Effects of ivacaftor on systemic inflammation and the plasma proteome in people with CF and G551D

被引:13
作者
Hoppe, Jordana E. [1 ]
Wagner, Brandie D. [2 ]
Harris, J. Kirk [1 ]
Rowe, Steven M. [3 ]
Heltshe, Sonya L. [4 ]
DeBoer, Emily M. [1 ]
Sagel, Scott D. [1 ]
机构
[1] Univ Colorado, Dept Pediat, Anschutz Med Campus, Aurora, CO 80045 USA
[2] Univ Colorado, Colorado Sch Publ Hlth, Dept Biostat & Informat, Anschutz Med Campus, Aurora, CO USA
[3] Univ Alabama Birmingham, Dept Med Pediat & Cell Dev & Integrat Biol, Birmingham, AL USA
[4] Univ Washington, Cyst Fibrosis Fdn, Therapeut Dev Network Coordinating Ctr, Dept Pediat, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
CFTR modulation; Proteomics; Inflammation; Extrapulmonary; FIBROSIS LUNG-DISEASE; CYSTIC-FIBROSIS; REGULATOR MODULATORS; LEPTIN LEVELS; DEPRESSION; ANXIETY; POTENTIATOR; EXPRESSION; GHRELIN; RISK;
D O I
10.1016/j.jcf.2022.03.012
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Ivacaftor is a cystic fibrosis transmembrane conductance regulator (CFTR) potentiator for people with CF and the G551D mutation. We aimed to investigate the biology of CFTR modulation and systemic effects of CFTR restoration by examining changes in circulating measurements of inflammation and growth and novel proteins with ivacaftor treatment. Methods: Blood samples from 64 CF subjects with G551D-CFTR were analyzed for inflammatory and growth-related proteins at baseline, 1 and 6 months after ivacaftor initiation. In 30 subjects, plasma was assayed for 1,322 proteins using the SomaScan proteomic platform at baseline and 6 months post-ivacaftor. Correlations with clinical outcomes were assessed. Measurements and Main Results: Significant reductions in high mobility group box-1 protein (HMGB-1), calprotectin, serum amyloid A, and granulocyte colony-stimulating factor (G-CSF), and an increase in insulin-like growth factor (IGF-1) occurred 1 month after ivacaftor. This treatment effect was sustained at 6 months for HMGB-1 and calprotectin. Correcting for multiple comparisons in the proteomic analysis, 9 proteins (albumin, afamin, leptin, trypsin, pancreatic stone protein [PSP], pituitary adenylate cyclase-activating polypeptide-38, repulsive guidance molecule A [RGMA], calreticulin, GTPase KRas) changed significantly with ivacaftor. Proteins changing with treatment are involved in lipid digestion and transport and extracellular matrix organization biological processes. Reductions in calprotectin and G-CSF and increases in calreticulin, and RGMA correlated with improved lung function, while increasing IGF-1, leptin and afamin and decreasing PSP correlated with increased weight. Conclusions: Ivacaftor led to changes in inflammatory, lipid digestion, and extracellular matrix proteins, lending insights into the extrapulmonary effects of CFTR modulation. (c) 2022 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:950 / 958
页数:9
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