Serum trimethylamine N-oxide levels among coronary artery disease and acute coronary syndrome patients: a systematic review and meta-analysis

Author:

Dean Yomna E.12,Rouzan Samah S.1,Loayza Pintado Jose J.3,Talat Nesreen Elsayed1,Mohamed Alaa R. H.4,Verma Suman5,Anwar Kamdi Zainab6,Gir Deepak7,Helmy Ahmed8,Helmy Zakaria9,Afzal Ahson6,Mady Tamer10,Hazimeh Yusef1112,Aiash Hani913

Affiliation:

1. Alexandria University, Faculty of Medicine, Alexandria

2. Alexandria Medical Center (AMC)

3. Universidad de San Martin de Porres Facultad de Medicina Humana, Peru

4. Suez Canal University, Faculty of Medicine, Ismailia

5. Maharishi Markandeshwar Medical College and Hospital, Solan, India

6. Dow University of Health Sciences, Karachi, Pakistan

7. St. Joseph’s Medical Center, Stockton, CA, USA

8. Kharkiv National Medical University, Kharkiv, Ukraine

9. 6th October University, Faculty of Medicine, Giza, Egypt

10. International American University, College of Medicine, Saint Lucia, Caribbean

11. Lebanese University

12. Zahraa Hospital, University Medical Center, Beirut, Lebanon

13. SUNY Upstate Medical University, Syracuse

Abstract

Background and Aim: Recent studies have linked trimethylamine N-oxide (TMAO) to cardiovascular diseases; our study aimed to analyze the association between coronary artery disease (CAD), acute coronary syndrome (ACS), and TMAO. Methods: PubMed, Scopus, Embase, and Web of Science were searched using terms such as ʻCADʼ and ʻTMAOʼ. Only observational controlled studies were included. RevMan software version 5.4 was used for the analysis. Results: A significant association was found between the CAD group and increased serum TMAO levels compared with the control group (MD=1.16, 95% CI=0.54–1.78, P=0.0003). This association remained significant among acute coronary syndrome patients (MD=0.98, 95% CI=0.73–1.23, P<0.00001) and was also detected among young and old CAD patients (MD=0.35, 95% CI=0.06–0.64, P=0.02 and MD=1.36, 95% CI=0.71–2.01, P<0.0001, respectively). On further analysis of intestinal metabolites, the authors detected an insignificant association between choline, betaine, carnitine, and CAD. According to our sensitivity analysis, TMAO is an acceptable diagnostic marker for CAD (0.721, SE was 0.0816, 95% CI: 0.561–0.881). Conclusion: TMAO is an acceptable diagnostic marker for CAD, with significantly higher levels among these patients regardless of their age. Other metabolites did not show such an association. The role of serum level TMAO in the early diagnosis of CAD should be further explored.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine,Surgery

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