Rosiglitazone evaluated for cardiovascular outcomes in oral agent combination therapy for type 2 diabetes (RECORD): a multicentre, randomised, open-label trial
Randomized controlled trial published in Lancet (London, England) (2009)
Abstract
BACKGROUND: Rosiglitazone is an insulin sensitiser used in combination with metformin, a sulfonylurea, or both, for lowering blood glucose in people with type 2 diabetes. We assessed cardiovascular outcomes after addition of rosiglitazone to either metformin or sulfonylurea compared with the combination of the two over 5-7 years of follow-up. We also assessed comparative safety. METHODS: In a multicentre, open-label trial, 4447 patients with type 2 diabetes on metformin or sulfonylurea monotherapy with mean haemoglobin A(1c) (HbA(1c)) of 7.9% were randomly assigned to addition of rosiglitazone (n=2220) or to a combination of metformin and sulfonylurea (active control group, n=2227). The primary endpoint was cardiovascular hospitalisation or cardiovascular death, with a hazard ratio (HR) non-inferiority margin of 1.20. Analysis was by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00379769. FINDINGS: 321 people in the rosiglitazone group and 323 in the active control group experienced the primary outcome during a mean 5.5-year follow-up, meeting the criterion of non-inferiority (HR 0.99, 95% CI 0.85-1.16). HR was 0.84 (0.59-1.18) for cardiovascular death, 1.14 (0.80-1.63) for myocardial infarction, and 0.72 (0.49-1.06) for stroke. Heart failure causing admission to hospital or death occurred in 61 people in the rosiglitazone group and 29 in the active control group (HR 2.10, 1.35-3.27, risk difference per 1000 person-years 2.6, 1.1-4.1). Upper and distal lower limb fracture rates were increased mainly in women randomly assigned to rosiglitazone. Mean HbA(1c) was lower in the rosiglitazone group than in the control group at 5 years. INTERPRETATION: Addition of rosiglitazone to glucose-lowering therapy in people with type 2 diabetes is confirmed to increase the risk of heart failure and of some fractures, mainly in women. Although the data are inconclusive about any possible effect on myocardial infarction, rosiglitazone does not increase the risk of overall cardiovascular morbidity or mortality compared with standard glucose-lowering drugs. FUNDING: GlaxoSmithKline plc, UK.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Zusammenfassung
Rosiglitazone is an insulin sensitiser used in combination with metformin, a sulfonylurea, or both, for lowering blood glucose in people with type 2 diabetes.
Warum dies für die Hirudotherapie relevant ist
Diese multizentrische, randomisierte, offene Studie untersuchte kardiovaskuläre Endpunkte bei 4.447 Patienten mit Typ-2-Diabetes, die randomisiert zusätzlich Rosiglitazon oder eine Metformin-Sulfonylharnstoff-Kombination über eine mittlere Nachbeobachtungszeit von 5,5 Jahren erhielten. Rosiglitazon erreichte Nicht-Unterlegenheit für den primären Endpunkt der kardiovaskulären Hospitalisierung oder des kardiovaskulären Todes (HR 0,99; 95-%-KI 0,85–1,16), erhöhte jedoch signifikant das Risiko für Herzinsuffizienz-Hospitalisierung oder -Tod (HR 2,10; 95-%-KI 1,35–3,27) sowie die Frakturraten der oberen und distalen unteren Extremitäten, vorwiegend bei Frauen. Dieser Artikel behandelt die Thiazolidindion-Sicherheit und blutzuckersenkende Strategien im Diabetesmanagement. Er weist keinerlei Verbindung zu Blutegeln, Hirudotherapie oder dem Blutegelsekretom auf, und es besteht keine vertretbare Relevanz für die Domäne der ASH.
Zitation
Rosiglitazone evaluated for cardiovascular outcomes in oral agent combination therapy for type 2 diabetes (RECORD): a multicentre, randomised, open-label trial
Home PD et al. · Lancet (London, England), 2009
Verwandter klinischer Kontext
Erfahren Sie, wie diese Forschung mit der klinischen Praxis verknüpft ist
Zur ASH-Bibliothek hinzugefügt: May 27, 2026 · Letzte Aktualisierung der Website: 18. Juni 2026