44 research outputs found
Research priorities for improving infant and young child feeding in humanitarian emergencies
Background
There are many challenges during emergencies to ensure that optimal infant and young child feeding is protected, promoted and supported, but there is a dearth of evidence on strategies and programmes to improve Infant and Young Child Feeding in Emergencies (IYCF-E) and a need to determine research priorities.
Methods
Based on interviews with key informants who are experts in the subject, we developed a list of 48 research questions on IYCF-E. A framework, following the Child Health and Nutrition Research Initiative method to set priorities in child health research, was developed to rank the research questions. Four criteria were applied to create a ranking based on answerability, operational relevance, disease burden reduction and prevention, and originality. Using an on-line survey, prioritisation of research questions was done by 27 people from 14 NGOs, universities and research institutions, and UN organisations.
Results
The top-ten research questions identified focused on the following:
• Use of cash-transfer to buy breast-milk substitutes;
• Effectiveness of complementary feeding strategies;
• Long-term effect of IYCF-E interventions;
• Design of IYCF-E programmes in a context where breastfeeding rates are low and breast milk substitutes use is high;
• Design of effective re-lactation interventions;
• Provision of psychological support to young children’s care-takers;
• Determination of number of beneficiaries and coverage of IYCF-E programmes;
• Pros and cons of distributing ready-to-use infant formula compared with distributing powdered infant formula plus kit for safer use of BMS, when use of infant formula is necessary;
• Assessment of the impact of specific IYCF-E programmes on nutritional status, morbidity and mortality;
• Linking and mainstreaming IYCF-E interventions with other sectors such as health, WASH, food security and child protection.
Conclusion
The questions found by this study could form the basis of future research on IYCF-E and could be integrated into the agenda of relevant stakeholders. Results of studies based on these questions will be fundamental to fill the evidence gap in IYCF-E, improve IYCF-E programming and ultimately contribute to the reduction in morbidity and mortality among infants and young children in humanitarian emergencies
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A20 Modulates Lipid Metabolism and Energy Production to Promote Liver Regeneration
Background: Liver Regeneration is clinically of major importance in the setting of liver injury, resection or transplantation. We have demonstrated that the NF-B inhibitory protein A20 significantly improves recovery of liver function and mass following extended liver resection (LR) in mice. In this study, we explored the Systems Biology modulated by A20 following extended LR in mice. Methodology and Principal Findings: We performed transcriptional profiling using Affymetrix-Mouse 430.2 arrays on liver mRNA retrieved from recombinant adenovirus A20 (rAd.A20) and rAd.galactosidase treated livers, before and 24 hours after 78% LR. A20 overexpression impacted 1595 genes that were enriched for biological processes related to inflammatory and immune responses, cellular proliferation, energy production, oxidoreductase activity, and lipid and fatty acid metabolism. These pathways were modulated by A20 in a manner that favored decreased inflammation, heightened proliferation, and optimized metabolic control and energy production. Promoter analysis identified several transcriptional factors that implemented the effects of A20, including NF-B, CEBPA, OCT-1, OCT-4 and EGR1. Interactive scale-free network analysis captured the key genes that delivered the specific functions of A20. Most of these genes were affected at basal level and after resection. We validated a number of A20's target genes by real-time PCR, including p21, the mitochondrial solute carriers SLC25a10 and SLC25a13, and the fatty acid metabolism regulator, peroxisome proliferator activated receptor alpha. This resulted in greater energy production in A20-expressing livers following LR, as demonstrated by increased enzymatic activity of cytochrome c oxidase, or mitochondrial complex IV. Conclusion: This Systems Biology-based analysis unravels novel mechanisms supporting the pro-regenerative function of A20 in the liver, by optimizing energy production through improved lipid/fatty acid metabolism, and down-regulated inflammation. These findings support pursuit of A20-based therapies to improve patients' outcomes in the context of extreme liver injury and extensive LR for tumor treatment or donation
Community Perceptions of Bloody Diarrhoea in an Urban Slum in South Asia: Implications for Introduction of a Shigella Vaccine
Understanding local perceptions of disease causation could help public health officials improve strategies to prevent bloody diarrhoea. A cross-sectional survey was conducted in Dhaka, Bangladesh to elicit community beliefs about the causes of and prevention strategies for bloody diarrhoea. Between March and June 2003, we interviewed 541 randomly selected respondents. Overall, 507 (93%) respondents perceived that a vaccine could prevent bloody diarrhoea. If a vaccine provided lifetime protection, 445 (83%) respondents stated that they would opt to get the vaccine and would pay a median of 0·01-0·15) for it, equivalent to \u3c1% of their median weekly income. There was almost universal perception that an effective vaccine to prevent bloody diarrhoea was highly beneficial and acceptable. While respondents valued a vaccine for prevention of bloody diarrhoea, they were only willing to pay minimally for it. Therefore, achieving a high rate of Shigella vaccine coverage may require subsidy of vaccine purchase
Informing Building Strategies to Reduce Infectious Aerosol Transmission Risk by Integrating DNA Aerosol Tracers with Quantitative Microbial Risk Assessment
Using aerosol-based tracers to estimate
risk of infectious aerosol
transmission aids in the design of buildings with adequate protection
against aerosol transmissible pathogens, such as SARS-CoV-2 and influenza.
We propose a method for scaling a SARS-CoV-2 bulk aerosol quantitative
microbial risk assessment (QMRA) model for impulse emissions, coughing
or sneezing, with aerosolized synthetic DNA tracer concentration measurements.
With point-of-emission ratios describing relationships between tracer
and respiratory aerosol emission characteristics (i.e., volume and
RNA or DNA concentrations) and accounting for aerosolized pathogen
loss of infectivity over time, we scale the inhaled pathogen dose
and risk of infection with time-integrated tracer concentrations measured
with a filter sampler. This tracer-scaled QMRA model is evaluated
through scenario testing, comparing the impact of ventilation, occupancy,
masking, and layering interventions on infection risk. We apply the
tracer-scaled QMRA model to measurement data from an ambulatory care
room to estimate the risk reduction resulting from HEPA air cleaner
operation. Using DNA tracer measurements to scale a bulk aerosol QMRA
model is a relatively simple method of estimating risk in buildings
and can be applied to understand the impact of risk mitigation efforts