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1.
Public Health Nutr ; 15(11): 1999-2004, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-22929414

RESUMO

OBJECTIVE: To assess and develop a consensus among a European panel of public health nutrition workforce stakeholders (academics and employers) regarding core functions required for effective public health nutrition practice. DESIGN: A modified Delphi study involving data from two rounds of questionnaires administered among a panel of public health nutrition workforce stakeholders. SETTING: Europe. SUBJECTS: A panel of fifty-three public health nutrition development stakeholders, including thirty-three academics and twenty employers, sampled from eighteen European countries. RESULTS: Panellists rated 50 % (19/38) of the initially listed functions as core (i.e. without which public health capacity is limited), using a majority cut-off (>50 %). Out of the nineteen core functions seven were categorised under the heading Intervention management, emphasising high agreement on the importance of managing interventions in public health nutrition work. Only one of the identified core public health nutrition functions was rated differently between academics and employers, suggesting consistent identification of core functions between stakeholder groups. CONCLUSIONS: This consensus on core functions of the public health nutrition workforce in Europe can be used to promote a consistent understanding of the role and value of public health nutritionists as a discrete disciplinary sub-specialty of the public health workforce. The convergence of opinions of academics and employers, as well as comparison with previous international studies, indicates that there is a set of core public health nutrition functions transferable between countries that can be used as a benchmark to guide further development of the public health nutrition workforce in Europe.


Assuntos
Consenso , Dietética , Ciências da Nutrição , Papel Profissional , Prática de Saúde Pública , Saúde Pública , Técnica Delphi , Emprego , Europa (Continente) , Humanos , Internacionalidade , Inquéritos e Questionários , Universidades
2.
BMC Med Genet ; 11: 76, 2010 May 17.
Artigo em Inglês | MEDLINE | ID: mdl-20478055

RESUMO

BACKGROUND: Recent whole genome analysis and follow-up studies have identified many new risk variants for coeliac disease (CD, gluten intolerance). The majority of newly associated regions encode candidate genes with a clear functional role in T-cell regulation. Furthermore, the newly discovered risk loci, together with the well established HLA locus, account for less than 50% of the heritability of CD, suggesting that numerous additional loci remain undiscovered. Linkage studies have identified some well-replicated risk regions, most notably chromosome 5q31 and 11q23. METHODS: We have evaluated six candidate genes in one of these regions (11q23), namely CD3E, CD3D, CD3G, IL10RA, THY1 and IL18, as risk factors for CD using a 2-phase candidate gene approach directed at chromosome 11q. 377 CD cases and 349 ethnically matched controls were used in the initial screening, followed by an extended sample of 171 additional coeliac cases and 536 additional controls. RESULTS: Promotor SNPs (-607, -137) in the IL18 gene, which has shown association with several autoimmune diseases, initially suggested association with CD (P < 0.05). Follow-up analyses of an extended sample supported the same, moderate effect (P < 0.05) for one of these. Haplotype analysis of IL18-137/-607 also supported this effect, primarily due to one relatively rare haplotype IL18-607C/-137C (P < 0.0001), which was independently associated in two case-control comparisons. This same haplotype has been noted in rheumatoid arthritis. CONCLUSION: Haplotypes of the IL18 promotor region may contribute to CD risk, consistent with this cytokine's role in maintaining inflammation in active CD.


Assuntos
Doença Celíaca/genética , Cromossomos Humanos Par 11/genética , Cromossomos Humanos Par 5/genética , Estudos de Associação Genética/métodos , Estudos de Casos e Controles , Mapeamento Cromossômico , Ligação Genética , Predisposição Genética para Doença , Variação Genética , Humanos , Interleucina-10/genética , Subunidade alfa de Receptor de Interleucina-10/genética , Interleucina-18/genética , Polimorfismo de Nucleotídeo Único/genética , Risco , Fatores de Risco
3.
Nat Genet ; 40(4): 395-402, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18311140

RESUMO

Our genome-wide association study of celiac disease previously identified risk variants in the IL2-IL21 region. To identify additional risk variants, we genotyped 1,020 of the most strongly associated non-HLA markers in an additional 1,643 cases and 3,406 controls. Through joint analysis including the genome-wide association study data (767 cases, 1,422 controls), we identified seven previously unknown risk regions (P < 5 x 10(-7)). Six regions harbor genes controlling immune responses, including CCR3, IL12A, IL18RAP, RGS1, SH2B3 (nsSNP rs3184504) and TAGAP. Whole-blood IL18RAP mRNA expression correlated with IL18RAP genotype. Type 1 diabetes and celiac disease share HLA-DQ, IL2-IL21, CCR3 and SH2B3 risk regions. Thus, this extensive genome-wide association follow-up study has identified additional celiac disease risk variants in relevant biological pathways.


Assuntos
Biomarcadores , Doença Celíaca/genética , Marcadores Genéticos/genética , Predisposição Genética para Doença , Genoma Humano , Polimorfismo de Nucleotídeo Único , Animais , Estudos de Casos e Controles , Doença Celíaca/imunologia , Mapeamento Cromossômico , Estudos de Coortes , Diabetes Mellitus Tipo 1/genética , Feminino , Antígenos HLA-DQ/metabolismo , Humanos , Subunidade p35 da Interleucina-12/genética , Subunidade beta de Receptor de Interleucina-18/sangue , Subunidade beta de Receptor de Interleucina-18/genética , Desequilíbrio de Ligação , Masculino , Camundongos , Reação em Cadeia da Polimerase , Proteínas RGS/genética , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Receptores CCR3/genética , Fatores de Risco , Distribuição Tecidual
4.
Br J Nutr ; 89(1): 137-45, 2003 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12568673

RESUMO

Anthropometric screening has been recommended for the detection of undernutrition as it is simple, inexpensive and non-invasive. However, a recent study estimating the prevalence of undernutrition on admission to hospital in Dublin, Republic of Ireland, highlighted that the anthropometric reference data currently available in the UK and Republic of Ireland are inadequate to accurately determine nutritional status. In order to provide current anthropometric data, we carried out a cross-sectional study of 874 free-living, apparently healthy Irish-born elderly individuals aged over 65 years. Height, weight, triceps skinfold thickness, mid-arm and calf circumference were measured, values for BMI, mid-arm muscle circumference and arm muscle area were calculated and smoothed centile data derived for each variable. One-third of these elderly individuals had a BMI between 20-25 kg/m2, approximately two-thirds (68.5 % of males and 61 % of females) were classified as overweight or obese, almost one-fifth having a BMI over 30 kg/m2 (17 % of men and 20 % of women). Very few were underweight, only 3 % having a BMI below 20 kg/m2. Height, weight, BMI and muscle reserves decreased with increasing age. The reduction in muscle size was associated with lower handgrip strength. Fat reserves declined with age in females only. Just over half of elderly Irish women reported participating in active leisure of 20 min duration four or more times/week, although 13 % reported having no involvement in active leisure. These data for the Irish elderly extend the data generated from a recent countrywide survey of Irish adults aged 18-64 years, thus providing suitable reference standards for nutritional assessment of elderly Irish individuals.


Assuntos
Antropometria/métodos , Avaliação Geriátrica/métodos , Estado Nutricional , Idoso , Idoso de 80 Anos ou mais , Envelhecimento/patologia , Estatura , Índice de Massa Corporal , Peso Corporal , Estudos Transversais , Exercício Físico , Feminino , Humanos , Irlanda , Masculino , Músculo Esquelético/anatomia & histologia , Valores de Referência , Fatores Sexuais , Dobras Cutâneas
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