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Performance of the Pediatric Asthma Risk Score across Diverse Populations.
Biagini, Jocelyn M; Martin, Lisa J; He, Hua; Bacharier, Leonard B; Gebretsadik, Tebeb; Hartert, Tina V; Jackson, Daniel J; Kim, Haejin; Miller, Rachel L; Rivera-Spoljaric, Katherine; Schauberger, Eric M; Singh, Anne Marie; Visness, Cynthia M; Wegienka, Ganesa; Ownby, Dennis R; Gold, Diane R; Martinez, Fernando D; Johnson, Christine C; Wright, Anne L; Gern, James E; Khurana Hershey, Gurjit K.
Afiliação
  • Biagini JM; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati.
  • Martin LJ; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati.
  • He H; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati.
  • Bacharier LB; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati.
  • Gebretsadik T; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati.
  • Hartert TV; Department of Pediatrics, Vanderbilt University Medical Center, Nashville.
  • Jackson DJ; Department of Biostatistics, Vanderbilt University Medical Center, Nashville.
  • Kim H; Department of Pediatrics, Vanderbilt University Medical Center, Nashville.
  • Miller RL; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison.
  • Rivera-Spoljaric K; Department of Internal Medicine, Henry Ford Health, Detroit.
  • Schauberger EM; Department of Medicine, Division of Clinical Immunology, Icahn School of Medicine at Mount Sinai, New York.
  • Singh AM; Department of Pediatrics, Washington University School of Medicine, St. Louis.
  • Visness CM; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison.
  • Wegienka G; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison.
  • Ownby DR; Rho, Inc., Federal Research Operations, Durham, NC.
  • Gold DR; Department of Public Health Sciences, Henry Ford Health System, Detroit.
  • Martinez FD; Department of Public Health Sciences, Henry Ford Health System, Detroit.
  • Johnson CC; The Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston.
  • Wright AL; Department of Environmental Health, Harvard T.H. Chan School of Public Health, Boston.
  • Gern JE; Asthma and Airways Disease Research Center, Department of Pediatrics, College of Medicine, University of Arizona, Tucson.
  • Khurana Hershey GK; Division of Pulmonary and Sleep Medicine, Department of Pediatrics, College of Medicine, University of Arizona, Tucson.
NEJM Evid ; 2(10): EVIDoa2300026, 2023 Oct.
Article em En | MEDLINE | ID: mdl-38320177
ABSTRACT

BACKGROUND:

Methods to determine whether a toddler is likely to develop asthma are of value to parents and clinical trialists testing primary prevention strategies. The Pediatric Asthma Risk Score (PARS) is a 14-point score of six factors designed to predict asthma in early life. PARS was developed and validated in relatively homogenous populations, so its generalizability is unknown.

METHODS:

We computed PARS using the six factors of self-declared race (parent-reported as "Black" or "not Black"), parental asthma, eczema, any wheezing, wheezing without a cold, and polysensitization in 5634 children from birth to 3 years of age. The primary outcome of our analysis was the ability of PARS to predict asthma development at 5 to 10 years of age using the area under the receiver operating curve in each cohort and across all cohorts with varying ethnicity, sex, cohort type, birth decades, missing PARS factors, and polysensitization definition. We also performed a meta-analysis across all the cohorts. Finally, we compared PARS predictive ability with the binary Asthma Predictive Index (API).

RESULTS:

Across 10 cohorts, the area under the receiver operating curve for PARS was 0.76. PARS performance did not differ by ethnicity, sex, cohort type, enrollment decade, missing PARS factors, or polysensitization definition (all P>0.05). The weights of each factor in the meta-analysis were similar to the original PARS weights. PARS and API equally identified children at high risk for developing asthma or not; API missed 31% of children at moderate asthma risk.

CONCLUSIONS:

PARS provided robust estimates of asthma risk in children from a wide range of ethnicities, backgrounds, and susceptibility. (Funded by the National Institute of Allergy and Infectious Diseases and others.)
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article