دورية أكاديمية

The effects of polyunsaturated fatty acid (PUFA) administration on the microbiome-gut-brain axis in adolescents with anorexia nervosa (the MiGBAN study): study protocol for a longitudinal, double-blind, randomized, placebo-controlled trial

التفاصيل البيبلوغرافية
العنوان: The effects of polyunsaturated fatty acid (PUFA) administration on the microbiome-gut-brain axis in adolescents with anorexia nervosa (the MiGBAN study): study protocol for a longitudinal, double-blind, randomized, placebo-controlled trial
المؤلفون: Lara Keller, Astrid Dempfle, Brigitte Dahmen, Samira Schreiber, Roger A. H. Adan, Nadia Andrea Andreani, Unna N. Danner, Albrecht Eisert, Sergueï Fetissov, Florian Ph. S. Fischmeister, Andreas Karwautz, Kerstin Konrad, Karlijn L. Kooij, Stefanie Trinh, Benny van der Vijgh, Annemarie A. van Elburg, Michael Zeiler, John Baines, Jochen Seitz, Beate Herpertz-Dahlmann
المصدر: Trials, Vol 23, Iss 1, Pp 1-15 (2022)
بيانات النشر: BMC, 2022.
سنة النشر: 2022
المجموعة: LCC:Medicine (General)
مصطلحات موضوعية: Anorexia nervosa, Gut microbiome, Gut microbiota, Microbiome-gut-brain axis, Supplementation, Polyunsaturated fatty acids, Medicine (General), R5-920
الوصف: Abstract Background Anorexia nervosa (AN) is a severe psychiatric disease that often takes a chronic course due to insufficient treatment options. Emerging evidence on the gut-brain axis offers the opportunity to find innovative treatments for patients with psychiatric disorders. The gut microbiome of patients with AN shows profound alterations that do not completely disappear after weight rehabilitation. In previous studies, the administration of polyunsaturated fatty acids (PUFA) resulted in effects that might be beneficial in the treatment of AN, affecting the microbiome, body weight and executive functions. Therefore, the MiGBAN study aims to examine the effects of a nutritional supplementation with PUFA on the gut microbiome and body mass index (BMI) in patients with AN. Methods This is a longitudinal, double-blind, randomized, placebo-controlled trial. Within 2 years, 60 adolescent patients aged 12 to 19 years with AN will receive either PUFA or placebo for 6 months additional to treatment as usual. After 1 year, the long-term effect of PUFA on the gut microbiome and consecutively on BMI will be determined. Secondary outcomes include improvement of gastrointestinal symptoms, eating disorder psychopathology, and comorbidities. Additionally, the interaction of the gut microbiome with the brain (microbiome-gut-brain axis) will be studied by conducting MRI measurements to assess functional and morphological changes and neuropsychological assessments to describe cognitive functioning. Anti-inflammatory effects of PUFA in AN will be examined via serum inflammation and gut permeability markers. Our hypothesis is that PUFA administration will have positive effects on the gut microbiota and thus the treatment of AN by leading to a faster weight gain and a reduction of gastrointestinal problems and eating disorder psychopathology. Discussion Due to previously heterogeneous results, a systematic and longitudinal investigation of the microbiome-gut-brain axis in AN is essential. The current trial aims to further analyse this promising research field to identify new, effective therapeutic tools that could help improve the treatment and quality of life of patients. If this trial is successful and PUFA supplementation contributes to beneficial microbiome changes and a better treatment outcome, their administration would be a readily applicable additional component of multimodal AN treatment. Trial registration German Clinical Trials Register DRKS00017130 . Registered on 12 November 2019.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1745-6215
Relation: https://doaj.org/toc/1745-6215
DOI: 10.1186/s13063-022-06413-7
URL الوصول: https://doaj.org/article/28e12969d4164977be2b9af856cd67d2
رقم الأكسشن: edsdoj.28e12969d4164977be2b9af856cd67d2
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:17456215
DOI:10.1186/s13063-022-06413-7