Evidence map›Paper›PMID 40813961›Full record

ArticleBMC microbiology2025

The association between gut microbiota composition and cardiometabolic parameters in healthy adults.

Seyda Silan Okalin, Nazli Arslan, Ebru Demiray Gürbüz, Mine Arayıcı, Nevin Deniz Kırca, Duygu Ozel Demiralp, Didem Dereli-Akdeniz, Pınar Akan, Ayse Aydan Ozkutuk

Abstract read
In one paragraph

Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Seyda Silan OkalinBioIzmir - Izmir Health Technologies Development and Accelerator Research and Application Center, Dokuz Eylul University, Izmir, Türkiye.
Nazli ArslanFaculty of Medicine, Department of Medical Microbiology, Dokuz Eylul University, Izmir, Türkiye.
Ebru Demiray GürbüzFaculty of Medicine, Department of Medical Microbiology, Dokuz Eylul University, Izmir, Türkiye.
Mine ArayıcıDepartment of Neurosciences, Institute of Health Sciences, Dokuz Eylul University, Izmir, Türkiye.
Nevin Deniz KırcaDepartment of Neurosciences, Institute of Health Sciences, Dokuz Eylul University, Izmir, Türkiye.
Duygu Ozel DemiralpOncology Institute, Dokuz Eylul University, Izmir, Türkiye.
Didem Dereli-AkdenizFaculty of Medicine, Department of Internal Medicine, Bakırcay University, Izmir, Türkiye.
Pınar AkanFaculty of Medicine, Department of Medical Biochemistry, Dokuz Eylul University, Izmir, Türkiye.
Ayse Aydan OzkutukFaculty of Medicine, Department of Medical Microbiology, Dokuz Eylul University, Izmir, Türkiye. aydan.ozkutuk@deu.edu.tr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe human gut microbiota comprises approximately 100 trillion microbial cells and produces a wide range of metabolites. Its composition is shaped by factors such as geography, dietary habits, and genetic background. Dysbiosis-an imbalance in this microbial ecosystem-has been associated with the development of metabolic diseases. This study aimed to characterize the gut microbiota composition in adults without diagnosed chronic diseases and assess its potential associations with cardiometabolic parameters.

methodsVolunteers over the age of 18 residing in Izmir province who met the inclusion criteria were enrolled in the study. Fecal and blood samples were collected from all participants. Bacterial DNA from fecal samples was extracted, and the full-length 16 S rRNA was amplified. Full-length 16 S rRNA PCR amplicons were sequenced using Oxford Nanopore Technologies. Taxonomic classification, Firmicutes/Bacteroidetes ratio, and Shannon index were determined using Massbiome Fecal Microbiome Analysis (Massive Bioinformatics, Türkiye). Dominant bacterial genera were also analyzed using the Epi2Me database. Blood samples were analyzed for metabolic health markers. Associations between bacterial taxa and blood-based metabolic parameters were examined statistically.

resultsA total of 82 participants were included in the study. According to BMI, 34 (41.4%) of the participants were classified as having a healthy weight, 23 (28.1%) as overweight, and 25 (30.5%) as obese. Segatella (Prevotella) copri was identified as the dominant species in most participants (51%). Other dominant species included Ruminococcus torques (13%), Faecalibacterium prausnitzii (13%), Faecalitalea cylindroides (5%), Bacteroides uniformis (4%), and Phocaeicola vulgatus (3%). S. copri was identified as the dominant bacterial species in 45 participants (54.8%) according to the Epi2Me database. The Shannon index and Firmicutes/Bacteroidetes ratio varied among the three BMI groups. Both Lachnospira and Ruminococcus genera had a significant negative correlation with BMI, indicating that higher levels of BMI are associated with lower abundances of these genera. In the regression analysis, Lachnospira was found to be less abundant at higher HbA1c levels. HOMA-IR was found to be a significant predictor for the relative abundance of Vescimonas. Ruthenibacterium is found to be more abundant at higher HDL levels.

conclusionThe dominant bacterial taxa differed from those reported in other populations, suggesting region-specific microbial profiles. Notably, specific gut microbial genera were associated with metabolic health indicators, including BMI, HbA1c, HOMA-IR, and HDL level. These findings underscore the potential role of gut microbiota in metabolic regulation and support the need for further region-specific research. This study is among the few in Türkiye focusing on healthy adults and contributes to the understanding of gut microbiota in relation to cardiometabolic parameters.

Indexed as

BacteriaGastrointestinal MicrobiomeAdultDNA, BacterialDysbiosisFecesFemaleHealthy VolunteersHumansMaleMiddle AgedObesityRNA, Ribosomal, 16SYoung AdultDNA, BacterialRNA, Ribosomal, 16SCardiometabolic parametersGut microbiotaHealthy adult individualOxford nanopore sequencing

Identifiers

PMID40813961
PMCPMC12351950

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.