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Glycocalyx breakdown is increased in African children with cerebral and uncomplicated falciparum malaria.

Publication ,  Journal Article
Yeo, TW; Bush, PA; Chen, Y; Young, SP; Zhang, H; Millington, DS; Granger, DL; Mwaikambo, ED; Anstey, NM; Weinberg, JB
Published in: FASEB J
December 2019

Cerebral malaria (CM) from Plasmodium falciparum infection is associated with endothelial dysfunction and parasite sequestration. The glycocalyx (GCX), a carbohydrate-rich layer lining the endothelium, is crucial in vascular homeostasis. To evaluate the role of its loss in the pathogenesis of pediatric CM, we measured GCX degradation in Tanzanian children with World Health Organization-defined CM (n = 55), uncomplicated malaria (UM; n = 20), and healthy controls (HCs; n = 25). Urine GCX breakdown products [glycosaminoglycans (GAGs)] were quantified using dimethylmethylene blue (DMMB) and liquid chromatography-tandem mass spectrometry assays. DMMB-GAG and mass spectrometry (MS)-GAG (g/mol creatinine) were increased in CM and UM compared with HCs (P < 0.001), with no differences in DMMB-GAG and MS-GAG between CM and UM children or between those with and without a fatal outcome. In CM survivors, urinary GCX DMMB-GAG normalized by d 3. After adjusting for disease severity, DMMB-GAG was significantly associated with parasitemia [partial correlation coefficient (Pcorr) = 0.34; P = 0.01] and plasma TNF (Pcorr = 0.26; P = 0.04) and inversely with plasma and urine NO oxidation products [Pcorr = -0.31 (P = 0.01) and Pcorr = -0.26 (P = 0.03), respectively]. GCX breakdown is increased in children with falciparum malaria, with similar elevations in CM and UM. Endothelial GCX degradation may impair endothelial NO production, exacerbate adhesion-molecule expression, exposure, and parasite sequestration, and contribute to malaria pathogenesis.-Yeo, T. W., Bush, P. A., Chen, Y., Young, S. P., Zhang, H., Millington, D. S., Granger, D. L., Mwaikambo, E. D., Anstey, N. M., Weinberg, J. B. Glycocalyx breakdown is increased in African children with cerebral and uncomplicated falciparum malaria.

Duke Scholars

Published In

FASEB J

DOI

EISSN

1530-6860

Publication Date

December 2019

Volume

33

Issue

12

Start / End Page

14185 / 14193

Location

United States

Related Subject Headings

  • Tanzania
  • Parasitemia
  • Methylene Blue
  • Male
  • Malaria, Falciparum
  • Malaria, Cerebral
  • Infant
  • Humans
  • Glycosaminoglycans
  • Glycocalyx
 

Citation

APA
Chicago
ICMJE
MLA
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Yeo, T. W., Bush, P. A., Chen, Y., Young, S. P., Zhang, H., Millington, D. S., … Weinberg, J. B. (2019). Glycocalyx breakdown is increased in African children with cerebral and uncomplicated falciparum malaria. FASEB J, 33(12), 14185–14193. https://doi.org/10.1096/fj.201901048RR
Yeo, Tsin W., Peggy A. Bush, Youwei Chen, Sarah P. Young, Haoyue Zhang, David S. Millington, Donald L. Granger, Esther D. Mwaikambo, Nicholas M. Anstey, and J Brice Weinberg. “Glycocalyx breakdown is increased in African children with cerebral and uncomplicated falciparum malaria.FASEB J 33, no. 12 (December 2019): 14185–93. https://doi.org/10.1096/fj.201901048RR.
Yeo TW, Bush PA, Chen Y, Young SP, Zhang H, Millington DS, et al. Glycocalyx breakdown is increased in African children with cerebral and uncomplicated falciparum malaria. FASEB J. 2019 Dec;33(12):14185–93.
Yeo, Tsin W., et al. “Glycocalyx breakdown is increased in African children with cerebral and uncomplicated falciparum malaria.FASEB J, vol. 33, no. 12, Dec. 2019, pp. 14185–93. Pubmed, doi:10.1096/fj.201901048RR.
Yeo TW, Bush PA, Chen Y, Young SP, Zhang H, Millington DS, Granger DL, Mwaikambo ED, Anstey NM, Weinberg JB. Glycocalyx breakdown is increased in African children with cerebral and uncomplicated falciparum malaria. FASEB J. 2019 Dec;33(12):14185–14193.

Published In

FASEB J

DOI

EISSN

1530-6860

Publication Date

December 2019

Volume

33

Issue

12

Start / End Page

14185 / 14193

Location

United States

Related Subject Headings

  • Tanzania
  • Parasitemia
  • Methylene Blue
  • Male
  • Malaria, Falciparum
  • Malaria, Cerebral
  • Infant
  • Humans
  • Glycosaminoglycans
  • Glycocalyx