<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Amat-Bou M</submitter><funding>Barcelona Magic Line</funding><pagination>E3123</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7650793</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(10)</volume><pubmed_abstract>Prader-Willi syndrome (PWS) is a rare genetic disorder characterized by a wide range of clinical manifestations, including obesity, hyperphagia, and behavioral problems. &lt;i>Bifidobacterium animalis&lt;/i> subsp. &lt;i>lactis&lt;/i> 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 (&lt;i>n&lt;/i> = 19) or BPL1-placebo (&lt;i>n&lt;/i> = 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 ab</pubmed_abstract><journal>Nutrients</journal><pubmed_title>Effects of &lt;i>Bifidobacterium animalis&lt;/i> Subsp. &lt;i>lactis&lt;/i> (BPL1) Supplementation in Children and Adolescents with Prader-Willi Syndrome: A Randomized Crossover Trial.</pubmed_title><pmcid>PMC7650793</pmcid><funding_grant_id>n.a.</funding_grant_id><pubmed_authors>Garcia-Ribera S</pubmed_authors><pubmed_authors>Sanchez-Infantes D</pubmed_authors><pubmed_authors>Ramon-Krauel M</pubmed_authors><pubmed_authors>Amat-Bou M</pubmed_authors><pubmed_authors>Lerin C</pubmed_authors><pubmed_authors>Piquer-Garcia I</pubmed_authors><pubmed_authors>Elias M</pubmed_authors><pubmed_authors>Corripio R</pubmed_authors><pubmed_authors>Ramon D</pubmed_authors><pubmed_authors>Climent E</pubmed_authors><pubmed_authors>Jimenez-Chillaron JC</pubmed_authors><pubmed_authors>Chenoll E</pubmed_authors><pubmed_authors>Ibanez L</pubmed_authors><pubmed_authors>Villalta L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effects of &lt;i>Bifidobacterium animalis&lt;/i> Subsp. &lt;i>lactis&lt;/i> (BPL1) Supplementation in Children and Adolescents with Prader-Willi Syndrome: A Randomized Crossover Trial.</name><description>Prader-Willi syndrome (PWS) is a rare genetic disorder characterized by a wide range of clinical manifestations, including obesity, hyperphagia, and behavioral problems. &lt;i>Bifidobacterium animalis&lt;/i> subsp. &lt;i>lactis&lt;/i> 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 (&lt;i>n&lt;/i> = 19) or BPL1-placebo (&lt;i>n&lt;/i> = 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 ab</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2026-04-07T17:42:55.104Z</modification><creation>2020-11-19T16:56:59Z</creation></dates><accession>S-EPMC7650793</accession><cross_references><pubmed>33066107</pubmed><doi>10.3390/nu12103123</doi></cross_references></HashMap>