Aims/hypothesis In a population-based setting, we investigated whether diabetes-related morbidity and all-cause mortality within 2 years of HbA 1c measurement were associated with that HbA 1c level in individuals with type 2 diabetes. The main objective was to compare outcomes in those with HbA 1c ≥ and <7% (53 mmol/mol). Methods Individuals with type 2 diabetes from Aarhus County, Denmark, were identified from public data files in a 3 year period (2001)(2002)(2003). Stratifying the 17,760 individuals by HbA 1c , we estimated HRs for diabetes-related morbidities and all-cause mortality using Cox regression. Results were also stratified by treatment modality. Results In total, 1,805 individuals experienced at least one diabetes-related morbidity and 1,859 individuals died. In general, the HRs in adjusted analyses of diabetes-related morbidity and mortality were increased for HbA 1c ≥7% (53 mmol/ mol): morbidity, HR 1.48 (95% CI 1.34, 1.63); and mortality, HR 1.26 (95% CI 1.15, 1.39). On grouping individuals according to HbA 1c <5% (31 mmol/mol), 5.0-5.9% (31-41 mmol/mol), 6.0-6.9% (42-52 mmol/mol), 7.0-7.9% (53-63 mmol/mol), 8.0-8.9% (64-74 mmol/mol) and ≥9% (75 mmol/mol), the HRs for mortality formed a U shape, with HbA 1c 6.0-6.9% (42-52 mmol/mol) at the lowest point. For diabetes-related morbidity, a dose-response pattern appeared (lowest for HbA 1c <5% [31 mmol/mol]). Patterns of HR differed with treatment modality. Conclusions/interpretation An HbA 1c level ≥7% (53 mmol/ mol) was associated with increased morbidity and mortality. Both high and very low levels of HbA 1c were associated with increased mortality. A dose-response pattern appeared for morbidity. The impact of HbA 1c level on morbidity and mortality depended on treatment modality.