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Impact of lumacaftor/ivacaftor on nutrition and growth in modulator-naïve children over 24 weeks.
Tindall, Alyssa; Bass, Rosara; Maqbool, Asim; Stallings, Virginia A.
Affiliation
  • Tindall A; Division of Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA, USA. Electronic address: tindalla@chop.edu.
  • Bass R; Division of Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Maqbool A; Division of Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Stallings VA; Division of Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
J Cyst Fibros ; 23(4): 758-763, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38789320
ABSTRACT

BACKGROUND:

Cystic fibrosis transmembrane conductance regulator (CFTR) modulators improve nutritional status and are of importance in achieving normal growth among younger children with CF. The study was designed to examine CFTR modulator-associated changes in nutrition status, including bile acids and fatty acids after lumacaftor/ivacaftor therapy for 24 weeks.

METHODS:

Children 2 to 5.9 years were recruited from US and Canadian CF Centers. Eligible children were lumacaftor/ivacaftor naïve and approved to initiate therapy. Anthropometrics, diet, energy expenditure, nutrition biomarkers, pancreatic status, serum and fecal calprotectin, serum bile acids and plasma fatty acids were measured. Changes from baseline at 12 and 24 weeks were examined using mixed effects linear regression modeling.

RESULTS:

Weight-for-age z-score (WAZ) increased at 12 (0.15 ± 0.1, p = 0.01) and 24 weeks (0.23 ± 0.1, p = 0.001) from baseline following modulator therapy. Head circumference-for-age (HCZ) increased at 12 weeks compared to baseline (0.22 ± 0.1, p = 0.03) and subscapular Z score increased from baseline at 24 weeks following therapy (0.33 ± 0.1, p = 0.02). There were no changes in energy expenditure. Serum total bile acids (6.7 ± 2.0, p = 0.001), chenodeoxycholic acid (CDCA) (2.4 ± 1.1, p = 0.001), and cholic acid (CA) (3.5 ± 0.8, p < 0.0001) increased at 24 weeks compared to baseline. Fecal calprotectin decreased at 12 and 24 weeks compared to baseline (-463 ± 310, p = 0.03 and 566 ± 347, p = 0.047). A number of plasma fatty acids changed over the course of 24 weeks of therapy. Noteably, alpha-linolenic acid (ALA) decreased at 12 and 24 weeks (-24 ± 10,p = 0.03 and -18 ± 10, p = 0.02, respectively).

CONCLUSIONS:

Overall, young children experienced favorable changes in nutritional and growth, with the exception of plasma ALA status in the first 24 weeks of lumacaftor/ivacaftor therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nutritional Status / Quinolones / Cystic Fibrosis / Drug Combinations / Benzodioxoles / Chloride Channel Agonists / Aminophenols / Aminopyridines Limits: Child, preschool / Female / Humans / Male Country/Region as subject: America do norte Language: En Journal: J Cyst Fibros Year: 2024 Document type: Article Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nutritional Status / Quinolones / Cystic Fibrosis / Drug Combinations / Benzodioxoles / Chloride Channel Agonists / Aminophenols / Aminopyridines Limits: Child, preschool / Female / Humans / Male Country/Region as subject: America do norte Language: En Journal: J Cyst Fibros Year: 2024 Document type: Article Country of publication: Netherlands