Persistent Identifier
|
doi:10.7910/DVN/I4EYDR |
Publication Date
|
2023-07-21 |
Title
| Replication Data for: Intestinal Disturbances Associated with Mortality of Children with Complicated Severe Malnutrition |
Author
| Wen, BijunUniversity of Toronto and Hospital for Sick Children, Toronto, CanadaORCIDhttps://orcid.org/0000-0001-6278-8188
Farooqui,AmberHospital for Sick Children, Toronto, Canada
Bourdon, CelineHospital for Sick Children, Toronto, Canada
Ngari,Moses M.KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya
Chimwezi, EmmanuelKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya
Thitiri, JohnstoneKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya
Mwalekwa,LauraThe Childhood Acute Illness & Nutrition Network, Nairobi, Kenya
Walson,Judd L.The Childhood Acute Illness & Nutrition Network, Nairobi, Kenya
Voskuijl,WiegerAmsterdam University Medical Centres, Amsterdam, The Netherlands
Berkley, James A.KEMRI-Wellcome Trust Research Programme, Kilifi, KenyaORCIDhttp://orcid.org/0000-0002-1236-849X
Bandsma,Robert H.J.University of Toronto and Hospital for Sick Children, Toronto, CanadaORCIDhttps://orcid.org/0000-0001-6358-4750 |
Point of Contact
|
Use email button above to contact.
Mwango, Lillian (KEMRI-Wellcome Trust Research programme) |
Description
| This is a replication dataset for the manuscript titled: "Replication Data for: Intestinal Disturbances Associated with Mortality of Children with Complicated Severe Malnutrition."
This is data is from a case-control study nested within the F75 intervention trial. By comparing the fecal metabolomic profiles and enteropathy markers between cases (children who died, n=68) and controls (children who were discharged alive, n=68), this study aimed to understand the association between intestinal disturbances wnad mortality among children with severe malnutrition admitted to hospitals in Kenya and Malawi. Targeted fecal metabolomics were performed using nuclear magnetic resonance spectroscopy. A total 68 metabolites were targeted. Four enteropathy markers, myeloperoxidase, calprotectin, alpha-1-antitrypsin, and intestinal fatty acid binding protein were quantified by ELISA. Lyophilization was used to determine water content of fecal samples. |
Subject
| Medicine, Health and Life Sciences |
Keyword
| Severe malnutrition
mortality
enteropathy
metabolomics |
Related Publication
| R. H. J. Bandsma et al., A reduced-carbohydrate and lactose-free formulation for stabilization among hospitalized children with severe acute malnutrition: A double-blind, randomized controlled trial. PLoS medicine 16, e1002747 (2019) doi 10.1371/journal.pmed.1002747 https://doi.org/10.1371/journal.pmed.1002747
Wen et al. Predicting the risk of mortality during hospitalization in sick severely malnourished children using daily evaluation of key clinical warning signs. BMC Medicine 19, 222, 2021. doi 10.1186/s12916-021-02074-6 https://doi.org/10.1186/s12916-021-02074-6
Wen et al. Systemic inflammation and metabolic disturbances underlie inpatient mortality among ill children with severe malnutrition. Science Advances 8(7), 2022. doi 10.1126/sciadv.abj6779 https://doi.org/10.1126/sciadv.abj6779
Gonzales et al. The role of albumin and the extracellular matrix on the pathophysiology of oedema formation in severe malnutrition. EBioMedicine 79:103991, 2022 doi 10.1016/j.ebiom.2022.103991 https://doi.org/10.1016/j.ebiom.2022.103991 |
Depositor
| Wen, Bijun |
Deposit Date
| 2023-07-21 |