https://www.selleckchem.com/mTOR.html
5 ± 2.8 vs. 5.8 ± 2.6, P less then 0.001) and received fewer automated boluses (3.5 ± 1.0 vs. 6.0 ± 1.6, P less then 0.001). Participants in the lowest (vs. the highest) TIR-quartile received more insulin per body weight (1.13 ± 0.27 vs. 0.87 ± 0.20 U/kg/d, P = 0.008). However, in a multivariate model adjusting for baseline TIR, user-initiated boluses and insulin-per-body-weight were no longer significant. Conclusions Higher baseline TIR is the strongest predictor of TIR on CLC in children with T1D. However, lower baseline TIR is associated wit
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