The American Journal of Gastroenterology · 2013 · 206 citations · 22 references
Life SciencesImmunologyPathologyAutoimmunityClinical ImmunologyImmunopathologyAutoimmune DiseasesCeliac DiseaseGastrointestinal ImmunologyGastrointestinal PathologyImmunodeficiency DisordersSerological DiagnosisAntibodiesCeliac Disease SerologyCeliac SerologyHla AllelesHla Risk AllelesImmunosuppressive Drug TherapySeronegative Celiac DiseaseVillous Atrophy
OBJECTIVES: Patients with villous atrophy (VA) and negative celiac disease (CD) serologies pose a diagnostic and therapeutic dilemma. When a definitive etiology for VA is not determined, patients are characterized as having unclassified sprue (US), the optimal management of which is unknown. METHODS: We studied adult patients with VA on biopsy and negative celiac serologies, evaluated at our tertiary referral center over a 10-year period. Testing for HLA DQ2/8 alleles, antienterocyte antibodies, giardia stool antigen, bacterial overgrowth, total serum immunoglobulins, and HIV was noted. Treatment, response, and repeat-biopsy findings were recorded. RESULTS: The most common diagnoses of the 72 patients were seronegative CD, medication-related villous atrophy, and US. Of those with US, the majority reported symptomatic improvement with immunosuppressive therapy. Some patients initially labeled as unclassified were found to have VA associated with olmesartan use. CONCLUSIONS: The role of medications in the development of VA and the optimal dose and length of immunosuppression for patients with US should be investigated further.
22
Severe Spruelike Enteropathy Associated With Olmesartan
Alberto Rubio‐Tapia, Margot L. Herman, Jonas F. Ludvigsson et al. · Mayo Clinic Proceedings · 2012 · 494 citations · Full text
Ulrich Wahnschaffe, Jörg–Dieter Schulzke, Martin Zeitz et al. · Clinical Gastroenterology and Hepatology · 2007 · 235 citations · Full text