Nani Alessandro, Carrara Federica, Paulesu Chiara Maria Eleonora, Dalle Fratte Chiara, Padroni Matteo, Enisci Silvia, Bilancio Maria Concetta, Romio Maria Silvia, Bertuzzi Federico, Pintaudi Basilio
Department of Medical Biotechnology and Translational Medicine, University of Milan, 20133 Milan, Italy.
Hospital Pharmacy, Humanitas Gavazzeni, 24125 Bergamo, Italy.
J Clin Med. 2023 Jun 9;12(12):3958. doi: 10.3390/jcm12123958.
Our aim was to evaluate osteomyelitis and other major lower limb safety outcomes (i.e., peripheral artery disease or PAD, ulcers, atraumatic fractures, amputations, symmetric polyneuropathy, and infections) in patients affected by type 2 diabetes mellitus (T2DM) and treated with sodium-glucose cotransporter 2 inhibitors (SGLT2-is). We thus performed a systematic review and meta-analysis of randomised controlled trials (RCTs) comparing SGLT2-is at approved doses for T2DM with a placebo or standard of care. MEDLINE, Embase, and Cochrane CENTRAL were searched through August 2022. Separate intention-to-treat analyses were implemented for each molecule to calculate Mantel-Haenszel risk ratios (RR) with 95% confidence intervals (CIs) through a random-effects model. We processed data from 42 RCTs for a total of 29,491 and 23,052 patients, respectively assigned to SGLT2-i and comparator groups. SGLT2-is showed a pooled neutral effect on osteomyelitis, PAD, fractures, and symmetric polyneuropathy, whereas slightly deleterious sway on ulcers (RR 1.39 [1.01-1.91]), amputations (RR 1.27 [1.04-1.55]), and infections (RR 1.20 [1.02-1.40]). In conclusion, SGLT2-is appear to not significantly interfere with the onset of osteomyelitis, PAD, lower limb fractures, or symmetric polyneuropathy, even though the number of these events proved consistently higher in the investigational groups; otherwise, local ulcers, amputations, and overall infections may be favoured by their employment. This study is registered with the Open Science Framework (OSF).
我们的目的是评估2型糖尿病(T2DM)患者使用钠-葡萄糖协同转运蛋白2抑制剂(SGLT2-i)治疗后的骨髓炎及其他主要下肢安全性结局(即外周动脉疾病或PAD、溃疡、非创伤性骨折、截肢、对称性多发性神经病和感染)。因此,我们对随机对照试验(RCT)进行了系统评价和荟萃分析,比较了SGLT2-i治疗T2DM的批准剂量与安慰剂或标准治疗。检索了截至2022年8月的MEDLINE、Embase和Cochrane CENTRAL。对每个分子进行单独的意向性分析,通过随机效应模型计算Mantel-Haenszel风险比(RR)及95%置信区间(CI)。我们处理了来自42项RCT的数据,共有29491例和23052例患者,分别分配到SGLT2-i组和对照组。SGLT2-i对骨髓炎、PAD、骨折和对称性多发性神经病显示出汇总中性效应,而对溃疡(RR 1.39 [1.01-1.91])、截肢(RR 1.27 [1.04-1.55])和感染(RR 1.20 [1.02-1.40])有轻微有害影响。总之,SGLT2-i似乎不会显著干扰骨髓炎发作、PAD、下肢骨折或对称性多发性神经病的发生,尽管这些事件的数量在研究组中一直较高;否则,使用它们可能会增加局部溃疡、截肢和总体感染的风险。本研究已在开放科学框架(OSF)注册。