Ве молиме користете го овој идентификатор да го цитирате или поврзете овој запис: http://hdl.handle.net/20.500.12188/12027
DC FieldValueLanguage
dc.contributor.authorSzarek Men_US
dc.contributor.authorPitt Ben_US
dc.contributor.authorCannon CPen_US
dc.contributor.authorLeiter LAen_US
dc.contributor.authorMcGuire DKen_US
dc.contributor.authorLewis JBen_US
dc.contributor.authorRiddle MCen_US
dc.contributor.authorInzucchi SEen_US
dc.contributor.authorKosiborod MNen_US
dc.contributor.authorCherney DZIen_US
dc.contributor.authorDwyer JPen_US
dc.contributor.authorBhatt DLen_US
dc.contributor.authorScirica BMen_US
dc.contributor.authorSCORED Investigatorsen_US
dc.contributor.authorMilenkovic Tatjanaen_US
dc.date.accessioned2021-04-23T07:59:32Z-
dc.date.available2021-04-23T07:59:32Z-
dc.date.issued2021-01-14-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/12027-
dc.description.abstractBACKGROUND The efficacy and safety of sodium–glucose cotransporter 2 inhibitors such as sotagliflozin in preventing cardiovascular events in patients with diabetes with chronic kidney disease with or without albuminuria have not been well studied. METHODS We conducted a multicenter, double-blind trial in which patients with type 2 diabetes mellitus (glycated hemoglobin level, ≥7%), chronic kidney disease (estimated glomerular filtration rate, 25 to 60 ml per minute per 1.73 m2 of body-surface area), and risks for cardiovascular disease were randomly assigned in a 1:1 ratio to receive sotagliflozin or placebo. The primary end point was changed during the trial to the composite of the total number of deaths from cardiovascular causes, hospitalizations for heart failure, and urgent visits for heart failure. The trial ended early owing to loss of funding. RESULTS Of 19,188 patients screened, 10,584 were enrolled, with 5292 assigned to the sotagliflozin group and 5292 assigned to the placebo group, and followed for a median of 16 months. The rate of primary end-point events was 5.6 events per 100 patient-years in the sotagliflozin group and 7.5 events per 100 patient-years in the placebo group (hazard ratio, 0.74; 95% confidence interval [CI], 0.63 to 0.88; P<0.001). The rate of deaths from cardiovascular causes per 100 patient-years was 2.2 with sotagliflozin and 2.4 with placebo (hazard ratio, 0.90; 95% CI, 0.73 to 1.12; P=0.35). For the original coprimary end point of the first occurrence of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke, the hazard ratio was 0.84 (95% CI, 0.72 to 0.99); for the original coprimary end point of the first occurrence of death from cardiovascular causes or hospitalization for heart failure, the hazard ratio was 0.77 (95% CI, 0.66 to 0.91). Diarrhea, genital mycotic infections, volume depletion, and diabetic ketoacidosis were more common with sotagliflozin than with placebo. CONCLUSIONS In patients with diabetes and chronic kidney disease, with or without albuminuria, sotagliflozin resulted in a lower risk of the composite of deaths from cardiovascular causes, hospitalizations for heart failure, and urgent visits for heart failure than placebo but was associated with adverse events.en_US
dc.language.isoenen_US
dc.publisherMassachusetts Medical Societyen_US
dc.relation.ispartofNew England Journal of Medicineen_US
dc.titleSotagliflozin in Patients with Diabetes and Chronic Kidney Diseaseen_US
dc.typeArticleen_US
dc.identifier.doi10.1056/NEJMoa2030186-
dc.identifier.if74.699-
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
Прикажи едноставен запис

Page view(s)

51
Last Week
0
Last month
checked on 17.8.2025

Google ScholarTM

Проверете

Altmetric


Записите во DSpace се заштитени со авторски права, со сите права задржани, освен ако не е поинаку наведено.