104 research outputs found
Levels of antinutritional factors in some wild edible fruits of Northern Nigeria
Sixteen wild fruits commonly consumed in northern Nigeria were assessed chemically for the presence of oxalate, phytate, saponin, and tannin. The highest level of oxalate was found in Zizyphus spinachristi,Zizyphus mauritiana and Balanite aegyptiaca (16.20±2.12%, 15.50±1.50% and 14.50±2.08%, respectively). Phytate was highest in Sclerocarya birrea (3.56±0.54%) and Haematostaphis barteri(3.30±0.10%). B. aegyptiaca, Detarium microcarpum and Parkia biglobosa had the highest saponin values of 16.01±0.02, 12.10±0.05 and 12.23±0.46% respectively. While tannin was highest in B.aegyptiaca (7.40±0.14%), closely followed by Hyphaena thebaica (6.39±0.5%) and Borassus aethiopum (5.90±0.13%). Though these antinutrients can interfere with nutrients utilization when in highconcentration, the values obtained for the fruits analysed were not up to the toxic levels of the antinutrients. Fruits such as Vittaleria paradoxum, Adansonia digitata, Diospyros mespiliformis Phoenixdactylifera and young shoot of Bor. aethiopum are highly recommended for consumption as they contain low amount of the antinutrients analysed
Effect of sodium selenite on sub-acute paraquat-induced toxicity in male rats
Acute paraquat (PQ) toxicity induces redox cycling leading to fatality in both man and animals with clinical management being supportive therapy due to lack of specific and effective antidote. This study thus aimed at determining the sero-biochemical and pathological changes induced by acute PQ administration in male rats and the mitigating role of sodium selenite. Forty male rats were used for the study and were grouped into 5 of eight rats viz: Group I (control) administered distilled water (2 ml/kg), group II (15 mg/kg of PQ), group III (15 mg/kg of PQ + 0.3 mg/kg sodium selenite), group IV (30 mg/kg of PQ) and group V (30 mg/kg of PQ + 0.3 mg/kg sodium selenite). Administration were achieved per os and lasted for a week. Sera, lungs, liver and kidney samples were harvested at the end of the experiment. Result showed a significant (p < 0.05) higher liver enzymes, urea and creatinine in treated groups when compared to control. Biomarkers of oxidative stress revealed a significant (p < 0.05) increased superoxide dismutase and malondealdehyde activities of the lungs and liver. A dose-dependent pathologic lesion was also observed with milder lesions in selenium supplemented groups. The results demonstrate that selenium supplementation may be a promising therapy and should further be clinically validated
Studies on Serum Haemolytic Complement and Haematological Parameters in Apparently Healthy Dromedary Camels (Camelus Dromedarius) in Northern Nigeria
Studies on serum haemolytic compliment and haematological parameters in 330 apparently healthy dromedary camels (Camelus dromedarius) were conducted in northern, Nigeria. The survey was conducted in the abattoirs of three major northern cities of Maiduguri, Kano and Sokoto. The parameters measured using standard procedures were complement level via the classicalpathway (CH ), packed cell volume (PCV), red blood cell 50 (RBC) and white blood cell counts (WBC). Mean CH units in 50 the camels investigated was 360 ± 15.8. In addition, PCV 12 (32.9 ± 1.5), total RBC (10.2 x 10 /L ± 1.2) and WBC (7.2 x 109 ± 1.3) values were obtained. There was no significant(p>0.05) differences between sexes and ages in all the parameters studied. The result obtained can be used as preliminary data in the investigation of the role of complement and blood cells in some immune mediated parasitic, bacterial and viral diseases of the dromedary camel in the study area
Two decades of neuroscience publication trends in Africa.
