Literature DB >> 23403437

High serum retinol and lung function in young patients with cystic fibrosis.

M Francisco Rivas-Crespo1, David González Jiménez, Maria D Acuña Quirós, Amaia Sojo Aguirre, Soledad Heredia González, Juan J Díaz Martín, Jesús M Garagorri Otero, Aurora Lázaro Almarza, Carlos Bousoño-García.   

Abstract

OBJECTIVE: The aim of the present study was to explore the relation between lung function and serum retinol (SR) in cystic fibrosis (CF) patients.
METHODS: This was a cross-sectional study conducted in a group of 98 young patients with CF (6.8-22.3 years), after the exclusion of those with pulmonary exacerbation, vitamin A deficiency, or other risks, from an initial group of 124 cases.
RESULTS: Data of forced expiratory volume in 1 second (FEV₁) were widely scattered (87.7% ± 16.9%). These were similar in the 78 pancreatic insufficient and 11 pancreatic sufficient patients. SR (56.6 ± 18.4 μg/dL) was >2.5th percentile of healthy people in the whole group, although 31 patients were situated above the 97.5th percentile (higher value: 110 μg/dL). The FEV₁ was noticeably higher in these than in those within the normal range (93.6 ± 14.0 vs 85.0 ± 17.6 μg/dL; P < 0.05). The z score of SR correlated positively with FEV₁ (r = 0.364; P = 0.000), after adjusting data for sex, age, body mass index, and pancreatic function. The odds ratio for a FEV₁ >80% is 3.78 in patients with SR above the 97.5th percentile, versus only 0.26 in those within the normal range. There were no cases with retinol toxicity.
CONCLUSIONS: FEV₁ of young patients with CF correlates positively with SR, regardless of age, pancreatic function, or nutritional condition. Those with a moderately high retinol (up to 110 μg/dL) maintain the best respiratory function (FEV₁ ≥80% in >90% of them) without any signs of toxicity.

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Year:  2013        PMID: 23403437     DOI: 10.1097/MPG.0b013e31828b1d90

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  3 in total

1.  Retinoic acid signaling is essential for airway smooth muscle homeostasis.

Authors:  Felicia Chen; Fengzhi Shao; Anne Hinds; Sean Yao; Sumati Ram-Mohan; Timothy A Norman; Ramaswamy Krishnan; Alan Fine
Journal:  JCI Insight       Date:  2018-08-23

Review 2.  Update on the management of vitamins and minerals in cystic fibrosis.

Authors:  Senthilkumar Sankararaman; Sara J Hendrix; Terri Schindler
Journal:  Nutr Clin Pract       Date:  2022-08-23       Impact factor: 3.204

3.  Association of vitamin A status with lung function in children and adolescents with cystic fibrosis.

Authors:  Ioanna Loukou; Maria Moustaki; Olympia Sardeli; Marina Plyta; Christina N Katsagoni; Konstantinos Douros
Journal:  Pediatr Investig       Date:  2021-06-18
  3 in total

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