TMAO: Eggs, Meats and Your Cardio-Metabolic Health | You Can Sill Eat Eggs & Meat, If You Got ‘the Right Gut Bugs’
If you have been following the SuppVersity News on Facebook (a must, btw ;-)), you will be aware of the “TMAO”-issue. If not, here’s the gist: The ingestion of certain dietary nutrients – primarily choline, phosphatidylcholine, and its precursor l-carnitine can serve as a precursor for the ultimate generation of an atherogenic metabolite, trimethylamine N-oxide (TMAO). TMAO, in turn, has been linked to all sorts of diseases, most prominently cardiovascular disease and the formation of atherosclerotic plaque.
More recent research suggests that these TMAO-mediated effects can be traced back to your gut and, more specifically, to a certain microbial composition of the commensal bacteria in your digestive tract (Koeth (2018). In their recently published paper, Koeth et al. write about the choline/carnitine-gut/microbiome-TMAO/heart disease link that all seems to start with the microbial formation of TMA in the gut and ends with the final conversion of TMA to TMAO (see Figure 1).
|Figure 1: This excellent graphical summary came with the FT of the original paper by Koeth et al. (2018)|
Very high levels of TMAO can trigger a disease that is known as “Fish-Odor-Syndrome” (check out Messenger et al. 2013 for a free review). Whether or not you stink when you consume high amounts of choline depends on (a) your genes and hence ability to metabolize and excrete TMA, the unoxidized fish-reeking precursor to TMAO, and (b) your dietary choline intake. Unfortunately, ill effects on your cardio-metabolic health have been observed in the absence of a flawed “flavin monooxygenase 3”-gene, and in spite of a flawless TMA metabolism. Hence, you may be at risk, even if you don’t reek of rancid fish. After all, it’s the TMA, not the TMAO that causes the unwanted body odor, and the latter, i.e. trimethylamine n-oxide (TMAO), are the ones that have been linked to cardiovascular and cardio-metabolic disease (CVD, CVMD) in multiple observational studies.
Evidence has been emerging over the past decades that suggests that an increased intake in choline or its precursor carnitine from eggs and meats is yet not sufficient to explain the increased TMA-formation in the gut, its oxidation in the bloodstream and the subsequent/concomitant development of atherosclerosis and thrombosis, as well as chronic kidney disease and heart failure.
|Figure 2: Yes, both dietary and supplemental carnitine may increase your atherosclerosis risk (Koeth 2014). If and to which extent they will do this, however, depends on both other dietary factors, as well as the microbial composition of your microbiome.|
This research lead many (but not all scientists) to postulate that the commonly observed links between meat consumption and cardiovascular disease could eventually be a function of the interaction of the high amount of dietary carnitine/choline with a dysbiotic microbiome… a hypothesis that is in line with isotope tracer studies in mice and (wo)men which prove the version of carnitine to choline and choline to to TMA and eventually TMAO, which has in turn been shown to promote the formation of atherosclerosis in murine models of the disease (Koeth 2014 | see Figure 2).
Moreover, parallel clinical studies in humans confirm the existence of a link between meat/carnitine intake and the risk of heart disease – a link that seems to be modulated by elevated TMAO levels in the egg/meat eaters.
|Table 1: Trimethylamine-producing capacity of various foods (mg trimethylamine/g food) following chemical hydrolysis and biological liberation (Mitchell 2002).|
One thing we still don’t fully understand is why fish is the exception to the rule: Fish is by far the worst offender when it comes to elevations in serum TMAO after a meal (Cho 2006) – with levels being ∼50 times higher than you’d see for comparable egg- or beef-based meals. The reason why it’s still a high egg- and meat-intake, not the amount of fish people are eating that has been linked to cardio-metabolic disease in large-scale epidemiological trials is still not clear. Especially in view of the fact that rodent studies seem to suggest that TMAO-supplemented diets seem to exert the same ill health effects that have been described in the previously mentioned observational trials in Western-diet-style, this seems to be odd, since pork w/ only 23mg/g TMAO should be healthier than cod w/ 1335 mg/g (Table 1).
It would appear prudent, however, to assume that (a) the co-ingestion of other nutrients in fish (such as taurine | see “Taurine Boosts Good Gut Bacteria” in the archives) and/or (b) the absence of general dysbiotic effects of increased fish consumption (and hence overall increases in TMAO exposure from choline sources) are at the heart of the cardio- and metabo-protective effects of fish (note: Saltwater fish contain ∼3 g/kg TMAO – the highest levels of all food sources | Mitchell 2002).
Add indeed, many of the previously cited human studies show that omnivores have higher circulating concentrations of l-carnitine than vegans or vegetarians, and that elevated plasma concentrations of l-carnitine in subjects is associated with incident CVD risks (e.g., heart attack, stroke, and death) independent of traditional CVD risk factors, but only in the presence of elevated TMAO (Koeth 2013). As you can see in Figure 3, however, this risk increase depends not on the amount of carnitine the subjects consumed and/or the carnitine or choline levels in their blood but was crucially dependent on its conversion to TMA/O.
|Figure 3: Kaplan-Meyer plot (depicting the event-free survival (%) over time) stratified for high vs. low carnitine and TAMO levels; based on data from N > 2,500 subjects undergoing standard cardiac evaluation (Kloeth 2013).|
Higher carnitine levels, alone (see the light and dark blue lines of the Kaplan-Meyer plots at the top of Figure 3), have no effect on one’s cardiovascular disease risk. In fact, the subjects in the high carnitine + low TMAO group (light blue) had the highest event-free survival of all groups.
