This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Salomaa-Räsänen, A.
Right arrow Articles by Rautelin, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Salomaa-Räsänen, A.
Right arrow Articles by Rautelin, H.

 Previous Article  |  Next Article 

Clinical and Diagnostic Laboratory Immunology, November 2004, p. 1185-1188, Vol. 11, No. 6
1071-412X/04/$08.00+0     DOI: 10.1128/CDLI.11.6.1185-1188.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Age-Dependent Accuracy of Helicobacter pylori Antibody Assays for Adults, with Special Emphasis on Atrophic Gastritis

A. Salomaa-Räsänen,1,2* T. U. Kosunen,1 J. Mattila,3 S. Sarna,4 and H. Rautelin1,5

Department of Bacteriology and Immunology, Haartman Institute,1 Department of Public Health, University of Helsinki,4 Department of Microbiology, HUSLAB, Helsinki University Central Hospital, Helsinki,5 Vammala Health Center, Vammala,2 Department of Pathology, Tampere University Hospital, Tampere, Finland3

Received 8 June 2004/ Returned for modification 19 July 2004/ Accepted 8 September 2004


arrow
ABSTRACT
 
The accuracy of Helicobacter pylori antibody assays for 561 consecutive adult outpatients who had undergone gastroscopy was studied. The sensitivity of an immunoglobulin G test was 99 to 100% for all age groups, but the specificity declined by age group, from 99% for those aged 15 to 49 years to 75% for those aged ≥65 years. The exclusion of false-positive results for patients with atrophic gastritis improved the specificity to 93 to 97% for the older age groups.


arrow
TEXT
 
Helicobacter pylori infection is associated with gastritis, peptic ulcer disease, and gastric malignancies (1). In about one-third or up to one-half of those infected with H. pylori, gastritis proceeds to atrophic gastritis, resulting in a loss of mucosal glands, decreased helicobacter colonization and, when affecting the corpus mucosa, decreased secretion of pepsinogen I (PGI) (10, 23).

Most helicobacter-infected subjects have specific circulating immunoglobulin G (IgG) antibodies. However, IgA antibodies are found in approximately two-thirds of infected subjects (9). Of infected individuals, 2 to 7% show an elevated level of IgA antibody only (5, 9). Patients with atrophic corpus gastritis often have positive helicobacter serology, although microscopic examination (6, 22), culture of biopsy samples, and even the urea breath test remain helicobacter negative (8). These particular patients may still be infected, as shown by rapidly falling antibody titers after therapy (7).

Enzyme immunoassay (EIA) is the most commonly used serological method for detecting antibodies to H. pylori. The best commercial kits have shown sensitivities and specificities of 90% to in excess of 95% (3, 12). The present study focuses on the diagnostic accuracy of H. pylori IgG and IgA antibody tests for adults in different age groups, with special emphasis on the presence of atrophic gastritis.

(This study was presented in part at the XVth and the XVIth International Workshops on Gastrointestinal Pathology and Helicobacter, Athens, Greece, 11 to 14 September 2002, and Stockholm, Sweden, 3 to 6 September 2003.)

Patients. We analyzed the data from 561 consecutive adult outpatients (age range, 16 to 91 years; median age, 56 years; 60.4% [339] female), who had undergone gastroscopy due to clinical indications at the primary care level at Vammala Health Center, Vammala, Finland, from December 1998 to November 2002. Patients who had been treated successfully for helicobacter infection were excluded.

Biopsy samples. Gastroscopies were performed by one of the authors (A.S.-R.) in a routine manner, with two biopsies from the gastric antrum (2 cm or more from the pylorus), two biopsies from the large curve of the gastric corpus for histological examination, and additional biopsies (one from the antrum and one from the corpus) for culture.

Formalin-fixed biopsy specimens were embedded in paraffin. Tissue sections of 3 µm were cut at three levels per biopsy and placed on one slide. The tissue sections were stained with hematoxylin and eosin, Alcian blue (pH 2.5)-periodic acid-Schiff, and modified Giemsa. Gastritis was classified according to the Sydney System, in a blinded fashion, by one pathologist (J.M.) (20).

The biopsies were mailed for culture in Transpocult tubes (Orion Diagnostica, Espoo, Finland). The specimens were cultured for H. pylori for up to 12 days on Brucella agar plates (Becton Dickinson, Sparks, Md.) (18) supplemented with whole horse blood (7%) and on selective Brucella agar plates containing Iso-Vitalex (1%), vancomycin (6 mg/liter), amphotericin B (2 mg/liter), and nalidixic acid (20 mg/liter).

Results were considered helicobacter positive if culture or histology or both were positive.

