In a previous study, Dr Stanley Hazen's, Vice Chair of Translational Research, Chair of the Department of Cellular and Molecular Medicine for the Lerner Research Institute, found that a chemical byproduct called trimethylamine N-oxide (TMAO) is produced when intestinal bacteria digest the nutrient phosphatidylcholine, commonly known as lecithin.
The prior research showed that TMAO levels in the blood were associated with heart disease.
Hazen, who is also section head of Preventive Cardiology & Rehabilitation in the Miller Family Heart and Vascular Institute at Cleveland Clinic, along with colleagues have now confirmed that gut flora are essential in forming TMAO in humans.
To demonstrate the role of gut flora in forming TMAO, human subjects were asked to eat two hard-boiled eggs (a common dietary source of lecithin) and a capsule of labelled lecithin (as a tracer).
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After ingestion, TMAO levels in the blood increased. However, when these same subjects were given a brief course of broad-spectrum antibiotics to suppress their gut flora, their TMAO levels were suppressed, and no additional TMAO was formed, even after ingesting lecithin.
In the second phase of the study, the researchers measured TMAO levels in a large, independent, clinical cohort - consisting of more than 4,000 adults undergoing cardiac evaluation at Cleveland Clinic - over a three-year follow-up period.
They found that higher TMAO blood levels were associated with higher future risks of death and nonfatal heart attack or stroke over the ensuing three-year period, independent of other risk factors and blood test results.
"These studies show that measuring blood levels of TMAO could serve as a powerful tool for predicting future cardiovascular risk, even for those without known risk factors," Hazen said.
The study was published in The New England Journal of Medicine.