BioMed Research International

BioMed Research International / 2014 / Article
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Peptic Ulcer Diseases: Genetics, Mechanism, and Therapies

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Research Article | Open Access

Volume 2014 |Article ID 568410 | 6 pages | https://doi.org/10.1155/2014/568410

The Utilization of a New Immunochromatographic Test in Detection of Helicobacter pylori Antibody from Maternal and Umbilical Cord Serum

Academic Editor: Seng-Kee Chuah
Received04 Jun 2014
Accepted09 Jul 2014
Published07 Aug 2014

Abstract

Background. Helicobacter pylori (H. pylori) was linked with several extragastrointestinal diseases, including preeclampsia and intrauterine growth restriction of fetus. One of the signals which can be transferred from mother to fetus is the H. pylori IgG antibody. Aims. We utilized a commercial immunochromatographic kit to detect the antibody in maternal and cord serum. Methods. Three hundred and forty-six females were enrolled and the blood samples were collected on antenatal examination and on delivery. The maternal H. pylori infection was determined by stool H. pylori antigen test. Results. One hundred and five females (30.3%) were H. pylori-infected, and the prevalence was higher in immigrants (43.5%) than in Taiwanese (28.7%, ). The sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of the kit were 77.1%, 88.0%, 73.6%, 89.8%, and 84.7%, respectively. This kit also had similar performance in cord serum. Comparing to the maternal result on delivery, this kit offered a consistent performance in antenatal maternal serum (kappa coefficient 0.92) and in cord serum (kappa coefficient 0.88). Conclusions. H. pylori IgG antibody can be transferred through the placenta into the fetal circulation. However, accuracy of the test kit needs to be evaluated before utilization in screening.

1. Introduction

Helicobacter pylori (H. pylori), a Gram-negative bacteria existing in the stomach, has been linked with many gastrointestinal diseases, such as peptic ulcer disease, gastric adenocarcinoma, and gastric mucosal-associated lymphoid tissue lymphoma [1]. Following the observation from public health studies, however, H. pylori was thought to be associated with several extragastrointestinal diseases [2], such as hematological disease (idiopathic thrombocytopenic purpura, unexplained iron deficiency anemia) [3, 4], cardiovascular disease [5], and neurological disorders [6]. Recently, studies focusing on the obstetric field mentioned the possible influence of H. pylori infection in pregnant female. The high prevalence of the H. pylori was observed in population who had preeclampsia during pregnancy [7]. The specific gastrointestinal symptom, hyperemesis gravidarum, was also linked with this bacterium [8], although the other study showed conflicting result [9]. These observations raise a concern about the necessity of knowing the H. pylori infection status for female in gestational age.

There are several methods to detect of H. pylori infection. One of them is the urease test using gastric mucosal tissue obtained during gastroendoscopy. Despite being proven that procedure is safe when performing on the pregnant women [10], the general unwillingness, the high cost, the invasiveness of the procedure, and the possible sampling error make it not the ideal choice for screening the H. pylori infection during pregnancy. The noninvasive tests include the urea breath test (UBT), the stool antigen test and the serum H. pylori IgG antibody test. The latest one is easy to perform during antenatal examination and the existence of the antibody was found to be associated with the intrauterine growth restriction [11]. How the maternal H. pylori antibody influences the growth of the fetus is still elusive, but, interestingly, the antibody can be transmitted transplacentally to the fetus [12, 13]. However, the detection of the serological antibody was frustrated because of the inconsistent accuracy caused by several factors, including the different antigen extracts the kit uses and variable H. pylori strain in different region [14, 15]. In the present study, we will evaluate the performance of a new immunochromatographic test kit and detect the existence of the H. pylori IgG antibody in both maternal and cord serum.

