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Treatment by biomarker-informed endotype vs guideline care in children with difficult-to-treat asthma.
Guilbert, Theresa W; Biagini, Jocelyn M; Ramsey, Rachelle R; Keidel, Kristina; Curtsinger, Kristi; Kroner, John W; Durrani, Sandy R; Stevens, Mariana; Pilipenko, Valentina; Martin, Lisa J; Kercsmar, Carolyn M; Hommel, Kevin; Hershey, Gurjit K Khurana.
Afiliação
  • Guilbert TW; Division of Pulmonary Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Biagini JM; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Ramsey RR; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Behavioral Medicine and Clinical Psychology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Keidel K; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Curtsinger K; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Kroner JW; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Durrani SR; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Allergy and Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Stevens M; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Pilipenko V; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Martin LJ; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Kercsmar CM; Division of Pulmonary Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Hommel K; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Behavioral Medicine and Clinical Psychology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Hershey GKK; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio. Electronic address: Gurjit.Hershey@cchmc.org.
Ann Allergy Asthma Immunol ; 128(5): 535-543.e6, 2022 05.
Article em En | MEDLINE | ID: mdl-35123074
ABSTRACT

BACKGROUND:

Asthma is heterogeneous, contributing to difficulty in disease management.

OBJECTIVE:

To develop a biomarker-informed treatment model for difficult-to-treat (DTT) asthma and conduct a pilot feasibility study.

METHODS:

School-aged children (n = 21) with DTT asthma were enrolled and completed 3 medical visits (V1-V3). V2 and V3 were completed approximately 3.5 months and 12 months after V1, respectively. At V1, guideline care and adherence interventions were initiated, and blood samples were collected for asthma biomarker assessment. A personalized treatment algorithm was developed based on biomarkers (treatment by endotype) and was implemented at V2. Asthma outcomes were compared from V1 to V2 (guideline-based care) to V2 to V3 (guideline + biomarker-informed care).

RESULTS:

Overall retention was 86%. There was an even distribution of participants with allergy, without allergy, and with mixed allergies. The participants received an average of 5.9 interventions (range, 3-9). The allergic phenotype was characterized by increased CDHR3 risk genotype and high transepidermal water loss. High serum interleukin-6 level was most notable in the mixed allergic subgroup. The nonallergic phenotype was characterized by vitamin D deficiency and poor steroid treatment responsiveness. The personalized treatment plans were associated with decreased emergency department visits (median, 1 vs 0; P = .04) and increased asthma control test scores (median, 22.5 vs 23.0; P = .01).

CONCLUSION:

The biomarker-based treatment algorithm triggered interventions on top of guideline care in all children with DTT asthma studied, supporting the need for this type of multipronged approach. Our findings identify the minimal biomarker set that is informative, reveal that this treatment-by-endotype intervention is feasible and may be superior to guideline care alone, and provide a strong foundation for a definitive trial. TRIAL REGISTRATION ClinicalTrials.gov identifier NCT04179461.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Hipersensibilidade Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Child / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Hipersensibilidade Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Child / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article