22 research outputs found
Swallowing abnormalities in HIV infected children : an important cause of morbidity
Publication of this article was funded by the Stellenbosch University Open Access Fund.The original publication is available at http://www.biomedcentral.com/bmcpediatrBackground: Swallowing disorders, well recognised in adults, contribute to HIV-infection morbidity. Little data
however is available for HIV-infected children. The purpose of this study is to describe swallowing disorders in a group of HIV-infected children in Africa after the introduction of combined anti-retroviral therapy.
Methods: We describe 25 HIV-infected children referred for possible swallowing disorders. Clinical and
videofluoroscopic assessment of swallowing (VFSS), HIV stage, and respiratory and neurological examination were recorded.
Results: Median age was 8 months (range 2.8-92) and 15 (60%) were male. Fifteen (60%) were referred for
recurrent respiratory complaints, 4 (16%) for poor growth, 4 (16%) for poor feeding and 2 (8%) patients for
respiratory complaints and either poor growth or feeding. Twenty patients (80%) had clinical evidence of
swallowing abnormalities: 11 (44%) in the oral phase, 4 (16%) in the pharyngeal phase, and 5 (25%) in both the oral and pharyngeal phases. Thirteen patients had a videofluoroscopic assessment of which 6 (46%) where abnormal. Abnormalities were detected in the oral phase in 2, in the pharyngeal phase in 3, and in the oral and pharyngeal phase in 1; all of these patients also had evidence of respiratory involvement. Abnormal swallowing occurred in 85% of children with central nervous system disease. CNS disease was due to HIV encephalopathy (8) and miscellaneous central nervous system diseases (5). Three of 4 (75%) patients with thrush had an abnormal oral phase on assessment. No abnormalities of the oesophagus were found.
Conclusions: This report highlights the importance of swallowing disorders in HIV infected children. Most patients have functional rather than structural or mucosal abnormalities. VFSS makes an important contribution to the diagnosis and management of these patients.Stellenbosch University Open Access FundPublishers' versio
Gene-environment and gene-gene interactions of specific MTHFR, MTR and CBS gene variants in relation to homocysteine in a black South Africans
The methylenetetrahydrofolate reductase (MTHFR), cystathione-β-synthase (CBS) and methionine synthase
(MTR) genes interact with each other and the environment. These interactions could influence homocysteine
(Hcy) and diseases contingent thereon. We determined single nucleotide polymorphisms (SNPs) within these
genes, their relationships and interactions with total Hcy concentrations within black South Africans to address
the increased prevalence of diseases associated with Hcy. The MTHFR 677 TT and MTR 2756 AA genotypes
were associated with higher Hcy concentrations (16.6 and 10.1 μmol/L; p b 0.05) compared to subjects harboring
the MTHFR 677 CT/CC and the MTR 2756 AG genotypes (10.5, 9.7 and 9.5 μmol/L, respectively). The investigated
CBS genotypes did not influence Hcy.We demonstrated interactions between the area of residence and the
CBS T833C/844ins68 genotypes (p = 0.005) so that when harboring the wildtype allele, rural subjects had significantly
higher Hcy than their urban counterparts, but when hosting the variant allele the environment made
no difference to Hcy. Between the CBS T833C/844ins68 or G9276A and MTHFR C677T genotypes, there were
two-way interactions (p = 0.003 and = 0.004, respectively), with regard to Hcy. Subjects harboring the
MTHFR 677 TT genotype in combination with the CBS 833 TT/homozygous 844 non-insert or the MTHFR 677
TT genotype in combination with the CBS 9276 GA/GG displayed higher Hcy concentrations.
Therefore, some of the investigated genotypes affected Hcy; residential area changed the way in which the CBS
T833C/844ins68 SNPs influenced Hcy concentrations highlighting the importance of environmental factors;
and gene–gene interactions allude to epistatic effectsSANPAD (South Africa-
Netherlands Research Programme on Alternatives in Development),
South African National Research Foundation (NRF),North-West University
(NWU), Population Health Research Institute (PHRI), Medical Research
Council (MRC) and the NorthWest Province Health Departmen
D4.3 – Initial version of game applications for scenario pilots
This intermediate report provides an overview of the current versions of the RAGE games made using the RAGE assets for the first round of pilot testing and formative evaluation. The document serves as internal communication and discussion in RAGE among game companies and asset developers together with case owners and evaluators. Whilst detailed description of the design of the games, together with their learning outcomes and piloting can be found in D4.2 and D5.1, updates and changes to the designs, game flow and use of assets are included here.This study is part of the RAGE project. The RAGE project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 644187. This publication reflects only the author's view. The European Commission is not responsible for any use that may be made of the information it contains
Pineal Gland from the Cell Culture to Animal Models: A Review
This review demonstrates current literature on pineal gland physiology, pathology, and animal model experiments to concisely explore future needs in research development with respect to pineal gland function and neuro-regenerative properties. The pineal gland plays an integral role in sleep and recovery by promoting physiologic circadian rhythms via production and release of melatonin. Yet, the current literature shows that the pineal gland has neuroprotective effects that modulate both peripheral and central nerve injuries through several direct and indirect mechanisms, such as angiogenesis and induction of growth factors and anti-inflammatory mediators. Animal models have also shown correlations between pineal gland function and metabolic homeostasis. Studies have shown that a functional pineal gland is essential in preventing and slowing the progression of certain diseases such as diabetes, osteoporosis, vertebral osteoarthritis, and neurodegenerative processes. Lastly, the array of cell culturing methods and animal models that can be used to further develop the study of pineal gland function and nervous system injury were reviewed