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  Vol. 162 No. 1, January 14, 2002 TABLE OF CONTENTS
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Methylmalonic Acid and Clinical Practice

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

We read with much interest the article published by Hvas et al.1 It reaches very interesting conclusions and deserves some careful considerations.

The follow-up study of individuals with slightly increased levels of plasma methylmalonic acid (P-MMA) during a period of up to 3.9 years, with no evidence of clinical manifestations of vitamin B12 deficiency, supports the thesis of its doubtful clinical significance as a marker for vitamin B12 deficiency.2-3

We reached similar conclusions during a study we performed4 to examine vitamin B12 deficiency in a group of healthy elderly patients (aged >60 years) who had partial gastrectomies for more than 5 years. In such a study, levels of urinary methylmalonic acid were measured using the Norman method5 together with measurement of total plasma homocysteine. Of the 47 individuals selected for the study, who had no symtoms and normal clinical examination findings, including a Mini-Mental State examination,6 9 individuals (19%) showed . . . [Full Text of this Article]







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