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The excellent report by Talwar et al. (1) promotes the measurement of thiamin diphosphate (TDP) for the assessment of vitamin B1 status. My experience with >30 000 people supports this, but only for the investigation of untreated patients. The TDP assay is more precise than the transketolase activation (ETK) test, and the method described is an important advance for which I thank the authors. In comparing the two methods, Talwar et al. (1) found TDP slightly advantageous in the identification of B1 deficiency. They and most workers using the ETK test agree that the cutoff point is 25%. I have found it useful to report results in the range 15–25% as borderline. When this is done, there is little to choose between TDP and ETK in terms of clinical usefulness. Much as I would like to use the more precise TDP assay, there is a problem that surfaces when one wishes to use the laboratory to follow repletion with thiamin. It is very rare for the TDP concentration to remain low after a few days of supplemental B1, and in many cases, TDP normalizes after a single 100-mg dose. This is not the case for the ETK test. In some cases, several weeks of daily supplementation are needed to normalize the results. I am in the fortunate position of receiving considerable feedback from the clinicians using our laboratory service and have carefully studied their findings in relation to the laboratory results. In my experience, it is the ETK test that parallels the clinical improvement in supplemented patients. I support the use of the more precise TDP (HPLC method) in untreated people, but I caution against its use in following supplementation. For this, the ETK test, even with its many limitations, remains the method of choice. A more precise method for measuring this enzyme would be enormously helpful. I hope this letter will open some further discussion on the use of functional tests in nutrient-related clinical chemistry.
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John M. Howard (2000) studied this question.
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