2. Materials and Methods

2.1. Subjects and Data Collection

This study was carried out according to the principles of the Declaration of Helsinki and was approved by the Institutional Review Board of E-Da Hospital (EMRP-096-092 and EMRP-099-052). Subjects were recruited from mothers who received regular antenatal examinations and/or delivered their babies at department of Gynecology and Obstetrics of E-Da Hospital in southern Taiwan between April 2008 and September 2011. Participation was voluntary. Informed consent was obtained from each subject and personal data regarding demographic characteristics and obstetric history was collected via questionnaire after interviewing with trained interviewers on participation and/or after baby delivery. Those who have history of gastric surgery, peptic ulcer, H. pylori-eradication treatment, or antibiotics or proton pump inhibitor prescription within two month before delivery were excluded. Blood samples from mothers were collected on receiving antenatal examination and/or on admission for delivery. After delivery, blood samples were also collected from umbilical cord vessels representing the existence of H. pylori antibody in baby’s circulation. The heparinized whole blood was centrifuged at 2,000 rpm for 10 min to isolate plasma supernatant. Stool samples from mothers were supplied during hospitalization for baby delivery. Both stool and serum samples were stored under −20°C until utilized.

2.2. Serum H. pylori IgG Detection

The IgG antibody to H. pylori in serum was detected using a commercial immunochromatographic test kit (ASSURE H. pylori Rapid Test, MP Biomedicals, USA). The procedure followed the manufacture’s protocol. In summary, 25 μL defrozen serum sample were added into the square well at the lower end of the kit. When the sample front moved upstream the viewing window and reached the pink control line labeled “A,” 2 drops of chase buffer were added into the oval well at upper end of the kit. Then pull the “Hp” marked tab until resistance was felt and add 1 drop of chase buffer into the square well. The result was read after 15 minutes by two trained technicians independently. Positive and negative controls were run simultaneously. The results were determined as both technicians had the same interpretation. The one which had invalid test result or discrepant interpretation was retested using a new device.

2.3. Stool H. pylori Antigen Detection

Another commercial kit (ImmunoCard STAT! HpSA, Meridian bioscience, Cincinnati, OH, USA), based on a lateral flow chromatography technique using monoclonal antibodies, was utilized for detection of H. pylori antigens in human stool. The procedure followed the manufacture’s protocol. In summary, stool specimen (5-6 mm in diameter) was transferred into diluent vial and mixed with sample diluent. After vortexing for 15 seconds, break the tip of the vial and dispense 4 drops into the round window at the lower end of the device and read the results after 5 minutes. The results were also interpreted independently by two technicians.

2.4. Statistical Analysis

Distribution of demographic and clinical characteristics of participants by H. pylori status was reported as means (± standard deviations (SD)) or number (frequency) and was analyzed by independent -test, Chi-square test, and Fischer’s exact test, whenever appropriate. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of H. pylori status in maternal and umbilical cord serum during delivery were presented, using H. pylori status in maternal stool specimens as gold standard. The reliability of H. pylori status in maternal serum during delivery and before delivery as well as in maternal serum and umbilical cord serum during delivery was compared by Kappa coefficient. All tests were performed by SAS 9.2 statistical software (SAS Institute Inc., Cary, NC); two-sided value less than 0.05 was considered statistically significant.

3. Results

Total 346 pregnant women were enrolled. The demographic characteristics were listed in Tables 1 and 2. Based on the result of stool H. pylori antigen detection, 105 subjects were infected with H. pylori on baby delivery, 241 subjects had negative stool test results, and the overall infection rate was 30.3%. There was no significant difference between these two groups in body mass index (BMI), education, daily habit (alcohol, smoking, and exercise), underline disease (diabetes mellitus (DM) and hypertension), and obstetric characteristics (parity, history of miscarriage, gestation age (GA), prematurity of infant, placenta weight, and gender of infant). The only difference but without significance was the nationality (). Within the enrolled subjects, 39 were immigrants from Singapore (2), Thailand (2), Cambodia (3), Vietnam (14), and China (18), respectively. Seventeen (43.5%) belonged to the H. pylori-infected group, and the prevalence was higher than in Taiwanese (28.7%).


H. pylori status determined by HpSA value
H. pylori (+)H. pylori (−)
Mean ± SDMean ± SD

Age (yrs) 10529.24 ± 4.5224129.15 ± 4.490.872
Height (cm)105157.99 ± 5.04241158.88 ± 4.920.124
Prepregnant weight (kg)10253.94 ± 7.8423755.63 ± 9.610.119
Prepregnant BMI10221.58 ± 2.7923722.03 ± 3.640.209
Weight gain (kg)10213.46 ± 4.0223713.02 ± 5.070.436
Placenta weight (g)105652.09 ± 126.10240645.42 ± 152.050.694
GA (weeks)10538.57 ± 1.1724138.45 ± 1.420.451

SD: standard deviation.

