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Evolution in coeliac disease diagnosis and management
被引:3
|作者:
Tye-Din, Jason A.
[1
,2
,3
,4
]
机构:
[1] Walter & Eliza Hall Inst Med Res, Immunol Div, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Dept Med Biol, Parkville, Vic, Australia
[3] Royal Melbourne Hosp, Dept Gastroenterol, Parkville, Vic, Australia
[4] Murdoch Childrens Res Inst, Ctr Food & Allergy Res, Parkville, Vic, Australia
来源:
JGH OPEN
|
2024年
/
8卷
/
07期
关键词:
coeliac disease;
diagnostics;
gluten;
novel therapies;
GLUTEN-FREE DIET;
PERSISTENT VILLOUS ATROPHY;
HISTOLOGICAL FOLLOW-UP;
MUCOSAL RECOVERY;
DOUBLE-BLIND;
LYMPHOPROLIFERATIVE MALIGNANCY;
ADULT PATIENTS;
ADHERENCE;
PREDICTORS;
SAFETY;
D O I:
10.1002/jgh3.13107
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
The traditional gut-centric view of coeliac disease is evolving as immune and genetic insights underscore the central importance of a systemic, T cell immune response to gluten in disease pathogenesis. As the field increasingly recognize the limitations of small intestinal histology as the diagnostic standard, data supporting the accuracy of an immune (serologic) diagnosis of coeliac disease - well demonstrated in children - are growing for adults. Novel biomarkers such as interleukin-2 that identify the gluten-specific T cell demonstrate high sensitivity and specificity for coeliac disease and offer the potential for a diagnostic approach that avoids the need for gluten challenge. Asymptomatic disease and manifestations outside the gut pose considerable challenges for diagnosis using a case-finding strategy and enthusiasm for population screening is growing. The gluten-free diet remains a highly restrictive treatment and there is a paucity of controlled data to inform a safe gluten intake threshold. Ongoing symptoms and enteropathy are common and require systematic evaluation. Slowly-responsive disease is prevalent in the older patient diagnosed with coeliac disease, and super-sensitivity to gluten is an emerging concept that may explain many cases of nonresponsive disease. While there is great interest in developing novel therapies for coeliac disease, no drug has yet been registered. Efficacy studies are generally assessing drugs in patients with treated coeliac disease who undergo gluten challenge or in patients with nonresponsive disease; however, substantial questions remain around specific endpoints relevant for patients, clinicians and regulatory agencies and optimal trial design. Novel immune tools are providing informative readouts for clinical trials and are now shaping their design. Our understanding of coeliac disease is evolving from a gut-centric view to recognizing it as a systemic illness driven by an aberrant T cell-mediated response to gluten. Interest in population screening is growing due to the failure of traditional case finding and reliance on small bowel histology is waning as serologic tests, now validated in both children and adults, prove effective. Novel biomarkers like interleukin-2 demonstrate high sensitivity and specificity for coeliac disease, potentially revolutionizing diagnostic approaches and aiding drug development. Despite significant interest in novel treatments, challenges persist in the design and execution of effective clinical trials. image
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