Effects of Bifidobacterium animalis Subsp. lactis (BPL1) Supplementation in Children and Adolescents with Prader-Willi Syndrome

Prader-Willi syndrome (PWS) is a rare genetic disorder characterized by a wide range of clinical manifestations, including obesity, hyperphagia, and behavioral problems. Bifidobacterium animalis subsp. lactis strain BPL1 has been shown to improve central adiposity in adults with simple obesity. To e...

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Detalles Bibliográficos
Autores: Amat-Bou, Montse, Garcia-Ribera, Sonika, Climent, Eric, Piquer García, Irene|||0000-0002-6746-3558, Corripio, Raquel|||0000-0003-3344-8269, Sánchez-Infantes, David|||0000-0001-6086-7501, Villalta, Laia, Elias, Maria, Jiménez-Chillarón, Josep C., Chenoll, Empar|||0000-0002-6891-3573, Ramón, Daniel, Ibáñez, Lourdes|||0000-0003-4595-7191, Ramon-Krauel, Marta|||0000-0003-3027-9105, Lerin, Carles|||0000-0003-0950-4363
Tipo de recurso: artículo
Fecha de publicación:2020
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:252994
Acceso en línea:https://ddd.uab.cat/record/252994
https://dx.doi.org/urn:doi:10.3390/nu12103123
Access Level:acceso abierto
Palabra clave:Obesity
Prader-Willi syndrome
Insulin sensitivity
Hyperphagia
Gut microbiota
Probiotic supplementation
Mental health
Descripción
Sumario:Prader-Willi syndrome (PWS) is a rare genetic disorder characterized by a wide range of clinical manifestations, including obesity, hyperphagia, and behavioral problems. Bifidobacterium animalis subsp. lactis strain BPL1 has been shown to improve central adiposity in adults with simple obesity. To evaluate BPL1's effects in children with PWS, we performed a randomized crossover trial among 39 patients (mean age 10.4 years). Participants were randomized to placebo-BPL1 (n = 19) or BPL1-placebo (n = 20) sequences and underwent a 12-week period with placebo/BPL1 treatments, a 12-week washout period, and a 12-week period with the crossover treatment. Thirty-five subjects completed the study. The main outcome was changes in adiposity, measured by dual-energy X-ray absorptiometry. Secondary outcomes included lipid and glucose metabolism, hyperphagia, and mental health symptoms. Generalized linear modeling was applied to assess differences between treatments. While BPL1 did not modify total fat mass compared to placebo, BPL1 decreased abdominal adiposity in a subgroup of patients older than 4.5 years (n = 28). BPL1 improved fasting insulin concentration and insulin sensitivity. Furthermore, we observed modest improvements in some mental health symptoms. A follow-up trial with a longer treatment period is warranted to determine whether BPL1 supplementation can provide a long-term therapeutic approach for children with PWS (ClinicalTrials.gov NCT03548480).