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Performance evaluation of a rapid whole-blood immunoassay for the detection of IgG antibodies against Helicobacter pylori in daily clinical practice
Annals of Clinical Microbiology and Antimicrobials volume 15, Article number: 47 (2016)
A growing number of rapid Helicobacter pylori antibody tests are commercially available now, however, some of these tests are often used without sufficient evaluation. The aim of this study was to evaluate the performance of a commercially available rapid whole-blood immunoassay (gabControl® H. pylori; gabmed GmbH, Köln, Germany), for the qualitative detection of IgG antibodies against H. pylori with the 13C-urea breath test (13C-UBT) serving as a reference method.
A total of 108 consecutive outpatients, who were referred for 13C-UBT by general practitioners and specialists, were also tested for H. pylori infection by the gabControl® H. pylori immunoassay. The clinical performance of this rapid whole-blood test was evaluated by determining the sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) compared to the 13C-UBT. The agreement between the two tests was calculated using Cohen’s Kappa (κ) with 95 % confidence intervals (CI).
The agreement between the gabControl® H. pylori assay and the 13C-UBT was 0.62 [95 % confidence intervals (CIs) 0.47–0.76; P < 0.001]. With the 13C-UBT serving as the non-invasive gold standard method of H. pylori diagnosis, the gabControl® H. pylori assay demonstrated a sensitivity and specificity of 91.4 and 76.7 %, respectively, with a PPV of 65.3 % and a NPV of 94.9 %. Seventeen (15.7 %) individuals with a positive H. pylori anamnesis showed a negative 13C-UBT and were typed positive by the gabControl® H. pylori assay. Of these, 13 (76.5 %) and 3 individuals (17.6 %) had completed one and two eradication therapies, respectively.
The gabControl® H. pylori immunoassay is a rapid and easy to use first line screening tool for H. pylori IgG antibody detection in daily clinical practice. However, this assay should not be used for confirmation of the successful H. pylori eradication after antibiotic treatment.
Helicobacter pylori infection is still a common condition worldwide. In North Europe and North America, about one-third of adults are infected, whereas in South-East Europe, South America, and in Asia, the H. pylori prevalence is reported to be higher than 50 % .
Since the H. pylori infection was recognized as a causative agent of chronic active gastritis and a risk factor for ulcer disease, gastric cancer and the mucosa-associated lymphoid tissue (MALT) lymphoma, numerous invasive and non-invasive methods for the accurate detection of this bacterium have been developed. Invasive techniques include biopsy-based histological methods, culture of the bacterium, the rapid urease test, and molecular tests (e.g. real-time PCR). Non-invasive methods encompass the 13C-urea breath test (13C-UBT), the stool antigen test, and the H. pylori antibody detection by serological tests [2–4].
The 13C-UBT is considered the non-invasive gold standard method of H. pylori diagnosis [5–7]. It is a simple and safe test, which is easily repeated and provides excellent accuracy for the initial diagnosis of H. pylori infection, as well as the confirmation of its eradication after treatment [7, 8]. In the presence of the H. pylori produced enzyme urease, the ingested labeled urea (13C-urea) is metabolized into labeled carbon dioxide (13CO2) and ammonia (NH3). The produced 13CO2 diffuses into the blood vessels and is eliminated via the lungs. The expired air is collected in order to measure the activity of labeled carbon so as to detect individuals with H. pylori infection [5, 9, 10].
Since individuals infected with H. pylori develop a local and systematic immune response [11, 12], specific H. pylori antibodies can be detected by rapid serological assays. These tests are easy to perform, inexpensive, and enable immediate patient testing for H. pylori antibodies in general practice surgeries . A previous study, which evaluated a rapid whole-blood test, demonstrated, that there was no difference in diagnostic accuracy between capillary (fingerstick) and venous blood (venipuncture) collection . A growing number of rapid H. pylori antibody tests are commercially available now, however, some of these tests are often used without sufficient evaluation.
The aim of this study was to evaluate the performance of a commercially available rapid whole blood immunoassay (gabControl® H. pylori; gabmed GmbH, Köln, Germany), for the qualitative detection of IgG antibodies against H. pylori with the 13C-UBT serving as a reference method.
