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Several of the essential nutrients also have well-documented toxic, perhaps even fatal, effects when taken in excess: Iron is an essential nutrient but iron poisoning from dietary supplements intended for their parents is also the most common cause of accidental poisoning in children Vitamin A (retinol) is known to be acutely toxic in high doses It may also cause increased risk of fracture in elderly people at doses around twice the usual recommended intake and it is also thought to cause malformations in unborn children if consumed in excess during pregnancy -carotene has very low acute toxicity but there is evidence that chronic high consumption may promote tumour growth in smokers and others at high risk of lung cancer Large folic acid supplements may interfere with the actions of a number of drugs that work by antagonising the effects of folic acid.

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7.9 Work through the steps of Lemma 7.5. (a) Explain why there must by polynomials Q l ( x ) and Q 2 ( x ) such that N ( x ) - W ( x ) P ( x )= Q l ( x ) n ( x ) and M ( x ) - V ( x ) P ( x )= Q ~ ( x ) ~ ( x ) . (b) Show that ( N V - M W ) P = ( M Q l - N Q 2 ) I l (c) Explain why ( l T ( x ) ,P ( x ) ) N ( x ) and (n(x), ( x ) ) M ( x ) . (Here, (n(x), ( x ) ) is the P P GCD.) (d) Show that ( N ( x ) V ( x ) - M ( x ) W ( x ) ) P ( x )= ( M ( x ) Q l ( x ) - N ( x ) Q 2 ( x ) ) n ( x ) . (e) Show that

It may also mask the anaemia caused by vitamin B12 de ciency (including pernicious anaemia) so that the irreversible neuropathy of B12 de ciency is left untreated A recent Expert Group on Vitamins and Minerals produced a 350 page report for the Food Standards Agency (FSA 2003) that tried to establish Tolerable Upper Intake Levels (UL) for all vitamins, essential minerals and other trace elements using previously published data The UL is the total chronic daily intake of the substance that is judged to be unlikely to pose a risk to health This UL is ideally based upon the No Observed Adverse Effect Level (NOAEL), the highest intake at which no adverse effects are observed.

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In several cases the committee had less than ideal data to work with, for example they may have had to: Infer doses that were chronically acceptable from relatively short-term studies Rely to some extent on animal data Use data from studies where the substance was not administered via the normal oral route Essentially the same types of observational and particularly experimental methods that are used to assess ef cacy are also used to assess safety In this case the outcome measure is some adverse effect , a physiological, developmental or other effect that in expert opinion is either directly damaging to individuals functioning or makes them more vulnerable to other stresses or environmental in uences..

[Lam73] [Lam81]

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P1: KTX WY022-34 WY022/Pfaffenberger WY022/Pfaffenberger-v3.cls June 9, 2004 15:11

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