105 research outputs found

    Vitamin D status among female handball and football elite athletes in Norway at latitude 60°N

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    Bakgrunn: En overhyppighet av suboptimal vitamin D-status er blitt rapportert pĂ„ verdensbasis, men lite er kjent nĂ„r det gjelder nivĂ„et hos idrettsutĂžvere. Vitamin D er kjent for sin funksjon i skjelettet og betydning for beinhelse. I tillegg har vitamin D en funksjon i muskel og immunforsvaret, og lave nivĂ„er er trolig forbundet med bĂ„de nedsatt muskelstyrke og kroniske sykdommer. Om disse funksjonene kan pĂ„virke helsestatus og prestasjon hos idrettsutĂžvere er ennĂ„ ikke bekreftet. Hensikt: Å mĂ„le serum vitamin D-konsentrasjon, som 25-hydroksyvitamin D (25(OH)D), hos kvinnelige toppidrettsutĂžvere innen hĂ„ndball og fotball pĂ„ Østlandet i Norge, ved breddegrad 60ÂșN. Vi ville ogsĂ„ se pĂ„ mulige eksponeringsfaktorer for 25(OH)D-nivĂ„et i denne gruppen, ved Ă„ se pĂ„ kosthold, bruk av kosttilskudd og solvaner. Metoder: Serum 25(OH)D-konsentrasjon ble mĂ„lt for 48 kvinnelige toppidrettsutĂžvere (26 hĂ„ndball/22 fotball) i oktober/november 2010. Utilstrekkelig 25(OH)D-nivĂ„ ble definert som <80 nmol/l. UtĂžverne registrerte kostholdet sitt med vekt i fire dager. Bruk av kosttilskudd og solvaner ble rapportert ved intervjuer-baserte spĂžrreskjemaer. Resultater: Gjennomsnittlig serum 25(OH)D-konsentrasjon var 99 (SD=32) nmol/l. Utilstrekkelig vitamin D-nivĂ„ ble funnet hos 27 prosent av utĂžverne. HĂ„ndballspillerne hadde signifikant hĂžyere serum 25(OH)D-nivĂ„ enn fotballspillerne (p=0.001). Deltakerne som kun oppholdt seg i Norden om sommeren, hadde signifikant lavere 25(OH)D-nivĂ„ enn deltakerne som reiste utenfor Norden (p=0.039). HĂ„ndballspillerne reiste signifikant mer utenfor Norden enn fotballspillerne (p=0.004). Vitamin D-inntaket var under anbefalt nivĂ„, 7,5 ”g/dag, for 73 prosent av alle deltakerne. Konklusjon: I denne studien, gjort pĂ„ kvinnelige utĂžvere fra hĂžy nordlig breddegrad, var gjennomsnittlig 25(OH)D-nivĂ„ om hĂžsten tilsvarende optimalt nivĂ„, og utilstrekkelig 25(OH)D-nivĂ„ ble funnet hos en av fire utĂžvere. Å reise utenfor Norden om sommeren sĂ„ ut til Ă„ vĂŠre den faktoren av stĂžrst betydning for 25(OH)D-nivĂ„ene. Siden deltakerne bor ved hĂžy nordlig breddegrad og siden vitamin D-inntaket var under anbefalt nivĂ„ for Ÿ av deltakerne, er det sannsynlig at 25(OH)D-nivĂ„ene deres vil synke i lĂžpet av vinteren. Derfor er det nĂždvendig Ă„ diskutere om generell screening av 25(OH)D-konsentrasjon for kvinnelige toppidrettsutĂžvere bĂžr anbefales

    Vocation and avocation: Leisure activities correlate with professional engagement, but not burnout, in a cross-sectional survey of UK doctors

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    RIGHTS : This article is licensed under the BioMed Central licence at http://www.biomedcentral.com/about/license which is similar to the 'Creative Commons Attribution Licence'. In brief you may : copy, distribute, and display the work; make derivative works; or make commercial use of the work - under the following conditions: the original author must be given credit; for any reuse or distribution, it must be made clear to others what the license terms of this work are.Abstract Background Sir William Osler suggested in 1899 that avocations (leisure activities) in doctors are related to an increased sense of vocation (professional engagement) and a decreased level of burnout. This study evaluated those claims in a large group of doctors practicing in the UK while taking into account a wide range of background variables. Methods A follow-up questionnaire was sent to 4,457 UK-qualified doctors who had been included in four previous studies of medical school selection and training, beginning in 1980, 1985, 1990 and 1989/1991. A total of 2,845 (63.8%) doctors returned the questionnaire. Questions particularly asked about work engagement, satisfaction with medicine as a career, and personal achievement (Vocation/engagement), stress, emotional exhaustion, and depersonalization (BurnedOut), and 29 different leisure activities (Avocation/Leisure), as well as questions on personality, empathy, work experience, and demography. Results Doctors reporting more Avocation/Leisure activities tended to be women, to have older children, to be less surface-rational, more extravert, more open to experience, less agreeable, and to fantasize more. Doctors who were more BurnedOut tended to be men, to be more sleep-deprived, to report a greater workload and less choice and independence in their work, to have higher neuroticism, lower extraversion and lower agreeableness scores, and to have lower self-esteem. In contrast, doctors with a greater sense of Vocation/engagement, tended to see more patients, to have greater choice and independence at work, to have a deep approach to work, to have a more supportive-receptive work environment, to be more extravert and more conscientious, and to report greater self-esteem. Avocation/Leisure activities correlated significantly with Vocation/engagement, even after taking into account 25 background variables describing demography, work, and personality, whereas BurnedOut showed no significant correlation with Avocation/Leisure activities. Popular Culture and High Culture did not differ in their influence on Vocation/engagement, although there was a suggestion that Depersonalization was correlated with more interest in Popular Culture and less interest in High Culture. Conclusion In this cross-sectional study there is evidence, even after taking into account a wide range of individual difference measures, that doctors with greater Avocation/Leisure activities also have a greater sense of Vocation/Engagement. In contrast, being BurnedOut did not relate to Avocation/Leisure activities (but did relate to many other measures). Osler was probably correct in recommending to doctors that, 'While medicine is to be your vocation, or calling, see to it that you also have an avocation'.Peer Reviewe