Serum tests. Serum samples were taken during each patient's visit to the endoscopic unit and were stored at –20°C until analyzed. Sera were tested for H. pylori IgG and IgA antibodies and PGI levels (16) by using commercially available EIAs (Pyloriset EIA-G III, Pyloriset EIA-A III, and Gastroset PGI; Orion Diagnostica). According to the manufacturer's instructions, PGI values below 28 µg/liter were considered low. After validation (results not shown) of Pyloriset EIA-G III and Pyloriset EIA-A III tests, titers of 30 or higher were considered positive instead of the cutoff value of 20 recommended by the manufacturer.

Statistics. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were determined for each test and compared with the prevalence of H. pylori based on histology or culture or both. The statistical significance of the improvement of the specificity figures was examined by using Pearson chi-square and Fisher's exact tests. The trend in proportion by age was evaluated by using a linear-by-linear test. Statistical analyses were done by using StatView 5.0 and SPSS 12.0 software packages (SPSS, Inc., Chicago, Ill.).

Presence of H. pylori and atrophic gastritis. Endoscopic findings are shown in Table 1. Of the 181 H. pylori-positive patients, culture was positive for 173 (95.6%), while microscopy of the histological preparations revealed the presence of the bacterium for 161 (88.9%) (P = 0.0305). Of the patients with a positive culture result without helicobacter in histological examination, all 19 demonstrated chronic gastritis and 12 showed atrophic changes in the gastric mucosa.


View this table:
[in this window]
[in a new window]
 
TABLE 1. Endoscopic findings for the 561 consecutive patients referred for upper endoscopy

Of the 181 patients with H. pylori gastritis, 66 (36.5%) showed atrophic gastritis in histology, while 54 (14.2%) of the 380 H. pylori-negative patients demonstrated atrophic gastritis in biopsy specimens (P < 0.0001). The grades of atrophic changes in the corpus mucosa and their relationship to low PGI values are shown in Table 2. Of the 24 H. pylori-infected patients with atrophic changes in the antrum mucosa, 17 (70.8%) demonstrated low-grade atrophic changes and only 2 patients showed advanced severe atrophy in the antrum mucosa. Similarly, 7 (70%) of the 10 H. pylori-negative patients with atrophic changes in the antrum mucosa had low-grade changes and no patients had severe changes. Atrophic gastritis based on histology or a low PGI value was more common in the older age groups, appearing in 10.2, 17.2, and 39.6% of the patients aged 15 to 49, 50 to 64, and >65 years, respectively (P = 0.0001).


View this table:
[in this window]
[in a new window]
 
TABLE 2. Elevated H. pylori antibody levels of the IgG class, atrophic corpus gastritis, and low serum pepsinogen I in H. pylori-positive and -negative patients

H. pylori antibodies. In young adults with a low prevalence of H. pylori infection, the IgG test demonstrated very high sensitivity and specificity figures (100 and 99%, respectively) and PPVs and NPVs (95 and 100%, respectively) (Table 3). In the older age groups, the sensitivity of the IgG test was high (over 98%). The number of false-positive results increased with patient age, resulting in a decrease in specificity to 75% for patients aged 65 years or older. After exclusion of the patients with false-positive antibody values and atrophic gastritis, the specificity for the older age groups increased to 93 to 97% (Table 3).


View this table:
[in this window]
[in a new window]
 
TABLE 3. Sensitivities, specificities, PPVs, and NPVs of H. pylori EIA antibody tests for different age groups for all patients and after excluding patients with atrophic gastritisa

The sensitivity of the IgA test increased and the specificity of the IgA test decreased with patient age (Table 3). For young adults the specificity was 97%. After exclusion of the false-positive results for patients with atrophic gastritis, the specificity was 92 to 95% for older age groups (Table 3).

Comments. In this study, we applied a novel approach to observe the effect of increasing age and presence of atrophic gastritis on the diagnostic performance of H. pylori IgG and IgA tests. The IgG test was highly sensitive in adult patients, which makes it an excellent choice for the test-and-treat approach recommended for young adult dyspeptic patients (15, 21). Both tests demonstrated high specificity in subjects below 50 years of age, with a low prevalence rate of H. pylori infection but a lower performance in older subjects due largely to atrophic gastritis. However, the specificity improved clearly after older patients with atrophic gastritis and false-positive antibody results were excluded. In addition, in serologic assays, the prior use of antibiotics, antisecretory treatments, or the location or the reduced number of helicobacters on the gastric mucosa had no effect on the diagnostic accuracy (4). However, antisecretory treatments before gastroscopy may lead to false-negative results for histology, culture, and urease tests (2, 14). It is also known that H. pylori is absent from areas of intestinal metaplasia, a common finding with chronic gastritis (19).

