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非类胰蛋白酶尿液和血液学生物标志物与肥大细胞扩增和肥大细胞活化:现状 2022 年。

Nontryptase Urinary and Hematologic Biomarkers of Mast Cell Expansion and Mast Cell Activation: Status 2022.

机构信息

Division of Allergic Diseases, Mayo Clinic and the Mayo Clinic Program for Mast Cell and Eosinophil Disorders, Rochester, Minn.

出版信息

J Allergy Clin Immunol Pract. 2022 Aug;10(8):1974-1984. doi: 10.1016/j.jaip.2022.03.008. Epub 2022 Mar 26.

Abstract

Quantitation of urinary metabolites of histamine, prostaglandin D, and leukotriene E can fill the gap in our current efforts to improve diagnosis and management of symptomatic patients with systemic mastocytosis, and/or mast cell activation syndrome, In addition, patients symptomatic due to mast cell activation but who do not meet all the criteria for mast cell activation syndrome can have elevated baseline mediator metabolites. Serum tryptase levels have been the workhorse in diagnosing these disorders, but it has several drawbacks including the need to obtain acute and baseline samples, which require 2 visits to health care facilities and 2 venipunctures. Recently, increased baseline tryptase level has been reported in hereditary alpha tryptasemia, complicating diagnostic possibilities of an increased baseline tryptase level. Furthermore, no treatment can specifically be targeted at tryptase itself. In contrast, the finding of 1 or more elevated urinary levels of histamine, prostaglandin D, and/or leukotriene E metabolites (1) greatly narrows diagnostic possibilities for causes of symptoms; (2) informs the practitioner what specific metabolic pathways are involved; and (3) targets the treatment in a specific, direct fashion. As a bonus, baseline spot/random urine samples can be obtained by the patients themselves and repeated at exactly the correct time when symptoms occur.

摘要

定量检测组胺、前列腺素 D 和白三烯 E 的尿代谢产物,可以填补我们当前改善系统性肥大细胞增多症和/或肥大细胞活化综合征有症状患者的诊断和治疗的空白。此外,由于肥大细胞活化而出现症状但不符合肥大细胞活化综合征所有标准的患者,其基线介质代谢物可能会升高。血清类胰蛋白酶水平一直是诊断这些疾病的主力,但它存在几个缺点,包括需要获得急性和基线样本,这需要到医疗机构就诊 2 次和静脉穿刺 2 次。最近,遗传性α-胰蛋白酶血症中报告了基线类胰蛋白酶水平升高,这使增加的基线类胰蛋白酶水平的诊断可能性变得复杂。此外,没有特定的治疗方法可以针对类胰蛋白酶本身。相比之下,发现 1 种或多种升高的组胺、前列腺素 D 和/或白三烯 E 代谢物尿水平(1)大大缩小了症状原因的诊断可能性;(2)告知医生具体涉及哪些代谢途径;(3)以特定、直接的方式靶向治疗。作为额外的好处,患者可以自行获得基线点/随机尿样,并在症状出现时准确地重复采集。

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