scholarly journals Defining the Path Forward for Biomarkers to Address Unmet Needs in Inflammatory Bowel Diseases

2020 ◽  
Vol 26 (10) ◽  
pp. 1451-1462
Author(s):  
Gerard Honig ◽  
Caren Heller ◽  
Andrés Hurtado-Lorenzo

Abstract Despite major advances in the inflammatory bowel diseases field, biomarkers to enable personalized and effective management are inadequate. Disease course and treatment response are highly variable, with some patients experiencing mild disease progression, whereas other patients experience severe or complicated disease. Periodic endoscopy is performed to assess disease activity; as a result, it takes months to ascertain whether a treatment is having a positive impact on disease progression. Minimally invasive biomarkers for prognosis of disease course, prediction of treatment response, monitoring of disease activity, and accurate diagnosis based on improved disease phenotyping and classification could improve outcomes and accelerate the development of novel therapeutics. Rapidly developing technologies have great potential in this regard; however, the discovery, validation, and qualification of biomarkers will require partnerships including academia, industry, funders, and regulators. The Crohn’s & Colitis Foundation launched the IBD Biomarker Summit to bring together key stakeholders to identify and prioritize critical unmet needs; prioritize promising technologies and consortium approaches to address these needs; and propose harmonization approaches to improve comparability of data across studies. Here, we summarize the outcomes of the 2018 and 2019 meetings, including consensus-based unmet needs in the clinical and drug development context. We highlight ongoing consortium efforts and promising technologies with the potential to address these needs in the near term. Finally, we summarize actionable recommendations for harmonization, including data collection tools for improved consistency in disease phenotyping; standardization of informed consenting; and development of guidelines for sample management and assay validation. Taken together, these outcomes demonstrate that there is an exceptional alignment of priorities across stakeholders for a coordinated effort to address unmet needs of patients with inflammatory bowel diseases through biomarker science.

2011 ◽  
Vol 17 (12) ◽  
pp. 2558-2565 ◽  
Author(s):  
Laszlo Lakatos ◽  
Lajos S. Kiss ◽  
Gyula David ◽  
Tunde Pandur ◽  
Zsuzsanna Erdelyi ◽  
...  

2010 ◽  
Vol 151 (8) ◽  
pp. 293-301 ◽  
Author(s):  
Lajos Sándor Kiss ◽  
Péter László Lakatos

A Crohn-betegség (CD) és a colitis ulcerosa (UC) klinikai megjelenése igen változatos lehet a betegség megjelenésekor és a betegség lefolyása során. A legtöbb Crohn-betegnél a betegség lefolyása során különböző szövődmények jelennek meg, szűkület alakulhat ki, illetve perforáció jelentkezhet. A szövődmények miatt a betegek egy része végül sebészi kezelésre szorul. Az utóbbi években éppen ezért a kutatások egyik középpontjába került a betegség progresszióját előrejelző faktorok vizsgálata. Mivel a potenciálisan súlyos lefolyású betegekben a korai immunmodulátor és/vagy biológiai kezelés indokolt, fontos a prediktív faktorok ismerete és minél korábbi meghatározása. Ebben az összefoglaló közleményben a szerzők az irodalomban elérhető azon klinikai, endoszkópiás, laboratóriumi és genetikai faktorokra vonatkozó adatokat szeretnék áttekinteni, amelyek segítséget nyújthatnak a mindennapi gyakorlatban a klinikusok számára a megfelelő kezelési stratégia kiválasztásához.


2020 ◽  
Vol 27 (1) ◽  
pp. 10-11
Author(s):  
Yejoo Jeon ◽  
Berkeley N Limketkai

The Mediterranean diet was recently shown to benefit hepatic steatosis and disease activity in inflammatory bowel diseases. These findings advance our knowledge on dietary approaches for IBD and motivate inquiry on the role of obesity in IBD pathogenesis.


Author(s):  
Yonghong Yang ◽  
Cui Zhang ◽  
Dehuai Jing ◽  
Heng He ◽  
Xiaoyu Li ◽  
...  

Abstract Background Inflammatory bowel diseases (IBDs), including ulcerative colitis (UC) and Crohn’s disease (CD), are chronic inflammatory disorders. As is well known, interferon regulatory factor (IRF) 5 is closely associated with the pathogenesis of various inflammatory diseases. But the exact role of IRF5 in IBD remains unclear. Methods In this study, we detected IRF5 expression in peripheral blood mononuclear cells (PBMCs) and inflamed mucosa from IBD patients by immunohistochemistry, western blot, and quantitative real-time polymerase chain reaction. Peripheral blood CD4+ T cells were stimulated with inflammatory cytokines and transfected by lentivirus. Results In active IBD patients, the expression of IRF5 in PBMCs and inflamed colonic tissues was obviously increased and significantly associated with disease activity. Ectopic overexpression of IRF5 could promote the differentiation of IBD CD4+ T cells into Th1 and Th17 cells by regulating T-bet and RAR related orphan receptor C, whereas knockdown of IRF5 had the opposite effects. Tumor necrosis factor (TNF)-α upregulated expression of IRF5 in CD4+ T cells, but anti-TNF treatment with infliximab could markedly reduce IRF5 expression in CD4+ T cells and intestinal mucosa of CD patients. Conclusion Our study reveals a novel mechanism that IRF5 levels are correlated with disease activity in IBD and might function as a possible marker for the management of IBD via regulating Th1 and Th17 immune responses and cytokine production.


2019 ◽  
Vol 13 (Supplement_1) ◽  
pp. S436-S437
Author(s):  
L Godskesen ◽  
M Lindholm ◽  
J Høg Mortensen ◽  
A Krag ◽  
T Manon-Jensen ◽  
...  

2014 ◽  
Vol 146 (5) ◽  
pp. S-435-S-436
Author(s):  
Xian-rui Wu ◽  
Feza H. Remzi ◽  
XiuLi Liu ◽  
Lei Lian ◽  
Luca Stocchi ◽  
...  

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