Neuroscience research in Africa remains sparse. Devising new policies to boost Africa's neuroscience landscape is imperative, but these must be based on accurate data on research outputs which is largely lacking. Such data must reflect the heterogeneity of research environments across the continent's 54 countries. Here, we analyse neuroscience publications affiliated with African institutions between 1996 and 2017. Of 12,326 PubMed indexed publications, 5,219 show clear evidence that the work was performed in Africa and led by African-based researchers - on average ~5 per country and year. From here, we extract information on journals and citations, funding, international coauthorships and techniques used. For reference, we also extract the same metrics from 220 randomly selected publications each from the UK, USA, Australia, Japan and Brazil. Our dataset provides insights into the current state of African neuroscience research in a global context
Natural multi-occurrence of mycotoxins in rice from Niger State, Nigeria
Twenty-one rice samples from field (ten), store (six) and market (five) from the traditional rice-growing areas of Niger State, Nigeria were analysed for aflatoxins (AFs), ochratoxin A (OTA), zearalenone (ZEA), deoxynivalenol (DON), fumonisin B1 (FB1) and B2 (FB2), and patulin (PAT) by thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC) respectively. T-2 toxin was determined using TLC only. AFs were detected in all samples, at total AF concentrations of 28–372 μg/kg. OTA was found in 66.7% of the samples, also at high concentrations (134–341 μg/kg) that have to be considered as critical levels in aspects of nephrotoxicity. ZEA (53.4%), DON (23.8), FB1 (14.3%) and FB2 (4.8%) were also found in rice, although at relatively low levels. T-2 toxin was qualitatively detected by TLC in only one sample. Co-contamination with AFs, OTA, and ZEA was very common, and up to five mycotoxins were detected in a single sample. The high AF and OTA levels as found in rice in this study are regarded as unsafe, and multi-occurrences of mycotoxins in the rice samples with possible additive or synergistic toxic effects in consumers raise concern with respect to public health
Voluntary Medical Male Circumcision: Strategies for Meeting the Human Resource Needs of Scale-Up in Southern and Eastern Africa
Kelly Curran and colleagues conducted a program review to identify human resource approaches that are being used to improve voluntary medical male circumcision volume and efficiency, identifying several innovative responses to human resource challenges
Feasibility and validity of telephone triage for adverse events during a voluntary medical male circumcision campaign in Swaziland
SPARC 2018 Internationalisation and collaboration : Salford postgraduate annual research conference book of abstracts
Welcome to the Book of Abstracts for the 2018 SPARC conference. This year we not only celebrate the work of our PGRs but also the launch of our Doctoral School, which makes this year’s conference extra special. Once again we have received a tremendous contribution from our postgraduate research community; with over 100 presenters, the conference truly showcases a vibrant PGR community at Salford. These abstracts provide a taster of the research strengths of their works, and provide delegates with a reference point for networking and initiating critical debate. With such wide-ranging topics being showcased, we encourage you to take up this great opportunity to engage with researchers working in different subject areas from your own. To meet global challenges, high impact research inevitably requires interdisciplinary collaboration. This is recognised by all major research funders. Therefore engaging with the work of others and forging collaborations across subject areas is an essential skill for the next generation of researchers
Population and fertility by age and sex for 195 countries and territories, 1950–2017: a systematic analysis for the Global Burden of Disease Study 2017
© 2018 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license Background: Population estimates underpin demographic and epidemiological research and are used to track progress on numerous international indicators of health and development. To date, internationally available estimates of population and fertility, although useful, have not been produced with transparent and replicable methods and do not use standardised estimates of mortality. We present single-calendar year and single-year of age estimates of fertility and population by sex with standardised and replicable methods. Methods: We estimated population in 195 locations by single year of age and single calendar year from 1950 to 2017 with standardised and replicable methods. We based the estimates on the demographic balancing equation, with inputs of fertility, mortality, population, and migration data. Fertility data came from 7817 location-years of vital registration data, 429 surveys reporting complete birth histories, and 977 surveys and censuses reporting summary birth histories. We estimated age-specific fertility rates (ASFRs; the annual number of livebirths to women of a specified age group per 1000 women in that age group) by use of