Sun Qinghua, Jia Qiong, Song Lijin, Duan Liping
Department of Gastroenterology, Peking University Third Hospital, No. 49 North Garden Rd., Haidian District, Beijing, 100191, China.
Medicine (Baltimore). 2019 Feb;98(7):e14513. doi: 10.1097/MD.0000000000014513.
Recent studies indicate that gut microbiota disorders potentially contribute to the pathogenesis of irritable bowel syndrome (IBS), which can be partly reflected by fecal short-chain fatty acids (SCFAs) generated from gut microbiota. Previous studies on SCFA alterations in patients with IBS have yielded conflicting results. No prior systematic review has been conducted on the alterations in fecal SCFAs in IBS patients.
We performed a meta-analysis to explore and clarify alterations in fecal SCFAs in IBS patients.
Case-control studies, randomized controlled trials (RCTs), and self-controlled studies were identified through electronic database searches. The standardized mean difference (SMD) with 95% confidence interval (CI) in fecal SCFA levels between different groups was calculated.
The proportion of fecal propionate in patients with IBS was significantly higher than in healthy controls (HCs) (SMD = 0.44, 95% CI = 0.12, 0.76). A subgroup analysis showed that the concentration of fecal propionate (SMD = -0.91, 95% CI = -1.41, -0.41) and butyrate (SMD = -0.53, 95% CI = -1.01, -0.04) in patients with constipation-predominant IBS (IBS-C) was significantly lower than that in HCs, and the concentration of fecal butyrate in patients with diarrhea-predominant IBS (IBS-D) was higher than that in HCs (SMD = 0.34, 95% CI = 0.00, 0.67). Finally, we found that restricted diets correlated with fecal butyrate reduction in IBS (SMD = -0.26, 95% CI = -0.51, -0.01).
In terms of fecal SCFAs, there were differences between patients with IBS and HCs. In IBS-C patients, propionate and butyrate were reduced, whereas butyrate was increased in IBS-D patients in comparison to HCs. Propionate and butyrate could be used as biomarkers for IBS diagnosis.
近期研究表明,肠道微生物群紊乱可能在肠易激综合征(IBS)的发病机制中起作用,这可部分通过肠道微生物群产生的粪便短链脂肪酸(SCFAs)反映出来。先前关于IBS患者SCFA改变的研究结果相互矛盾。此前尚未对IBS患者粪便SCFAs的改变进行系统评价。
我们进行了一项荟萃分析,以探索并阐明IBS患者粪便SCFAs的改变情况。
通过电子数据库检索确定病例对照研究、随机对照试验(RCT)和自身对照研究。计算不同组之间粪便SCFA水平的标准化均数差(SMD)及95%置信区间(CI)。
IBS患者粪便丙酸的比例显著高于健康对照(HCs)(SMD = 0.44,95%CI = 0.12,0.76)。亚组分析显示,便秘型IBS(IBS-C)患者粪便丙酸(SMD = -0.91,95%CI = -1.41,-0.41)和丁酸(SMD = -0.53,95%CI = -1.01,-0.04)的浓度显著低于HCs,腹泻型IBS(IBS-D)患者粪便丁酸的浓度高于HCs(SMD = 0.34,95%CI = 0.00,0.67)。最后,我们发现限制饮食与IBS患者粪便丁酸减少相关(SMD = -0.26,95%CI = -0.51,-0.01)。
在粪便SCFAs方面,IBS患者与HCs之间存在差异。与HCs相比,IBS-C患者的丙酸和丁酸减少,而IBS-D患者的丁酸增加。丙酸和丁酸可作为IBS诊断的生物标志物。