Fischer, N, Darmstadt, GL, Shahunja, K, Crowther, JM, Kendall, L, Gibson, RA, Ahmed, T and Relman, DA. 2021. Dataset and R code for article "Topical emollient therapy with sunflower seed oil alters the skin microbiota of young children with severe acute malnutrition in Bangladesh: a randomised, controlled study". [Online]. Stanford Digital Repository. Available from: https://purl.stanford.edu/dk954yp6586
Fischer, N, Darmstadt, GL, Shahunja, K, Crowther, JM, Kendall, L, Gibson, RA, Ahmed, T and Relman, DA. Dataset and R code for article "Topical emollient therapy with sunflower seed oil alters the skin microbiota of young children with severe acute malnutrition in Bangladesh: a randomised, controlled study" [Internet]. Stanford Digital Repository; 2021. Available from: https://purl.stanford.edu/dk954yp6586
Fischer, N, Darmstadt, GL, Shahunja, K, Crowther, JM, Kendall, L, Gibson, RA, Ahmed, T and Relman, DA (2021). Dataset and R code for article "Topical emollient therapy with sunflower seed oil alters the skin microbiota of young children with severe acute malnutrition in Bangladesh: a randomised, controlled study". [Data Collection]. Stanford Digital Repository. https://purl.stanford.edu/dk954yp6586
Description
A detailed description of the data analysis, along with all analysis code and raw data used to go from sequences to final results and figures.
Keywords
| Description of data capture | Background: Topical emollient therapy with sunflower seed oil (SSO) reduces risk of sepsis and mortality in very preterm infants in low- or middle-income countries (LMICs). Proposed mechanisms include modulation of skin and possibly gut barrier function. The skin and gut microbiota play important roles in regulating barrier function, but the effects of emollient therapy on these micro-biotas are poorly understood. Methods: We characterised microbiota structure and diversity with 16S rRNA gene amplicon sequence data and ecological statistics in 20 children with severe acute malnutrition (SAM) aged 2-24 months, at four skin sites and in stool, during a randomised, controlled trial of emollient therapy with SSO in Bangladesh. Microbes associated with therapy were identified with tree-based sparse discriminant analysis. Results: The skin microbiota of Bangladeshi children with SAM was highly di-verse and displayed significant variation in structure as a function of physical distance between sites. Microbiota structure differed between the study groups (P = 0.005), was more diverse in emollient-treated subjects–including on the forehead which did not receive direct treatment–and changed with each day (P = 0.005) at all skin sites. Overall, Prevotellaceae were the most differentially affected by emollient treatment; several genera within this family became more abundant in the emollient group than in the controls across several skin sites. Gut microbiota structure was associated with sample day (P = 0.045) and subject age (P = 0.045), but was not significantly affected by emollient treatment (P = 0.060). Conclusions: Emollient therapy altered the skin microbiota in a consistent and temporally coherent manner. We speculate that therapy with SSO enhances skin barrier function in part through alterations in the microbiota, and through systemic mechanisms. Strategies to strengthen skin and gut barrier function in populations at risk, such as children in LMICs like Bangladesh, might include deliberate manipulation of their skin microbiota. Trial registration ClinicalTrials.gov: NCT02616289. |
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| Data capture method | Unknown |
| Date (Published in a 3rd party system) | 25 November 2021 |
| Language(s) of written materials | English |
| Data Creators | Fischer, N, Darmstadt, GL, Shahunja, K, Crowther, JM, Kendall, L, Gibson, RA, Ahmed, T and Relman, DA |
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| LSHTM Faculty/Department | Faculty of Epidemiology and Population Health > Dept of Infectious Disease Epidemiology (-2023) |
| Participating Institutions | Stanford University School of Medicine, Stanford, California, United States, International Centre for Diarrhoeal Disease Research Bangladesh, Dhaka, Bangladesh, JMC Scientific Consulting Ltd, Egham, Surrey, United Kingdom, GlaxoSmithKline R&D, Global Health Catalyst, Stevenage, United Kingdom, Veterans Affairs Palo Alto Health Care System 154T, Palo Alto, California, United States |
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| Date Deposited | 25 Jan 2024 12:45 |
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| Last Modified | 25 Jan 2024 12:45 |
| Publisher | Stanford Digital Repository |
