Trimethylamine N-Oxide is Elevated in Type 2 Diabetes and Correlates with Gut Dysbiosis and Systemic Inflammation in a Nigerian Cohort

Authors

  • Jafaru Muhammad Bunza Department of Chemical Pathology, School of Medical Laboratory Sciences, Usmanu Danfodiyo University, Sokoto, Nigeria [and] Institute of One Health, Usmanu Danfodiyo University, Sokoto, Nigeria
  • Jidda Muhammad Lawal Department of Chemical Pathology, School of Medical Laboratory Sciences, Usmanu Danfodiyo University, Sokoto, Nigeria
  • Umar Asiya Imam Department of Medical Microbiology, School of Medical Laboratory Sciences, Usmanu Danfodiyo University, Sokoto, Nigeria
  • Aliyu Maimunatu Umar Department of Medical Microbiology, School of Medical Laboratory Sciences, Usmanu Danfodiyo University, Sokoto, Nigeria
  • Dallatu Muhammad Kabiru Department of Chemical Pathology, School of Medical Laboratory Sciences, Usmanu Danfodiyo University, Sokoto, Nigeria
  • Ogunwale Kolawole Ayobami Department of Chemical Pathology & Immunology, University of Ilorin Teaching Hospital, Ilorin, Nigeria
  • Yusuf Habeb Demilola Department of Medical Microbiology & Parasitology, University of Ilorin Teaching Hospital, Ilorin, Nigeria
  • Giwa Jamiah Ikeoluwa Nigeria Army Reference Hospital, Yaba, Lagos, Nigeria
  • Oladele Blessing Shina Department of Biomedical Science, University of Salford, Manchester, United Kingdom.

DOI:

https://doi.org/10.51152/jbarbiomed.v12i1.261

Keywords:

Trimethylamine N-oxide, Gut dysbiosis, Type 2 diabetes, Inflammation, Nigeria

Abstract

Background: Trimethylamine N-oxide (TMAO), a gut microbiota-derived metabolite linked to cardiometabolic disease, remains understudied in sub-Saharan Africa.

Objectives: To evaluate plasma TMAO concentrations and assess their associations with the Firmicutes/Bacteroidetes (F/B) ratio, pro-inflammatory cytokines, glycemic control, and body mass index in Nigerian T2DM patients.

Methods: This cross-sectional study enrolled 126 participants (63 with T2DM and 63 age-- and sex-matched healthy controls). Gut Firmicutes and Bacteroidetes were quantified by qPCR; dysbiosis was defined as total bacterial load > the 75th percentile of controls. ELISA was used to measure plasma TMAO and cytokines. Associations were tested using the Kruskal–Wallis test, logistic regression, and Spearman's correlation.

Results: TMAO was markedly elevated in T2DM patients compared with controls (medians 7.22 ng/mL in eubiotic T2DM, 6.80 ng/mL in dysbiotic T2DM vs 2.62 ng/mL in controls; η²H = 0.746, p < 0.001). TMAO levels were similarly high in both diabetic subgroups, demonstrating functional dysbiosis despite a normal F/B ratio. Among dysbiotic patients, TMAO showed positive correlations with the F/B ratio (r = 0.407, p = 0.002), Tumer Necrosis Factor-alpha (TNF-α) (r = 0.504, p < 0.001), and Interluken-6 (IL-6) (r = 0.386, p = 0.004). Hyperglycemia was independently associated with elevated TMAO (adjusted OR = 3.12, 95% CI 1.64–5.94, p = 0.001).

Conclusion: The disconnect between TMAO and conventional microbial composition highlights the need for functional microbiome assessment. TMAO may be a modifiable risk marker in this population.

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Published

2026-06-30

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

How to Cite

Trimethylamine N-Oxide is Elevated in Type 2 Diabetes and Correlates with Gut Dysbiosis and Systemic Inflammation in a Nigerian Cohort. (2026). Journal of Basic and Applied Research in Biomedicine, 12(1), 16-22. https://doi.org/10.51152/jbarbiomed.v12i1.261

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