprevalence (P < 0.01), and the younger age groups were less infected than the older age groups (Table 1). The greatest difference between H. pylori seropositivity was observed in the youngest group (20–34 years old) (Fig. 2). The variables of race, education, poverty income ratio, smoking, and blood lead and cadmium levels were also significantly associated with H. pylori seroprevalence (P < 0.01). Participants who were non-Hispanic White and wealthy with high educational level or with low blood lead and cadmium levels had lower H. pylori seroprevalence. A higher number of seropositive participants were also current smokers, as compared to the previous smoker or never smoked (P < 0.01). The percentage of underweight, overweight or obese participants with H. pylori seropositive status were higher than that of the participants with normal weight. However, this was not statistically significant (P > 0.05). Alcohol drinkers who drank less often tended to have a lower risk of H. pylori infection. Participants who consumed well water as their source of tap water tended to have higher seroprevalence than those with the water company. However, both the alcohol and source of tap water covariates were not statistically significant (P > 0.05). Vitamin C and caffeine intake also did not show significant associations with H. pylori seroprevalence.

Fig. 2.

Weighted percentage of participants who were H. pylori seropositive by age group among those taking or not taking contraceptive drugs: NHANES 1999–2000.

The logistic regression models of each adjusted variable with contraceptive use against H. pylori seroprevalence are provided in Table 2. Among all these models, the race-adjusted model obtained less difference between the contraceptive use and H. pylori infection, the OR was 0.54, however, it was the only adjusted model with a statistically insignificant 95% CI. The range of OR among all other adjusted models was 0.38–0.51. (Table 2)

Table 2.

Weighted associations of individual variable and contraceptive drug use against H. pylori seroprevalence in 799 participants, NHANES 1999–2000

H. pylori, Helicobacter pylori; NHANES, US National Health and Nutrition Examination Survey; BMI, body mass index.

Three multiple logistic regressions models are provided in Table 3. They were age and blood lead-adjusted, age and blood lead- and cadmium-adjusted and the final multivariate models. More multiple logistic regression analysis with all other covariates were conducted using forward stepwise modelling. These three models had the highest OR values and their 95% CI were statistically significant. The age and blood lead-adjusted model revealed that contraceptive users are 59% less likely of being H. pylori seropositive than non-contraceptive users (OR: 0.41, 95% CI: 0.27–0.76). This association was slightly stronger with the final multivariate model (OR: 0.46, 95% CI: 0.23–0.89).

Table 3.

Weighted association of contraceptive drug use and covariates with H. pylori seroprevalence in 799 participants, NHANES 1999–2000

H. pylori, Helicobacter pylori; NHANES, US National Health and Nutrition Examination Survey; BMI, body mass index.

Discussion

This cross-sectional study found the association between contraceptive drug use and H. pylori seroprevalence using the US NHANES dataset. Various brands of contraceptive drugs exist in the US, and each brand may contain different active ingredients in different amounts and dosages. The active ingredients involved in this study were ethinyloestradiol, ethynediol, desogestrel, levonorgestrel, medroxyprogesterone, mestranol, norethindrone, norgestrel and norgestimate. They are either synthetic oestrogen or progestational hormones with different chemical structures, which affect their clinical potencies and half-lives. Oestrogen and progestogen have been shown to have in vitro and in vivo antibacterial properties on various types of bacteria, including H. pylori [Reference Hosoda11]. There are many existing oestrogens and progestogens and their different chemical structures affect the strength of their effects on H. pylori. The exact pharmacological mechanism is unknown, but they may bind to the cholesterol-binding site of bacterial cell membranes, causing bacteriostatic or even bactericidal effects [Reference Hosoda11]. Literature searches on major scientific databases were performed to find the relationship between H. pylori and the active ingredients that were involved in this study, and no related information could be found. Thus, we believe this is a primitive study to support the anti-H. pylori effects of contraceptive drugs in humans.

In this study, the results of the bivariate chi-square tests indicated associations between H. pylori seroprevalence and the variables of age [Reference Graham21], race [Reference Graham21], education [Reference Moreira22], poverty [Reference Graham21], smoking [Reference Ogihara24] and levels of lead and cadmium in blood [Reference Krueger and Wade29] were similar to previously published literature. Whereas, the results on BMI [Reference Suki23], caffeine [Reference Monno26], vitamin C [Reference Simon, Hudes and Perez-Perez27], water treatment and source of drinking water [Reference Rolle-Kampczyk28] were different from some of the other published studies and had no association with H. pylori seroprevalence. The associations of these variables with H. pylori can be controversial. As both age and sex are identified covariates [Reference Graham21], the characteristics of the samples may affect their associations. For instance, Ogihara et al. [Reference Ogihara24] found that current smokers were at higher risk of being H. pylori seropositive than those who never smoked in 8837 participants older than 39 years of age. Whereas, Shinchi et al. [Reference Shinchi34] found no relationship between smoking and H. pylori infection in 566 Japanese men aged 50–55 years. Another example is caffeine intake, the study of Monno et al. [Reference Monno26] with 580 participants between 18 and 54 years of age found that coffee consumption was positively correlated with H. pylori status, whereas Shimamoto et al. [Reference Shimamoto35] showed that coffee consumption was not a risk factor for H. pylori infection in 8013 participants. The characteristics of the participants in this study were dissimilar with the above-mentioned studies, as they were female-only and most of them were 20–50 years of age.