spatiotemporal Gaussian process regression and used the ASFRs to estimate total fertility rates (TFRs; the average number of children a woman would bear if she survived through the end of the reproductive age span [age 10–54 years] and experienced at each age a particular set of ASFRs observed in the year of interest). Because of sparse data, fertility at ages 10–14 years and 50–54 years was estimated from data on fertility in women aged 15–19 years and 45–49 years, through use of linear regression. Age-specific mortality data came from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2017 estimates. Data on population came from 1257 censuses and 761 population registry location-years and were adjusted for underenumeration and age misreporting with standard demographic methods. Migration was estimated with the GBD Bayesian demographic balancing model, after incorporating information about refugee migration into the model prior. Final population estimates used the cohort-component method of population projection, with inputs of fertility, mortality, and migration data. Population uncertainty was estimated by use of out-of-sample predictive validity testing. With these data, we estimated the trends in population by age and sex and in fertility by age between 1950 and 2017 in 195 countries and territories. Findings: From 1950 to 2017, TFRs decreased by 49·4% (95% uncertainty interval [UI] 46·4–52·0). The TFR decreased from 4·7 livebirths (4·5–4·9) to 2·4 livebirths (2·2–2·5), and the ASFR of mothers aged 10–19 years decreased from 37 livebirths (34–40) to 22 livebirths (19–24) per 1000 women. Despite reductions in the TFR, the global population has been increasing by an average of 83·8 million people per year since 1985. The global population increased by 197·2% (193·3–200·8) since 1950, from 2·6 billion (2·5–2·6) to 7·6 billion (7·4–7·9) people in 2017; much of this increase was in the proportion of the global population in south Asia and sub-Saharan Africa. The global annual rate of population growth increased between 1950 and 1964, when it peaked at 2·0%; this rate then remained nearly constant until 1970 and then decreased to 1·1% in 2017. Population growth rates in the southeast Asia, east Asia, and Oceania GBD super-region decreased from 2·5% in 1963 to 0·7% in 2017, whereas in sub-Saharan Africa, population growth rates were almost at the highest reported levels ever in 2017, when they were at 2·7%. The global average age increased from 26·6 years in 1950 to 32·1 years in 2017, and the proportion of the population that is of working age (age 15–64 years) increased from 59·9% to 65·3%. At the national level, the TFR decreased in all countries and territories between 1950 and 2017; in 2017, TFRs ranged from a low of 1·0 livebirths (95% UI 0·9–1·2) in Cyprus to a high of 7·1 livebirths (6·8–7·4) in Niger. The TFR under age 25 years (TFU25; number of livebirths expected by age 25 years for a hypothetical woman who survived the age group and was exposed to current ASFRs) in 2017 ranged from 0·08 livebirths (0·07–0·09) in South Korea to 2·4 livebirths (2·2–2·6) in Niger, and the TFR over age 30 years (TFO30; number of livebirths expected for a hypothetical woman ageing from 30 to 54 years who survived the age group and was exposed to current ASFRs) ranged from a low of 0·3 livebirths (0·3–0·4) in Puerto Rico to a high of 3·1 livebirths (3·0–3·2) in Niger. TFO30 was higher than TFU25 in 145 countries and territories in 2017. 33 countries had a negative population growth rate from 2010 to 2017, most of which were located in central, eastern, and western Europe, whereas population growth rates of more than 2·0% were seen in 33 of 46 countries in sub-Saharan Africa. In 2017, less than 65% of the national population was of working age in 12 of 34 high-income countries, and less than 50% of the national population was of working age in Mali, Chad, and Niger. Interpretation: Population trends create demographic dividends and headwinds (ie, economic benefits and detriments) that affect national economies and determine national planning needs. Although TFRs are decreasing, the global population continues to grow as mortality declines, with diverse patterns at the national level and across age groups. To our knowledge, this is the first study to provide transparent and replicable estimates of population and fertility, which can be used to inform decision making and to monitor progress. Funding: Bill & Melinda Gates Foundation
The Rotterdam Study: 2012 objectives and design update
The Rotterdam Study is a prospective cohort study ongoing since 1990 in the city of Rotterdam in The Netherlands. The study targets cardiovascular, endocrine, hepatic, neurological, ophthalmic, psychiatric, dermatological, oncological, and respiratory diseases. As of 2008, 14,926 subjects aged 45 years or over comprise the Rotterdam Study cohort. The findings of the Rotterdam Study have been presented in over a 1,000 research articles and reports (see www.erasmus-epidemiology.nl/rotterdamstudy). This article gives the rationale of the study and its design. It also presents a summary of the major findings and an update of the objectives and methods
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