H. pyloric status determined by HpSA
H. pylori (+)H. pylori (−)-value
(%) (%)

Education
 <college48 (45.7)90 (37.5)0.152
 ≧college57 (54.3)150 (62.5)
Nationality
 Taiwan88 (83.8)218 (90.8)0.058
 Immigrant17 (16.2)22 (9.2)
Smoking status
 Yes2 (1.9)8 (3.3)0.729a
 No103 (98.1)233 (96.7)
Alcohol drinking
 Yes02 (0.8)1.000a
 No105 (100.0)238 (99.2)
Exercise
 ≧1 times/week37 (35.2)69 (28.8)0.229
 <1 times/week68 (64.8)171 (71.3)
Diabetes mellitus
 Yes4 (3.8)8 (3.3)0.760a
 No101 (96.2)233 (96.7)
Hypertension
 Yes3 (2.9)17 (7.1)0.124
 No102 (97.1)224 (92.9)
Parity
 151 (48.6)121 (50.2)0.806
 243 (41.0)100 (41.5)
 >311 (10.5)20 (8.3)
Miscarriage
 Yes13 (12.4)32 (13.3)0.820
 No92 (87.6)209 (86.7)
Type of delivery
 NSD/VED72 (68.6)158 (65.6)0.585
 C/S33 (31.4)83 (34.4)
Prematurity
 <37 weeks4 (3.8)11 (4.6)1.000a
 ≧37 weeks101 (96.2)230 (95.4)
Baby gender
 Male58 (55.2)140 (58.1)0.622
 Female47 (44.8)101 (41.9)

aFisher’s exact test.

Next, we evaluated the existence of H. pylori IgG antibody in maternal serum. Using the immunochromatographic device to test the serum sample collected on delivery, the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy were 77.1%, 88.0%, 73.6%, 89.8%, and 84.7%, respectively (Table 3). This commercial test also had similar performance when testing the serum collected from umbilical vein. Within 338 umbilical serum samples (100 from babies delivered from H. pylori-infected mothers), the sensitivity, specificity, and accuracy were 69.0%, 91.6%, and 84.9%, respectively, in comparison with maternal stool test results.


SensitivitySpecificityPPVNPVAccuracy
%%%%%
(n/N)(n/N)(n/N)(n/N)(n/N)

Maternal serum77.188.073.689.884.7
(81/105)(212/241)(81/110)(212/236)(293/346)
Umbilical serum69.091.677.587.684.9
(69/100)(218/238)(69/89)(218/249)(287/338)

: serum sample number; : stool sample number.

This commercial test also offers consistent results (Table 4). Within 324 participants who donated two blood samples (one collected when receiving antenatal examination and the other collected during admission for delivery), 314 had consistent result. Two participants were positive in antenatal test but negative in delivery. The situation of the other 8 cases was reversed, with negative result on antenatal but positive on delivery. The kappa coefficient was 0.92 (95% CI 0.88–0.97). Besides, when comparing between the maternal (on delivery) and the cord serum, 89 out of 105 H. pylori-infected mothers had positive cord serum antibody detection from their babies. On the other hand, none of the baby’s cord serum from H. pylori-negative mothers showed the existence of H. pylori antibody. The kappa coefficient was 0.88 (95% CI 0.83–0.93).


Maternal serum
on delivery
Kappa
coefficient
H. pylori (+)H. pylori (−)(95% CI)

Maternal serum, antenatal
H. pylori (+)9320.92
H. pylori (−)8221(0.88–0.97)
Cord serum
H. pylori (+)8900.88
H. pylori (−)16233(0.83–0.93)

4. Discussion

In the present study, we evaluated the H. pylori IgG antibody from maternal and cord serum using a commercial immunochromatographic test kit. It has been shown that the human immune system can produce variable antibodies with different molecular weight against H. pylori, either in serum (IgG) or in human milk (IgA) [13]. We found that, in cord serum, there was detectable H. pylori IgG antibody, and all these seropositive babies were delivered from seropositive mothers. The consistency of the H. pylori IgG antibody detection between maternal and cord serum suggested that the antibody in cord serum was transferred transplacentally, similar to the findings reported previously [12, 13]. However, the antibody was not detected from 16 infants who were delivered from H. pylori-seropositive mothers, and the relatively low antibody titer in cord serum might be the reason.

