Bent Rebekka Karolin, Kugler Claudia, Faihs Valentina, Darsow Ulf, Biedermann Tilo, Brockow Knut
Department of Dermatology and Allergy Biederstein, Faculty of Medicine, Technical University of Munich, Munich, Germany.
Department of Dermatology and Allergy Biederstein, Faculty of Medicine, Technical University of Munich, Munich, Germany.
J Allergy Clin Immunol Pract. 2023 Dec;11(12):3724-3731.e11. doi: 10.1016/j.jaip.2023.08.030. Epub 2023 Aug 28.
Histamine intolerance (HIT) is frequently diagnosed in patients with polysymptomatic otherwise unexplained symptoms.
To exclude HIT by a single-blind placebo-controlled histamine challenge (SBPCHC), to study clinical features of patients with positive challenge, and to examine the predictability of HIT by biomarkers.
SBPCHC was performed in 59 patients with suspected HIT. History and clinical data, including serum diamine oxidase (DAO) and histamine skin test wheal size of patients with positive versus negative SBPCHC, were compared.
Patients were predominantly middle-aged women (84.7%). Three-quarters reported improvement but never resolution of symptoms during a histamine-low diet. Histamine provocation was safe; only 1 patient was treated with antihistamines. Thirty-seven patients (62.7%) displayed symptoms to placebo. HIT was excluded in 50 patients (84.7%). Objective symptoms occurred in 4 of 59 cases (6.8%) after histamine but not after placebo challenge. These were diagnosed with "plausible HIT" because reactions occurring by chance could not be excluded. Another 5 patients (8.5%) were diagnosed with "possible HIT" after case-dependent detailed analysis. Patients with plausible/possible HIT had reported more gastrointestinal symptoms (P = .01), but comparable diet response and equal histamine skin prick test wheal sizes to those without HIT. Serum DAO activity tended to be lower in patients with HIT (P = .08), but was highly variable in those without, limiting its value as a biomarker.
SBPCHC disproves HIT in the majority of patients. Placebo-controlled challenges are needed as placebo reactions were frequent. Gastrointestinal symptoms after food intake and reduced DAO levels are markers for HIT; however, specificity is not sufficient enough for making the diagnosis.
组胺不耐受(HIT)在有多种症状但病因不明的患者中经常被诊断出来。
通过单盲安慰剂对照组胺激发试验(SBPCHC)排除HIT,研究激发试验阳性患者的临床特征,并通过生物标志物检验HIT的可预测性。
对59例疑似HIT患者进行SBPCHC。比较了SBPCHC阳性和阴性患者的病史及临床数据,包括血清二胺氧化酶(DAO)和组胺皮肤试验风团大小。
患者以中年女性为主(84.7%)。四分之三的患者报告在低组胺饮食期间症状有所改善,但从未完全缓解。组胺激发试验是安全的;只有1例患者接受了抗组胺药治疗。37例患者(62.7%)对安慰剂有反应。50例患者(84.7%)排除了HIT。59例中有4例(6.8%)在组胺激发试验后出现客观症状,但安慰剂激发试验后未出现。这些患者被诊断为“疑似HIT”,因为不能排除偶然发生的反应。另外5例患者(8.5%)在根据病例进行详细分析后被诊断为“可能HIT”。疑似/可能HIT患者报告的胃肠道症状更多(P = 0.01),但饮食反应和组胺皮肤点刺试验风团大小与无HIT患者相当。HIT患者的血清DAO活性往往较低(P = 0.08),但无HIT患者的血清DAO活性变化很大,限制了其作为生物标志物的价值。
SBPCHC在大多数患者中排除了HIT。由于安慰剂反应频繁,需要进行安慰剂对照激发试验。进食后出现的胃肠道症状和DAO水平降低是HIT的标志物;然而,特异性不足以用于诊断。