In total, 108 patients, who were consecutively referred for 13C-UBT by general practitioners and specialists to our outpatient clinic, were also tested for H. pylori infection by the gabControl® H. pylori immunoassay (gabmed GmbH, Köln, Germany). The study period was from January to December 2015. The inclusion criteria were a minimum age of >15 years, an overnight fasting state and a non-smoking period >12 h before the 13C-UBT. Patients with antibiotic-based therapy at least 4 weeks before and/or proton pump inhibitor (PPI) therapy at least 2 weeks before the 13C-UBT were excluded from the study. An anamnesis was carried out about the history of H. pylori infections, completed eradication therapies, and intake of medication. Written informed consent was provided from all the patients. The ethical approval for this study was obtained from the Ethical Committee of Upper Austria, Linz, Austria. The study was carried out in accordance with the latest version of the Declaration of Helsinki.
Isotope ratio mass spectrometry was employed using the IRIS®-13C-Infrared Isotope Analyzer System (Wagner Analysen Technik GmbH, Bremen, Germany). The 13C-UBT was performed according to the manufacturer’s instructions. Briefly: after a 12 h fasting period, breath samples were obtained before (baseline) and 30 min after the test drink intake (75 mg 13C-urea from the capsule dissolved in 200 mL fruit juice) early in the morning (8:00–10.00 a. m.). 13C/12C-isotope ratio differences between the value at 30 min and the baseline value were determined and expressed in delta over baseline (DOB, ‰). A sample was considered positive if the 30 min value was above a 4 ‰ cut-off level . Eating, drinking and/or smoking were not allowed until the 13C-UBT was completed.
GabControl® H. pylori
This commercially available test is a qualitative membrane based immunoassay for the qualitative detection of H. pylori IgG antibodies in whole-blood, serum or plasma. The test was performed in accordance with the manufacturer’s instructions. Approximately 50 µL of fingerstick whole-blood was sampled in a glass capillary tube and transferred to the specimen well (S) on the test device (Fig. 1a–c). One drop (approximately 40 µL) of dilution buffer containing H. pylori antigen-coated particles was added and allowed to migrate along a lateral-flow membrane thereby interacting with anti-human IgG antibodies immobilized as parallel lines. The test results were read after 10 min: a red control (C) line signal together with a red test (T) line signal (intense or faint) indicated the presence of H. pylori IgG antibody (Fig. 1a, b); showing a single red C line signal only, the assay was interpreted as negative (Fig. 1c). Assay read-out was performed independently by two physicians (i.e. four eyes principle), which were both blinded to the respective 13C-UBT result.
The agreement between the 13C-UBT and the gabControl® H. pylori assay was calculated using Cohen’s Kappa (κ) with 95 % confidence intervals (CIs) . Sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of the gabControl® H. pylori assay were calculated compared to the 13C-UBT. No adjustment for type I error was made. Therefore the concerning P values are only descriptive. Analyse-it® software version 2.30 (Analyse-it Software, Ltd, Leeds, United Kingdom) was used for statistical analysis.
Study population characteristics
Of 108 consecutively enrolled patients, 36 (33.3 %) were male and 72 (66.7 %) were female. The median age was 44.0 (range: 15–88) years. The main demographic and clinical characteristics of the study population are provided in Table 1. Fifty-eight (53.7 %) individuals had a positive history of previous H. pylori infections.
Performance of the gabControl® H. pylori assay
The gabControl® H. pylori assay was found positive and negative in 49/108 (45.4 %) and 59/108 (54.6 %) patients, respectively (Table 2). Of those patients with a positive result, fifteen (30.6 %) individuals showed faint red colored changes in the test line region (T) only (Fig. 1b).
The agreement between the gabControl® H. pylori assay and the 13C-UBT was 0.62 (95 % CI 0.47–0.76; P < 0.001). With the 13C-UBT serving as the non-invasive gold standard method of H. pylori diagnosis [5–7], the gabControl® H. pylori assay demonstrated a sensitivity and specificity of 91.4 and 76.7 %, respectively, with a PPV of 65.3 % and a NPV of 94.9 % (Table 2).
Thirty-five (32.4 %) individuals had a positive 13C-UBT. Twenty-seven (77.1 %) of these patients had a positive H. pylori anamnesis, whereas in 8 patients (22.9 %) H. pylori infection was detected for the first time. Seventeen (15.7 %) individuals with a positive H. pylori anamnesis showed a negative 13C-UBT and were typed positive by the gabControl® H. pylori assay. Of these, 13 (76.5 %) and 3 individuals (17.6 %) had completed one and two eradication therapies, respectively. One patient (5.9 %), however, did not undergo any kind of antibiotic treatment.
