Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Reduced production of sulfated glycosaminoglycans occurs in Zambian children with kwashiorkor but not marasmus

Amadi, Beatrice ; Fagbemi, Andrew O ; Kelly, Paul ; Mwiya, Mwiya ; Torrente, Franco ; Salvestrini, Camilla ; Day, Richard ; Golden, Michael H ; Eklund, Erik A LU and Freeze, Hudson H , et al. (2009) In The American journal of clinical nutrition 89(2). p.592-600
Abstract

BACKGROUND: Kwashiorkor, a form of severe malnutrition with high mortality, is characterized by edema and systemic abnormalities. Although extremely common, its pathophysiology remains poorly understood, and its characteristic physical signs are unexplained.

OBJECTIVE: Because kwashiorkor can develop in protein-losing enteropathy, which is caused by a loss of enterocyte heparan sulfate proteoglycan (HSPG), and previous observations suggest abnormal sulfated glycosaminoglycan (GAG) metabolism, we examined whether intestinal GAG and HSPG are abnormal in children with kwashiorkor.

DESIGN: Duodenal biopsy samples collected from Zambian children with marasmus (n = 18), marasmic kwashiorkor (n = 8), and kwashiorkor (n = 15) were... (More)

BACKGROUND: Kwashiorkor, a form of severe malnutrition with high mortality, is characterized by edema and systemic abnormalities. Although extremely common, its pathophysiology remains poorly understood, and its characteristic physical signs are unexplained.

OBJECTIVE: Because kwashiorkor can develop in protein-losing enteropathy, which is caused by a loss of enterocyte heparan sulfate proteoglycan (HSPG), and previous observations suggest abnormal sulfated glycosaminoglycan (GAG) metabolism, we examined whether intestinal GAG and HSPG are abnormal in children with kwashiorkor.

DESIGN: Duodenal biopsy samples collected from Zambian children with marasmus (n = 18), marasmic kwashiorkor (n = 8), and kwashiorkor (n = 15) were examined for expression of HSPG, GAGs, and immunologic markers and compared against reference samples from healthy UK control children. GAG and HSPG expression density and inflammatory cell populations were quantitated by computerized analysis.

RESULTS: The kwashiorkor group was less wasted and had a lower HIV incidence than did the other groups. All duodenal biopsy samples showed inflammation compared with the histologically uninflamed control samples. Biopsy samples from marasmic children had greater inflammation and greater CD3+ and HLA-DR (human leukocyte antigen DR)-positive cell densities than did samples from children with kwashiorkor. Expression of both HSPG and GAGs was similar between marasmic and well-nourished UK children but was markedly lower in children with kwashiorkor in both the epithelium and lamina propria. Although underglycosylated and undersulfated, epithelial syndecan-1 protein was normally expressed in kwashiorkor, which confirmed that abnormalities arise after core protein synthesis.

CONCLUSIONS: Intestinal HSPG loss occurs in kwashiorkor, which may precipitate protein-losing enteropathy to cause edema. If occurring systemically, impaired HSPG expression could cause several previously unexplained features of kwashiorkor. We speculate that a genetic predisposition to reduced HSPG biosynthesis may offer a contrasting selective advantage, by both diminishing protein catabolism during transient undernutrition and protecting against specific infectious diseases.

