PEDIATRICS Vol. 104 No. 2 August 1999, p. e22
Received Nov 24, 1998; accepted Mar 12, 1999.
,
From the * Department of Pediatrics, Tohoku University School of
Medicine; and
Department of Pediatrics, Sendai City Hospital,
Sendai, Japan.
Objective. There have been few studies concerning serum titers of anti-Helicobacter pylori immunoglobulin G (IgG) antibody >12 months after eradication of the original infection. Moreover, clinical usefulness of immunoglobulin A (IgA) antibody levels remains to be established. The purpose of this study was to investigate long-term responses of serum IgG-specific and IgA-specific antibodies to H pylori in children after eradication therapy.
Study Design. A total of 34 children, 2 to 17 years of age
(mean: 11.7 years) with H pylori-associated
gastroduodenal disease received eradication therapy (proton pump
inhibitor-based dual or triple regimens). Diagnoses included nodular
gastritis (n = 8), gastric ulcer
(n = 7), and duodenal ulcer (n = 19). Upper gastrointestinal endoscopy and biopsy were performed
before the therapy and at 1 to 2 months' posttreatment. H
pylori infection and eradication were defined by biopsy-based
tests; eradication was successful in 28 patients and unsuccessful in 6. Pretreatment IgG was positive in 30 patients (88.2%), and the IgA was
positive in 31 (91.2%), who were entered into this study (duration
24 months). Serum samples were obtained before treatment and at 1, 3, 6, 12, 18, and 24 months' posttreatment. IgG and IgA antibodies were
measured using commercial enzyme immunoassay kits (HM-CAP and PP-CAP;
Enteric Products, Inc, New York, NY).
Results. Compared with pretreatment values, IgG and IgA
antibodies significantly and steadily decreased at 1 through 24 months' posttreatment in successfully treated patients. A decrease in
titer of the IgA class was significantly greater than that of the IgG
class at 1 to 12 months' follow-up. There was no significant decrease
in titer of either antibody in all but 2 patients with eradication failure. A
30% decrease in titer of the IgA antibody at 6 months indicated eradication with sensitivity of 90.5% and specificity of
100%. For the IgG antibody, a 30% decrease at 12 months showed equal
sensitivity and specificity. Seroreversion rates of IgG and IgA
antibodies were 53% and 48% at 12 months and were 86% and 81% at 24 months, respectively. The mean periods from the completion of
eradication therapy to seroreversion of IgG and IgA antibodies were
11.2 ± 7.0 and 11.6 ± 7.8 months, respectively (not
significantly different). A higher pretreatment titer of IgG antibody
was related to a longer period of seroreversion (r = 0.44). In one patient, 13C-urea breath
test-confirmed reinfection was accompanied by reappearance of
significant titers of the IgG and IgA antibodies.
Conclusions. A serology test is useful for evaluating
eradication in children. Approximately half of patients with successful
eradication remained to be IgG-seropositive and IgA-seropositive at 12 months' posttreatment. When a decrease titer in antibody is used for
assessing eradication, an endpoint of
6 months is required. The IgA
antibody may be a more convenient indicator of H pylori
status than is the IgG antibody.
Key words:
Helicobacter
pylori,
serum antibody,
eradication,
IgG,
IgA.
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