Trimethylamine-N-oxide and 5-year mortality: the role of gut microbiota-generated metabolite from the CORE-Thailand cohort
Issued Date
2024-12-01
Resource Type
eISSN
20452322
Scopus ID
2-s2.0-85203683604
Journal Title
Scientific Reports
Volume
14
Issue
1
Rights Holder(s)
SCOPUS
Bibliographic Citation
Scientific Reports Vol.14 No.1 (2024)
Suggested Citation
Senthong V., Kiatchoosakun S., Wongvipaporn C., Phetcharaburanin J., Sritara P., Phrommintikul A., Worasuwannarak S., Dutsadeevettakul S., Suksuphew S., Cheewatanakornkul S., Suwanugsorn S., Taweesangsuksakul P., Senthong V., Tatsanaviva P., Kiatchoosakun S., Wongvipaporn C., Simtharakaew T., Sukanandachai B., Dinchuthai P., Kositchaiwat J., Siriaree K., Siriwattana K., Chotechuang Y., Phengtham U., Watcharasaksilp K., Buranapin S., Prasertwitayakij N., Wongcharoen W., Phrommintikul A., Paspitsanu P., Laksomya T., Maraprasertsak M., Jai-aue S., Wongtheptien W., Deerochanawong C., Hutayanon P., Changsirikulchai S., Porapakkham P., Kanaderm C., Suraamornkul S., Satirapoj B., Tiyanon W., Rattanasumawong K., Wongpraparut N., Boonyasirinant T., Krittayaphong R., Udol K., Lertsuwunseri V., Satitthummanid S., Boonyaratavej S., Srimahachota S., Yamwong S., Sritara P. Trimethylamine-N-oxide and 5-year mortality: the role of gut microbiota-generated metabolite from the CORE-Thailand cohort. Scientific Reports Vol.14 No.1 (2024). doi:10.1038/s41598-024-71479-z Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/101266
Title
Trimethylamine-N-oxide and 5-year mortality: the role of gut microbiota-generated metabolite from the CORE-Thailand cohort
Author(s)
Senthong V.
Kiatchoosakun S.
Wongvipaporn C.
Phetcharaburanin J.
Sritara P.
Phrommintikul A.
Worasuwannarak S.
Dutsadeevettakul S.
Suksuphew S.
Cheewatanakornkul S.
Suwanugsorn S.
Taweesangsuksakul P.
Senthong V.
Tatsanaviva P.
Kiatchoosakun S.
Wongvipaporn C.
Simtharakaew T.
Sukanandachai B.
Dinchuthai P.
Kositchaiwat J.
Siriaree K.
Siriwattana K.
Chotechuang Y.
Phengtham U.
Watcharasaksilp K.
Buranapin S.
Prasertwitayakij N.
Wongcharoen W.
Phrommintikul A.
Paspitsanu P.
Laksomya T.
Maraprasertsak M.
Jai-aue S.
Wongtheptien W.
Deerochanawong C.
Hutayanon P.
Changsirikulchai S.
Porapakkham P.
Kanaderm C.
Suraamornkul S.
Satirapoj B.
Tiyanon W.
Rattanasumawong K.
Wongpraparut N.
Boonyasirinant T.
Krittayaphong R.
Udol K.
Lertsuwunseri V.
Satitthummanid S.
Boonyaratavej S.
Srimahachota S.
Yamwong S.
Sritara P.
Kiatchoosakun S.
Wongvipaporn C.
Phetcharaburanin J.
Sritara P.
Phrommintikul A.
Worasuwannarak S.
Dutsadeevettakul S.
Suksuphew S.
Cheewatanakornkul S.
Suwanugsorn S.
Taweesangsuksakul P.
Senthong V.
Tatsanaviva P.
Kiatchoosakun S.
Wongvipaporn C.
Simtharakaew T.
Sukanandachai B.
Dinchuthai P.
Kositchaiwat J.
Siriaree K.
Siriwattana K.
Chotechuang Y.
Phengtham U.
Watcharasaksilp K.
Buranapin S.
Prasertwitayakij N.
Wongcharoen W.
