HbA1c levels and all-cause mortality in type 2 diabetic patients: Epidemiological evidence of the need for personalised therapeutic targets |
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Authors: | M Monami V Vitale C Lamanna N Bartoli D Martelli S Zannoni A Antenore G Toffanello N Marchionni E Mannucci |
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Institution: | 1. Section of Geriatric Cardiology and Medicine, Department of Cardiovascular Medicine, University of Florence, Careggi Teaching Hospital, Florence, Italy;2. Diabetes Agency, Careggi Teaching Hospital, Azienda Ospedaliero-Universitaria Careggi, Via delle Oblate n. 4, 50141 Florence, Italy |
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Abstract: | Background and AimThe aim of the present case-control study is to explore the effect of case mix on the relationship between glycated haemoglobin (HbA1c) and mortality in type 2 diabetic patients.Methods and ResultsA nested case-control study data set was generated from the cohort-study data set (n = 4140 type 2 diabetic outpatients) by sampling controls from the risk sets. Cases (n = 427) were compared with an equal number of controls chosen from those members of the cohort who were at risk for the same follow-up time of the case, matched for age (±3 years), sex, body mass index (BMI) (±2 kg m?2), duration of diabetes (±5 years), and Charlson's Comorbidity Score (CCS) (±1). The main predefined analysis was the comparison of cases and controls for proportion of patients with each HbA1c class (<6.5%, 6.5–7.4%, 7.5–8.4% and ≥8.5%).During a mean follow-up of 5.7 ± 3.5 years, 427 deaths were recorded. The lowest risk of death was observed in the HbA1c 6.5–7.4% category; a lower HbA1c was associated with a non-significant trend towards a higher risk. The risk associated with a low (<6.5%) HbA1c was significantly greater in patients who were insulin-treated than in the rest of the sample.ConclusionsThe present study suggests that glycaemic targets should be individualised on the basis of the characteristics of each patient, considering age, co-morbidity and duration of diabetes. Caution should be used in prescribing insulin to reach near-normoglycaemia, particularly in older, frail patients. |
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