Reduced stress-associated FKBP5 DNA methylation together with gut microbiota dysbiosis is linked with the progression of obese PCOS patients

Autor: Miaoqiong Ou, Yongsong Chen, Fu Chen, Wencan Xu, Zhangran Chen, Xiaoping Yang, Luanhong Wang, Chujia Lin, Guoshu Yin, Guishan Chen, Huihuang Yin, Qingxia Huang, Hong Lin, Minjie Chen, Weichun Zhang, Lan Chen
Jazyk: angličtina
Rok vydání: 2021
Předmět:
0301 basic medicine
endocrine system diseases
medicine.medical_treatment
Gut flora
Applied Microbiology and Biotechnology
Microbial ecology
chemistry.chemical_compound
0302 clinical medicine
biology
QR100-130
Biodiversity
Middle Aged
Polycystic ovary
female genital diseases and pregnancy complications
DNA methylation
Metabolome
Female
Disease Susceptibility
Biotechnology
Polycystic Ovary Syndrome
Adult
medicine.medical_specialty
030209 endocrinology & metabolism
Microbiology
Article
Anovulation
Tacrolimus Binding Proteins
03 medical and health sciences
Young Adult
Dehydroepiandrosterone sulfate
Estrone sulfate
Stress
Physiological

Internal medicine
medicine
Humans
Metabolomics
Obesity
Clinical microbiology
business.industry
Insulin
Computational Biology
nutritional and metabolic diseases
DNA Methylation
medicine.disease
biology.organism_classification
Gastrointestinal Microbiome
030104 developmental biology
Endocrinology
chemistry
Case-Control Studies
Dysbiosis
business
Biomarkers
Zdroj: npj Biofilms and Microbiomes, Vol 7, Iss 1, Pp 1-12 (2021)
NPJ Biofilms and Microbiomes
ISSN: 2055-5008
Popis: Polycystic ovary syndrome (PCOS) is a common endocrine disease in females that is characterized by hyperandrogenemia, chronic anovulation, and polycystic ovaries. However, the exact etiology and pathogenesis of PCOS are still unknown. The aim of this study was to clarify the bacterial, stress status, and metabolic differences in the gut microbiomes of healthy individuals and patients with high body mass index (BMI) PCOS (PCOS-HB) and normal BMI PCOS (PCOS-LB), respectively. Here, we compared the gut microbiota characteristics of PCOS-HB, PCOS-LB, and healthy controls by 16S rRNA gene sequencing, FK506-binding protein 5 (FKBP5) DNA methylation and plasma metabolite determination. Clinical parameter comparisons indicated that PCOS patients had higher concentrations of total testosterone, androstenedione, dehydroepiandrosterone sulfate, luteinizing hormone, and HOMA-IR while lower FKBP5 DNA methylation. Significant differences in bacterial diversity and community were observed between the PCOS and healthy groups but not between the PCOS-HB and PCOS-LB groups. Bacterial species number was negatively correlated with insulin concentrations (both under fasting status and 120 min after glucose load) and HOMA-IR but positively related to FKBP5 DNA methylation. Compared to the healthy group, both PCOS groups had significant changes in bacterial genera, including Prevotella_9, Dorea, Maihella, and Slackia, and plasma metabolites, including estrone sulfate, lysophosphatidyl choline 18:2, and phosphatidylcholine (22:6e/19:1). The correlation network revealed the complicated interaction of the clinical index, bacterial genus, stress indices, and metabolites. Our work links the stress responses and gut microbiota characteristics of PCOS disease, which might afford perspectives to understand the progression of PCOS.
Databáze: OpenAIRE