Kaur Simran, Sojitra Vani, Zahra Anam, Hutchinson Jhenelle, Folawemi Oluwa, Bittla Parikshit, Ramphall Shivana
Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Medicine, Bavadia Hospital, Una, IND.
Cureus. 2023 Sep 22;15(9):e45789. doi: 10.7759/cureus.45789. eCollection 2023 Sep.
Non-alcoholic fatty liver disease (NAFLD) is a complication related to obesity and metabolic syndrome. There are increased incidences of NAFLD/non-alcoholic steatohepatitis (NASH) due to rising obesity and type 2 diabetes mellitus (T2DM). This has resulted in significant morbidity and mortality. The two promising therapeutic agents for treating NAFLD/NASH are sodium-glucose cotransporter 2 (SGLT2) inhibitors and pioglitazone. The reason is their potential to target underlying pathophysiological mechanisms. SGLT2 inhibitors may help treat NAFLD/NASH by reducing insulin resistance and improving glucose control, thereby lowering hepatic fat accumulation and inflammation, although their exact mechanism in this context is still being studied. This systematic review aims to compare the efficacy of SGLT2 inhibitors and pioglitazone in treating NAFLD/NASH. Major research literature databases were searched, and appropriate keywords were used to find relevant articles published in the last three years. Eighteen studies were critically evaluated using standardized quality assessment tools. Among those, nine studies qualified as medium or high quality and were included in the review. Both SGLT2 inhibitors and pioglitazone showed promising results in improving NAFLD/NASH. The efficacy outcomes assessed liver fat content, liver enzyme levels, histological improvement, and metabolic parameters. The safety outcomes considered adverse events and cardiovascular events. The conducted review suggests that SGLT2 inhibitors and pioglitazone are potential treatment options for NAFLD/NASH. Having said that, individualized considerations are essential. It includes patient comorbidities, preferences, and overall safety profiles. Further research is needed to assess long-term effects and outcomes. It would provide more definitive evidence of these treatment options' comparative efficacy and safety for NAFLD/NASH.
非酒精性脂肪性肝病(NAFLD)是一种与肥胖和代谢综合征相关的并发症。由于肥胖率上升和2型糖尿病(T2DM),NAFLD/非酒精性脂肪性肝炎(NASH)的发病率有所增加。这已导致显著的发病率和死亡率。治疗NAFLD/NASH的两种有前景的治疗药物是钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂和吡格列酮。原因是它们有针对潜在病理生理机制的潜力。SGLT2抑制剂可能通过降低胰岛素抵抗和改善血糖控制来帮助治疗NAFLD/NASH,从而减少肝脏脂肪堆积和炎症,尽管其在这种情况下的确切机制仍在研究中。本系统评价旨在比较SGLT2抑制剂和吡格列酮治疗NAFLD/NASH的疗效。检索了主要的研究文献数据库,并使用适当的关键词查找过去三年发表的相关文章。使用标准化质量评估工具对18项研究进行了严格评估。其中,9项研究被判定为中等或高质量,并纳入本评价。SGLT2抑制剂和吡格列酮在改善NAFLD/NASH方面均显示出有前景的结果。疗效指标评估了肝脏脂肪含量、肝酶水平、组织学改善和代谢参数。安全性指标考虑了不良事件和心血管事件。所进行的评价表明,SGLT2抑制剂和吡格列酮是NAFLD/NASH的潜在治疗选择。话虽如此,个体化考量至关重要。这包括患者的合并症、偏好和总体安全性概况。需要进一步研究来评估长期影响和结果。这将为这些治疗选择对NAFLD/NASH的比较疗效和安全性提供更确凿的证据。