Phrommintikul A.
Paspitsanu P.
Laksomya T.
Maraprasertsak M.
Jai-aue S.
Wongtheptien W.
Deerochanawong C.
Hutayanon P.
Changsirikulchai S.
Porapakkham P.
Kanaderm C.
Suraamornkul S.
Satirapoj B.
Tiyanon W.
Rattanasumawong K.
Wongpraparut N.
Boonyasirinant T.
Krittayaphong R.
Udol K.
Lertsuwunseri V.
Satitthummanid S.
Boonyaratavej S.
Srimahachota S.
Yamwong S.
Sritara P.
Author's Affiliation
Ramathibodi Hospital
Siriraj Hospital
Faculty of Medicine, Chiang Mai University
Nakornping Hospital
Lampang Hospital
Suranaree University of Technology
Faculty of Medicine, Khon Kaen University
Faculty of Medicine, Prince of Songkla University
Police General Hospital
Naresuan University
Vajira Hospital
Khon Kaen University
Faculty of Medicine Ramathibodi Hospital, Mahidol University
Faculty of Medicine, Thammasat University
Maharaj Nakhon Ratchasima Hospital
Khon Kaen Regional Hospital
Mahidol University
Burapha University
Phramongkutklao College of Medicine
Faculty of Medicine, Srinakharinwirot University
Rajavithi Hospital
Faculty of Medicine, Chulalongkorn University
Central Chest Institute of Thailand
Phrapokklao Hospital
Phrae Hospital
Chiangrai Prachanukroh Hospital
Pranangklao Hospital
Siriraj Hospital
Faculty of Medicine, Chiang Mai University
Nakornping Hospital
Lampang Hospital
Suranaree University of Technology
Faculty of Medicine, Khon Kaen University
Faculty of Medicine, Prince of Songkla University
Police General Hospital
Naresuan University
Vajira Hospital
Khon Kaen University
Faculty of Medicine Ramathibodi Hospital, Mahidol University
Faculty of Medicine, Thammasat University
Maharaj Nakhon Ratchasima Hospital
Khon Kaen Regional Hospital
Mahidol University
Burapha University
Phramongkutklao College of Medicine
Faculty of Medicine, Srinakharinwirot University
Rajavithi Hospital
Faculty of Medicine, Chulalongkorn University
Central Chest Institute of Thailand
Phrapokklao Hospital
Phrae Hospital
Chiangrai Prachanukroh Hospital
Pranangklao Hospital
Corresponding Author(s)
Other Contributor(s)
Abstract
The gut microbiota metabolite trimethylamine-N-oxide (TMAO)—derived from dietary phosphatidylcholine—is mechanistically linked to cardiovascular disease (CVD) and increased cardiovascular risk. This study examined the relationship between fasting plasma TMAO levels and 5-year all-cause mortality in a cohort of patients at high risk of cardiovascular events (CORE-Thailand Registry). Of the 134 patients, 123 (92%) had established cardiovascular disease, and 11 (8%) had multiple risk factors. Fasting plasma TMAO levels were measured using nuclear magnetic resonance spectroscopy. Within this prospective cohort study, the median TMAO was 3.81 μM [interquartile range (IQR) 2.89–5.50 μM], with a mean age of 65 ± 11 years; 61% were men, and 39.6% had type II diabetes. Among 134 patients, 65 (49%) were identified as the high-TMAO group (≥ 3.8 μM), and 69 (51%) were identified as the low-TMAO group (< 3.8 μM). After a median follow-up of 58.8 months, the high-TMAO group was associated with a 2.88-fold increased mortality risk. Following adjustment for traditional risk factors, high-sensitivity cardiac troponin-T, estimated glomerular filtration rate, angiotensin-converting enzyme (ACEI), or angiotensin-receptor blocker (ARB) use, the high-TMAO group remained predictive of 5-year all-cause mortality risk (the high-TMAO vs. the low-TMAO group, adjusted hazard ratio 2.73, 95% CI 1.13–6.54; P = 0.025). Among Thai patients at high risk of cardiovascular events, increased plasma TMAO levels portended greater long-term mortality risk.