Summary of Study ST000877

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR000608. The data can be accessed directly via it's Project DOI: 10.21228/M83105 This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST000877
Study TitleMicronutrient deficiencies, environmental exposures and severe malaria: Risk factors for adverse neurodevelopmental outcomes in Ugandan children
Study TypeUntargeted high-resolution mass spectrometry profiling
Study SummaryMicronutrient deficiencies and environmental exposures have been to known to adversely impact brain and nervous system functions in adults and children worldwide. However, few studies have examined the short and long-term impact of these risk factors on neurodevelopmental outcomes in children in low-income countries, where the effects are likely to be more pronounced due to limited resources for monitoring and insufficient regulations. Biological risk factors of relevance include micronutrient deficiencies such as zinc and exposure to heavy metals such as lead and mercury. Studies have suggested an association between neurodevelopmental impairment and micronutrient deficiency as well as exposure to a number of heavy metals and environmental toxins. Moreover, findings also suggest that risk factors for adverse developmental outcomes that are independently significant may have the potential for causing cumulative increases in adverse effects. In Sub-Saharan Africa, severe malaria is a leading risk factor for long-term neurocognitive impairment in children. Zinc deficiency or exposure to heavy metals could influence risk of severe malaria, modify the risk of neurocognitive impairment in children with severe malaria, or independently affect risk of neurocognitive impairment. Untargeted analyses for potential environmental exposures or metabolomic changes in children with cerebral malaria vs. without cognitive impairment or in children with higher vs. lower cognitive scores, could also identify new risk factors for neurodevelopmental impairment in Ugandan children with cerebral malaria.In our completed study in Kampala, we assessed neurologic and developmental impairment in children with cerebral malaria [CM] or severe malarial anemia [SMA], as compared to health community children from the same extended household as the children with CM or SMA. As an extension of this study, we are interested in determining levels of micronutrients such as zinc in the population, and in addition, determining exposure levels of heavy metals (lead, mercury, copper, manganese etc.) in samples collected from children with severe malaria and community controls. The primary hypotheses of this study is that nutrient deficiencies or exposure to heavy metals influence short and long term neurocognitive outcomes in healthy community children and in children with severe malaria, and that children with cerebral malaria have specific metabolomic changes that relate to long-term neurocognitive impairment. The specific aims of our study are:Aim 1: To determine levels of zinc, heavy metals, and biomarkers associated with inflammation in children presenting with different forms of severe malaria (SM) and in healthy community children (CC). The working hypothesis of this aim is that 1) children with SM will have lower zinc levels compared to CC; 2) children with SM will present with higher toxic metal exposure and higher levels of biomarkers associated with inflammation than CC.Aim 2: To investigate how micronutrient deficiency, toxic metal exposure and inflammatory biomarkers affect short and long term neurodevelopmental outcomes and growth in children with severe malaria and community children (CC).The working hypothesis of this aim is that the lower levels of zinc, and presence of toxic metals in high concentrations will independently contribute to worsening neurodevelopmental outcomes and worsening growth over time in children with severe malaria and in community children. An alternate hypothesis is that micronutrient deficiency, toxic metal exposure and inflammatory states may interact with each other and with severe malaria to produce greater neurodevelopmental impairment, i.e., that the contribution is not independent but interactive.Aim 3: To determine whether the CSF metabolome differs according to level of neurodevelopmental impairment in children with cerebral malaria. The working hypothesis of this aim is that neurodevelopmental impairment in children with cerebral malaria is associated with changes in the CSF metabolome.
Institute
Emory University
DepartmentSchool of Medicine, Division of Pulmonary, Allergy, Critical Care Medicine
LaboratoryClincal Biomarkers Laboratory
Last NameWalker
First NameDouglas
Address615 Michael St. Ste 225, Atlanta, GA, 30322, USA
Emaildouglas.walker@emory.edu
Phone(404) 727 5984
Submit Date2017-09-27
Total Subjects141
Study CommentsCSF pools from elderly individuals included for QA/QC. Study specific pools were not created due to limited sample volumes provided (<100uL).
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Chear StudyYes
Analysis Type DetailLC-MS
Release Date2021-08-31
Release Version1
Douglas Walker Douglas Walker
https://dx.doi.org/10.21228/M83105
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Factors:

Subject type: Cerebrospinal Fluid; Subject species: Homo sapiens (Factor headings shown in green)