In this study, the 20–34 years old age group exhibited the greatest difference of seropositive rates between the contraceptive drug users and non-users (Fig. 2). This age group may have less exposure to H. pylori than the older groups because of their younger age. This may allow the contraceptive drug to exert their potential anti-H. pylori effects in an earlier stage of the infection. Also, older age participants are more likely to have other pathophysiological conditions that may make them prone to the infection, such as diabetes, systemic inflammation and other health concerns [Reference Zhou36].

This study has several limitations. The common weaknesses of a cross-sectional study are the lack of control variables and the absence of following the participants over time. These may introduce recall bias, detection bias and information bias. A cross-sectional study may not be able to study the temporal association between the variables and outcomes. Thus, the results of this study cannot decide if the contraceptive use affected the H. pylori infection, or the H. pylori infection affected the contraceptive use.

All the participants involved in this study had been taking contraceptives drugs for at least 90 days; however, their actual length of time of taking the drugs was not considered. Bacteria are prone to develop drug resistance after long-term exposure to a drug [Reference Megraud37]. Hence, there is a chance that H. pylori may react differently with different lengths of drug exposure. Analysis of the types of oestrogen and progestogen, their dosages and formulations may help to generate more meaningful results, but they were also not considered here. This is because the limited sample size restricted the possibility of categorising the various types, and the NHANES dataset did not contain information on dosages and formulations.

With regard to the smoking variables, this study only considered whether the participants were current smokers, previous smoker or never smoked and did not consider some other more precise but unavailable measurements, such as the number of cigarettes smoked per day. The water-related data obtained in the NHANES may not truly reflect the type of drinking water of the participants. For example, some participants work long shifts, and their major source of drinking water was from their workplace. The BMI variable may not be truly independent of the exposure variable and contraceptive drug use. This is because weight gain may be considered as a side effect of certain types of contraceptive drugs [Reference Gallo38]. Also, the number of underweight participants involved in this study was too small (2.5%). This may underestimate the effects of this group of participants. With regards to alcohol consumption, a high proportion of participants did not report their alcohol drinking status (31.2%). Again, this may have affected the association between alcohol and H. pylori status found in this study.

Another limitation is the exclusion of other confounders shown in the literature. Examples are blood group and diet. Participants with blood groups O and A were found to have higher risks of H. pylori infection, whereas blood group AB was less prone to the infection [Reference Kanbay39]. Dietary compounds, such as capsaicin in chilli peppers, affect the growth of H. pylori [Reference Zeyrek and Oguz40]. The inclusion of these covariates may help to strengthen our multiple logistic regression models; however, the 1999–2000 NHANES dataset did not contain this information.

Conclusions

This study found an association between contraceptive drug use and H. pylori seroprevalence. However, the effect of individual active ingredients and their corresponding dose-dependent relationship with H. pylori seroprevalence could not be found in this study. This was due to the sample size of each active ingredient being too small for adequate statistical power, and the dosage of each drug was not recorded in the NHANES dataset. Thus far, this study revealed the hidden protective effects of oral contraceptives against H. pylori infection and served as a foundation for further investigations. Future studies may investigate the pharmacological mechanism and dose-dependent relationship of the individual contraceptive ingredients on H. pylori prevalence. This study only considered the US population, future studies may include participants in other parts of the world with different dietary habits.

Financial support

This work was supported by the Macao Polytechnic Institute (grant number RP/ESS-03/2018).

Conflict of interest

None.

Data availability statement

All data used for analysis are freely available via online public domains (https://www.cdc.gov/nchs/nhanes/index.htm).

