2020
DOI: 10.7326/m20-0864
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Comparative Effectiveness of Glucose-Lowering Drugs for Type 2 Diabetes

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Cited by 224 publications
(145 citation statements)
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“…Second, the present study only assessed the clinical effectiveness of GLP-1RAs in terms of short-term clinical biochemical marker changes (e.g., HbA1c, eGFR), while the hard endpoints of treatments (e.g., cardiovascular disease, death, progression to end-stage renal disease) were not measured. To date, there is a lack of direct head-to-head comparative trials of GLP-1RAs on the long-term cardiovascular safety and mortality, but there are indirect comparisons from three network meta-analysis studies [ 42 44 ]. This suggests that future studies with the long-term follow-up period on hard outcomes among GLP-1RAs are needed.…”
Section: Discussionmentioning
confidence: 99%
“…Second, the present study only assessed the clinical effectiveness of GLP-1RAs in terms of short-term clinical biochemical marker changes (e.g., HbA1c, eGFR), while the hard endpoints of treatments (e.g., cardiovascular disease, death, progression to end-stage renal disease) were not measured. To date, there is a lack of direct head-to-head comparative trials of GLP-1RAs on the long-term cardiovascular safety and mortality, but there are indirect comparisons from three network meta-analysis studies [ 42 44 ]. This suggests that future studies with the long-term follow-up period on hard outcomes among GLP-1RAs are needed.…”
Section: Discussionmentioning
confidence: 99%
“…Similar considerations are applied in patients who require a third agent to achieve glycemic goals. A recent systematic review and network metaanalysis suggests greatest reductions in A1C level with insulin regimens and specific GLP-1 RAs added to metformin-based background therapy (52). In all cases, treatment regimens need to be continuously reviewed for efficacy, side effects, and patient burden ( Table 9.1).…”
Section: Combination Therapymentioning
confidence: 99%
“…In addition, most patients with T2DM progress to requiring combination therapy soon after baseline metformin therapy. A recent meta-analysis examining comparative effectiveness of GLTs concluded that the use of metformin as first-line treatment in treatment-naïve individuals with low cardiovascular risk remains justified and given the lack of evidence, they could not reach a conclusion about the optimal initial treatment of treatment-naïve patients at increased cardiovascular risk [44]. Future studies will need to address whether SGLT2i and GLP-1RAs should be used for the prophylaxis of ASCVD and CKD in uncomplicated newly diagnosed treatment-naïve individuals with T2D to address this further.…”
Section: The European Society Of Cardiology (Esc) 2019 Guidelines On mentioning
confidence: 99%
“…HbA1c not only reflects longer-term glycaemic control but improvement in HbA1c correlates with reduced risk of cardiovascular complications [59][60][61]. In a recent meta-analysis, metformin reduced mean HbA1c by −0.92% (95% CI −1.07, −0.77) in treatment-naïve individuals which was lower only to canagliflozin (−1.02% [95% CI −1.68, −0.36]) and oral semaglutide (−1.10%, 95% CI −1.7, −0.45) amongst oral GLTs [44]. Metformin has been found to improve glycaemic variables significantly (both fasting blood glucose and HbA1c) compared to placebo in a dose-dependent fashion at dosages of 500 to 2000 mg daily, with maximal benefits observed at upper limits of recommended daily dosage [62].…”
Section: Efficacy Of Metformin As a Glucose-lowering Agentmentioning
confidence: 99%