Does the 5-Aminosalicylate Concentration Correlate with the Efficacy of Oral 5-Aminosalicylate and Predict Response in Patients with Inflammatory Bowel Disease? A Systematic Review

被引:11
|
作者
van de Meeberg, Maartje M. [1 ,2 ]
Schultheiss, Johannes P. D. [1 ]
Oldenburg, Bas [1 ]
Fidder, Herma H. [1 ]
Huitema, Alwin D. R. [2 ,3 ]
机构
[1] Univ Utrecht, Univ Med Ctr Utrecht, Dept Gastroenterol & Hepatol, Utrecht, Netherlands
[2] Univ Utrecht, Univ Med Ctr Utrecht, Dept Clin Pharm, Utrecht, Netherlands
[3] Netherlands Canc Inst, Dept Pharm & Pharmacol, Amsterdam, Netherlands
关键词
Therapeutic drug monitoring; Mesalazine; Ulcerative colitis; Systematic review; ACCELERATED INTESTINAL TRANSIT; COLONIC MUCOSAL CONCENTRATIONS; DELAYED-RELEASE MESALAZINE; TISSUE DRUG CONCENTRATIONS; ACTIVE ULCERATIVE-COLITIS; DISODIUM AZODISALICYLATE; CLINICAL PHARMACOKINETICS; GASTROINTESTINAL-TRACT; HEALTHY-VOLUNTEERS; DELIVERING DRUGS;
D O I
10.1159/000499331
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Oral 5-aminosalicylic acid (5-ASA, mesalazine) is the first choice therapeutic agent for treating mild-to-moderate ulcerative colitis (UC). Unfortunately a significant group of patients fail to respond. Therapeutic drug monitoring might help to maintain or induce remission by providing a tool for optimization of 5-ASA therapy. However, plasma and urine concentrations of 5-ASA reflect systemic uptake and are not useful to evaluate therapeutic effect. Objectives: To explore if mucosal and faecal 5-ASA values correlate with disease activity and/or therapeutic effects in patients with inflammatory bowel disease, especially UC. Method: We identified studies that analysed 5-ASA in faeces or mucosa of humans using an oral 5-ASA formulation, using PubMed and Embase. Results: In total, 39 studies (n = 939) were included, 27 on faecal 5-ASA, 9 on mucosal concentrations, and 3 on both faecal and mucosal values. We included 33 cross-sectional studies, 3 randomised clinical trials, 2 longitudinal cohorts and 1 randomized cross-over study. Mucosal 5-ASA concentrations in healthy subjects and patients on equivalent doses of 5-ASA were not found to differ remarkably. In the sub-analysis of mucosal 5-ASA concentrations in patients with active or quiescent UC, a higher concentration was seen during remission. Faecal concentrations were associated with 5-ASA doses but not with disease activity. Differences in faecal or mucosal 5-ASA values could not be ascribed to different 5-ASA formulations. Conclusions: An increase of the mucosal 5-ASA concentrations was observed during remission in patients with UC. No clear relationship between the faecal 5-ASA excretion and the therapeutic efficacy was identified.
引用
收藏
页码:245 / 261
页数:17
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