Hod Keren, Ringel-Kulka Tamar, Martin Christopher F, Maharshak Nitsan, Ringel Yehuda
Departments of *Epidemiology and Preventive Medicine, School of Public Health §Gastroenterology and Liver Diseases, Tel Aviv Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel Departments of †Medicine, Division of Gastroenterology and Hepatology ‡Maternal and Child Health, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC.
J Clin Gastroenterol. 2016 Mar;50(3):227-32. doi: 10.1097/MCG.0000000000000327.
Recent studies demonstrated low-grade inflammation in patients with irritable bowel syndrome (IBS). However, these studies have been relatively small and do not enable examination of this factor in different subtypes of IBS and the possibility of confounding effects of comorbidities that may be associated with inflammatory responses.
To investigate the association between high-sensitive C-reactive protein (hs-CRP) and the diagnosis of IBS, IBS subtypes, symptoms' severity, and IBS-associated comorbidities.
This cross-sectional study uses data from a large matched case-control study of IBS subjects and healthy controls (HC). hs-CRP levels were measured in all subjects. IBS diagnosis was determined by Rome III criteria, negative screening blood tests, and normal colonoscopy. Subjects were evaluated for IBS severity and associated pain and psychological comorbidities.
A total of 242 IBS patients and 244 HC were studied. Median hs-CRP levels in the IBS group were significantly higher than in HC (1.80; interquartile range, 0.7 to 4.04 mg/L vs. 1.20, interquartile range, 0.5 to 2.97 mg/L respectively, P<0.006). Levels were highest in IBS-D patients with greater disease severity. Hs-CRP levels mildly correlated with symptoms severity (r=0.169, P=0.009); this correlation was stronger for the IBS-D patients (r=0.27, P=0.006). IBS was a significant independent predictor (P=0.025) for higher hs-CRP levels, whereas other pain and psychological comorbidities were not.
Given these observations of cross-sectional differences in hs-CRP between IBS subtypes and severity, independent of pain and comorbidities, more research is needed to explore a possible role of low-grade inflammation in the pathogenesis and/or clinical presentation of IBS.
近期研究表明,肠易激综合征(IBS)患者存在低度炎症。然而,这些研究规模相对较小,无法对IBS不同亚型中的这一因素进行检测,也无法探讨可能与炎症反应相关的合并症的混杂效应。
研究高敏C反应蛋白(hs-CRP)与IBS诊断、IBS亚型、症状严重程度以及IBS相关合并症之间的关联。
这项横断面研究使用了一项针对IBS患者和健康对照(HC)的大型匹配病例对照研究的数据。对所有受试者测量hs-CRP水平。IBS诊断依据罗马III标准、血液筛查阴性以及结肠镜检查正常来确定。对受试者进行IBS严重程度以及相关疼痛和心理合并症的评估。
共研究了242例IBS患者和244例HC。IBS组的hs-CRP中位数水平显著高于HC(分别为1.80;四分位间距,0.7至4.04mg/L,相比之下HC为1.20,四分位间距,0.5至2.97mg/L,P<0.006)。在疾病严重程度较高的IBS-D患者中水平最高。hs-CRP水平与症状严重程度呈轻度相关(r=0.169,P=0.009);这种相关性在IBS-D患者中更强(r=0.27,P=0.006)。IBS是hs-CRP水平升高的显著独立预测因素(P=0.025),而其他疼痛和心理合并症则不是。
鉴于观察到IBS亚型和严重程度之间hs-CRP存在横断面差异,且独立于疼痛和合并症,需要更多研究来探讨低度炎症在IBS发病机制和/或临床表现中的可能作用。