References

Zamani, M et al. (2018) Systematic review with meta-analysis: the worldwide prevalence of Helicobacter pylori infection. Alimentary Pharmacology & Therapeutics 47, 868–876.CrossRefGoogle ScholarPubMed
Suerbaum, S and Michetti, P (2002) Helicobacter pylori infection. New England Journal of Medicine 347, 1175–1186.CrossRefGoogle ScholarPubMed
Carmel, R, Perez-Perez, GI and Blaser, MJ (1994) Helicobacter pylori infection and food-cobalamin malabsorption. Digestive Diseases and Sciences 39, 309–314.CrossRefGoogle ScholarPubMed
Guevara, B and Cogdill, AG (2020) Helicobacter pylori: a review of current diagnostic and management strategies. Digestive Diseases and Sciences 65, 1917–1931.CrossRefGoogle ScholarPubMed
Wang, X et al. (2001) Inhibition of Helicobacter pylori infection by bovine milk glycoconjugates in a BAlb/cA mouse model. Journal of Medical Microbiology 50, 430–435.CrossRefGoogle Scholar
Fahey, JW et al. (2002) Sulforaphane inhibits extracellular, intracellular, and antibiotic-resistant strains of Helicobacter pylori and prevents benzo [a] pyrene-induced stomach tumors. Proceedings of the National Academy of Sciences 99, 7610–7615.CrossRefGoogle ScholarPubMed
Wolf, VG et al. (2017) Octyl gallate, a food additive with potential beneficial properties to treat Helicobacter pylori infection. Food & Function 8, 2500–2511.CrossRefGoogle ScholarPubMed
Al-Kuraishy, HM, Al-Gareeb, AI and Al-Buhadily, AK (2018) Rosuvastatin as forthcoming antibiotic or as adjuvant additive agent: in vitro novel antibacterial study. Journal of Laboratory Physicians 10, 271–275.Google ScholarPubMed
Lüthje, P et al. (2013) Estrogen supports urothelial defense mechanisms. Science Translational Medicine 5, 190ra80.CrossRefGoogle ScholarPubMed
Ohtani, M et al. (2011) 17β-Estradiol suppresses Helicobacter pylori-induced gastric pathology in male hypergastrinemic INS-GAS mice. Carcinogenesis 32, 1244–1250.CrossRefGoogle ScholarPubMed
Hosoda, K et al. (2011) Steroid hormones as bactericidal agents to Helicobacter pylori. FEMS Microbiology Letters 318, 68–75.CrossRefGoogle ScholarPubMed
Johnson, CL et al. (2013) National health and nutrition examination survey: analytic guidelines, 1999–2010. Vital and Health Statistics 161, 1–24.Google Scholar
Prakash, AV et al. (2020) Repositioned drugs for inflammatory diseases such as sepsis, asthma, and atopic dermatitis. Biomolecules & Therapeutics 28, 222–229.CrossRefGoogle ScholarPubMed
Dong, G et al. (2019) A systematic framework for drug repurposing based on literature mining. 2019 IEEE International Conference on Bioinformatics and Biomedicine, pp. 939–942.CrossRefGoogle Scholar
Centers for Disease Control and Prevention (2013) Overview of NHANES Survey Design and Weights. Available at https://www.cdc.gov/Nchs/tutorials/environmental/orientation/sample_design/index.htm (Accessed 13 July 2020).Google Scholar
Centers for Disease Control and Prevention. NHANES 1999–2001 Data Documentation: Codebook, and Frequencies - H. pylori https://wwwn.cdc.gov/Nchs/Nhanes/1999-2000/LAB11.htm#LBXHP1 (Accessed 3 July 2020).Google Scholar
Meier, HCS et al. (2020) Helicobacter pylori seropositivity is associated with antinuclear antibodies in US adults, NHANES 1999–2000. Epidemiology and Infection 148, 1–5.CrossRefGoogle Scholar
Centers for Disease Control and Prevention. NHANES 1999-2001 Data Documentation: Codebook, and Frequencies - Prescription Medications. Available at https://wwwn.cdc.gov/Nchs/Nhanes/1999-2000/RXQ_RX.htm#FDACODE1 (Accessed 6 July 2020).Google Scholar
U.S. Food and Drug Administration (2020) National Drug Code Directory. Available at https://www.accessdata.fda.gov/scripts/cder/ndc/index.cfm (Accessed 6 July 2020).Google Scholar
Laine, L et al. (1998) Effect of proton-pump inhibitor therapy on diagnostic testing for Helicobacter pylori. Annals of internal medicine 129, 547–550.CrossRefGoogle ScholarPubMed
Graham, DY et al. (1991) Epidemiology of Helicobacter pylori in an asymptomatic population in the United States: effect of age, race, and socioeconomic status. Gastroenterology 100, 1495–1501.CrossRefGoogle Scholar
Moreira, ED et al. (2004) Risk factors for Helicobacter pylori infection in children: is education a main determinant? Epidemiology and Infection 132, 327–335.CrossRefGoogle ScholarPubMed
