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Abstract
Objective To assess the association of serum vitamin D (VD) levels and Helicobacter pylori (H. pylori) cytotoxic-associated gene A (CagA) seropositivity, and further explore potential effect modifiers in this association.
Design Cross-sectional study.
Setting Data from phase I of the National Health and Nutrition Examination Survey (NHANES III, 1988–1991) led by the Center for Disease Control and Prevention.
Participants A total of 3512 US adults (≥20 years) with both serum VD levels and H. pylori CagA antibody data from NHANES III were included in the analysis.
Methods VD deficiency was defined as serum 25(OH)D concentrations<20 ng/mL. Logistic regression models were used to assess the association of serum VD levels and H. pylori CagA seropositivity (VD–Hp CagA+), and stratification analyses were used to explore potential effect modifiers.
Results There was no significant association of VD–Hp CagA+ in the general population. But serum 25(OH)D concentrations were associated with H. pylori CagA+ in non-Hispanic whites (adjusted OR=1.02, 95% CI: 1.00 to 1.03), other races/ethnicities (adjusted OR=1.08, 95% CI: 1.01 to 1.06), populations born in other countries (adjusted OR=1.09, 95% CI: 1.04 to 1.15) or occasional drinkers (adjusted OR=0.93, 95% CI: 0.88 to 0.99). VD deficiency was associated with H. pylori CagA+ in non-Hispanic whites (adjusted OR=0.69, 95% CI: 0.53 to 0.92), populations born in other countries (adjusted OR=0.47, 95% CI: 0.25 to 0.89), non-drinkers (adjusted OR=0.80, 95% CI: 0.65 to 0.99), occasional drinkers (adjusted OR=2.53, 95% CI: 1.06 to 6.05), population with first quartile level of serum ferritin (adjusted OR=0.70, 95% CI: 0.51 to 0.96) or fourth quartile level of serum folate (adjusted OR=0.63, 95% CI: 0.46 to 0.87).
Conclusions Racial/ethnic differences and different serum ferritin or serum folate levels may be effect modifiers for the association of VD–Hp CagA+.
- epidemiology
- gastrointestinal infections
- public health
Data availability statement
Data are available in a public, open access repository. All data used in article analyses are publicly available on the NHANES website: https://www.cdc.gov/nchs/nhanes/index.htm.
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
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Strengths and limitations of this study
To our best knowledge, this is the first study to explore the association of serum vitamin D (VD) levels with Helicobacter pylori cytotoxic-associated gene A (CagA) seropositivity using nationally representative data from the National Health and Nutrition Examination Survey.
We used a method based on statistical considerations to screen potential confounding factors and a comprehensive stratification analysis to explore potential effect modifiers in the association of serum VD levels with H. pylori CagA seropositivity.
This cross-sectional study did not allow us to determine the temporality and the causality between serum VD levels and H. pylori CagA seropositivity.
The lack of international, unequivocal threshold values for diagnosing VD deficiency might affect our study’s intensity.
We lacked data on participants’ time spent on sun exposure behaviours that could affect their serum VD levels.
Introduction
Helicobacter pylori (H. pylori) is a spiral-shaped gram-negative bacterium that colonises the human gastric mucosa.1 2 H. pylori infection, with the prevalence being approximately 44.3% worldwide, is believed to trigger several gastrointestinal diseases, including chronic gastritis, atrophic gastritis, peptic ulcer disease and mucosa-associated lymphoid tissue lymphoma.1–4 In addition, over 75% of all gastric cancer cases are associated with H. pylori infection.5 H. pylori strains may become more virulent when they are able to produce and secrete cytotoxin-associated gene A (cagA) protein.6 CagA gene, a part of the cag pathogenicity island that cagA is injected into the host cell and then it tethered with the inner surface of the cytoplasmic membrane during H. pylori attaching host cells, promotes the epithelial–mesenchymal transition, contributing to carcinogenesis.5–10 Clinically, it is verified that individuals with CagA seropositivity (CagA+) have an increased risk of gastric cancer.11 12 Therefore, in view of CagA’s significance for H. pylori pathogenicity, further exploring factors that influence CagA expression are needed.
