| Trimethylaminuria is a rare genetic metabolic disorder occurring in oil to 0.1 to 1% of the
population and is due to deficiency of the enzyme trimethylamine-N-oxide synthetase.
Trimethylamine, which is produced from Choline, is excreted from the body by the urine,
sweat, breath and other bodily secretions. It has a nauseating, rotten-fish-smelling odor.
Trimethylamine-N-oxide is non-odorous. Individuals with primary genetic trimethyluria should
restrict intake of Choline. Individuals with certain types of liver disease caused by any of
the hepatitis viruses or from other etiologies might develop fishy body odor when taking
supplemental Choline. Choline intake should be restricted in these cases. Choline doses of
up to 3 grams daily are generally well tolerated although there are occasional reports of
diarrhea, loose stools, and nausea. Higher doses have been associated with fishy body odor,
particularly in individuals with trimethylaminuria. Trimethylaminuria might also occur in
individuals with liver damage who are using high doses of Choline. High intakes of Choline
have been linked with excessive sweating and hypotension. There are reports of depression or
increased symptoms of depression in individuals using high doses of choline bitartrate.
There are no adequate data demonstrating a no-observed-adverse-effect level for excess
Choline intake. Based on two clinical studies in humans, a lowest-observed-adverse-effect
level of 7.5 grams daily has been determined. At 7.5 grams of Choline daily, diarrhea,
nausea, and a small decrease in blood pressure were reported in some patients. The upper
limit for adults is 3.5 grams daily. Individuals that might be at increased risk of side
effects with Choline intakes at the upper limit include those with depression, liver
disease, renal disease, Parkinson's disease, and trimethylaminuria. Methotrexate might
diminish pools of all Choline metabolites. Choline supplementation reverses fatty liver
caused by methotrexate administration in rats. Choline works in concert with vitamins B6,
B12, and folic acid in the metabolism of homocysteine. This website is intended to educate
and inform, and should not replace discussions with your doctor. |