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. Author manuscript; available in PMC: 2022 May 2.
Published in final edited form as: Ann N Y Acad Sci. 2021 Feb 6;1495(1):40–54. doi: 10.1111/nyas.14572

Figure 1.

Figure 1.

β cell secretory capacity data from an individual with adult-onset T1D, initially diagnosed with T2D and at the time of glucose-potentiated arginine testing before initiating insulin therapy. Under fasting conditions, the acute insulin (A) or C-peptide (B) response to arginine appear “normal” (although not when considering the fasting glucose was elevated at 162.5 mg/dL (not shown)), and further elevation of the glucose cannot further potentiate insulin release as the entire reserve capacity for secretion (~15% of normal) is already engaged under the fasting condition. The normal data are 95% CI based on 28 nondiabetic individuals.