mb_sample_id local_sample_id Sample Type
SA050837chearplasma_2cCHEAR Plasma
SA050838chearplasma_3aCHEAR Plasma
SA050839chearplasma_2bCHEAR Plasma
SA050840chearplasma_2aCHEAR Plasma
SA050841chearplasma_1dCHEAR Plasma
SA050842chearplasma_3bCHEAR Plasma
SA050843chearplasma_3dCHEAR Plasma
SA050844chearplasma_4cCHEAR Plasma
SA050845chearplasma_4dCHEAR Plasma
SA050846chearplasma_4bCHEAR Plasma
SA050847chearplasma_4aCHEAR Plasma
SA050848chearplasma_1cCHEAR Plasma
SA050849chearplasma_3cCHEAR Plasma
SA050850chearplasma_2dCHEAR Plasma
SA050851chearplasma_1aCHEAR Plasma
SA050852chearplasma_1bCHEAR Plasma
SA050853csfpool_4dCSF Pool
SA050854csfpool_4cCSF Pool
SA050855csfpool_2eCSF Pool
SA050856csfpool_4aCSF Pool
SA050857csfpool_3cCSF Pool
SA050858csfpool_2fCSF Pool
SA050859csfpool_1eCSF Pool
SA050860csfpool_2aCSF Pool
SA050861csfpool_2bCSF Pool
SA050862csfpool_1fCSF Pool
SA050863csfpool_1aCSF Pool
SA050864csfpool_3dCSF Pool
SA050865csfpool_4bCSF Pool
SA050866csfpool_2cCSF Pool
SA050867csfpool_1bCSF Pool
SA050868csfpool_3fCSF Pool
SA050869csfpool_3eCSF Pool
SA050870csfpool_4fCSF Pool
SA050871csfpool_4eCSF Pool
SA050872csfpool_1dCSF Pool
SA050873csfpool_1cCSF Pool
SA050874csfpool_3bCSF Pool
SA050875csfpool_3aCSF Pool
SA050876csfpool_2dCSF Pool
SA050877C-XBVS6-CF-00CSF Study Sample
SA050878C-XBXF3-CF-00CSF Study Sample
SA050879C-XCU28-CF-00CSF Study Sample
SA050880C-X7R50-CF-00CSF Study Sample
SA050881C-XB7F6-CF-00CSF Study Sample
SA050882C-XA7K7-CF-00CSF Study Sample
SA050883C-XAKS9-CF-00CSF Study Sample
SA050884C-XA870-CF-00CSF Study Sample
SA050885C-X7WK7-CF-00CSF Study Sample
SA050886C-XLGH4-CF-00CSF Study Sample
SA050887C-XR6V7-CF-00CSF Study Sample
SA050888C-XR6R6-CF-00CSF Study Sample
SA050889C-XQQ05-CF-00CSF Study Sample
SA050890C-XS193-CF-00CSF Study Sample
SA050891C-XSRV6-CF-00CSF Study Sample
SA050892C-XUWS3-CF-00CSF Study Sample
SA050893C-XUJF5-CF-00CSF Study Sample
SA050894C-XTRX9-CF-00CSF Study Sample
SA050895C-XPYG9-CF-00CSF Study Sample
SA050896C-XP6C3-CF-00CSF Study Sample
SA050897C-XGTT5-CF-00CSF Study Sample
SA050898C-XEA72-CF-00CSF Study Sample
SA050899C-XDCN1-CF-00CSF Study Sample
SA050900C-XHD99-CF-00CSF Study Sample
SA050901C-XKRU6-CF-00CSF Study Sample
SA050902C-XM3V1-CF-00CSF Study Sample
SA050903C-XM0D3-CF-00CSF Study Sample
SA050904C-X7AU7-CF-00CSF Study Sample
SA050905C-XCVE5-CF-00CSF Study Sample
SA050906C-X70K6-CF-00CSF Study Sample
SA050907C-WXAL5-CF-00CSF Study Sample
SA050908C-WX0F5-CF-00CSF Study Sample
SA050909C-WWY21-CF-00CSF Study Sample
SA050910C-WXGE4-CF-00CSF Study Sample
SA050911C-WXJQ5-CF-00CSF Study Sample
SA050912C-X0LF4-CF-00CSF Study Sample
SA050913C-WYEH8-CF-00CSF Study Sample
SA050914C-WXNN7-CF-00CSF Study Sample
SA050915C-WW0Q4-CF-00CSF Study Sample
SA050916C-WV7M8-CF-00CSF Study Sample
SA050917C-WRW40-CF-00CSF Study Sample
SA050918C-WQZA0-CF-00CSF Study Sample
SA050919C-WPSW1-CF-00CSF Study Sample
SA050920C-WRZP5-CF-00CSF Study Sample
SA050921C-WSMA8-CF-00CSF Study Sample
SA050922C-WUS96-CF-00CSF Study Sample
SA050923C-WTKE9-CF-00CSF Study Sample
SA050924C-X0RN0-CF-00CSF Study Sample
SA050925C-X1BV7-CF-00CSF Study Sample
SA050926C-X6NS0-CF-00CSF Study Sample
SA050927C-X66K2-CF-00CSF Study Sample
SA050928C-X65W7-CF-00CSF Study Sample
SA050929C-X6UX2-CF-00CSF Study Sample
SA050930C-XUXR5-CF-00CSF Study Sample
SA050931C-Z6TH7-CF-00CSF Study Sample
SA050932C-Z9710-CF-00CSF Study Sample
SA050933C-X5XU8-CF-00CSF Study Sample
SA050934C-X5P15-CF-00CSF Study Sample
SA050935C-X2G11-CF-00CSF Study Sample
SA050936C-X2C64-CF-00CSF Study Sample
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