Evidence map›Paper›PMID 42555686›Full record

ArticleThe Indian journal of medical research2026

Gut microbiota-derived trimethylamine N-oxide (TMAO) and its association with neuroinflammation in migraine.

Yasemin Atıcı, Esra Eruyar, Zeynep Ökten, Ceyhan Ceran Serdar, Muhittin A Serdar, Doğan Yücel

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Article in The Indian journal of medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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6 authors.

Yasemin AtıcıDepartment of Medical Biochemistry, Lokman Hekim University, Ankara, Turkey.
Esra EruyarDepartment of Neurology, Lokman Hekim University, Ankara, Turkey.
Zeynep ÖktenDepartment of Faculty of Medicine, Lokman Hekim University, Ankara, Turkey.
Ceyhan Ceran SerdarDepartment of Medical Biology and Genetics, Faculty of Medicine, Ankara Medipol University, Ankara, Turkey.
Muhittin A SerdarDepartment of Medical Biochemistry, Faculty of Medicine, Acibadem Mehmet Ali Aydinlar University, Istanbul, Turkey.
Doğan YücelDepartment of Medical Biochemistry, Lokman Hekim University, Ankara, Turkey.

Funding

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6 · The paper itself

Abstract

Background and objectives Migraine is a common primary headache disorder associated with neuroinflammation, with evidence implicating gut microbiota and metabolites in neurological mechanisms pathways. Since trimethylamine-N-oxide (TMAO), derived from dietary precursors by gut microbial metabolism, is associated with cardiovascular and neurodegenerative conditions, and its role in migraines is unclear, we aimed to evaluate whether serum TMAO level and related metabolites in migraine patients can be biomarkers. Methods A total of 106 participants were enrolled, consisting of healthy controls (n=46; mean age ± SD=39±8 yr old) and migraine patients (n=60). The migraine cohort was divided into migraine with aura (n=18; mean age±SD=33±11 yr old) and migraine without aura (n=42; mean age±SD=37±10 yr old), according to the International Classification of Headache Disorders, 3rd edition (ICHD-3). Blood samples were centrifuged, stored at -80°C, and analysed for TMAO, carnitine, betaine, and choline levels using liquid chromatography-mass spectrometry (LC-MS/MS). Results There were no significant differences between the groups for age, smoking, or body mass index (BMI). Serum TMAO levels were significantly higher in patients with migraine with aura [2.75 (1.98-3.91) ng/mL] and migraine without aura [2.85 (2.08-5.53) ng/mL] compared to controls [1.40 (1.00-3.01) ng/mL] (P<0.001). Serum choline, betaine, and carnitine levels were significantly higher in the migraine groups (all P < 0.01). Interpretation and conclusions These findings indicate elevated TMAO levels in patients with migraine, suggesting a possible involvement of TMAO in migraine-associated neuroinflammatory processes. Targeted studies and cohort-based investigations are needed to clarify its role in migraine and evaluate its potential as a biomarker.

Indexed as

Gastrointestinal MicrobiomeInflammationMethylaminesMigraine DisordersMigraine with AuraNeuroinflammatory DiseasesAdultBetaineBiomarkersCarnitineCholineFemaleHumansMaleMiddle AgedBetaineBiomarkersCarnitineCholineMethylaminestrimethyloxamineGut–brain axisInflammatory pathwaysMicrobiota-derived metabolitesMigraineNeuroinflammationTrimethylamine-N-oxide

Identifiers

PMID42555686
PMCPMC13466871

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