Vitamin D (VD) is functionally a hormone rather than a vitamin and is an essential regulator of cell proliferation, differentiation, apoptosis and angiogenesis.13 14 In addition to osteoporosis and rickets, low serum VD levels also contribute to the increased risk of infections, chronic diseases and even cancers.15–19 Previous studies have indicated that lower serum VD levels could contribute to H. pylori infection in adults.1 17 20–25 Currently, a study showed that H. pylori CagA might be involved in inhibiting the MCOLN3 protein expression of the Ca2+ channel, leading to Ca2+ accumulation and impaired lysosomal acidification, which further inhibited autolysosomal degradation functions and promoted H. pylori infection.26 In contrast, VD3 could reverse the downregulated MCOLN3 protein expression and reactivate autolysosomal degradation functions to remove H. pylori in host cells.26 Based on the above studies, it is suggested that serum VD levels may also be associated with H. pylori CagA seropositivity. However, observational studies on their association are scarce. Therefore, using publicly available data from a national representative sample of the US adults, we assessed the association of serum VD levels with H. pylori CagA seropositivity (VD–Hp CagA+) and further explored potential effect modifiers in this association.
Methods
Study design and participants
The data of this cross-sectional study were from the National Health and Nutrition Examination Survey (NHANES). The NHANES, a series of surveys led by the Center for Disease Control and Prevention (CDC), provides multistage, national representative nutrition and health data of the civilian, non-institutionalised US population, which is used to assess the health and nutritional status of US adults and children since 1960s.27 NHANES includes in-person household interviews and health examinations from a mobile examination centre.
Data were selected from phase I of NHANES III (1988–1991) because serum 25(OH)D concentrations and H. pylori CagA antibody were only measured in this cycle. Participants aged 20 years or older were eligible to measure H. pylori CagA antibody from collected blood samples. Final samples were those with both serum 25(OH)D concentrations and H. pylori CagA antibody measurements.
Additionally, we excluded participants who were H. pylori seronegative because H. pylori CagA status was shown only in those with H. pylori seropositivity. Participants who reported taking VD supplements within the last month were also excluded in the present study because their serum VD levels might be inflated (figure 1).
Flowchart of the study population. CagA, cytotoxic-associated gene A; H. pylori, Helicobacter pylori; NHANES, National Health and Nutrition Examination Survey.
Measures of serum 25(OH)D concentrations
Serum 25(OH)D concentrations were measured at the National Center for Environmental Health, CDC, Atlanta, Georgia, USA, using a radioimmunoassay kit (Diasorin, Stillwater, Minnesota, USA) and the coefficients of variations were 13%–19% in the NHANES III.28 VD deficiency was defined as serum 25(OH)D concentrations <20 ng/mL.14
Measures of H. pylori CagA antibody
H. pylori CagA antibody was measured on participants 20 years or older from phase I of NHANES III by an immunoglobulin G enzyme-linked immunosorbent assay (Wampole Laboratories, Cranbury, New Jersey, USA) with sensitivity and specificity of 96%.29 30
Covariates
First, covariates in this study were selected based on previous studies, including age, sex, race/ethnicity, family income to poverty ratio, place of birth, marital status, education level, smoking status, alcohol consumption, physical exercise, source of drinking water, peptic ulcer, cardiovascular disease (eg, congestive heart failure, hypertension, heart attack and stroke), respiratory disease (eg, asthma, chronic bronchitis and emphysema), diabetes, osteoporosis, body mass index, haemoglobin, serum cholesterol, serum triglycerides, serum ferritin, serum folate, serum vitamin A, serum vitamin E, serum vitamin C, serum α-carotene, serum β-carotene, plasma glucose, glycated haemoglobin, serum C reactive protein, serum creatinine, serum thyroid stim hormone and serum thyroxine.1 14 20 21 31
Second, the above covariates with an estimated variance inflation factor (VIF) value of more than 5 would be excluded because of leading to multicollinearity.32 There was no multicollinearity among covariates showed by VIF tests (online supplemental table S1).
Supplemental material
Third, we selected the above covariates as potential confounders if they changed the estimates of serum 25(OH)D concentrations on H. pylori CagA+ more than 10%, or were significantly associated with H. pylori CagA+ (significant association was defined as p value<0.10) (online supplemental tables S2 and S3).33 34 Finally, the following covariates were selected as potential confounders in this study: age, sex (male, female), race/ethnicity (non-Hispanic white/black, Mexican American, other), place of birth (50 United States, Mexico, other), education level (less than high school, high school, high school above), alcohol consumption (never, <1 time/month, 2–4 times/month, >4 times/month), haemoglobin (g/dL), serum ferritin (ng/mL), serum folate (ng/mL), serum vitamin A (µg/dL), serum vitamin E (µg/dL) and serum β-carotene (µg/dL) (online supplemental table S4).
