Persistent Mucosal Damage and Risk of Fracture in Celiac Disease
2014 (English)In: Journal of Clinical Endocrinology and Metabolism, ISSN 0021-972X, E-ISSN 1945-7197, Vol. 99, no 2, 609-616 p.Article in journal (Refereed) Published
Context: Celiac disease (CD) is associated with an increased fracture risk, an increase that persists after diagnosis. A significant proportion of patients with CD have persistent villous atrophy (VA) on follow-up biopsy.
Objective: The objective of the study was to determine whether persistent VA impacts long-term fracture risk.
Design: This was a cohort study.
Setting and Patients: We identified all patients in Sweden with histological evidence of CD who underwent a follow-up biopsy and compared patients with persistent VA with those with mucosal healing.
Main Outcome Measures: The following were measured: 1) any fracture; 2) likely osteoporotic fracture (defined as fractures of the hip, distal forearm, thoracic and lumbar spine, or proximal humerus); and 3) hip fracture.
Results: Of 7146 patients, VA was present on follow-up biopsy in 43%. There was no significant association between persistent VA and overall fractures [hazard ratio (HR) of persistent VA compared with those with healing 0.93, 95% confidence interval (CI) 0.82-1.06] or with likely osteoporotic fractures (HR 1.11, 95% CI 0.84-1.46). Persistent VA was associated with an increased risk of hip fracture (HR 1.67, 95% CI 1.05-2.66). Hip fracture risk increased, depending on the degree of VA (HR for partial VA compared with those with healing 1.70, 95% CI 0.82-3.49, HR for subtotal/total VA compared with those with healing 2.16, 95% CI 1.06-4.41).
Conclusions: Persistent VA on follow-up biopsy is predictive of hip fracture risk. The association between persistent VA and hip fractures, but not fractures overall, implies that thinner sc tissue
Place, publisher, year, edition, pages
Endocrine Society , 2014. Vol. 99, no 2, 609-616 p.
Endocrinology and Diabetes
IdentifiersURN: urn:nbn:se:oru:diva-56576DOI: 10.1210/jc.2013-3164ISI: 000333460300061PubMedID: 24432993ScopusID: 2-s2.0-84896701102OAI: oai:DiVA.org:oru-56576DiVA: diva2:1082959