The sensitivities and specificities of the commercial H. pylori antibody tests seemed to vary between 60 and 100% (3, 12). The accuracy of serological tests is strongly dependent on the prevalence of H. pylori infection (13, 17). Although it has been recommended that antibody assays be evaluated locally (4, 13), this has rarely been carried out for different age groups. Our results of the accuracy of the H. pylori IgG and IgA tests were superior to those reported earlier (3, 11, 12, 24). To avoid any misjudgment in the validation of serological tests for H. pylori antibodies in adult subjects, the validation should be carried out separately for different age groups with special emphasis not only on the known H. pylori status but also on the presence of atrophic gastritis.


arrow
ACKNOWLEDGMENTS
 
This study was supported in part by grants from Helsinki University's Research Fund and The Medical Research Fund of Tampere University Hospital.

We thank Pirjo Kosonen for her technical assistance and Orion Diagnostica for the Pyloriset and Gastroset kits.


arrow
FOOTNOTES
 
* Corresponding author. Mailing address: Department of Bacteriology and Immunology, Haartman Institute, P.O. Box 21 (Haartmaninkatu 3), FIN-00014 University of Helsinki, Helsinki, Finland. Phone: 358-9-19126296. Fax: 358-9-19126382. E-mail: anniina.salomaa{at}helsinki.fi. Back


