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The journal of allergy and clinical immunology. In practice · 2025

Real-World Evidence on the Management of Hereditary Angioedema With Normal C1 Inhibitor.

СтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Lobão Nyla Thyara Melo, Bardou Maine Luellah Demaret, Vila Shirley Yajaira Cerinza, Sousa Ferreira Lucas Salomão de, Arruda Luisa Karla, Lemos José Eduardo Seneda, Ferriani Mariana Paes Leme, Dias Marina Mendonça, Toledo Eliana Cristina, Serpa Faradiba Sarquis, Moyses Therezinha Ribeiro, Chong-Neto Herberto J, Rosário Filho Nelson Augusto, de Moraes Caroline Guth de Freitas Batista, Marcelino Fernanda Casares, Mansour Eli, Coutinho Caroline Rosa Emergente, Mendes Ronney Corrêa, Gonçalves Rozana de Fátima, Valle Solange Oliveira Rodrigues, Oliva-Alonso Maria Luiza, Dortas Junior Sérgio Duarte, da Silva Jane, de Souza Aline Lara Fonseca, Ensina Luis Felipe, Morato Vanessa, de Albuquerque Campos Regis, Pesquero João Bosco, Constantino-Silva Rosemeire Navickas, Grumach Anete Sevciovic

Аннотация

BACKGROUND: Hereditary angioedema (HAE) with normal C1 inhibitor (HAE-nC1INH) is a rare and heterogeneous group of bradykinin-mediated disorders, characterized by diagnostic challenges and limited evidence-based recommendations.

OBJECTIVE: To describe the clinical features and therapeutic strategies of Brazilian patients with HAE-nC1INH, supporting individualized, subtype-oriented management.

METHODS: This multicenter, cross-sectional analytical study was conducted through the Brazilian Group for the Study of Hereditary Angioedema (GEBRAEH). Data were collected in December 2024 using a standardized online questionnaire and analyzed descriptively and inferentially.

RESULTS: A total of 116 symptomatic patients were included: 92 with HAE with mutation in coagulation factor XII, 21 with HAE of unknown genetic cause, and 3 with HAE with mutation in angiopoietin-1. Females accounted for 96%. Abdominal symptoms were predominant, and diagnostic delay decreased in more recent generations. Initial interventions most often involved isolated combined estrogen-progestin oral contraceptive (COC) withdrawal (33 of 116; 28%) or combined with progestins (35 of 116; 30%). In HAE with mutation in coagulation factor XII, COC withdrawal was effective in 97% (29 of 30), further enhanced with progestins (30 of 30; 100%). COC withdrawal reduced median attack days (4.5 to 1; P < .001) and prolonged attack-free intervals (P < .001). Four patients relapsed after more than 10 years of remission, associated with hormonal changes. Tranexamic acid demonstrated variable efficacy (2 of 10 achieved complete cessation, 5 of 10 partial reduction, and 3 of 10 no response). Lanadelumab showed clinical efficacy in HAE of unknown genetic cause (2 of 2) and HAE with mutation in angiopoietin-1 (1 of 1). Androgens showed only limited benefit (7 of 7; all partial reduction).

CONCLUSIONS: COC withdrawal is the most effective first-line intervention in HAE with mutation in coagulation factor XII, with greater efficacy when combined with progestins. Tranexamic acid and lanadelumab may serve as complementary options in selected cases. Late relapse highlights the need for long-term follow-up, with intensified monitoring during periods of hormonal fluctuation.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты