Shastri Sanjana Aditya, Kantamneni Raveena, Rashid Muhammed, Chandran Viji Pulikkel, Suhita Ramadugula, Begum Izwath, Nair Sreedharan, Thunga Girish
Department of Pharmacy Practice, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, India.
Centre for Toxicovigilance and Drug Safety, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, India.
Med Pharm Rep. 2022 Oct;95(4):357-369. doi: 10.15386/mpr-2259. Epub 2022 Oct 27.
Proton Pump Inhibitors (PPIs) reduce gastric acid production and they are indicated for myriad gastrointestinal conditions. Prolonged use of PPI has been linked to the risk of inflammatory bowel disease (IBD) though this fact is not well established. We aimed to conduct a systematic review and meta-analysis to estimate the risk of IBD occurrence with PPI use.
The databases such as PubMed, Scopus, and Cochrane Library were accessed from inception to December 2020. Additionally, the bibliographic search and a random search in Google, Google Scholar, and ResearchGate were performed to find additional sources. The observational studies estimating the risk of IBD following the use of PPI, published in the English language were considered for this review. The methodological quality of included studies was assessed using the Modified Downs and Black checklist.
Eight out of 2038 studies with 157,758 participants were included in this meta-analysis. A significantly higher risk of IBD (adjusted odds ratio [aOR] 2.43; 95% Confidence Interval [CI] 1.18-5.02; P=0.02; n=6) was observed in participants taking PPIs for any indication. Moreover, a significant association was observed between PPI exposure on the different types of IBD such as ulcerative colitis and Crohn's disease together (aOR: 3.60; 95% CI: 1.10-11.74), collagenous colitis (OR: 4.73; 95% CI: 1.99-11.22) and lymphocytic Colitis (OR: 3.77; 95% CI: 2.91-4.87), but not with ulcerative colitis (P=0.47) and microscopic colitis (P=0.07) alone. Similarly, a significant association was observed among Europeans (aOR: 3.98; 95% CI: 2.36-6.71), but not with North American (aOR: 0.48; 95% CI: 0.01-26.71) studies. Overall the study quality was good.
The current evidence indicates that exposure to PPI is significantly associated with increased risk of IBD. Further, adequately powered studies from various parts of the world are needed for better quantification and generalizability of our findings.
CRD42020209674.
质子泵抑制剂(PPIs)可减少胃酸分泌,适用于多种胃肠道疾病。长期使用PPIs与炎症性肠病(IBD)风险增加有关,不过这一关联尚未完全明确。我们旨在进行一项系统评价和荟萃分析,以评估使用PPIs后患IBD的风险。
检索了PubMed、Scopus和Cochrane图书馆等数据库,检索时间从建库至2020年12月。此外,还进行了文献检索,并在谷歌、谷歌学术和ResearchGate上进行随机搜索,以寻找其他来源。纳入本评价的是那些用英文发表的、评估使用PPIs后患IBD风险的观察性研究。采用改良的唐斯和布莱克清单评估纳入研究的方法学质量。
本荟萃分析纳入了2038项研究中的8项,共157,758名参与者。在因任何适应症服用PPIs的参与者中,观察到患IBD的风险显著更高(调整后的优势比[aOR]为2.43;95%置信区间[CI]为1.18 - 5.02;P = 0.02;n = 6)。此外,观察到PPIs暴露与不同类型的IBD之间存在显著关联,如溃疡性结肠炎和克罗恩病合并(aOR:3.60;95% CI:1.10 - 11.74)、胶原性结肠炎(OR:4.73;95% CI:1.99 - 11.22)和淋巴细胞性结肠炎(OR:3.77;95% CI:2.91 - 4.87),但与单独的溃疡性结肠炎(P = 0.47)和微观性结肠炎(P = 0.07)无关。同样,在欧洲人的研究中观察到显著关联(aOR:3.98;95% CI:2.36 - 6.71),但在北美人的研究中未观察到(aOR:0.48;95% CI:0.01 - 26.71)。总体而言,研究质量良好。
目前的证据表明,暴露于PPIs与IBD风险增加显著相关。此外,需要来自世界各地的有足够样本量的研究,以便更好地量化我们的研究结果并提高其可推广性。
国际前瞻性系统评价注册库(PROSPERO)注册号:CRD42020209674。