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Long-term laboratory follow-up is essential in pediatric patients with celiac
Alexander Krauthammer1,2, Anat Guz-Mark1,2, Noam Zevit1,2
1Institute of Gastroenterology, Nutrition and Liver Diseases, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
Insights
Monitoring hemoglobin, ferritin, folate, liver, and thyroid function is crucial for pediatric celiac disease (CeD) patients during long-term follow-up, alongside celiac serology. These tests help detect potential abnormalities that may arise over time.
Area of Science:
- Pediatric Gastroenterology
- Clinical Diagnostics
- Autoimmune Diseases
Background:
- Celiac disease (CeD) necessitates lifelong monitoring.
- The utility of non-serological laboratory tests in CeD follow-up remains incompletely understood.
Purpose of the Study:
- To identify essential laboratory tests for monitoring pediatric celiac disease patients.
- To determine the prevalence and timing of laboratory abnormalities during long-term follow-up.
Main Methods:
- Retrospective chart review of 500 children diagnosed with CeD between 1999 and 2018.
- Analysis of demographic, clinical, and laboratory data from diagnosis through follow-up.
Main Results:
- Common initial abnormalities included low ferritin (64.3%), vitamin D (33.6%), zinc (29.9%), and hemoglobin (29.2%).
- Anemia developed during follow-up in 14.8% of patients; folate deficiency and abnormal liver enzymes also emerged later.
- Elevated TSH was noted in 5% of patients during follow-up.
Conclusions:
- Pediatric celiac disease patients exhibit diverse laboratory abnormalities at diagnosis and during follow-up.
- Continued monitoring of hemoglobin, ferritin, folate, liver function, and thyroid function is recommended alongside celiac serology.
Objectives:
Celiac disease (CeD) requires long-term follow. The role of laboratory testing other than celiac serology during follow up is unclear. We aimed to determine which laboratory tests are required during follow up based on the prevalence of abnormal tests and timing of abnormalities appearance.
Methods:
Retrospective chart-review of children diagnosed with CeD between 1999 and 2018 was conducted. Demographic, clinical and laboratory data were recorded from diagnosis and during follow-up.
Results:
The cohort included 500 children with CeD [59.8% females, median(IQR) age at diagnosis 5.7(3.7-8.9) years]. Mean follow-up time was 5.5 years (range 1.5-16.2). The most frequently abnormal laboratory tests at time of diagnosis were low ferritin (64.3%), vitamin D (33.6%), zinc (29.9%), hemoglobin (29.2%), and folate (14.7%). In 74 (14.8%) patients, anemia developed only during follow up, while in another 46 patients, anemia resolved after diagnosis and reappeared later (after a mean ± SD 2.8 ± 2.1 years from CeD diagnosis, for the entire group). Abnormal values that developed during follow up were low folate in 40 patients (3.9 ± 2.6 years), and abnormal liver enzymes in 18 patients (3.1 ± 2.7 years). Elevated TSH during follow-up was observed in 14/280 (5%) patients, after a mean ± SD of 2.2 ± 1.6 years from diagnosis. Patients diagnosed as teenagers (12-18 years) had shorter intervals to reappearance of anemia and folate deficiency.
Conclusions:
Multiple laboratory abnormalities may occur in pediatric patients with CeD, both at diagnosis and during long-term follow-up. We suggest continued monitoring of hemoglobin, ferritin, folate, liver, and thyroid function in addition to celiac serology during follow-up of CeD.
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