Effects of inulin on intestinal flora and metabolism-related indicators in obese polycystic ovary syndrome patients Original paper
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Dr. Umar
Read MoreClinical Pharmacist and Clinical Pharmacy Master’s candidate focused on antibiotic stewardship, AI-driven pharmacy practice, and research that strengthens safe and effective medication use. Experience spans digital health research with Bloomsbury Health (London), pharmacovigilance in patient support programs, and behavioral approaches to mental health care. Published work includes studies on antibiotic use and awareness, AI applications in medicine, postpartum depression management, and patient safety reporting. Developer of an AI-based clinical decision support system designed to enhance antimicrobial stewardship and optimize therapeutic outcomes.
Microbiome Signatures identifies and validates condition-specific microbiome shifts and interventions to accelerate clinical translation. Our multidisciplinary team supports clinicians, researchers, and innovators in turning microbiome science into actionable medicine.
Karen Pendergrass is a microbiome researcher specializing in microbiome-targeted interventions (MBTIs). She systematically analyzes scientific literature to identify microbial patterns, develop hypotheses, and validate interventions. As the founder of the Microbiome Signatures Database, she bridges microbiome research with clinical practice. In 2012, based on her own investigative research, she became the first documented case of FMT for Celiac Disease—four years before the first published case study.
What was studied?
The focus keyphrase inulin and PCOS gut microbiota anchors this study, which examined how three months of dietary inulin supplementation affected gut microbiota composition, metabolic markers, inflammatory cytokines, and sex steroid hormones in obese women with polycystic ovary syndrome (PCOS). Drawing on stool sequencing and detailed plasma biomarker panels, the research tracked shifts across the gut microbiota–inflammation–hormone axis. According to the figures and microbial bar plots, the investigators compared pre- and post-inulin states alongside obese and non-obese controls, capturing changes in both microbial diversity and specific taxa such as Firmicutes, Bacteroidetes, Actinobacteria, Proteobacteria, Lachnospira, Sutterella, Enterobacter, Lactobacillus, and Bifidobacterium.
Who was studied?
Fifty-five women from a reproductive medicine center in China participated, grouped into obese PCOS patients, obese controls, and non-obese controls. Thirteen obese PCOS participants who adhered strictly to the protocol completed the three-month inulin intervention, forming the core analysis group (FDA). All participants provided blood and stool samples before and after the intervention. Inclusion and exclusion criteria ensured that only PCOS cases defined by the Rotterdam criteria were included, and that no recent antibiotic, hormone, or probiotic exposures confounded gut microbiome results. The clinical and microbial comparisons across groups, described in Tables and PCA plots, allowed clear interpretation of obesity- and PCOS-specific microbiome patterns.
Most important findings
Inulin supplementation improved clinical, hormonal, inflammatory, and microbial parameters relevant to obese PCOS. BMI and waist-to-hip ratio trended downward, while sex steroid abnormalities—including elevated LH, LH/FSH ratio, testosterone, AMH, and estradiol—shifted toward healthier ranges. Pro-inflammatory cytokines (TNF-α, IL-1β, IL-6, MCP-1) were significantly reduced after the intervention, as shown in the inflammatory scatterplots. Microbiome analysis revealed key taxonomic rebalancing. At the phylum level, inulin lowered the Firmicutes/Bacteroidetes (F/B) ratio and reduced Proteobacteria abundance, a phylum linked to dysbiosis and endotoxin (LPS) load. Actinobacteria and Fusobacteria increased following treatment. At the genus level, inulin increased beneficial Lachnospira and Bifidobacterium while decreasing Sutterella, Lactobacillus, Lactococcus, and Enterobacter—patterns displayed clearly in the LEfSe biomarker charts. Correlation heatmaps showed strong associations between microbial taxa, inflammatory markers, lipid profiles, and anthropometrics, indicating that microbial shifts accompanied measurable clinical improvements.
Key implications
This study demonstrates that dietary inulin can beneficially modulate the gut microbiota–inflammation–sex hormone axis in obese women with PCOS. The intervention improved dysbiosis, reduced pro-inflammatory cytokines, and incrementally corrected sex hormone imbalances, suggesting that microbiota-targeted therapy may complement existing PCOS treatments. The consistent reduction in Proteobacteria and restoration of Actinobacteria and Lachnospira highlight potential microbial signature candidates for monitoring therapeutic response. While the sample size is limited, the findings underscore the value of prebiotic interventions as accessible, low-risk adjuncts for managing metabolic-hormonal dysfunction in PCOS.
Citation
Li X, Jiang B, Gao T, et al. Effects of inulin on intestinal flora and metabolism-related indicators in obese polycystic ovary syndrome patients. European Journal of Medical Research. 2024;29:443. doi:10.1186/s40001-024-02034-9
Polycystic ovary syndrome (PCOS) is a common endocrine disorder that affects women of reproductive age, characterized by irregular menstrual cycles, hyperandrogenism, and insulin resistance. It is often associated with metabolic dysfunctions and inflammation, leading to fertility issues and increased risk of type 2 diabetes and cardiovascular disease.
Lipopolysaccharide (LPS), a potent endotoxin present in the outer membrane of Gram-negative bacteria that causes chronic immune responses associated with inflammation.