AI Article Synopsis

  • The standard of care for Type 1 diabetes (T1D) has not significantly changed since the 1920s, relying mainly on various insulin types to manage symptoms without addressing the root cause, the autoimmune response.
  • There is a pressing need for new treatment options that target both the symptoms and the underlying immune issues associated with T1D.
  • Progress towards effective therapies in humans could hinge on using biomarkers in clinical trials, which may help establish a new standard of care that tackles autoimmunity alongside symptom management.

Article Abstract

The standard of care (SoC) for Type 1 diabetes (T1D) today is much the same as it was in the early 1920s, simply with more insulin options-fast-acting, slow-acting, injectable, and inhalable insulins. However, these well-tolerated treatments only manage the symptoms and complications, but do nothing to halt the underlying immune response. There is an unmet need for better treatment options for T1D that address all aspects of the disease. For decades, we have successfully treated T1D in preclinical animal models with immune-modifying therapies that have not demonstrated comparable efficacy in humans. The path to bringing such options to the clinic will depend on the implementation and standard inclusion of biomarkers of immune and therapeutic efficacy in T1D clinical trials, and dictate if we can create a new SoC that treats the underlying autoimmunity as well as the symptoms it causes.

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Source
http://dx.doi.org/10.1016/j.clim.2015.05.021DOI Listing

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