Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters











Database
Language
Publication year range
1.
J Clin Gastroenterol ; 51(2): 127-135, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27479142

ABSTRACT

BACKGROUND: The diagnosis and management of eosinophilic esophagitis (EoE) often requires multiple endoscopies. Serum biomarkers can be elevated in EoE patients, but their clinical utility in diagnosis and assessing response to treatment is not well established. GOALS: To evaluate serum biomarkers in EoE subjects compared with controls and assess longitudinally in response to treatment. STUDY: We conducted a prospective cohort study of children and adults undergoing esophagogastroduodenoscopy for suspected EoE. After completing an 8-week course of proton-pump inhibitor therapy, esophageal mucosal biopsies were obtained, as well as, serum analysis of absolute eosinophil count (AEC), eotaxin-3, eosinophil-derived neurotoxin (EDN), eosinophil cationic protein (ECP) and interleukin-5. Subjects with normal endoscopic and histologic findings constituted controls. Those meeting criteria for EoE underwent repeat esophagogastroduodenoscopy and biomarker measurements following treatment with topical steroids for 8 weeks. RESULTS: Median levels of AEC (263.50 vs. 102 cu/mm, P<0.001), ECP (26.98 vs. 5.20 ng/mL, P<0.001) and EDN (31.70 vs. 14.18 ng/mL, P=0.004) were significantly elevated in EoE subjects compared with controls and correlated with esophageal eosinophilia. Levels of AEC (odds ratio, 1.79; 95% confidence interval, 1.28-2.64) and ECP (odds ratio, 1.61; 95% confidence interval, 1.23-2.36) were associated with a diagnosis of EoE. Among the 5 biomarkers evaluated, only AEC significantly predicted esophageal eosinophilia following topical steroid therapy in EoE subjects (P=0.006). CONCLUSIONS: AEC, ECP, and EDN were higher in EoE subjects compared with controls and correlated with degree of esophageal eosinophilia. Furthermore, AEC predicted post-treatment eosinophilia, suggesting a potential role in monitoring EoE disease activity.


Subject(s)
Eosinophil Cationic Protein/blood , Eosinophil-Derived Neurotoxin/blood , Eosinophilic Esophagitis/blood , Eosinophilic Esophagitis/drug therapy , Eosinophils , Steroids/administration & dosage , Administration, Topical , Adolescent , Adult , Biomarkers/analysis , Biopsy , Case-Control Studies , Child , Child, Preschool , Drug Therapy, Combination , Endoscopy, Digestive System , Eosinophilic Esophagitis/pathology , Esophageal Mucosa/pathology , Female , Humans , Infant , Leukocyte Count , Longitudinal Studies , Male , Middle Aged , Predictive Value of Tests , Prospective Studies , Proton Pump Inhibitors/therapeutic use , Severity of Illness Index , Treatment Outcome , Young Adult
2.
J Pediatr Endocrinol Metab ; 28(9-10): 1101-6, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26024243

ABSTRACT

OBJECTIVE: The purpose of this study was to examine the effect of chronic swallowed glucocorticoids on adrenal function during the treatment of eosinophilic esophagitis (EoE) in children. METHODS: Serum cortisol levels were obtained in children with EoE pre- and post-treatment with swallowed glucocorticoids. Exclusion criteria included those on any additional steroid therapy. Once diagnosed with EoE by esophageal biopsy, subjects were treated based on current standard of care with either swallowed fluticasone or budesonide. At the time of follow-up, esophagogastroduodenoscopy and blood sampling was repeated. Both pre- and post-treatment serum cortisol samples were collected fasting, between 07:00 and 10:00, and determined using a competitive binding method assay. The distribution of differences in cortisol levels between the pre- and post-treatment samples satisfied the assumption for normality and were subsequently analyzed using the paired t-test. RESULTS: Pre- and post-treatment serum cortisol levels were examined in 14 children who met clinical and histological diagnostic criteria for EoE. Mean age was 10.1 years (range 2-17 years) with 71% male and 29% female subjects. Swallowed glucocorticoid treatment included fluticasone in 79% and budesonide in 21% of subjects. Mean dosage of fluticasone was 704 µg daily (range 220-880 µg daily) and budesonide 0.8 mg daily (range 0.5-1 mg daily), along with a mean treatment length of 17 weeks (range 8-43 weeks). No significant difference in serum cortisol was found following treatment with swallowed fluticasone or budesonide (mean change 1.9 µg/dL, p=0.75, SD of the change=21.2). CONCLUSIONS: Swallowed glucocorticoid therapy does not appear to significantly affect the adrenal axis in children, and therefore, may represent a safe therapy for EoE.


Subject(s)
Adrenal Glands/drug effects , Eosinophilic Esophagitis/drug therapy , Glucocorticoids/therapeutic use , Adolescent , Adrenal Glands/physiopathology , Child , Child, Preschool , Eosinophilic Esophagitis/blood , Eosinophilic Esophagitis/physiopathology , Female , Glucocorticoids/administration & dosage , Humans , Hydrocortisone/blood , Longitudinal Studies , Male , Prospective Studies
SELECTION OF CITATIONS
SEARCH DETAIL