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Mast Cell Activation Syndromes: Comparison Between Two Scoring Models to Predict for Mast Cell Clonality.
Rama, Tiago Azenha; Torrado, Inés; Henriques, Ana Filipa; Sánchez-Muñoz, Laura; Jara-Acevedo, Maria; Navarro-Navarro, Paula; Caldas, Carolina; Mayado, Andrea; Muñoz-González, Javier; García-Montero, Andrés; Mollejo, Manuela; Redondo, Elba; Garbán, Andrea; Moreira, André; Órfão, Alberto; Álvarez-Twose, Iván.
Afiliação
  • Rama TA; Serviço de Imunoalergologia, Centro Hospitalar Universitário São João, Porto, Portugal; Serviço de Imunologia Básica e Clínica, Departamento de Patologia, Faculdade de Medicina da Universidade do Porto, Porto, Portugal; EPIUnit, Institute of Public Health, University of Porto, Porto, Portugal; Labor
  • Torrado I; Instituto de Estudios de Mastocitosis de Castilla La Mancha, Reference Center for Mastocytosis, Hospital Virgen del Valle, Complejo Hospitalario Universitario de Toledo, Toledo, Spain.
  • Henriques AF; Instituto de Estudios de Mastocitosis de Castilla La Mancha, Reference Center for Mastocytosis, Hospital Virgen del Valle, Complejo Hospitalario Universitario de Toledo, Toledo, Spain; Spanish Network on Mastocytosis, Toledo and Salamanca, Spain.
  • Sánchez-Muñoz L; Instituto de Estudios de Mastocitosis de Castilla La Mancha, Reference Center for Mastocytosis, Hospital Virgen del Valle, Complejo Hospitalario Universitario de Toledo, Toledo, Spain; Spanish Network on Mastocytosis, Toledo and Salamanca, Spain; Centro de Investigación Biomédica en Red de Cáncer, I
  • Jara-Acevedo M; Spanish Network on Mastocytosis, Toledo and Salamanca, Spain; Centro de Investigación Biomédica en Red de Cáncer, Instituto de Salud Carlos III, Madrid, Spain; DNA Sequencing Service, Instituto de Investigación Biomédica de Salamanca, University of Salamanca, Salamanca, Spain.
  • Navarro-Navarro P; Spanish Network on Mastocytosis, Toledo and Salamanca, Spain; Centro de Investigación Biomédica en Red de Cáncer, Instituto de Salud Carlos III, Madrid, Spain; DNA Sequencing Service, Instituto de Investigación Biomédica de Salamanca, University of Salamanca, Salamanca, Spain.
  • Caldas C; Spanish Network on Mastocytosis, Toledo and Salamanca, Spain; Centro de Investigación Biomédica en Red de Cáncer, Instituto de Salud Carlos III, Madrid, Spain; DNA Sequencing Service, Instituto de Investigación Biomédica de Salamanca, University of Salamanca, Salamanca, Spain.
  • Mayado A; Spanish Network on Mastocytosis, Toledo and Salamanca, Spain; Centro de Investigación Biomédica en Red de Cáncer, Instituto de Salud Carlos III, Madrid, Spain; Cancer Research Center, Department of Medicine, Cytometry Service, Instituto de Investigación Biomédica de Salamanca, University of Salamanc
  • Muñoz-González J; Spanish Network on Mastocytosis, Toledo and Salamanca, Spain; Centro de Investigación Biomédica en Red de Cáncer, Instituto de Salud Carlos III, Madrid, Spain; Cancer Research Center, Department of Medicine, Cytometry Service, Instituto de Investigación Biomédica de Salamanca, University of Salamanc
  • García-Montero A; Spanish Network on Mastocytosis, Toledo and Salamanca, Spain; Centro de Investigación Biomédica en Red de Cáncer, Instituto de Salud Carlos III, Madrid, Spain; Cancer Research Center, Department of Medicine, Cytometry Service, Instituto de Investigación Biomédica de Salamanca, University of Salamanc
  • Mollejo M; Pathology Department, Hospital Virgen de la Salud, Complejo Hospitalario Universitario de Toledo, Toledo, Spain.
  • Redondo E; Servicio de Alergologia, Hospital Clínico San Carlos, Madrid, Spain.
  • Garbán A; Servicio de Alergologia, Hospital Clínico San Carlos, Madrid, Spain.
  • Moreira A; Serviço de Imunoalergologia, Centro Hospitalar Universitário São João, Porto, Portugal; Serviço de Imunologia Básica e Clínica, Departamento de Patologia, Faculdade de Medicina da Universidade do Porto, Porto, Portugal; EPIUnit, Institute of Public Health, University of Porto, Porto, Portugal; Labor
  • Órfão A; Spanish Network on Mastocytosis, Toledo and Salamanca, Spain; Centro de Investigación Biomédica en Red de Cáncer, Instituto de Salud Carlos III, Madrid, Spain; Cancer Research Center, Department of Medicine, Cytometry Service, Instituto de Investigación Biomédica de Salamanca, University of Salamanc
  • Álvarez-Twose I; Instituto de Estudios de Mastocitosis de Castilla La Mancha, Reference Center for Mastocytosis, Hospital Virgen del Valle, Complejo Hospitalario Universitario de Toledo, Toledo, Spain; Spanish Network on Mastocytosis, Toledo and Salamanca, Spain; Centro de Investigación Biomédica en Red de Cáncer, I
J Allergy Clin Immunol Pract ; 11(3): 908-919.e4, 2023 03.
Article em En | MEDLINE | ID: mdl-36535520
ABSTRACT