Statistical analysis
The descriptive analysis of population characteristics was performed to examine the distribution of each variable, including count and weighted proportion, weighted means and SD. χ2 test or Fisher’s exact test was used to analyse categorical variables, and Mann-Whitney U test or Kruskal-Wallis test was used to compare continuous variables.
Logistic regression models were used to assess the association of continuous serum 25(OH)D concentrations and VD deficiency with H. pylori CagA seropositivity. In model 1, we adjusted no factors. In model 2, we adjusted potential confounders that changed the estimates of serum 25(OH)D concentrations on H. pylori CagA seropositivity more than 10%, including age, sex, race/ethnicity, education level, serum folate, serum vitamin A, serum vitamin E and serum β-carotene. In model 3, we further adjusted potential confounders significantly associated with H. pylori CagA seropositivity (p value < 0.10), including place of birth, alcohol consumption, haemoglobin and serum ferritin. Finally, we stratified the above analyses by potential effect modifiers, including age groups, sex, race/ethnicity, place of birth, education level, alcohol consumption, haemoglobin, ferritin, folate, vitamin A, vitamin E and β-carotene. In addition, based on the Analytic and Reporting Guidelines of NHANES III,35 age was categorised into age groups with 10 years in each group. Serum concentrations of haemoglobin, ferritin, folate, vitamin A, vitamin E and β-carotene were categorised into quartiles to maximise the sample size in each stratum. The regression analyses were reported as ORs and 95% CIs.
Besides, to maximise statistical power and minimise bias that might occur if participants with missing data were excluded from analyses, we used multiple imputations (MI), based on five replications and a chained equation approach method in the MI procedure of R statistical software, to account for missing data.36 37 The MI data were only used for regression analyses. We repeated regression analyses using complete data for the comparison of primary outcomes (online supplemental tables S5 and S6).
All analyses used appropriate statistical weights provided in NHANES, and all tests were two sided with a p value < 0.05 considered statistically significant. All analyses were conducted with R’s statistical software packages (https://www.R-project.org, The R Foundation) and EmpowerStats (https://www.empowerstats.net/en/, X&Y Solution, Boston, Massachusetts, USA).
Patient and public involvement
There was no patient or public involvement in this study.
Results
A total of 3512 participants were included in our study, and the weighted prevalence of H. pylori CagA+ and VD deficiency was 53.69% and 37.81%, respectively (table 1). A majority reported non-Hispanic whites (64.89%), born in the USA (78.24%), high school education (52.14%) and non-drinkers (53.60%). The prevalence of H. pylori CagA seropositivity was higher with 20–49 years old (eg, 60.72% in 40–49 age group), race/ethnicity other than non-Hispanic white (eg, 77.63% in non-Hispanic black), populations born in other countries (64.77%), population with education level other than high school (eg, 56.63% in high school above) and drinkers (eg, 63.37% in occasional drinkers who had alcohol consumption<1 time/month). Significantly lower serum 25(OH)D concentrations with higher VD deficiency prevalence were shown in females and race/ethnicity other than non-Hispanic white.
Distribution characteristics of Helicobacter pylori CagA seropositive prevalence and vitamin D levels among 3512 US adults from the NHANES III
The association of serum 25(OH)D concentrations with H. pylori CagA+ was shown in table 2. In the general population, H. pylori CagA+ was negatively associated with serum 25(OH)D concentrations (OR=0.98, 95% CI: 0.97 to 0.99). While the direction of the association was reversed after adjusting for potential confounders in model 2 and model 3, the association was neither statistically significant (models 2 and 3: OR=1.02, 95% CI: 0.99 to 1.04). In stratified analyses, the adjusted association of serum 25(OH)D concentrations with H. pylori CagA+ was statistically significant in non-Hispanic white (adjusted OR=1.02, 95% CI: 1.00 to 1.03), other race/ethnicity (adjusted OR=1.08, 95% CI: 1.01 to 1.06), populations born in other countries (adjusted OR=1.09, 95% CI: 1.04 to 1.15) and occasional drinkers (adjusted OR=0.93, 95% CI: 0.88 to 0.99). No statistically significant association was shown in any other strata.
