NETwork of Linoleic Acid Supplementation in Cystic Fibrosis

Last updated: November 25, 2024
Sponsor: Karolinska Institutet
Overall Status: Completed

Phase

N/A

Condition

Cystic Fibrosis

Scar Tissue

Lung Disease

Treatment

linoleic acid supplementation

oleic acid supplementation

Clinical Study ID

NCT04531410
2020-02871
  • Ages 5-15
  • All Genders

Study Summary

Undernutrition is a common problem in patients with cystic fibrosis (CF) despite international consensus that the patients shall be given 120-200% of energy recommendations. Studies imply that one problem might be that the patients are not compensated for the essential fatty acid deficiency (linoleic acid, LA), which is well known in these patients. This deficiency is shown not to be due to fat malabsorption, but related to an increased turnover of arachidonic acid, a transformation product of LA. This abnormality is related to mutations associated with a more severe clinical phenotype. The most common and typical symptom of LA deficiency is poor growth. Studies in animals have further indicated that many of the symptoms in CF are related to the deficiency. A series of recent prospective studies from Wisconsin corroborate the importance of LA for growth. In Sweden LA has been supplemented to most patients since the late 70´, and the condition of patients have been among the leading in the world regarding growth, pulmonary function and survival. Short-term studies have shown better effect of LA supplementation compared to similar supply of energy without including extra LA. There are few long-term studies, performed before the gene was identified, giving very heterogeneous patient groups in regard to genotype, but with some positive results on growth and physiology. It´s of interest that modern personalized extremely expensive therapy with correctors and potentiators for Cystic Fibrosis Transmembrane Conductance Regulator may influence lipid metabolism. LA might thus tentatively be a cheap adjuvant to this modern therapy, but this has to be specially studied.

The aim of the study is to find if there are differences in clinical and metabolic outcome between two groups, blindly given similar amount of extra calories, in one group consisting of linoleic acid.The benefit for the patients would be great if the expected positive effect can be proved in the planned study. The treatment will be cheap and without adverse effects. From socioeconomic point of view is would be a great advantage.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Two mutations related to severe clinical status such as dF508, or other stopmutations or class II mutations. Severe status includes pancreatic insufficiency

Exclusion

Exclusion Criteria:

  • Liver cirrhosis and/or portal hypertension, transplantation or on transplantationlist, intake of lipid supplements the latest 2 months

Study Design

Total Participants: 50
Treatment Group(s): 2
Primary Treatment: linoleic acid supplementation
Phase:
Study Start date:
October 25, 2021
Estimated Completion Date:
November 05, 2024

Study Description

Two group of matched children with CF were randomized to two type of oils given 20 g oil and 600 mg DHA daily for one year and anthropometry, pulmonary function, biochemistry, resting energy expenditure, lipid mediators, inflammatory and intestinal markers were studied at start and at 6 months and 1 year. Dietary intake was controlled and life quality recording at start and end of study.

Connect with a study center

  • Centro Regionale di Supporto per la Fibrosei Cistica, ASST Spedali civili, Univ of Brescia

    Brescia, Brescia - Lombardia 25123
    Italy

    Site Not Available

  • Università degli Studi di Milan

    Milan,
    Italy

    Site Not Available

  • Norwegian Resourse Center for Cystic Fibrosis, Oslo University Hospital

    Oslo,
    Norway

    Site Not Available

  • Poznan University of Medical Sciences

    Poznań,
    Poland

    Site Not Available

  • Center of Cystic fibrosis, Dept of Pediatrics, Lund University Hospital

    Lund, Skåne 22242
    Sweden

    Site Not Available

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