BACKGROUND:

The Red Española de Mastocitosis (Spanish Network on Mastocytosis) score (REMAs) and the National Institutes of Health idiopathic clonal anaphylaxis score (NICAS) were developed for more efficient screening of mast cell (MC) clonality in MC activation syndromes. In a limited idiopathic anaphylaxis case series, the NICAS showed higher accuracy compared with the REMAs.

OBJECTIVE:

To compare the performance of the REMAs against the NICAS in the diagnosis of MC clonality.

METHODS:

We compared the diagnostic value of the REMAs against the NICAS in 182 patients (63% men, median age 56 years) who presented with anaphylaxis triggered by Hymenoptera venom allergy (45%), drugs (15%), food (11%), idiopathic anaphylaxis (20%), and mixed causes (10%). KIT mutation was assessed in parallel in whole blood and bone marrow (BM) and, when negative, in highly purified BM MC. TPSAB1 was genotyped in a subset of 71 patients.

RESULTS:

We found higher accuracy and rates of correctly classified patients for the REMAs (82% and 84%) compared with the NICAS (75% and 75%; P = .02 and P = .03, respectively), particularly among men (P = .05), patients with systemic mastocytosis (P = .05), those presenting anaphylaxis owing to any cause featuring urticaria (P = .04), cardiovascular symptoms (P = .02), and/or presyncope (P = .02) and those with a blood-negative/BM-positive KIT mutational profile (P = .002), but not hereditary α-tryptasemia-associated genotypes. Combined assessment of the REMAs and KITD816V in blood yielded an overall improved classification efficiency of 86% versus 84% for REMAs.

CONCLUSIONS:

The combined use of the REMAs and blood detection of KITD816V is recommended, but more sensitive blood-based molecular assays to detect KITD816V are needed.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Venenos de Artrópodes / Mastocitose / Mastocitose Sistêmica / Síndrome da Ativação de Mastócitos / Anafilaxia Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Allergy Clin Immunol Pract Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Venenos de Artrópodes / Mastocitose / Mastocitose Sistêmica / Síndrome da Ativação de Mastócitos / Anafilaxia Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Allergy Clin Immunol Pract Ano de publicação: 2023 Tipo de documento: Article