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1.
J Endocrinol Invest ; 38(12): 1265-75, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26219612

RESUMO

A considerable number of studies have examined vitamin D status during pregnancy. Although data from observational studies denote vitamin D hypovitaminosis (deficiency or insufficiency) during pregnancy is associated with a plethora of adverse maternal and neonatal outcomes, data from interventional (supplementation) trials fail to reveal a significant impact on maternal and offspring health. The aim of this narrative review was to critically appraise the methodology of the most representative published randomized controlled trials in an attempt to explain the difference between observational and supplementation results. We found that this difference could be attributed to a variety of factors, namely: (i) study design (lack of a specific outcome in conjunction with timing of supplementation, enrolment of participants with heterogeneous vitamin D status); (ii) pitfalls in the interpretation of vitamin D equilibrium (lack of determination of plasma half-life); (iii) supplementation regimen (administration of a wide range of regimens, in terms of dose, bolus and form); (iv) geographical characteristics (vitamin D needs could vary significantly within a country, particularly in areas with a wide range of latitude gradient); (v) adaptations of vitamin D metabolism during pregnancy (vitamin D and calcium equilibrium are changed during pregnancy compared with the non-pregnant state) and (vi) supplementation of populations with low baseline 25(OH)D values would likely manifest beneficial effects. All these parameters should be taken into consideration in the design of future vitamin D supplementation trials.


Assuntos
Estudos Observacionais como Assunto , Avaliação de Resultados em Cuidados de Saúde , Complicações na Gravidez/tratamento farmacológico , Ensaios Clínicos Controlados Aleatórios como Assunto , Deficiência de Vitamina D/tratamento farmacológico , Vitamina D/uso terapêutico , Feminino , Humanos , Gravidez , Vitamina D/sangue
2.
Osteoporos Int ; 25(3): 795-805, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23907574

RESUMO

Data from animal and human studies implicate maternal vitamin D deficiency during pregnancy as a significant risk factor for several adverse outcomes affecting maternal, fetal, and child health. The possible associations of maternal vitamin D status and offspring bone development comprise a significant public health issue. Evidence from randomized trials regarding maternal vitamin D supplementation for optimization of offspring bone mass is lacking. In the same field, data from observational studies suggest that vitamin D supplementation is not indicated. Conversely, supplementation studies provided evidence that vitamin D has beneficial effects on neonatal calcium homeostasis. Nevertheless, a series of issues, such as technical difficulties of current vitamin D assays and functional interplay among vitamin D analytes, prohibit arrival at safe conclusions. Future studies would benefit from adoption of a gold standard assay, which would unravel the functions of vitamin D analytes. This narrative review summarizes and discusses data from both observational and supplementation studies regarding maternal vitamin D status during pregnancy and offspring bone development.


Assuntos
Desenvolvimento Ósseo/fisiologia , Gravidez/sangue , Efeitos Tardios da Exposição Pré-Natal , Vitamina D/sangue , Densidade Óssea/fisiologia , Cálcio/uso terapêutico , Suplementos Nutricionais , Feminino , Humanos , Recém-Nascido , Complicações na Gravidez/diagnóstico , Complicações na Gravidez/prevenção & controle , Cuidado Pré-Natal/métodos , Fenômenos Fisiológicos da Nutrição Pré-Natal/fisiologia , Raquitismo/prevenção & controle , Deficiência de Vitamina D/diagnóstico , Deficiência de Vitamina D/prevenção & controle
3.
Scand J Med Sci Sports ; 23(2): 244-52, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22092778

RESUMO

Nutritional supplement (NS) use is widespread in sport. This study applied an integrated social cognitive approach to examine doping attitudes, beliefs, and self-reported doping use behavior across NS users (n = 96) and nonusers (n = 116). Following ethical approval, 212 competitive athletes (age mean = 21.4, s = 4.5; 137 males) completed self-reported measures of doping-related social cognitions and behaviors, presented in an online format where completion implied consent. Significantly more NS users (22.9%) reported doping compared with nonusers (6.0%; U = 4628.0, P < 0.05). NS users presented significantly more positive attitudes toward doping (U = 3152.0, P < 0.05) and expressed a significantly greater belief that doping is effective (U = 3152.0, P < 0.05). When presented with the scenario that performance-enhancing substances are effective and increase the possibility of winning, NS users were significantly more in favor of competing in situations that allow doping (U = 3504.5, P < 0.05). In sum, doping use is three-and-a-half times more prevalent in NS users compared with nonusers. This finding is accompanied by significant differences in doping attitudes, norms, and beliefs. Thus, this article offers support for the gateway hypothesis; athletes who engage in legal performance enhancement practices appear to embody an "at-risk" group for transition toward doping. Education should be appropriately targeted.


Assuntos
Atletas/psicologia , Atitude , Suplementos Nutricionais , Dopagem Esportivo/estatística & dados numéricos , Feminino , Humanos , Masculino , Autorrelato , Fatores Sexuais , Inquéritos e Questionários , Adulto Jovem
4.
Food Chem Toxicol ; 49(2): 393-402, 2011 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21087651

RESUMO

Dietary supplements are widely used across all ages and user groups and constitute a considerable business sector in most developed countries. Hazards relating to concentration, composition, individual contaminants and supplement interactions present an increasing public health concern. The aim of this paper is to review the literature for reported supplement contaminations (occurs in ca 25% of supplements, with anabolic steroids being the most common) and complement these findings with notifications logged in the EU's Rapid Alert System for Food and Feed (RASFF) through imports or market surveillance, typically logged for poor quality control issues. Notifications in the RASFF have steadily increased by sixfold for supplements in the past 7 years with the USA and China being the major transgressors. Finland and Italy lead in detections, mainly notifying unpermitted substances and contaminants in sexual-enhancing or weight-loss supplements. This paper highlights the paucity of enforcement. Regulating supplements as a foodstuff and not a medicine, coupled with the fact that a significant proportion of the supplement market is distributed via the Internet (hence absent from routine border control and surveillance), make ensuring and enforcing safety a very challenging task. The need for better quality control, compliance and public awareness is evident.


Assuntos
Qualidade de Produtos para o Consumidor/legislação & jurisprudência , Suplementos Nutricionais/efeitos adversos , Rotulagem de Alimentos/legislação & jurisprudência , Saúde Global , Política de Saúde , Humanos , Legislação de Medicamentos , Legislação sobre Alimentos , Saúde Pública
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