{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,23]],"date-time":"2026-06-23T22:56:27Z","timestamp":1782255387409,"version":"3.54.5"},"reference-count":50,"publisher":"Oxford University Press (OUP)","issue":"5","license":[{"start":{"date-parts":[[2024,10,25]],"date-time":"2024-10-25T00:00:00Z","timestamp":1729814400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"funder":[{"DOI":"10.13039\/100000065","name":"National Institute of Neurological Disorders and Stroke","doi-asserted-by":"publisher","award":["R01 NS055349"],"award-info":[{"award-number":["R01 NS055349"]}],"id":[{"id":"10.13039\/100000065","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000061","name":"Fogarty International Center","doi-asserted-by":"publisher","award":["D43TW010928"],"award-info":[{"award-number":["D43TW010928"]}],"id":[{"id":"10.13039\/100000061","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000060","name":"National Institute of Allergy and Infectious Diseases","doi-asserted-by":"publisher","award":["T32AI007637"],"award-info":[{"award-number":["T32AI007637"]}],"id":[{"id":"10.13039\/100000060","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,6,2]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:sec>\n                  <jats:title>Background<\/jats:title>\n                  <jats:p>Children with severe malarial anemia (SMA) typically have low in-hospital mortality but have a high risk of postdischarge readmission or death. We hypothesized that the dysregulation of hematopoiesis, vascular growth factors, and endothelial function that occurs in SMA might affect risk of readmission or death.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Methods<\/jats:title>\n                  <jats:p>Plasma was obtained from children 18 months to 12 years old with SMA (n = 145) in Kampala, Uganda on admission, and outcomes were assessed over 12-month follow-up. Admission plasma levels of 10 biomarkers of vascular growth, hematopoiesis, and endothelial function were compared to risk of readmission or death over 12-month follow-up.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>Over 12-month follow-up, 19 of 145 children with SMA were either readmitted or died: 15 children were readmitted (13 with malaria) and 4 children died. In multivariable analyses adjusted for age and sex, elevated plasma levels of platelet-derived growth factor-BB (PDGF-BB) and vascular endothelial growth factor (VEGF) on admission were independently associated with a decreased risk of all-cause readmission or death (adjusted hazard ratios [95% confidence intervals], 0.28 [.16\u2013.51] and 0.19 [.08\u2013.48], respectively) and a decreased risk of readmission due to severe malaria (0.27 [.15\u2013.51] and 0.16 [.05\u2013.47]) but not with risk of uncomplicated malaria (1.01 [.53\u20131.95] and 2.07 [.93\u20134.64]).<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusions<\/jats:title>\n                  <jats:p>In children with severe malarial anemia, elevated plasma levels of PDGF-BB and VEGF, 2 factors that promote angiogenesis, are associated with a decreased risk of readmission or death in the year following admission, primarily driven by a decrease in the risk of recurrent severe malaria.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1093\/infdis\/jiae527","type":"journal-article","created":{"date-parts":[[2024,10,25]],"date-time":"2024-10-25T08:05:27Z","timestamp":1729843527000},"page":"1258-1266","source":"Crossref","is-referenced-by-count":1,"title":["Elevated Levels of PDGF-BB and VEGF Are Associated With a Decreased Risk of Readmission or Death in Children With Severe Malarial Anemia"],"prefix":"10.1093","volume":"231","author":[{"ORCID":"https:\/\/orcid.org\/0009-0007-1565-0806","authenticated-orcid":false,"given":"Mary G","family":"Slaughter","sequence":"first","affiliation":[{"name":"Ryan White Center for Pediatric Infectious Disease and Global Health, Department of Pediatrics, Indiana University School of Medicine , Indianapolis, Indiana 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,","place":["USA"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2459-6526","authenticated-orcid":false,"given":"Ruth","family":"Namazzi","sequence":"additional","affiliation":[{"name":"Department of Paediatrics and Child Health, Makerere University , Kampala ,","place":["Uganda"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3240-2058","authenticated-orcid":false,"given":"Robert O","family":"Opoka","sequence":"additional","affiliation":[{"name":"Department of Pediatrics and Child Health, Aga Khan University Medical College East Africa , Nairobi ,","place":["Kenya"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1634-1411","authenticated-orcid":false,"given":"Chandy C","family":"John","sequence":"additional","affiliation":[{"name":"Ryan White Center for Pediatric Infectious Disease and Global Health, Department of Pediatrics, Indiana 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