Su1200 The Contribution of Clinical Factors, Serology and Genetics in Differentiating Inflammatory Bowel Disease Type Unclassified

2015 ◽  
Vol 148 (4) ◽  
pp. S-435-S-436
Author(s):  
Thomas Billiet ◽  
Isabelle Cleynen ◽  
Vera Ballet ◽  
Karolien Claes ◽  
Fred Princen ◽  
...  
2017 ◽  
Vol 64 (2) ◽  
pp. e52-e54 ◽  
Author(s):  
Nicole T. Lawrence ◽  
Tayoot Chengsupanimit ◽  
Laurie M. Brown ◽  
Terry G.J. Derks ◽  
G. Peter A. Smit ◽  
...  

Author(s):  
Alyce Anderson ◽  
Cynthia Cherfane ◽  
Benjamin Click ◽  
Claudia Ramos-Rivers ◽  
Ioannis E Koutroubakis ◽  
...  

Abstract Background Inflammatory bowel disease (IBD) is associated with alterations of the innate and adaptive immune systems. Monocytes respond to inflammation and infection, yet the relationship between monocytosis and IBD severity is not fully understood. We aimed to characterize the prevalence of monocytosis in IBD and the association between monocytosis and disease severity and IBD-related health care utilization. Methods We used a multiyear, prospectively collected natural history registry to compare patients with IBD with monocytosis to those without monocytosis, among all patients and by disease type. Results A total of 1290 patients with IBD (64.1% with Crohn disease; 35.9% with ulcerative colitis) were included (mean age 46.4 years; 52.6% female). Monocytosis was found in 399 (30.9%) of patients with IBD (29.3% with Crohn disease; 33.9% with ulcerative colitis). Monocytosis was significantly associated with abnormal C-reactive protein level and erythrocyte sedimentation rate, anemia, worse quality of life, active disease, and increased exposure to biologics (all P < 0.001). Compared with patients without monocytosis, patients with monocytosis had a 3-fold increase in annual financial health care charges (median: $127,013 vs. $32,925, P < 0.001) and an increased likelihood of hospitalization (adjusted odds ratio [AOR], 4.5; P < 0.001), IBD-related surgery (AOR, 1.9; P = 0.002), and emergency department (ED) use (AOR, 2.8; P < 0.001). Patients with monocytosis had a shorter time to surgery, hospitalization, and ED visit after stratifying by disease activity (all P < 0.05). Conclusions Patients with IBD with monocytosis, regardless of disease type, are at increased risk for worse clinical outcomes, hospitalization, surgery, and ED use. Peripheral monocytosis may represent a routinely available biomarker of a distinct subgroup with severe disease.


2008 ◽  
Vol 134 (4) ◽  
pp. A-346 ◽  
Author(s):  
Thomas A. Ullman ◽  
Daniel Wild ◽  
Seamus J. Murphy ◽  
Adam S. Cheifetz ◽  
Miles Sparrow ◽  
...  

Blood ◽  
2020 ◽  
Vol 136 (9) ◽  
pp. 1033-1043 ◽  
Author(s):  
Saskia B. Wortmann ◽  
Johan L. K. Van Hove ◽  
Terry G. J. Derks ◽  
Nathalie Chevalier ◽  
Vijaya Knight ◽  
...  

Abstract Neutropenia and neutrophil dysfunction cause serious infections and inflammatory bowel disease in glycogen storage disease type Ib (GSD-Ib). Our discovery that accumulating 1,5-anhydroglucitol-6-phosphate (1,5AG6P) caused neutropenia in a glucose-6-phosphatase 3 (G6PC3)–deficient mouse model and in 2 rare diseases (GSD-Ib and G6PC3 deficiency) led us to repurpose the widely used antidiabetic drug empagliflozin, an inhibitor of the renal glucose cotransporter sodium glucose cotransporter 2 (SGLT2). Off-label use of empagliflozin in 4 GSD-Ib patients with incomplete response to granulocyte colony-stimulating factor (GCSF) treatment decreased serum 1,5AG and neutrophil 1,5AG6P levels within 1 month. Clinically, symptoms of frequent infections, mucosal lesions, and inflammatory bowel disease resolved, and no symptomatic hypoglycemia was observed. GCSF could be discontinued in 2 patients and tapered by 57% and 81%, respectively, in the other 2. The fluctuating neutrophil numbers in all patients were increased and stabilized. We further demonstrated improved neutrophil function: normal oxidative burst (in 3 of 3 patients tested), corrected protein glycosylation (2 of 2), and normal neutrophil chemotaxis (1 of 1), and bactericidal activity (1 of 1) under treatment. In summary, the glucose-lowering SGLT2 inhibitor empagliflozin, used for type 2 diabetes, was successfully repurposed for treating neutropenia and neutrophil dysfunction in the rare inherited metabolic disorder GSD-Ib without causing symptomatic hypoglycemia. We ascribe this to an improvement in neutrophil function resulting from the reduction of the intracellular concentration of 1,5AG6P.


2019 ◽  
Vol 35 (6) ◽  
pp. 988-993
Author(s):  
Sang Hyoung Park ◽  
Sung Wook Hwang ◽  
Byong Duk Ye ◽  
Soomin Noh ◽  
Jae Cheol Park ◽  
...  

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