(Less)
Please use this url to cite or link to this publication:
author
; ; ; ; ; ; ; ; and , et al. (More)
; ; ; ; ; ; ; ; ; and (Less)
publishing date
type
Contribution to journal
publication status
published
keywords
Analysis of Variance, Biomarkers, Case-Control Studies, Duodenum/immunology, Edema/etiology, Female, Glycosaminoglycans/metabolism, HIV Infections/complications, Heparan Sulfate Proteoglycans/metabolism, Humans, Infant, Inflammation/complications, Kwashiorkor/metabolism, Male, Prevalence, Protein-Energy Malnutrition/complications, Protein-Losing Enteropathies/etiology, Zambia/epidemiology
in
The American journal of clinical nutrition
volume
89
issue
2
pages
592 - 600
publisher
Oxford University Press
external identifiers
  • scopus:59649101628
  • pmid:19116330
ISSN
1938-3207
DOI
10.3945/ajcn.2008.27092
language
English
LU publication?
no
id
97e70793-93f1-4525-bbf4-f8643b4f8918
date added to LUP
2021-10-12 00:00:19
date last changed
2024-03-23 11:54:04
@article{97e70793-93f1-4525-bbf4-f8643b4f8918,
  abstract     = {{<p>BACKGROUND: Kwashiorkor, a form of severe malnutrition with high mortality, is characterized by edema and systemic abnormalities. Although extremely common, its pathophysiology remains poorly understood, and its characteristic physical signs are unexplained.</p><p>OBJECTIVE: Because kwashiorkor can develop in protein-losing enteropathy, which is caused by a loss of enterocyte heparan sulfate proteoglycan (HSPG), and previous observations suggest abnormal sulfated glycosaminoglycan (GAG) metabolism, we examined whether intestinal GAG and HSPG are abnormal in children with kwashiorkor.</p><p>DESIGN: Duodenal biopsy samples collected from Zambian children with marasmus (n = 18), marasmic kwashiorkor (n = 8), and kwashiorkor (n = 15) were examined for expression of HSPG, GAGs, and immunologic markers and compared against reference samples from healthy UK control children. GAG and HSPG expression density and inflammatory cell populations were quantitated by computerized analysis.</p><p>RESULTS: The kwashiorkor group was less wasted and had a lower HIV incidence than did the other groups. All duodenal biopsy samples showed inflammation compared with the histologically uninflamed control samples. Biopsy samples from marasmic children had greater inflammation and greater CD3+ and HLA-DR (human leukocyte antigen DR)-positive cell densities than did samples from children with kwashiorkor. Expression of both HSPG and GAGs was similar between marasmic and well-nourished UK children but was markedly lower in children with kwashiorkor in both the epithelium and lamina propria. Although underglycosylated and undersulfated, epithelial syndecan-1 protein was normally expressed in kwashiorkor, which confirmed that abnormalities arise after core protein synthesis.</p><p>CONCLUSIONS: Intestinal HSPG loss occurs in kwashiorkor, which may precipitate protein-losing enteropathy to cause edema. If occurring systemically, impaired HSPG expression could cause several previously unexplained features of kwashiorkor. We speculate that a genetic predisposition to reduced HSPG biosynthesis may offer a contrasting selective advantage, by both diminishing protein catabolism during transient undernutrition and protecting against specific infectious diseases.</p>}},
  author       = {{Amadi, Beatrice and Fagbemi, Andrew O and Kelly, Paul and Mwiya, Mwiya and Torrente, Franco and Salvestrini, Camilla and Day, Richard and Golden, Michael H and Eklund, Erik A and Freeze, Hudson H and Murch, Simon H}},
  issn         = {{1938-3207}},
  keywords     = {{Analysis of Variance; Biomarkers; Case-Control Studies; Duodenum/immunology; Edema/etiology; Female; Glycosaminoglycans/metabolism; HIV Infections/complications; Heparan Sulfate Proteoglycans/metabolism; Humans; Infant; Inflammation/complications; Kwashiorkor/metabolism; Male; Prevalence; Protein-Energy Malnutrition/complications; Protein-Losing Enteropathies/etiology; Zambia/epidemiology}},
  language     = {{eng}},
  number       = {{2}},
  pages        = {{592--600}},
  publisher    = {{Oxford University Press}},
  series       = {{The American journal of clinical nutrition}},
  title        = {{Reduced production of sulfated glycosaminoglycans occurs in Zambian children with kwashiorkor but not marasmus}},
  url          = {{http://dx.doi.org/10.3945/ajcn.2008.27092}},
  doi          = {{10.3945/ajcn.2008.27092}},
  volume       = {{89}},
  year         = {{2009}},
}