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Loss of bronchoprotection with ICS plus LABA treatment, ß-receptor dynamics, and the effect of alendronate.
Cardet, Juan Carlos; Jiang, Xiaofeng; Lu, Quan; Gerard, Norma; McIntire, Kristen; Boushey, Homer A; Castro, Mario; Chinchilli, Vernon M; Codispoti, Christopher D; Dyer, Anne-Marie; Holguin, Fernando; Kraft, Monica; Lazarus, Stephen; Lemanske, Robert F; Lugogo, Njira; Mauger, Dave; Moore, Wendy C; Moy, James; Ortega, Victor E; Peters, Stephen P; Smith, Lewis J; Solway, Julian; Sorkness, Christine A; Sumino, Kaharu; Wechsler, Michael E; Wenzel, Sally; Israel, Elliot.
Afiliação
  • Cardet JC; Department of Medicine, Brigham and Women's Hospital, Boston, Mass.
  • Jiang X; Departments of Environmental Health, Genetics & Complex Diseases, Harvard T.H. Chan School of Public Health, Boston, Mass.
  • Lu Q; Departments of Environmental Health, Genetics & Complex Diseases, Harvard T.H. Chan School of Public Health, Boston, Mass.
  • Gerard N; Department of Pediatrics, Boston Children's Hospital, Boston, Mass.
  • McIntire K; Department of Medicine, Brigham and Women's Hospital, Boston, Mass.
  • Boushey HA; Department of Medicine, University of California San Francisco, San Francisco, Calif.
  • Castro M; Department of Medicine, Washington University, St Louis, Mo.
  • Chinchilli VM; Department of Public Health Sciences, Penn State College of Medicine, Hershey, Pa.
  • Codispoti CD; Department of Medicine, Rush University Medical Center and Department of Pediatrics, Stroger Hospital of Cook County, Chicago, Ill.
  • Dyer AM; Department of Public Health Sciences, Penn State College of Medicine, Hershey, Pa.
  • Holguin F; Department of Medicine, Pittsburgh University, Pittsburgh, Pa.
  • Kraft M; Department of Medicine, University of Arizona, Tucson, Ariz.
  • Lazarus S; Department of Medicine, University of California San Francisco, San Francisco, Calif.
  • Lemanske RF; Departments of Medicine and Pharmacy Practice, University of Wisconsin, Madison, Wis.
  • Lugogo N; Department of Medicine, Duke University, Durham, NC.
  • Mauger D; Department of Public Health Sciences, Penn State College of Medicine, Hershey, Pa.
  • Moore WC; Department of Internal Medicine, Wake Forest University, Winston-Salem, NC.
  • Moy J; Department of Medicine, Rush University Medical Center and Department of Pediatrics, Stroger Hospital of Cook County, Chicago, Ill.
  • Ortega VE; Department of Internal Medicine, Wake Forest University, Winston-Salem, NC.
  • Peters SP; Department of Internal Medicine, Wake Forest University, Winston-Salem, NC.
  • Smith LJ; Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Ill.
  • Solway J; Department of Medicine, University of Chicago, Chicago, Ill.
  • Sorkness CA; Departments of Medicine and Pharmacy Practice, University of Wisconsin, Madison, Wis.
  • Sumino K; Department of Medicine, Washington University, St Louis, Mo.
  • Wechsler ME; Department of Medicine, National Jewish University, Denver, Colo.
  • Wenzel S; Department of Medicine, Pittsburgh University, Pittsburgh, Pa.
  • Israel E; Department of Medicine, Brigham and Women's Hospital, Boston, Mass. Electronic address: eisrael@bwh.harvard.edu.
J Allergy Clin Immunol ; 144(2): 416-425.e7, 2019 08.
Article em En | MEDLINE | ID: mdl-30872116
ABSTRACT

BACKGROUND:

Loss of bronchoprotection (LOBP) with a regularly used long-acting ß2-adrenergic receptor agonist (LABA) is well documented. LOBP has been attributed to ß2-adrenergic receptor (B2AR) downregulation, a process requiring farnesylation, which is inhibited by alendronate.

OBJECTIVE:

We sought to determine whether alendronate can reduce LABA-associated LOBP in inhaled corticosteroid (ICS)-treated patients.

METHODS:

We conducted a randomized, double-blind, placebo-controlled, parallel-design, proof-of-concept trial. Seventy-eight participants with persistent asthma receiving 250 µg of fluticasone twice daily for 2 weeks were randomized to receive alendronate or placebo while initiating salmeterol for 8 weeks. Salmeterol-protected methacholine challenges (SPMChs) and PBMC B2AR numbers (radioligand binding assay) and signaling (cyclic AMP ELISA) were assessed before randomization and after 8 weeks of ICS plus LABA treatment. LOBP was defined as a more than 1 doubling dose reduction in SPMCh PC20 value.

RESULTS:

The mean doubling dose reduction in SPMCh PC20 value was 0.50 and 0.27 with alendronate and placebo, respectively (P = .62). Thirty-eight percent of participants receiving alendronate and 33% receiving placebo had LOBP (P = .81). The after/before ICS plus LABA treatment ratio of B2AR number was 1.0 for alendronate (P = .86) and 0.8 for placebo (P = .15; P = .31 for difference between treatments). The B2AR signaling ratio was 0.89 for alendronate (P = .43) and 1.02 for placebo (P = .84; P = .44 for difference). Changes in lung function and B2AR number and signaling were similar between those who did and did not experience LOBP.

CONCLUSION:

This study did not find evidence that alendronate reduces LABA-associated LOBP, which relates to the occurrence of LOBP in only one third of participants. LOBP appears to be less common than presumed in concomitant ICS plus LABA-treated asthmatic patients. B2AR downregulation measured in PBMCs does not appear to reflect LOBP.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Corticosteroides / Receptores Adrenérgicos beta 2 / Alendronato / Xinafoato de Salmeterol / Fluticasona Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Corticosteroides / Receptores Adrenérgicos beta 2 / Alendronato / Xinafoato de Salmeterol / Fluticasona Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article