Allegretti Jessica R, Kassam Zain, Mullish Benjamin H, Chiang Austin, Carrellas Madeline, Hurtado Jonathan, Marchesi Julian R, McDonald Julie A K, Pechlivanis Alexandros, Barker Grace F, Miguéns Blanco Jesús, Garcia-Perez Isabel, Wong Wing Fei, Gerardin Ylaine, Silverstein Michael, Kennedy Kevin, Thompson Christopher
Division of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Finch Therapeutics Group, Somerville, Massachusetts.
Clin Gastroenterol Hepatol. 2020 Apr;18(4):855-863.e2. doi: 10.1016/j.cgh.2019.07.006. Epub 2019 Jul 10.
BACKGROUND & AIMS: Studies in mice have shown that the intestinal microbiota can contribute to obesity via the anorexigenic gut hormone glucagon-like peptide 1 (GLP1) and bile acids, which affect lipid metabolism. We performed a randomized, placebo-controlled, pilot study of the effects of fecal microbiota transplantation (FMT) in obese, metabolically uncompromised patients.
We performed a double-blind study of 22 obese patients (body mass index [BMI] ≥5 kg/m) without a diagnosis of diabetes, nonalcoholic steatohepatitis, or metabolic syndrome. Participants were assigned randomly (1:1) to groups that received FMT by capsules (induction dose of 30 capsules at week 4 and maintenance dose of 12 capsules at week 8) or placebo capsules. FMT capsules were derived from a single lean donor (BMI, 17.5 kg/m). Patients were followed up through week 26; the primary outcome was safety. Stool and serum samples were collected from patients at baseline and at weeks 1, 4, 6, 8, and 12 after administration of the first dose of FMT or placebo and analyzed by 16S RNA gene sequencing. Stool and serum samples were analyzed for metabolomics by liquid chromatography-mass spectrometry. Additional outcomes were the change in area under the curve for GLP1 at week 12.
We observed no significant differences in adverse events between patients who received FMT vs placebo. There was no increase in the area under the curve of GLP1 in either group. Patients who received FMT had sustained shifts in microbiomes associated with obesity toward those of the donor (P < .001). Patients who received FMT had a sustained decrease in stool levels of taurocholic acid (P < .05) compared with baseline; bile acid profiles began to resemble those of the donor more closely. We did not observe significant changes in mean BMI at week 12 in either group.
In a placebo-controlled pilot study, we found that FMT capsules (derived from a lean donor) were safe but did not reduce BMI in obese metabolically uncompromised patients. The FMT capsules were well tolerated and led to sustained changes in the intestinal microbiome and bile acid profiles that were similar to those of the lean donor. ClinicalTrials.gov number: NCT02741518.
对小鼠的研究表明,肠道微生物群可通过影响脂质代谢的厌食性肠道激素胰高血糖素样肽1(GLP1)和胆汁酸导致肥胖。我们开展了一项随机、安慰剂对照的初步研究,以评估粪便微生物群移植(FMT)对肥胖且代谢未受损患者的影响。
我们对22名未诊断出患有糖尿病、非酒精性脂肪性肝炎或代谢综合征的肥胖患者(体重指数[BMI]≥5kg/m²)进行了一项双盲研究。参与者被随机(1:1)分配到接受胶囊FMT(第4周诱导剂量为30粒胶囊,第8周维持剂量为12粒胶囊)或安慰剂胶囊的组中。FMT胶囊来自一名单一的瘦素供体(BMI,17.5kg/m²)。对患者进行随访至第26周;主要结局是安全性。在基线以及首次给予FMT或安慰剂后第1、4、6、8和12周从患者处收集粪便和血清样本,并通过16S RNA基因测序进行分析。通过液相色谱 - 质谱联用对粪便和血清样本进行代谢组学分析。其他结局是第12周时GLP1曲线下面积的变化。
我们观察到接受FMT与接受安慰剂的患者在不良事件方面无显著差异。两组中GLP1曲线下面积均未增加。接受FMT的患者与肥胖相关的微生物群持续向供体的微生物群转变(P <.001)。与基线相比,接受FMT的患者粪便中牛磺胆酸水平持续下降(P <.α5);胆汁酸谱开始更接近供体的胆汁酸谱。我们未观察到两组在第12周时平均BMI有显著变化。
在一项安慰剂对照的初步研究中,我们发现(来自瘦素供体的)FMT胶囊是安全的,但在肥胖且代谢未受损的患者中并未降低BMI。FMT胶囊耐受性良好,并导致肠道微生物群和胆汁酸谱持续发生变化,这些变化与瘦素供体的相似。ClinicalTrials.gov编号:NCT02741518。