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Fish Oil Supplementation in Overweight/Obese Patients with Uncontrolled Asthma. A Randomized Trial.
Lang, Jason E; Mougey, Edward B; Hossain, Md Jobayer; Livingston, Floyd; Balagopal, P Babu; Langdon, Scott; Lima, John J.
  • Lang JE; 1 Division of Allergy/Immunology and Pulmonary Medicine, Duke University, Durham, North Carolina.
  • Mougey EB; 2 Center for Pharmacogenomics and Translational Research, Nemours Children's Health System, Jacksonville, Florida.
  • Hossain MJ; 3 Center for Pediatric Research, Alfred I. DuPont Hospital of Children, Wilmington, Delaware.
  • Livingston F; 4 Nemours Children's Hospital, Orlando, Florida.
  • Balagopal PB; 5 Biomedical Analysis Laboratory, Nemours Children's Specialty Care, Jacksonville, Florida; and.
  • Langdon S; 6 Department of Immunology, Duke University School of Medicine, Durham, North Carolina.
  • Lima JJ; 2 Center for Pharmacogenomics and Translational Research, Nemours Children's Health System, Jacksonville, Florida.
Ann Am Thorac Soc ; 16(5): 554-562, 2019 05.
Article en En | MEDLINE | ID: mdl-30678465
ABSTRACT
Rationale Omega-3 fatty acid (n3PUFA) supplementation has been proposed as a promising antiasthma strategy. The rs59439148 ALOX5 polymorphism affects leukotriene production and possibly inflammatory responses to n3PUFA.

Objectives:

Assess the effects of n3PUFA supplementation and ALOX5 genotype on asthma control in patients with obesity and uncontrolled asthma.

Methods:

This multicenter trial among 12- to 25-year-olds with overweight/obesity and uncontrolled asthma randomized subjects in a 31 allotment to n3PUFA (4 g/d) or soy oil control for 24 weeks. Asthma Control Questionnaire was the primary outcome; secondary outcomes included blood leukocyte n3PUFA levels, urinary leukotriene-E4, spirometry, and asthma-related events. The number of SP1 tandem repeats in rs59439148 determined ALOX5 genotype status. Simple and multivariable generalized linear models assessed effects on outcomes.

Results:

Ninety-eight participants were randomized (77 to PUFA, 21 to control), and more than 86% completed all visits. Asthma and demographic characteristics were similar among treatment groups. n3PUFA treatment increased the n3-to-n6 PUFA ratio in circulating granulocytes (P = 0.029) and monocytes (P = 0.004) but did not affect mean Asthma Control Questionnaire change at 6 months (n3PUFA mean, -0.09; 95% confidence interval [CI], 0.09 to 0.10; vs. control mean, -0.18; 95% CI, -0.42 to 0.06; P = 0.58). Changes in urinary leukotriene-E4 (P = 0.24), forced expiratory volume in 1 second % predicted (P = 0.88), and exacerbations (relative risk [RR], 0.92; 95% CI, 0.30-2.89) at 6 months were similar in both groups. n3PUFA treatment was associated with reduced asthma-related phone contacts (RR, 0.34; 95% CI, 0.13-0.86; P = 0.02). ALOX5 genotype did not affect n3PUFA treatment responses.

Conclusions:

We did not find evidence that n3PUFA use improves most asthma-related outcomes and cannot recommend it as a prevention strategy for overweight/obese patients with asthma. Clinical trial registered with www.clinicaltrials.gov (NCT01027143).
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Asma / Aceites de Pescado / Ácidos Grasos Omega-3 / Sobrepeso / Obesidad Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Asma / Aceites de Pescado / Ácidos Grasos Omega-3 / Sobrepeso / Obesidad Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Año: 2019 Tipo del documento: Article