Published online Apr 14, 2025. doi: 10.3748/wjg.v31.i14.104397
Revised: February 1, 2025
Accepted: March 21, 2025
Published online: April 14, 2025
Processing time: 113 Days and 9.4 Hours
Celiac disease (CD) is a systemic autoimmune disorder triggered by gluten ingestion ingenetically predisposed individuals. It is characterized by intestinal histological damage and the production of specific autoantibodies. The latest European Society for Paediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) 2020 guidelines have excluded human leukocyte antigen (HLA) genotyping from the no-biopsy diagnostic approach due to its weak positive predictive value, limited availability, and high cost in some countries. However, HLA genetic testing remains valuable in certain clinical contexts. This study provided practical indications for when to request and how to interpret HLA genotyping, emphasizing its continued relevance for CD diagnosis in specific cases. We also proposed a strategy for monitoring the risk of developing type 1 diabetes (T1D) in patients with CD, based on the risk stratification carried by different HLA genotypes. A retrospective analysis of 746 patients with CD and 627 controls was conducted at our hospital starting in 2012, when HLA geno
Core Tip: This guide explained how to interpret human leukocyte antigens (HLA) genetics associated with celiac disease (CD) and the different clinical situations where HLA genotyping can be useful in the diagnosis of CD. It also provided a strategy based on HLA genotyping for monitoring patients with CD at risk for the future development of type 1 diabetes (T1D). Only a subset of HLA genotypes linked to CD is associated with the development of T1D. Interestingly, some HLA genotypes that carry a high risk for CD may offer protection against T1D. Therefore, HLA genotyping in patients with CD could help in identifying those at high risk for T1D, enabling proactive interventions and therapies to preserve beta cell function.