Clinical Pharmacology Unit, São João Hospital University Centre, Porto, Portugal.
Department of Biomedicine, Unit of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal.
Pharmacol Res Perspect. 2020 Jun;8(3):e00601. doi: 10.1002/prp2.601.
Recently, the gut microbiome has become an important field of interest. Indeed, the microbiome has been associated to numerous drug interactions and it is thought to influence the efficacy of pharmacologic treatments. Although statins are widely prescribed medications, there remains considerable variability in its therapeutic response. In this context, we aimed to investigate how statins modulate the gut microbiome and, reversely, how can the microbiome influence the course of anti-hypercholesterolemic treatment. We conducted a systematic review by searching four online databases, in accordance with PRISMA guidelines. Studies addressing gut microbiome changes following statin treatment and those assessing statins' response and associating it with patients' microbiome were included. Due to the limited number of results, we decided to include studies enrolling both humans and animals. We summarized information from three human and seven animal studies and aimed to assess the influence of gut microbiome composition on statin response (Outcome 1) and to evaluate the impact of statin treatment on the gut microbiome (Outcome 2). An association between a certain microbiome composition that promoted the lipid-lowering effect of statins was found. However, what kind of microorganisms and how they can exert this effect remains uncertain. Furthermore, statins might have a role in the modulation of the gut microbiome, but then again, it is still unknown whether this change is directly caused by the drug or another metabolic mechanism. Even though gut microbiota may have several potential therapeutic implications, its use as a personalized predictive biomarker requires further studies.
最近,肠道微生物组已成为一个重要的研究领域。事实上,微生物组与许多药物相互作用有关,并且被认为会影响药物治疗的效果。尽管他汀类药物被广泛开处方,但它的治疗反应仍然存在很大的差异。在这种情况下,我们旨在研究他汀类药物如何调节肠道微生物组,以及微生物组如何影响抗高胆固醇血症治疗的进程。我们按照 PRISMA 指南,通过搜索四个在线数据库进行了系统综述。纳入了研究他汀类药物治疗后肠道微生物组变化的研究,以及评估他汀类药物反应并将其与患者微生物组相关联的研究。由于结果数量有限,我们决定同时纳入人类和动物研究。我们总结了三个人类和七项动物研究的信息,旨在评估肠道微生物组组成对他汀类药物反应的影响(结果 1),并评估他汀类药物治疗对肠道微生物组的影响(结果 2)。发现了一种特定的微生物组组成与他汀类药物的降脂效果之间存在关联。然而,什么样的微生物以及它们如何发挥这种作用仍然不确定。此外,他汀类药物可能在调节肠道微生物组方面发挥作用,但同样不清楚这种变化是否是由药物本身还是其他代谢机制直接引起的。尽管肠道菌群可能具有多种潜在的治疗意义,但将其用作个性化预测生物标志物仍需要进一步研究。