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The Role of Laboratory Tests in Crohn's Disease

机译:实验室检查在克罗恩病中的作用

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In the past, laboratory tests were considered of limited value in Crohn's disease (CD). In the era of biologics, laboratory tests have become essential to evaluate the inflammatory burden of the disease (C-reactive protein, fecal calprotectin) since symptoms-based scores are subjective, to predict the response to pharmacological options and the risk of relapse, to discriminate CD from ulcerative colitis, to select candidates to anti-tumor necrosis factors [screening tests looking for hepatitis B virus and hepatitis C virus status and latent tuberculosis], to assess the risk of adverse events (testing for thiopurine metabolites and thiopurine-methyltransferase activity), and to personalize and optimize therapy (therapeutic drug monitoring). Pharmacogenetics, though presently confined to the assessment of thiopurineme methyltransferase polymorphisms and hematological toxicity associated with thiopurine treatment, is a promising field that will contribute to a better understanding of the molecular mechanisms of the variability in response to the drugs used in CD with the attempt to expand personalized care and precision medicine strategies.
机译:过去,实验室测试被认为对克罗恩病(CD)的价值有限。在生物制剂时代,由于基于症状的评分是主观的,可以预测对药理学选择的反应和复发风险,因此实验室测试对于评估疾病的炎症负担(C反应蛋白,粪便钙卫蛋白)已变得至关重要。区分CD与溃疡性结肠炎,选择抗肿瘤坏死因子的候选物[筛选测试,寻找乙型肝炎病毒和丙型肝炎病毒的状况以及潜伏性结核病],评估不良事件的风险(测试硫代嘌呤代谢产物和硫代嘌呤甲基转移酶活性),以及个性化和优化治疗(治疗药物监测)。药物遗传学虽然目前仅限于评估硫嘌呤甲基转移酶多态性和与硫嘌呤治疗有关的血液学毒性,但它是一个有前途的领域,将有助于更好地了解CD中使用的药物对变异的分子机制,并尝试扩展个性化护理和精准医学策略。

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