Suki, M et al. (2018) Helicobacter pylori infection is positively associated with an increased BMI, irrespective of socioeconomic status and other confounders: a cohort study. European Journal of Gastroenterology & Hepatology 30, 143–148.CrossRefGoogle ScholarPubMed
Ogihara, A et al. (2000) Relationship between Helicobacter pylori infection and smoking and drinking habits. Journal of Gastroenterology and Hepatology 15, 271–276.CrossRefGoogle ScholarPubMed
Zhang, L et al. (2010) Relationship between alcohol consumption and active Helicobacter pylori infection. Alcohol & Alcoholism 45, 89–94.CrossRefGoogle ScholarPubMed
Monno, R et al. (2019) Helicobacter pylori infection: association with dietary habits and socioeconomic conditions. Clinics and Research in Hepatology and Gastroenterology 43, 603–607.CrossRefGoogle ScholarPubMed
Simon, JA, Hudes, ES and Perez-Perez, GI (2003) Relation of serum ascorbic acid to Helicobacter pylori serology in US adults: the third national health and nutrition examination survey. Journal of the American College of Nutrition 22, 283–289.CrossRefGoogle ScholarPubMed
Rolle-Kampczyk, UE et al. (2004) Well water–one source of Helicobacter pylori colonization. International Journal of Hygiene and Environmental Health 207, 363–368.CrossRefGoogle ScholarPubMed
Krueger, WS and Wade, TJ (2016) Elevated blood lead and cadmium levels associated with chronic infections among non-smokers in a cross-sectional analysis of NHANES data. Environmental Health 15, 16.CrossRefGoogle Scholar
Centers for Disease Control and Prevention (2020) All About Adult BMI. https://www.cdc.gov/healthyweight/assessing/bmi/adult_bmi/index.html (Accessed 6 July 2020).Google Scholar
Centers for Disease Control and Prevention. NHANES 1999-2001 Data Documentation: Codebook, and Frequencies - Alcohol Use. Available at https://wwwn.cdc.gov/Nchs/Nhanes/1999-2000/ALQ.htm#ALQ100 (Accessed 6 July 2020).Google Scholar
Centers for Disease Control and Prevention. NHANES 1999-2000 Data Documentation, Codebook, and Frequencies - Housing Characteristics. Available at https://wwwn.cdc.gov/Nchs/Nhanes/1999-2000/HOQ.htm#HOQ070 (Accessed 10 July 2020).Google Scholar
Rao, JNK and Scott, AJ (1987) On simple adjustments to chi-square tests with sample survey data. The Annals of Statistics 15, 385–397.CrossRefGoogle Scholar
Shinchi, K et al. (1997) Relationship of cigarette smoking, alcohol use, and dietary habits with Helicobacter pylori infection in Japanese men. Scandinavian Journal of Gastroenterology 32, 651–655.CrossRefGoogle ScholarPubMed
Shimamoto, T et al. (2013) No association of coffee consumption with gastric ulcer, duodenal ulcer, reflux esophagitis, and non-erosive reflux disease: a cross-sectional study of 8,013 healthy subjects in Japan. PloS One 8, e65996.CrossRefGoogle ScholarPubMed
Zhou, X et al. (2013) Association between Helicobacter pylori infection and diabetes mellitus: a meta-analysis of observational studies. Diabetes Research and Clinical Practice 99, 200–208.CrossRefGoogle ScholarPubMed
Megraud, F et al. (2013) Helicobacter pylori resistance to antibiotics in Europe and its relationship to antibiotic consumption. Gut 62, 34–42.CrossRefGoogle ScholarPubMed
Gallo, MF et al. (2014) Combination contraceptives: effects on weight. Cochrane Database of Systematic Reviews 1, CD003987.Google Scholar
Kanbay, M et al. (2005) The relationship of ABO blood group, age, gender, smoking, and Helicobacter pylori infection. Digestive Diseases and Sciences 50, 1214–1217.CrossRefGoogle ScholarPubMed
Zeyrek, FY and Oguz, E (2005) In vitro activity of capsaicin against Helicobacter pylori. Annals of Microbiology 55, 125–127.Google Scholar
Figure 0

Fig. 1.Flow chart of study populations.

Figure 1

Table 1.Weighted characteristics of 799 participants by H. pylori seroprevalence, NHANES 1999–2000

Figure 2

Fig. 2.Weighted percentage of participants who were H. pylori seropositive by age group among those taking or not taking contraceptive drugs: NHANES 1999–2000.

Figure 3

Table 2.Weighted associations of individual variable and contraceptive drug use against H. pylori seroprevalence in 799 participants, NHANES 1999–2000

Figure 4

Table 3.Weighted association of contraceptive drug use and covariates with H. pylori seroprevalence in 799 participants, NHANES 1999–2000