    Dietary nitrate and sports performance

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    New Opportunities to Advance Sport Nutrition

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    Sports nutrition is a relatively new discipline; with ~100 published papers/year in the 1990s to ~3,500+ papers/year today. Historically, sports nutrition research was primarily initiated by university-based exercise physiologists who developed new methodologies that could be impacted by nutrition interventions (e.g., carbohydrate/fat oxidation by whole body calorimetry and muscle glycogen by muscle biopsies). Application of these methods in seminal studies helped develop current sports nutrition guidelines as compiled in several expert consensus statements. Despite this wealth of knowledge, a limitation of the current evidence is the lack of appropriate intervention studies (e.g., randomized controlled clinical trials) in elite athlete populations that are ecologically valid (e.g., in real-life training and competition settings). Over the last decade, there has been an explosion of sports science technologies, methodologies, and innovations. Some of these recent advances are field-based, thus, providing the opportunity to accelerate the application of ecologically valid personalized sports nutrition interventions. Conversely, the acceleration of novel technologies and commercial solutions, especially in the field of biotechnology and software/app development, has far outstripped the scientific communities' ability to validate the effectiveness and utility of the vast majority of these new commercial technologies. This mini-review will highlight historical and present innovations with particular focus on technological innovations in sports nutrition that are expected to advance the field into the future. Indeed, the development and sharing of more “big data,” integrating field-based measurements, resulting in more ecologically valid evidence for efficacy and personalized prescriptions, are all future key opportunities to further advance the field of sports nutrition

    Leucine rich repeat kinase 2 (LRRK2) GLY2019SER mutation is absent in a second cohort of Nigerian Africans with Parkinson disease

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    To date the LRRK2 p.G2019S mutation remains the most common genetic cause of Parkinson disease (PD) worldwide. It accounts for up to 6% of familial and approximately 1.5% of sporadic cases. LRRK2 has a kinase enzymatic domain which provides an attractive potential target for drug therapies and LRRK2 kinase inhibitors are in development. Prevalence of the p.G2019S has a variable ethnic and geographic distribution, the highest reported among Ashkenazi Jews (30% in patients with familial PD, 14% in sporadic PD, 2.0% in controls) and North African Berbers (37% in patients with familial PD, 41% in sporadic PD, and 1% in controls). Little is known about the frequency of the LRRK2 p.G2019S among populations in sub-Saharan Africa. Our group and others previously reported that the p.G2019S is absent in a small cohort of Nigerian PD patients and controls. Here we used Kompetitive Allele Specific PCR (KASP) assay to screen for the p.G2019S in a larger cohort of Black African PD patients (n = 126) and healthy controls (n = 54) from Nigeria. Our analysis confirmed that all patients and controls are negative for the p.G2019S mutation. This report provides further evidence that the LRRK2 p.G2019S is not implicated in PD in black populations from Nigeria and support the notion that p.G2019S mutation originated after the early human dispersal from sub-Saharan Africa. Further studies using larger cohorts and advance sequencing technology are required to underpin the genetic causes of PD in this region

    Mitochondrial DNA analysis from exome sequencing data improves the diagnostic yield in neurological diseases

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    A rapidly expanding catalogue of neurogenetic disorders has encouraged a diagnostic shift towards early clinical whole exome sequencing (WES). Adult primary mitochondrial diseases (PMDs) frequently exhibit neurological manifestations that overlap with other nervous system disorders. However, mitochondrial DNA (mtDNA) is not routinely analyzed in standard clinical WES bioinformatic pipelines. We reanalyzed 11,424 exomes, enriched with neurological diseases, for pathogenic mtDNA variants. Twenty‐four different mtDNA mutations were detected in 64 exomes, 11 of which were considered disease causing based on the associated clinical phenotypes. These findings highlight the diagnostic uplifts gained by analyzing mtDNA from WES data in neurological diseases

    Truncating mutations in SPAST patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia.

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    BACKGROUND: The hereditary spastic paraplegias (HSPs) are a rare and heterogeneous group of neurodegenerative disorders that are clinically characterised by progressive lower limb spasticity. They are classified as either 'pure' or 'complex' where spastic paraplegia is complicated with additional neurological features. Mutations in the spastin gene (SPAST) are the most common cause of HSP and typically present with a pure form. METHODS: We assessed in detail the phenotypic and genetic spectrum of SPAST-related HSP focused on 118 patients carrying SPAST mutations. RESULTS: This study, one of the largest cohorts of genetically confirmed spastin patients to date, contributes with the discovery of a significant number of novel SPAST mutations. Our data reveal a high rate of complex cases (25%), with psychiatric disorders among the most common comorbidity (10% of all SPASTpatients). Further, we identify a genotype-phenotype correlation between patients carrying loss-of-function mutations in SPAST and the presence of psychiatric disorders
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