Carnitine, alone, is not the problem: it’s its conversion to TMAO
The mediating effect of having an (unfavorably) TMA-producing microbiome may also explain the heterogeneous results of previous studies on the link of high(er) carnitine intake (3g+/d), all-cause mortality, heart failure, unstable angina, or myocardial reinfarction in the setting of acute myocardial infarction as it was descibed by Shang & Hui Li. in 2014.
In the absence of a TMA-producing microbiome, on the other hand, both beneficial effects on cardiovascular risk factors and metabolic syndrome have been observed in response to l-carnitine supplementation (Johri 2014). As Tang & Hazen (2014) point out, the contemporary available evidence does, therefore, seem to confirm an “obligatory role of intestinal microbiota in the generation of TMAO from multiple dietary nutrients, and TMAO as the proatherogenic species likely promoting the striking associations noted between plasma levels and both prevalent and incident CVD risks” (Tang & Hazen 2014) – Important: the simple provision of allegedly health(ier) probiotic mixes (e.g. #VSL3 fails to re-establish a non-TMA promoting microbial composition | Boutagy 2015).
Update from 25.01.2019: The scientific research on TMAO is just really taking off. Reason enough to address two new studies in form of a short addendum to the original article; two studies that deal with supplements that can – through modulating your microbiome do what probiotics won’t do: significantly reduce the production of TMAO in your gut:
- grape seed extract – In the early 2000s it was in (almost) every preworkout; these days, GSE is harder to come by but still sold as a standalone antioxidant supplement – one you may want to buy to benefit from its anti-microbial effects and its downstream effects on TMAO (Annunziata 2019); tip: don’t buy in bulk, it’s almost impossible to stomach
- fermented apple puree – it doesn’t sound like much but if you blend lactobacilli into the original superfood apple, you get a puree, you get a superfood² which has just been shown to increase HDL-C (+61.8% | p = 0.0095), while decreasing TMAO levels by a whopping -63.1% (p = 0.0042) in N=90 human subjects (Tenore 2019)
I am pretty sure that other agents of which we already know that they promote heart health and have antimicrobial effects (green tea comes to mind) will soon show up on the “anti-TMAO” supplement list.
- Annunziata, Giuseppe, et al. “Effects of Grape Pomace Polyphenolic Extract (Taurisolo®) in Reducing TMAO Serum Levels in Humans: Preliminary Results from a Randomized, Placebo-Controlled, Cross-Over Study.” Nutrients 11.1 (2019): 139.
- Bergeron, Nathalie, et al. “Diets high in resistant starch increase plasma levels of trimethylamine-N-oxide, a gut microbiome metabolite associated with CVD risk.” British Journal of Nutrition 116.12 (2016): 2020-2029.
- Boutagy, Nabil E., et al. “Probiotic supplementation and trimethylamine‐N‐oxide production following a high‐fat diet.” Obesity 23.12 (2015): 2357-2363.
- Koeth, Robert A., et al. “Intestinal microbiota metabolism of L-carnitine, a nutrient in red meat, promotes atherosclerosis.” Nature medicine 19.5 (2013): 576.
- Koeth, Robert A., et al. “γ-Butyrobetaine is a proatherogenic intermediate in gut microbial metabolism of L-carnitine to TMAO.” Cell metabolism 20.5 (2014): 799-812.
- Koeth, Robert A., et al. “L-Carnitine in omnivorous diets induces an atherogenic gut microbial pathway in humans.” Journal of Clinical Investigation (2018): 10-1172.
- Leal‐Witt, María J., et al. “Lifestyle Intervention Decreases Urine Trimethylamine N‐Oxide Levels in Prepubertal Children with Obesity.” Obesity 26.10 (2018): 1603-1610.
- Messenger, Jeffrey, et al. “A review of trimethylaminuria:(fish odor syndrome).” The Journal of clinical and aesthetic dermatology 6.11 (2013): 45.
- Mitchell, S. C., A. Q. Zhang, and R. L. Smith. “Chemical and biological liberation of trimethylamine from foods.” Journal of Food Composition and Analysis 15.3 (2002): 277-282.
- Roberts, Adam B., et al. “Development of a gut microbe–targeted nonlethal therapeutic to inhibit thrombosis potential.” Nature medicine 24.9 (2018): 1407.
- Shang, Ruiping, Zhiqi Sun, and Hui Li. “Effective dosing of L-carnitine in the secondary prevention of cardiovascular disease: a systematic review and meta-analysis.” BMC cardiovascular disorders 14.1 (2014): 88.
- Simpson, Hannah Louise, and Barry J. Campbell. “dietary fibre–microbiota interactions.” Alimentary pharmacology & therapeutics 42.2 (2015): 158-179.
- Tang, WH Wilson, and Stanley L. Hazen. “The contributory role of gut microbiota in cardiovascular disease.” The Journal of clinical investigation 124.10 (2014): 4204-4211.
- Tenore, Gian Carlo, et al. “Lactofermented Annurca Apple Puree as a Functional Food Indicated for the Control of Plasma Lipid and Oxidative Amine Levels: Results from a Randomised Clinical Trial.” Nutrients 11.1 (2019): 122.