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Fluorescence-mediated Tomography for the Detection and Quantification of Macrophage-related Murine Intestinal Inflammation
Published on: December 15, 2017
Precision medicine in inflammatory bowel diseases
1Division of Gastroenterology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Abstract:
Inflammatory bowel diseases comprising Crohn's disease and ulcerative colitis have emerged as global diseases. Multiple distinct therapeutic mechanisms have allowed us to increase our rates of achieving remission and reducing permanent disease-related morbidity. However, there is limited data to inform relative positioning of different therapies. This review will summarize existing literature on use of clinical decision models to inform relative efficacy of one therapeutic mechanism compared to the other given individual patient characteristics. It will also demonstrate the value of serologic, transcriptomic (from biopsies), and microbiome-based biomarkers in identifying which therapy is most likely to work for a given patient. We will review the existing gaps in the literature in this field and suggest a path forward for future studies to better inform patient care, incorporating the principles of precision medicine in the management of inflammatory bowel disease.
Insights
Precision medicine can improve inflammatory bowel disease (IBD) treatment. Biomarkers and decision models help select the best therapy for individual patients, optimizing outcomes and reducing long-term complications.
Area of Science:
- Gastroenterology
- Immunology
- Genomics
Background:
- Inflammatory bowel diseases (IBD), including Crohn's disease and ulcerative colitis, are increasingly prevalent global health issues.
- Advances in therapeutic mechanisms have improved remission rates and reduced disease-related morbidity.
- Current data is insufficient to guide the optimal sequencing of these diverse therapies for individual patients.
Purpose of the Study:
- To review clinical decision models for comparing therapeutic efficacy based on patient characteristics.
- To highlight the utility of biomarkers (serologic, transcriptomic, microbiome) in predicting treatment response.
- To identify literature gaps and propose future research directions for precision medicine in IBD management.
Main Methods:
- Literature review of clinical decision models in IBD therapy.
- Analysis of studies utilizing biomarkers for treatment selection.
- Synthesis of existing evidence to identify research gaps.
Main Results:
- Clinical decision models show promise in guiding therapy selection.
- Biomarkers such as serologic, transcriptomic, and microbiome profiles can predict individual treatment efficacy.
- Significant gaps exist in understanding the comparative effectiveness of different therapeutic mechanisms.
Conclusions:
- Integrating clinical decision models and biomarkers is crucial for personalized IBD management.
- Future research should focus on validating these approaches to optimize patient care.
- Adopting precision medicine principles can enhance treatment outcomes for IBD patients.
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