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T., Moon, M
doi: 10.1016/0014-5793(81)80288-8 19 LundPKGoodmanRHDeePCHabenerJF
10.1016/j.ejogrb.2016.02.009 104 KovacsS
However, there may be brief fluctuations during the transition period when tirzepatide is at its starting dose
While the inflammation-reducing and fibrosis-attenuating effects of glucagon agonism are less well-characterized, the reductions in hepatic inflammation parameters and fibrosis observed in preclinical models likely reflect secondary effects consequent to improved steatosis, rather than direct anti-inflammatory actions [21]
35 (2), E48E54
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