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The US HAEA Scientific Registry: Triggers and Prodromes
Sandra C Christiansen1, Joyce Wilmot2, Christine Selva2
1Department of Medicine, University of California San Diego, La Jolla, CA.
Background:
Triggers and prodromes have been reported as preludes to hereditary angioedema (HAE) attacks.
Objective:
Utilizing data from the US HAE Association Scientific Registry, we describe the clinical characteristics of triggers, prodromes, and their relationships to attack onset.
Methods:
Clinical data concerning trigger and prodrome types, frequency, and the likelihood of having a subsequent attack were extracted from the Scientific Registry. Data were compiled from both HAE-C1INH and angioedema non-mast cell-mediated with normal C1INH (ANM-nl-C1INH) cohorts.
Results:
HAE-C1INH cohort: 458 of 485 subjects recorded triggers with stress the most frequent (91.5%) followed by minor trauma (83.2%) and infection (67.3%). Hormonal triggers were the most likely to always be followed by an attack. Prodromal symptoms were reported by 399 (82.3%) with the most frequent being non-itchy rash (78.7%), sense/hunch (52.6%), tiredness/fatigue (47.2%) and tightness/prickling (45.8%). A prodromal sense/hunch of an impending attack was the most likely to always be followed by an attack (47.4%). ANM-NL-C1INH COHORT: 83 of 96 subjects documented 1 or more triggers with stress the most common (81.25%) and menses the most likely to always be followed by an attack (38.5%). Prodromal symptoms were reported in 83 with the most common being tightness/prickling (58.3%), tiredness/fatigue (56.3%), non-itchy rash (51.0%), and a sense/hunch (45.8%). The prodrome that had the highest percentage of always being followed by an attack was a tightness/prickling sensation (62.2%).
Conclusion:
Our analysis highlighted the importance of stress and hormonal attack triggers. The sense/hunch of an impending attack was the most reliable prodrome for HAE-C1INH vs tightness/prickling in ANM-nl-C1INH. Erythema marginatum type eruptions were common in all subjects. We hypothesize that triggers and prodromes are fundamentally interconnected with attacks of HAE through activation of kinin generating pathways.
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