OR (95% CI) for the association of serum 25(OH)D concentrations with Helicobacter pylori cytotoxic-associated gene A seropositivity
The association of VD deficiency with H. pylori CagA+ was shown in table 3. Similarly, the adjusted association of VD deficiency with H. pylori CagA+ in the general population was neither statistically significant (models 2 and 3: adjusted OR=0.90, 95% CI: 0.77 to 1.05). In stratified analyses, the adjusted association was statistically significant in non-Hispanic white (adjusted OR=0.69, 95% CI: 0.53 to 0.92), populations born in other countries (adjusted OR=0.47, 95% CI: 0.25 to 0.89), non-drinkers (OR=0.80, 95% CI: 0.65 to 0.99), occasional drinkers (adjusted OR=2.53, 95% CI: 1.06 to 6.05), population with quartile 1 level (ranging from 2 to 48 ng/mL, weighted mean±SD: 26.58±13.69 ng/mL) of serum ferritin (adjusted OR=0.70, 95% CI: 0.51 to 0.96) or quartile 4 level (ranging from 6.9 to 60.7 ng/mL, weighted mean±SD: 11.57±4.76 ng/mL) of serum folate (adjusted OR=0.63, 95% CI: 0.46 to 0.87). No statistically significant association was shown in any other strata.
OR (95% CI) for the association of vitamin D deficiency with Helicobacter pylori cytotoxic-associated gene A seropositivity
Discussion
Previous studies have found that serum VD levels are associated with H. pylori infection, while the association of VD–Hp CagA+ is unclear.1 17 20–25 Therefore, using a national representative sample of US adults, we assessed the association of VD–Hp CagA+ and further explored potential effect modifiers in this association. The present study showed that serum VD levels trended to be positively associated with Hp CagA+ in the general population after adjusting potential confounders, although this association was not statistically significant. While in stratified analyses, we found that serum VD levels were significantly positively associated with Hp CagA+ in non-Hispanic white, other race/ethnicity, populations born in other countries, non-drinkers, populations with first quartile level of serum ferritin or fourth quartile level of serum folate. Possible explanations are as follows:
First, racial/ethnic differences in VD levels and the prevalence of H. pylori CagA+ are significant. In the US cross-sectional study of VD metabolism, white populations had higher baseline serum 25(OH)D and lower parathyroid hormone concentrations compared with black populations and other races/ethnicity.38 The other cohort study showed that the prevalence of H. pylori CagA+ among black populations were approximately two times higher than that among white populations.39 In comparison, almost all isolated H. pylori strains were CagA positive among East Asian populations.6 Such differences may vary VD–Hp CagA+ in different races/ethnicities, although we only observed significant VD–Hp CagA+ in non-Hispanic whites and other races/ethnicities. The present study showed that VD–Hp CagA+ was positively correlated among non-Hispanic whites with higher baseline serum 25(OH)D concentrations and lower Hp CagA+ prevalence. In comparison, a negative correlation of VD–Hp CagA+ was shown among non-Hispanic blacks with lower baseline serum 25(OH)D concentrations and higher Hp CagA+ prevalence. Besides, we also found a significant association of VD–Hp CagA+ in populations born in other countries. However, this association was more likely to go along with racial/ethnic differences. For instance, 75.43% of populations born in 50 United States were non-Hispanic white, and almost all of the populations born in Mexico were Mexican American (data not shown).
Second, the effect of alcohol intake on serum VD levels or H. pylori infection is still controversial. A recent review summarised that research before 2000 mainly was carried out among specific populations with small sample sizes. The results tended to show no correlation or negative correlation between alcohol intake and serum VD levels. In comparison, after 2000, research that had larger sample sizes and more extended follow-up periods trended to show a positive correlation.40 Additionally, although alcohol intake was found to be linked to the increased risk of gastric cancer, studies only demonstrated this association in individuals with heavy alcohol intake or H. pylori seronegativity.41 A recent systematic review further showed that no significant association could be found between H. pylori infection and alcohol consumption.42 The present study’s descriptive analysis of population characteristics showed significant differences in serum 25(OH)D as well as Hp CagA+ prevalence between occasional drinkers and populations with other alcohol intakes. Moreover, we found a significantly positive association of VD–Hp CagA+ among non-drinkers but a significantly negative association of VD–Hp CagA+ among occasional drinkers. In contrast, the association of VD–Hp CagA+ tended to be positive among populations with other alcohol intakes. It seems that occasional drinkers could be regarded as an effect modifier in the association of VD–Hp CagA+. However, we noted that the weighted proportion of occasional drinkers was deficient (5.41%) in the present study. Hence its association’s statistical significance might be inflated by stratified analyses. Besides, the significant association of VD–Hp CagA+ among non-drinkers could not indicate the effect of alcohol intake on the association of VD–Hp CagA+. Therefore, we considered that the effect of alcohol intake on the association of VD–Hp CagA+ was still limited.