This study aimed to compare the performance of the gabControl® H. pylori rapid immunoassay with the 13C-UBT in 108 patients, who were referred by general practitioners and specialists to our outpatient clinic. As the 13C-UBT was considered the non-invasive gold standard method of H. pylori diagnosis [5–7], the gabControl® H. pylori assay demonstrated a sensitivity and specificity of 91.4 and 76.7 %, respectively, with a PPV of 65.3 % and a NPV of 94.9 %.
Several previous studies have evaluated other rapid whole blood test kits for H. pylori antibody detection, reporting sensitivities and specificities of 80.3–89.5 % and 78.0–93.5 %, and PPVs and NPVs of 83–92.9 % and 57.4–93.5 %, respectively [13, 17–19].
Herein, seventeen patients (15.7 %), who had a negative 13C-UBT result were found positive for H. pylori antibody by the gabControl® H. pylori testing. Of these, 16 (94.1 %) individuals had a positive H. pylori anamnesis with one or two completed eradication therapies most likely responsible for the relatively low specificity of 76.7 % observed for the gabControl® H. pylori assay as well as the substantial agreement of 0.62 (95 % CI 0.47–0.76; P < 0.001) between the two methodologies investigated here. Patients with previous eradication therapy might recently have overcome their infection and the 13C-UBT, as an indicator of current active infection, might be negative [20, 21]. Furthermore, it is known that it may take more than 1 year for H. pylori antibody to disappear after successful eradication . Moreover, post-treatment circulating H. pylori antibodies are considered to remain positive for a significant period or perhaps indefinitely in some patients [3, 4, 20].
The intake of proton pump inhibitors (PPIs) may be another possible explanation of discrepant test results between the 13C-UBT and the gabControl® H. pylori assay. While PPI intake at least 2 weeks before the 13C-UBT was an exclusion criterion of this study, the authors cannot guarantee, that all individuals strictly followed this instruction. Individuals with PPI intake within 2 weeks before the 13C-UBT may have false-negative breath test results, whereas H. pylori antibodies are serologically detectable [23–25].
Previous studies, which were performed in various populations with different geographical and socio-economic status, demonstrated, that the prevalence of antibodies against H. pylori increases with age [26–28]. A cross-sectional population study in Germany comprising 1797 individuals showed a H. pylori antibody prevalence of 48 % . These seroprevalence data are in agreement with our study that found IgG antibodies against H. pylori in 49/108 (45.4 %) individuals.
In clinical practice, it should be considered, that a positive IgG serology does not necessarily indicate an ongoing infection . As a consequence the 13C-UBT may not be replaced through rapid whole-blood IgG antibody screening tests for confirmation of the successful H. pylori eradication after antibiotic treatment.
Using finger-stick blood samples the gabControl® H. pylori assay is rapid and easy to perform as centrifugation is no necessary and results are available within 10 min. However, low antibody titers resulting in faintest signal intensities may lead to false negative read-outs as interpretation becomes highly subjective and should therefore be based on the four eyes principle.
The major limitation of this study is the lack of invasive biopsy-based methods (e.g. histology, bacterial culture and real-time PCR) for H. pylori detection.
In conclusion, the gabControl® H. pylori immunoassay is a rapid and easy to use first-line screening tool for H. pylori IgG antibody detection in daily clinical practice. However, it should not be used for confirmation of the successful H. pylori eradication after antibiotic treatment.
Mucosa-associated lymphoid tissue
13C-urea breath test
- CO2 :
- NH3 :
Delta over baseline
Positive predictive value
Negative predictive value
proton pump inhibitor
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All authors contributed to the design of the study. DE and GK collected the data. DE analyzed the data and wrote the first draft of the manuscript. GK revised the paper critically. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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Enko, D., Halwachs-Baumann, G., Stolba, R. et al. Performance evaluation of a rapid whole-blood immunoassay for the detection of IgG antibodies against Helicobacter pylori in daily clinical practice. Ann Clin Microbiol Antimicrob 15, 47 (2016). https://doi.org/10.1186/s12941-016-0161-1
- Helicobacter pylori
- Laboratory diagnosis