The Journal of Allergy and Clinical Immunology
Volume 120, Issue 6 , Pages 1285-1291, December 2007

FCER2: A pharmacogenetic basis for severe exacerbations in children with asthma

  • Kelan G. Tantisira, MD, MPH

      Affiliations

    • Channing Laboratory, Brigham and Women's Hospital, Boston, Mass
    • Pulmonary Division, Brigham and Women's Hospital, Boston, Mass
    • Harvard Medical School, Boston, Mass
    • Corresponding Author InformationReprint requests: Kelan G. Tantisira, MD, MPH, Channing Laboratory, 181 Longwood Avenue, Boston, MA 02115.
  • ,
  • Eric S. Silverman, MD

      Affiliations

    • MetroWest Medical Center, Natick, Mass
  • ,
  • Thomas J. Mariani, PhD

      Affiliations

    • Pulmonary Division, Brigham and Women's Hospital, Boston, Mass
    • Harvard Medical School, Boston, Mass
  • ,
  • Jingsong Xu, PhD

      Affiliations

    • Pulmonary Division, Brigham and Women's Hospital, Boston, Mass
    • Harvard Medical School, Boston, Mass
  • ,
  • Brent G. Richter, MS

      Affiliations

    • Channing Laboratory, Brigham and Women's Hospital, Boston, Mass
  • ,
  • Barbara J. Klanderman, PhD

      Affiliations

    • Channing Laboratory, Brigham and Women's Hospital, Boston, Mass
    • Harvard Medical School, Boston, Mass
  • ,
  • Augusto A. Litonjua, MD, MPH

      Affiliations

    • Channing Laboratory, Brigham and Women's Hospital, Boston, Mass
    • Harvard Medical School, Boston, Mass
  • ,
  • Ross Lazarus, MD

      Affiliations

    • Channing Laboratory, Brigham and Women's Hospital, Boston, Mass
    • Harvard Medical School, Boston, Mass
  • ,
  • Lanny J. Rosenwasser, MD

      Affiliations

    • University of Missouri–Kansas City School of Medicine, Kansas City, Mo
  • ,
  • Anne L. Fuhlbrigge, MD, MS

      Affiliations

    • Channing Laboratory, Brigham and Women's Hospital, Boston, Mass
    • Pulmonary Division, Brigham and Women's Hospital, Boston, Mass
    • Harvard Medical School, Boston, Mass
  • ,
  • Scott T. Weiss, MD, MS

      Affiliations

    • Channing Laboratory, Brigham and Women's Hospital, Boston, Mass
    • Harvard Medical School, Boston, Mass

Received 16 March 2007; received in revised form 16 August 2007; accepted 5 September 2007. published online 05 November 2007.

Background

Although inhaled corticosteroids (ICSs) generally protect against severe exacerbations in asthma, they may result in elevated IgE levels, which are associated with exacerbations.

Objective

To determine whether variation in the low-affinity IgE receptor gene, FCER2, is associated with severe exacerbations defined as emergency department visits and/or hospitalizations in patients with asthma on ICSs.

Methods

We resequenced, then genotyped 10 FCER2 single nucleotide polymorphisms (SNPs) in 311 children randomized to inhaled budesonide as part of the Childhood Asthma Management Program. We evaluated the association of FCER2 variants with IgE levels and presence or absence of severe exacerbations over the 4-year clinical trial. We also evaluated differences in cellular expression of the novel FCER2 SNP, T2206C.

Results

In white subjects, 3 FCER2 SNPs were significantly associated (P < .05) with elevated 4-year IgE level; each was also associated with increased severe exacerbations. Final multivariable models demonstrated associations between T2206C and severe exacerbations in both white and African American children (hazard ratio, 3.95; 95% CI, 1.64-9.51; and hazard ratio, 3.08; 95% CI, 1.00-9.47), despite ICS use. Interaction models supported a true gene-environment effect in white subjects (interaction P = .004). T2206C was also associated with decreased FCER2 expression (P = .02).

Conclusion

FCER2 predicts the likelihood of treatment protocol success in asthma. The associations of T2206C with IgE level, severe exacerbations, and FCER2 expression may provide a mechanistic basis for the observed findings.

Clinical implications

Genetic variation in FCER2 may help form a prognostic model for ICS response in asthma.

Key words: Asthma, CD23, FCER2, exacerbation, corticosteroid, pharmacogenetic, hospitalization

Abbreviations used: CAMP, Childhood Asthma Management Program, FCER2, Fc fragment of IgE, low-affinity II receptor gene (the gene encoding for CD23), ICS, Inhaled corticosteroid, OR, Odds ratio, SNP, Single nucleotide polymorphism

 

 Supported by National Institutes of Health grants HL U01 65899 and HG K23 3983. The Childhood Asthma Management Program Genetics Ancillary Study was supported by the National Heart, Lung, and Blood Institute, NO1-HR-16049. Additional support for this research came from grants N01 HR16044, HR16045, HR16046, HR16047, HR16048, HR16049, HR16050, HR16051, and HR16052 from the National Heart, Lung and Blood Institute.

 Disclosure of potential conflict of interest: L. J. Rosenwasser has consulting arrangements with Biogen Idec Corp. A. L. Fuhlbrigge has consulting arrangements with GlaxoSmithKline and Merck; has received grant support from Boehringer Ingelheim, Merck, and GlaxoSmithKline; and is on the speakers' bureau for GlaxoSmithKline and Merck. The rest of the authors have declared that they have no conflict of interest.

PII: S0091-6749(07)01727-7

doi:10.1016/j.jaci.2007.09.005

The Journal of Allergy and Clinical Immunology
Volume 120, Issue 6 , Pages 1285-1291, December 2007