Third, Hp CagA+ may be associated with iron status and one-carbon metabolites. A recent study found that one-carbon metabolism (involving serum folate, vitamin B12 and homocysteine levels) was mainly mediated by iron status (involving serum ferritin levels and transferrin saturation), while H. pylori infection could increase reactive oxygen species (ROS) by weakening iron status or indirectly reducing one-carbon metabolism levels.43 Protein expression levels of CagA were subsequently upregulated in response to oxidative stress.44 It is suggested that lower levels of iron status or one-carbon metabolism may contribute to H. pylori CagA+. We found some evidence in the present study, which showed a significantly positive association of VD–Hp CagA+ among populations with first quartile level of serum ferritin and fourth quartile level of serum folate. But there are contradictions in our result: based on the outcomes of the above studies, populations with first quartile level may have lower serum folate levels and higher ROS levels, which should be more likely to result in H. pylori CagA+. However, respectively only 32.03% and 23.54% of this subgroup populations had their serum ferritin and folate levels lower than minimum cutoffs (data not shown), which might result from the study sample from national representative populations, rather than hospital inpatients or other specific people. Therefore, we inferred that their antioxidant status might still be equal to inhibit the protein expression of CagA and lead to decreased H. pylori CagA+. More observational and mechanistic studies on the role of iron status and one-carbon metabolites in the relationship between VD levels and H. pylori CagA+ are needed.
Not fully understanding the influencing factors of H. pylori CagA+ is a crucial research gap. To our knowledge, this is the first study to explore the association of VD–Hp CagA+ using nationally representative data. Based on previous studies on the relationship between VD levels and H. pylori infection, we further used a method based on statistical considerations to screen potential confounding factors. Moreover, we used a comprehensive stratification analysis to explore potential effect modifiers in this association, finding that racial/ethnic differences and different serum ferritin or folate levels may affect the association of VD–Hp CagA+. Future randomised controlled trials of VD–Hp CagA+ may need to fully consider the effects of race/ethnicity, serum ferritin and serum folate levels.
However, there are limitations to our studies. First, the data used in the present study are not current because the date of serum VD levels and H. pylori CagA antibody is only provided in NHANES III. Second, this study was designed as a cross-sectional study, which did not allow us to determine the temporality and the causality between VD levels and H. pylori CagA+. Third, the lack of international, unequivocal threshold values for diagnosing VD deficiency might affect our study’s intensity. Fourth, we also lacked data on participants’ time spent on sun exposure behaviours that could affect their VD levels. At last, the lack of data on quantity of alcohol or times of alcohol intake, which will affect the results.
Conclusions
In a nationally representative sample, VD levels may be not associated with H. pylori CagA seropositivity in the general population. Still, racial/ethnic differences and different serum ferritin or serum folate levels may be effect modifiers for the association of serum VD levels with H. pylori CagA seropositivity.
Data availability statement
Data are available in a public, open access repository. All data used in article analyses are publicly available on the NHANES website: https://www.cdc.gov/nchs/nhanes/index.htm.
Ethics statements
Patient consent for publication
Ethics approval
This study involves human participants but was not approved by Data used for analysis in this study is publicly available on the NHANES website. The National Center for Health Statistics Research Ethics Review Board provided approval for the NHANES data collection. Use of the public use data sets requires neither Institutional Review Board review nor an exempt determination. Participants gave informed consent to participate in the study before taking part.
References
Supplementary materials
Supplementary Data
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Footnotes
Contributors Conceptualisation: LH and W-mK; methodology: LH, W-mK and Y-jR; formal analysis: W-mK and Y-jR; original draft preparation: W-mK; review and editing: LH, XC, QL, WC and HP; supervision: LH, XC, QL, WC and H-gP; project administration and funding acquisition: LH; guarantor: LH.
Funding This work was supported by the National Natural Science Foundation of China, Grant numbers: 81774238 and 82174298.
Competing interests None declared.
Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Provenance and peer review Not commissioned; externally peer reviewed.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.