Conclusions
These results impact understanding of the differences in asthma features with pubertal maturation and the potential for new treatment. The androgen surge with puberty is likely to confer protective effects on lung growth in both males and females whereas estrogens may well have deleterious effects in females extending into adult development. A trial of weak androgen therapy in adolescent children with low androgen levels and poorly-controlled asthma could be considered to improve lung function. These data may help to explain the gender switch observed in asthma incidence during adolescence and likewise inform lung growth and asthma severity with subsequent maturation into adulthood.
Abbreviations
ACQ6: Asthma control questionnaire 6 item scale; DHEAS: Dehydroepiandrostenedione sulfate; FEV1%: Forced expired volume in one second percent predicted; FVC %: Forced expired vital capacity % predicted; NIH/NHLBI: National Institutes of Health/National Heart Lung Blood Institute; SARP: Severe Asthma Research Program
Acknowledgments
The authors wish to acknowledge the children and their parents who participated in the SARP III study, as well as the hard work of the site-based study coordinators and regulatory personnel, the oversight of the members of the Data Safety and Monitoring Board, and the diligent efforts of the NIH/NHLBI project officers and staff who administered the protocol.
SARP Principal/Co-Principal Investigators.
Eugene R. Bleecker, PI, Wake Forest University, U10 HL109164.
Mario Castro, PI, Washington University, U10 HL109257.
John V. Fahy, PI, University of California San Francisco, U10 HL109146.
Elliot Israel and Bruce Levy, Co-PI's, Brigham and Women's Hospital, U10 HL109172.
Benjamin Gaston, PI, Rainbow Babies and Children's Hospital Virginia-Cleveland Consortium, U10 HL109250.
Serpil Erzurum, Co-PI, Cleveland Clinic, Virginia-Cleveland Consortium, U10 HL109250.
W. Gerald Teague, Co-PI, Univ. of Virginia, Virginia-Cleveland Consortium, U10 HL109250.
Nizar N. Jarjour, PI, University of Wisconsin, U10 HL109168.
Sally E. Wenzel, PI, University of Pittsburgh, U10 HL109152.
David T. Mauger, PI, DCC, Penn State University, U10 HL109086-04.
Funding
This work was supported by the following grants: U10 HL109164, U10 HL109257, U10 HL109146, U10 HL109172, U10 HL109250, U10 HL109250, U10 HL109250, U10 HL109168, U10 HL109152, U10 HL109086–04.
Availability of data and materials
The datasets generated and/or analyzed during the current study are not currently publicly available but will be made available following completion of ongoing data collection. Contact: David T. Mauger, PhD, Pennsylvania State University School of Medicine, DMauger@phs.psu.edu.
Ethics approval and consent to participate
Study procedures were approved by the IRB at each institution and an independent Data Safety Monitoring Board. All subjects provided written informed consent and/or assent. For participants under 16 years-old consent was provided by a parent or legal guardian.
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Trial registration
ClinicalTrials.gov registration number: NCT01748175.
BMC Pulm Med. 2018;18(58) © 2018 BioMed Central, Ltd.
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