Type 2 diabetes is characterised by chronic hyperglycaemia and variable degrees of
insulin deficiency and resistance. Hyperglycaemia and elevated
fatty acids exert harmful effects on β-cell function, regeneration and apoptosis (gluco-lipotoxicity). Furthermore, chronic hyperglycaemia triggers a vicious cycle of
insulin resistance, low-grade
inflammation and a cascade of pro-atherogenic processes. Thus, timely near to normal
glucose control is of utmost importance in the management of type 2 diabetes and prevention of micro- and macroangiopathy. The majority of patients are multimorbid and obese, with critical comorbidities such as
cardiovascular disease,
heart failure and
chronic kidney disease. Recently published guidelines therefore recommend patient-centred risk/benefit-balanced use of oral
glucose-lowering drugs or a
glucagon-like peptide 1 (GLP-1) receptor agonist, or switching to
insulin with glycated haemoglobin (HbA1c) out of target. This article covers the indications of early
insulin treatment to prevent
diabetes-related complications, particularly in subgroups with severe
insulin deficit, and to achieve recovery of residual β-cell function. Furthermore, the individualised, risk/benefit-balanced, timely initiation of
insulin as second and third option is analysed. Timely
insulin initiation may prevent diabetes progression, reduce
diabetes-related complications and has less serious adverse effects. Basal
insulin is the preferred option in most clinical situations with consequences of undertreatment of chronic hyperglycaemia.