We utilized the stool antigen test as the gold standard of H. pylori infection. In fact, both UBT and stool antigen test are acceptable noninvasive test [16]. UBT has better performance, with a sensitivity of 88–95% and a specificity of 95%–100% [17]. It has also been proven that both 13C- (nonradioactive) and 14C-UBT (radioactive) are harmless in the pregnant female [18], with the possibility of the fetal radiation dose in the latter being much lower than the dose considered teratogenic [19]. However, the high cost and the unavailability in clinic limit its utilization. In the present study, we chose the stool antigen test for determining the H. pylori status and this test has been shown to have equal performance to UBT, with a sensitivity of 94% and a specificity of 92% [20].

Detection of the H. pylori IgG antibody in serum is an alternative method. The advantage of this test is that it is not affected by local changes in the stomach, such as bleeding, that could lead to false-negative results in the other tests. For female in pregnancy, it is an option to screen when they receive the regular antenatal examinations, using commercial available test kit. In the present study, we confirmed that the results obtained antenatally were consistent with the ones checked on baby delivery. However, this method has several disadvantages. Firstly, the performance of each test kit varies in different regions [21]. This depends on the H. pylori strain chosen for development of the IgG antibody and the prevalence of the strain in the given region, as the H. pylori strain differs in different countries or area [22]. Therefore, it is necessary to know the performance of a new test kit before utilizing it for screening. In the present study performed in southern Taiwan, the sensitivity, specificity, and accuracy of this test kit were 77.1%, 88.0%, and 84.7%, respectively, relatively lower than the data in manufacturer’s instructions which was tested in the other Asian countries. Secondary, the result cannot represent the current infection, as the antibody is still detectable months to years after successful H. pylori eradication [23, 24]. So it raises a concern about the interpretation of the association between disease and H. pylori when the infection is determined by the existence of H. pylori IgG antibody. All mentioned above might be the reasons to cause fluctuated association between H. pylori and variable disease, including preeclampsia [2527].

It has been mentioned that maternal H. pylori infection influences the development of the fetus [11]. The mechanism of intrauterine growth restriction is still elusive. Previous study proved that transmission of infection from mother to infant was not detected on delivery [28]. Therefore, the other factors associated with this bacterium, such as the transplacentally acquired antibody, should be taken into consideration. In fact, the human immune system responding to the H. pylori produces variable antibodies, and most of them can be detected in cord serum [13]. Although it has been shown that the transplacentally acquired antibody does not protect infants from colonization by H. pylori [12], it is necessary to further investigate its possible role during pregnancy.

Following the improvement of the hygiene condition and the comprehensive utilization of eradication, the prevalence of H. pylori infection is decreasing in Taiwan. The overall infection rate in the present study was 30.3%. Interestingly, when classifying the H. pylori-positive group, higher infection rate (43.5%) was found in immigrants who came from China and south-east Asian countries where the H. pylori prevalence was high [29]. It is worth observing how this situation will influence the prevalence of H. pylori in their next generation.

5. Conclusion

H. pylori is not only connected with gastrointestinal symptoms; in pregnant female, the related antibody can transfer through the placenta into the fetal circulation. The IgG antibody can be detected during antenatal examination using commercial test kit. However, accuracy of the test kit needs to be evaluated before utilization in screening. And the possible role of the H. pylori IgG antibody in the fetal development needs further investigation.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This study was supported by Grant from E-Da Hospital (Grant no. EDAHP99009), Kaohsiung Medical University Hospital (10104, KMUH102-2 M04), and Kaohsiung Medical University (KMU-Q103026).

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Copyright © 2014 Fu-Chen Kuo et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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