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1.
Nutr Bull ; 39(4): 322-350, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25635171

RESUMO

In recent years, there have been reports suggesting a high prevalence of low vitamin D intakes and vitamin D deficiency or inadequate vitamin D status in Europe. Coupled with growing concern about the health risks associated with low vitamin D status, this has resulted in increased interest in the topic of vitamin D from healthcare professionals, the media and the public. Adequate vitamin D status has a key role in skeletal health. Prevention of the well-described vitamin D deficiency disorders of rickets and osteomalacia are clearly important, but there may also be an implication of low vitamin D status in bone loss, muscle weakness and falls and fragility fractures in older people, and these are highly significant public health issues in terms of morbidity, quality of life and costs to health services in Europe. Although there is no agreement on optimal plasma levels of vitamin D, it is apparent that blood 25-hydroxyvitamin D [25(OH)D] levels are often below recommended ranges for the general population and are particularly low in some subgroups of the population, such as those in institutions or who are housebound and non-Western immigrants. Reported estimates of vitamin D status within different European countries show large variation. However, comparison of studies across Europe is limited by their use of different methodologies. The prevalence of vitamin D deficiency [often defined as plasma 25(OH)D <25 nmol/l] may be more common in populations with a higher proportion of at-risk groups, and/or that have low consumption of foods rich in vitamin D (naturally rich or fortified) and low use of vitamin D supplements. The definition of an adequate or optimal vitamin D status is key in determining recommendations for a vitamin D intake that will enable satisfactory status to be maintained all year round, including the winter months. In most European countries, there seems to be a shortfall in achieving current vitamin D recommendations. An exception is Finland, where dietary survey data indicate that recent national policies that include fortification and supplementation, coupled with a high habitual intake of oil-rich fish, have resulted in an increase in vitamin D intakes, but this may not be a suitable strategy for all European populations. The ongoing standardisation of measurements in vitamin D research will facilitate a stronger evidence base on which policies can be determined. These policies may include promotion of dietary recommendations, food fortification, vitamin D supplementation and judicious sun exposure, but should take into account national, cultural and dietary habits. For European nations with supplementation policies, it is important that relevant parties ensure satisfactory uptake of these particularly in the most vulnerable groups of the population.

2.
Eur J Clin Nutr ; 64 Suppl 3: S8-13, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-21045856

RESUMO

Regulation on nutrition and health claims number (EC) No. 1924/2006 came into force in the European Union (EU) in 2007. The Regulation aims to ensure that claims are truthful and do not mislead consumers. It also aims to stimulate innovation to produce healthier food products in the food industry. Nutrition claims are defined in an annex to the Regulation that states the wording of permitted claims and the conditions of use. The scientific support for potential health claims is being assessed by the European Food Safety Authority (EFSA), but consideration of other aspects and the final decision to accept or reject a claim lies with the European Commission. The final list of approved health claims was due to be published in early 2010, but work is behind schedule, and therefore decisions are being published in batches; the first batch of Article 13 claims based on generally accepted science was published in October 2009. Food composition data are vital in making accurate claims on food as the amount of the nutrient or food component in question must be defined. It is also important that the composition of a particular food or food category has been sufficiently defined in order for a health claim pertaining to this to be approved. In addition, to prevent claims being made on foods with a less healthy profile, nutrient profiles are being developed that will specify threshold amounts of saturated fat, sodium and sugar present in any product bearing a nutrition or health claim, and thus the composition of a food will be critical in determining whether it is eligible to carry a claim. Therefore, the access that the European Food Information Resource (EuroFIR) will provide to pan-European food composition data will be of great importance in making the Regulation workable. EuroFIR has been actively involved in EFSA's work on nutrient profiles, supplying data that have been used to develop the current profiling model. It is hoped that the EuroFIR Network and the not-for-profit organisation EuroFIR AISBL (Association Internationale Sans But Lucratif, that has been established to take forward EuroFIR's work) can continue to provide guidance to stakeholders as the Regulation develops.


Assuntos
Análise de Alimentos/estatística & dados numéricos , Rotulagem de Alimentos/normas , Alimentos Orgânicos/normas , Promoção da Saúde , Valor Nutritivo , Suplementos Nutricionais , União Europeia , Inocuidade dos Alimentos , Humanos , Legislação sobre Alimentos , Fenômenos Fisiológicos da Nutrição
3.
Biochim Biophys Acta ; 963(1): 61-9, 1988 Nov 04.
Artigo em Inglês | MEDLINE | ID: mdl-3179330

RESUMO

(1) Rats were given a diet deficient in vitamin E and selenium, or diets supplemented with either or both of these nutrients. The livers were subfractionated by standard procedures, and the purity of the fractions was assessed by marker enzyme techniques. alpha-Tocopherol was measured and profiles of phospholipid fatty acids were determined. (2) All the organelles studied were severely depleted of alpha-tocopherol in the rats deprived of vitamin E: no organelle was particularly severely depleted. There was a large rise in the alpha-tocopherol content in organelles of rats deprived of selenium but given adequate amounts of vitamin E, suggesting an increased uptake or mobilization of tocopherol to compensate for the detrimental effects of selenium deficiency. (3) The following general conclusions were reached from the results of the phospholipid fatty acid analyses. (i) vitamin E deficiency caused a consistent fall in the polyunsaturated fatty acid (PUFA) content (13-66% of the control level); (ii) selenium deficiency alone caused no consistent effect on phospholipid PUFA in the fractions studied; (iii) double deficiency of vitamin E and selenium caused a consistent rise in the proportion of PUFA in the fractions studied, ranging from 11 to 311%. (4) The result given in 3(i) is consistent with peroxidative destruction of membrane phospholipid PUFA during vitamin E deficiency. The result in 3(iii) is paradoxical: a possible explanation is that during severe disruption of antioxidant defences, there is an overshoot in the increased incorporation of unsaturated fatty acids into the membrane phospholipids, or in the chain-elongation and desaturation process required for the formation of PUFA, which may require vitamin E and/or selenium for its regulation.


Assuntos
Ácidos Graxos/análise , Fígado/análise , Fosfolipídeos/análise , Selênio/deficiência , Vitamina E/análise , Animais , Fígado/citologia , Masculino , Lipídeos de Membrana/análise , Ratos , Ratos Endogâmicos , Frações Subcelulares/análise
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