arrow
REFERENCES
 
    1
  1. Blaser, M. J. 2004. Helicobacter pylori persistence; biology and disease. J. Clin. Investig. 113:321-333.[CrossRef][Medline]
  2. 2
  3. Chey, W. D., M. Spybrook, S. Carpenter, T. T. Nostrant, G. H. Elta, and J. M. Scheiman. 1996. Prolonged effect of omeprazole on the 14C-urea breath test. Am. J. Gastroenterol. 91:89-92.[Medline]
  4. 3
  5. Feldman R. A., J. J. Deeks, S. J. W. Evans, and the Helicobacter pylori Serology Study Group. 1995. Multi-laboratory comparison of eight commercially available Helicobacter pylori serology kits. Eur. J. Clin. Microbiol. Infect. Dis. 14:428-433.[CrossRef][Medline]
  6. 4
  7. Herbrink, P., and L. van Doorn. 2000. Serological methods for diagnosis of Helicobacter pylori infection and monitoring of eradication therapy. Eur. J. Clin. Microbiol. Infect. Dis. 10:164-173.
  8. 5
  9. Jaskowski, T. D., T. B. Martins, H. R. Hill, and C. M. Litwin. 1997. Immunoglobulin A antibodies to Helicobacter pylori. J. Clin. Microbiol. 35:2999-3000.[Abstract]
  10. 6
  11. Karnes, W. E., Jr., I. M. Samloff, M. Siurala, M. Kekki, P. Sipponen, S. W. R. Kim, and J. H. Walsh. 1991. Positive serum antibody and negative tissue staining for Helicobacter pylori in subjects with atrophic body gastritis. Gastroenterology 101:167-174.[Medline]
  12. 7
  13. Kokkola, A., H. Rautelin, P. Puolakkainen, P. Sipponen, M. Färkkilä, R. Haapiainen, and T. Kosunen. 1998. Positive result by serology indicates active Helicobacter pylori infection in patients with atrophic gastritis. J. Clin. Microbiol. 36:1808-1810.[Abstract/Free Full Text]
  14. 8
  15. Kokkola, A., H. Rautelin, P. Puolakkainen, P. Sipponen, M. Farkkila, R. Haapiainen, and T. U. Kosunen. 2000. Diagnosis of Helicobacter pylori infection in patients with atrophic gastritis: comparison of histology, 13C-urea breath test, and serology. Scand. J. Gastroenterol. 35:138-141.[CrossRef][Medline]
  16. 9
  17. Kosunen, T. U., K. Seppälä, S. Sarna, and P. Sipponen. 1992. Diagnostic value of decreasing IgG, IgA, and IgM antibody titers after eradication of Helicobacter pylori. Lancet 339:893-895.[CrossRef][Medline]
  18. 10
  19. Kuipers, E. J., A. M. Uyterlinde, A. S. Peña, R. Roosendaal, G. Pals, G. F. Nelis, H. P. M. Festen, and S. G. M. Meuwissen. 1995. Long-term sequelae of Helicobacter pylori gastritis. Lancet 345:1525-1528.[CrossRef][Medline]
  20. 11
  21. Ladas, S. D., I. Varzakakos, H. Malamou, S. Georgopoulos, G. Giota, K. Triantafyllou, T. Rokkas, C. Spiliadi, and S. A. Raptis. 2002. Evaluation of a single-step serological assay for laboratory diagnosis of Helicobacter pylori infection. Eur. J. Clin. Microbiol. Infect. Dis. 21:56-59.[Medline]
  22. 12
  23. Laheij, R. J. F., H. Straatman, B. M. J. Jansen, and A. L. M. Verbeek. 1998. Evaluation of commercially available Helicobacter pylori serology kits: a review. J. Clin. Microbiol. 36:2803-2809.[Free Full Text]
  24. 13
  25. Leodolter, A., K. Wolle, and P. Malfertheiner. 2001. Current standards in the diagnosis of Helicobacter pylori infection. Dig. Dis. 19:116-122.[Medline]
  26. 14
  27. Lerang, F., B. Moum, P. Mowinckel, J. B. Haug, E. Ragnhildstveit, T. Berge, and A. Bjorneklett. 1998. Accuracy of seven different tests for the diagnosis of Helicobacter pylori infection and the impact of H12-receptor antagonists on test results. Scand. J. Gastroenterol. 33:364-369.[CrossRef][Medline]
  28. 15
  29. Malfertheiner, P., F. Mégraud, C. O'Morain, A. P. Hungin, R. Jones, A. Axon, D. Y. Graham, G. Tytgat, et al. 2002. Current concepts in the management of Helicobacter pylori infection—the Maastricht 2-2000 consensus report. Aliment. Pharmacol. Ther. 16:167-180.[Medline]
  30. 16
  31. Oksanen, A., P. Sipponen, R. Karttunen, A. Miettinen, L. Veijola, S. Sarna, and H. Rautelin. 2000. Atrophic gastritis and Helicobacter pylori infection in outpatients referred for gastroscopy. Gut 46:460-463.[Abstract/Free Full Text]
  32. 17
  33. Oksanen, A., P. Sipponen, S. Sarna, and H. Rautelin. 2001. Serologic diagnosis of Helicobacter pylori infection in outpatients aged 45 years or less. Eur. J. Clin. Microbiol. Infect. Dis. 20:554-557.[Medline]
  34. 18
  35. Oksanen, A., L. Veijola, P. Sipponen, K.-O. Schauman, and H. Rautelin. 1998. Evaluation of Pyloriset Screen, a rapid whole-blood diagnostic test for Helicobacter pylori infection. J. Clin. Microbiol. 36:955-957.[Abstract/Free Full Text]
  36. 19
  37. Price, A. B. 1988. Histological aspects of Campylobacter pylori colonisation and infection of gastric and duodenal mucosa. Scand. J. Gastroenterol. 23 (Suppl. 142):21-24.
  38. 20
  39. Price, A. B. 1991. The Sydney System: histological division. J. Gastroenterol. Hepatol. 6:209-222.[Medline]
  40. 21
  41. Sobala, G. M., J. E. Crabtree, J. A. Pentith, B. J. Rathbone, T. M. Shallcross, J. I. Wyatt, M. F. Dixon, R. V. Heatley, and A. T. Axon. 1991. Screening dyspepsia by serology to Helicobacter pylori. Lancet 338:94-96.[CrossRef][Medline]
  42. 22
  43. Testoni, P. A., E. Colombo, L. Cattani, M. Longhi, F. Bagnolo, F. Lella, M. Buizza, and R. Scelsi. 1996. Helicobacter pylori serology in chronic gastritis with antral atrophy and negative histology for Helicobacter-like organisms. J. Clin. Gastroenterol. 22:182-185.[Medline]
  44. 23
  45. Valle, J., M. Kekki, P. Sipponen, T. Ihamäki, and M. Siurala. 1996. Long-term course and consequences of Helicobacter pylori gastritis. Results of a 32-year follow-up study. Scand. J. Gastroenterol. 31:546-550.[Medline]
  46. 24
  47. Weijnen, C. F., H. A. Hendriks, A. W. Hoes, W. M. Verweij, T. J. M. Verheij, and H. J. de Wit. 2001. New immunoassay for the detection of Helicobacter pylori infection compared with urease test, 13C breath test and histology: validation in the primary care setting. J. Microbiol. Methods 46:235-240.[CrossRef][Medline]


Clinical and Diagnostic Laboratory Immunology, November 2004, p. 1185-1188, Vol. 11, No. 6
1071-412X/04/$08.00+0     DOI: 10.1128/CDLI.11.6.1185-1188.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.





This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Salomaa-Räsänen, A.
Right arrow Articles by Rautelin, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Salomaa-Räsänen, A.
Right arrow Articles by Rautelin, H.