Artificial intelligence-based personalized diet: A pilot clinical study for irritable bowel syndrome
dc.contributor.author | Karakan T. | |
dc.contributor.author | Gundogdu A. | |
dc.contributor.author | Alagözlü H. | |
dc.contributor.author | Ekmen N. | |
dc.contributor.author | Ozgul S. | |
dc.contributor.author | Tunali V. | |
dc.contributor.author | Hora M. | |
dc.contributor.author | Beyazgul D. | |
dc.contributor.author | Nalbantoglu O.U. | |
dc.date.accessioned | 2024-07-22T08:05:02Z | |
dc.date.available | 2024-07-22T08:05:02Z | |
dc.date.issued | 2022 | |
dc.description.abstract | We enrolled consecutive IBS-M patients (n = 25) according to Rome IV criteria. Fecal samples were obtained from all patients twice (pre-and post-intervention) and high-throughput 16S rRNA sequencing was performed. Six weeks of personalized nutrition diet (n = 14) for group 1 and a standard IBS diet (n = 11) for group 2 were followed. AI-based diet was designed based on optimizing a personalized nutritional strategy by an algorithm regarding individual gut microbiome features. The IBS-SSS evaluation for pre- and post-intervention exhibited significant improvement (p < .02 and p < .001 for the standard IBS diet and personalized nutrition groups, respectively). While the IBS-SSS evaluation changed to moderate from severe in 78% (11 out of 14) of the personalized nutrition group, no such change was observed in the standard IBS diet group. A statistically significant increase in the Faecalibacterium genus was observed in the personalized nutrition group (p = .04). Bacteroides and putatively probiotic genus Propionibacterium were increased in the personalized nutrition group. The change (delta) values in IBS-SSS scores (before-after) in personalized nutrition and standard IBS diet groups are significantly higher in the personalized nutrition group. AI-based personalized microbiome modulation through diet significantly improves IBS-related symptoms in patients with IBS-M. Further large-scale, randomized placebo-controlled trials with long-term follow-up (durability) are needed. © 2022 ENBIOSIS Biotechnologies Limited. Published with license by Taylor & Francis Group, LLC. | |
dc.identifier.DOI-ID | 10.1080/19490976.2022.2138672 | |
dc.identifier.issn | 19490976 | |
dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/12964 | |
dc.language.iso | English | |
dc.publisher | Taylor and Francis Ltd. | |
dc.rights | All Open Access; Gold Open Access; Green Open Access | |
dc.subject | Artificial Intelligence | |
dc.subject | Diet | |
dc.subject | Gastrointestinal Microbiome | |
dc.subject | Humans | |
dc.subject | Irritable Bowel Syndrome | |
dc.subject | RNA, Ribosomal, 16S | |
dc.subject | probiotic agent | |
dc.subject | RNA 16S | |
dc.subject | RNA 16S | |
dc.subject | adult | |
dc.subject | Article | |
dc.subject | artificial intelligence | |
dc.subject | bacterial microbiome | |
dc.subject | Bacteroides | |
dc.subject | body mass | |
dc.subject | clinical article | |
dc.subject | Clostridiaceae | |
dc.subject | cohort analysis | |
dc.subject | controlled study | |
dc.subject | Faecalibacterium | |
dc.subject | fecal microbiota transplantation | |
dc.subject | feces analysis | |
dc.subject | female | |
dc.subject | fluorometry | |
dc.subject | follow up | |
dc.subject | gastrointestinal tract | |
dc.subject | gene sequence | |
dc.subject | high throughput screening | |
dc.subject | high throughput sequencing | |
dc.subject | human | |
dc.subject | irritable colon | |
dc.subject | machine learning | |
dc.subject | male | |
dc.subject | middle aged | |
dc.subject | multivariate analysis of variance | |
dc.subject | personalized nutrition | |
dc.subject | pilot study | |
dc.subject | rank sum test | |
dc.subject | Ruminococcaceae | |
dc.subject | therapy effect | |
dc.subject | artificial intelligence | |
dc.subject | diet | |
dc.subject | intestine flora | |
dc.subject | microbiology | |
dc.title | Artificial intelligence-based personalized diet: A pilot clinical study for irritable bowel syndrome | |
dc.type | Article |