دورية أكاديمية

Comparative effectiveness of cardiovascular, renal and safety outcomes of second-line antidiabetic drugs use in people with type 2 diabetes: A systematic review and network meta-analysis of randomised controlled trials.

التفاصيل البيبلوغرافية
العنوان: Comparative effectiveness of cardiovascular, renal and safety outcomes of second-line antidiabetic drugs use in people with type 2 diabetes: A systematic review and network meta-analysis of randomised controlled trials.
المؤلفون: Sim, Ruth, Chun Wie Chong, Loganadan, Navin K., Fong, Alan Y. Y., Leenhapong Navaravong, Hussein, Zanariah, Khunti, Kamlesh, Wen Huey Lee, Shaun
المصدر: Diabetic Medicine; Mar2022, Vol. 39 Issue 3, p1-20, 20p
مصطلحات موضوعية: THERAPEUTIC use of protease inhibitors, CARDIOVASCULAR disease prevention, STROKE risk factors, KIDNEY disease prevention, SODIUM-glucose cotransporters, CHRONIC kidney failure, META-analysis, MEDICAL information storage & retrieval systems, CONFIDENCE intervals, FEMALE reproductive organ diseases, SYSTEMATIC reviews, MAJOR adverse cardiovascular events, HYPOGLYCEMIC agents, DISEASE incidence, SULFONYLUREAS, GASTROINTESTINAL diseases, TYPE 2 diabetes, TREATMENT effectiveness, NECROTIZING pancreatitis, MEDLINE, ODDS ratio, GLUCAGON-like peptide-1 agonists, MALE reproductive organ diseases, BLOOD volume, AMPUTATION, PATIENT safety, DIABETIC acidosis, DISEASE risk factors
مستخلص: Aims: To compare the cardiovascular, renal and safety outcomes of second-line glucose-lowering agents used in the management of people with type 2 diabetes. Methods: MEDLINE, EMBASE and CENTRAL were searched from inception to 13 July 2021 for randomised controlled trials comparing second-line glucose lowering therapies with placebo, standard care or one another. Primary outcomes included cardiovascular and renal outcomes. Secondary outcomes were non-cardiovascular adverse events. Risk ratios (RRs) and corresponding confidence intervals (CI) or credible intervals (CrI) were reported within pairwise and network meta-analysis. The quality of evidence was evaluated using the GRADE (Grading of Recommendations, Assessment, Development and Evaluation) criteria. Number needed to treat (NNT) and number needed (NNH) to harm were calculated at 5 years using incidence rates and RRs. PROSPERO (CRD42020168322). Results: We included 38 trials from seven classes of glucose-lowering therapies. Both sodium-glucose co-transporter-2 inhibitors (SGLT2i) and glucagon-like peptide 1 receptor agonists (GLP1RA) showed moderate to high certainty in reducing risk of 3-point major adverse cardiovascular events, 3P-MACE (network estimates: SGLT2i [RR 0.90; 95% CrI 0.84-0.96; NNT, 59], GLP1RA [RR 0.88; 95% CrI 0.83-0.93; NNT, 50]), cardiovascular death, all-cause mortality, renal composite outcome and macroalbuminuria. SGLT2i also showed high certainty in reducing risk of hospitalization for heart failure (hHF), ESRD, acute kidney injury, doubling in serum creatinine and decline in eGFR. GLP1RA were associated with lower risk of stroke (high certainty) while glitazone use was associated with an increased risk of hHF (very low certainty). The risk of developing ESRD was lower with the use of sulphonylureas (low certainty). For adverse events, sulphonylureas and insulin were associated with increased hypoglycaemic events (very low to low certainty), while GLP1RA increased the risk of gastrointestinal side effects leading to treatment discontinuation (low certainty). DPP-4i increased risk of acute pancreatitis (low certainty). SGLT2i were associated with increased risk of genital infection, volume depletion (high certainty), amputation and ketoacidosis (moderate certainty). Risk of fracture was increased with the use of glitazones (moderate certainty). Conclusions: SGLT2i and GLP1RA were associated with lower risk for different cardiorenal end points, when used as an adjunct to metformin in people with type 2 diabetes. Additionally, SGLT2i demonstrated benefits in reducing risk for surrogate end points in kidney disease progression. Safety outcomes differ among the available pharmacotherapies. [ABSTRACT FROM AUTHOR]
Copyright of Diabetic Medicine is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:07423071
DOI:10.1111/dme.14780