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1.
BMC Pulm Med ; 20(1): 234, 2020 Aug 31.
Artigo em Inglês | MEDLINE | ID: mdl-32867730

RESUMO

BACKGROUND: Cystic Fibrosis (CF) is a hereditary pulmonary and extra-pulmonary disease that occurs equally in men and women. However, a difference in morbidity and mortality rates between the sexes has been long documented. Similarly, a sex-disparity in disease severity has been reported in asthma as well. Studies done to date point to estrogen as a possible cause of this sex disparity in pulmonary outcomes in both conditions. CASE PRESENTATION: Here, we describe a case of a patient with CF and asthma/allergic bronchopulmonary aspergillosis (ABPA) undergoing sex reassignment therapy (male-to-female) and the negative impact it had on her lung function and frequency of pulmonary exacerbations in the context of increasing doses of exogenous estrogen. CONCLUSIONS: This case raises the possibility of a link between estrogen and worsening pulmonary outcomes and the need for further studies into transgender individuals with CF and/or asthma/ABPA as well as those undergoing high dose estrogen therapy for other indications.


Assuntos
Aspergilose Broncopulmonar Alérgica/complicações , Asma/complicações , Fibrose Cística/complicações , Estrogênios/efeitos adversos , Pulmão/fisiopatologia , Aspergilose Broncopulmonar Alérgica/fisiopatologia , Asma/fisiopatologia , Fibrose Cística/fisiopatologia , Estrogênios/administração & dosagem , Feminino , Humanos , Masculino , Testes de Função Respiratória , Cirurgia de Readequação Sexual , Pessoas Transgênero , Adulto Jovem
2.
J Cyst Fibros ; 19(5): 677-687, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-32522463

RESUMO

As CFTR modulator therapy transforms the landscape of cystic fibrosis (CF) care, its lack of uniform access across the globe combined with the shift towards a new standard of care creates unique challenges for the development of future CF therapies. The advancement of a full and promising CF therapeutics pipeline remains a necessary priority to ensure maximal clinical benefits for all people with CF. It is through collaboration across the global CF community that we can optimize the evaluation and approval process of new therapies. To this end, we must identify areas for which harmonization is lacking and for which efficiencies can be gained to promote ethical, feasible, and credible study designs amidst the changing CF care landscape. This article summarizes the counsel from core advisors across multiple international regions and clinical trial networks, developed during a one-day workshop in October 2019. The goal of the workshop was to identify, in consideration of the highly transitional era of CFTR modulator availability, the drug development areas for which global alignment is currently uncertain, and paths forward that will enable advancement of CF therapeutic development.


Assuntos
Regulador de Condutância Transmembrana em Fibrose Cística/efeitos dos fármacos , Fibrose Cística/tratamento farmacológico , Desenvolvimento de Medicamentos/organização & administração , Cooperação Internacional , Fibrose Cística/genética , Humanos
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