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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric nephrology 7 (1993), S. 515-519 
    ISSN: 1432-198X
    Keywords: Haemolytic uraemic syndrome ; Prostacyclin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The role of prostacyclin (PGI2) in the pathogenesis of haemolytic uraemic syndrome (HUS) is controversial. In part, confusion has been caused by failure to distinguish between two main sub-types of the syndrome: extrinsic, diarrhoea-associated HUS (D+ HUS), usually caused by infection with verocytotoxin-producingEscherichia coli orShigella dysenteriae, and the heterogeneous group of non-prodromal forms where intrinsic factors predominate (D− HUS). This paper critically reviews data confined to D+ HUS. Two methods have been used to assess PGI2 synthesis; the generation of PGI2 from endothelium in the presence of HUS plasma in vitro and the measurement of stable metabolites in body fluids. No concensus could be reached with regard to the former. The reported increase of PGI2 stable metabolites in plasma may represent reduced clearance or increased carriage by plasma lipids. Apparent differences between studies of urinary excretion of PGI2 metabolites may reflect the way excretion was expressed. If the metabolite concentration is factored for urinary creatinine, it appears that renal excretion and thus renal synthesis of PGI2 is reduced. However, these are insufficient data on which to attribute the pathogenesis of D+ HUS to disordered PGI2 metabolism.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-198X
    Keywords: Haemolytic uraemic syndrome ; Endothelium ; Soluble vascular cell adhesion molecule-1 ; Soluble intercellular adhesion molecule-1
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Plasma concentrations of soluble vascular cell adhesion molecule-1 (sVCAM-1), E-selectin (sE-selectin) and intercellular adhesion molecule-1 (sICAM-1) were measured by enzyme-linked immunosorbent assay in four groups of children. Group 1 consisted of 20 patients with acute diarrhoea-associated haemolytic uraemic syndrome (D+HUS), the aetiology of HUS being verocytotoxin-producingEscherichia coli infection in each case. Controls consisted of 11 patients who had previously had D+HUS (group 2), 12 with chronic renal failure (group 3) and 8 healthy controls (group 4). When compared with healthy controls, the acute D+HUS group had higher sVCAM-1 (median 1,875 ng/ml, range 1,200–6,450 ng/ml vs. 1,200 ng/ml, range 975–2,125 ng/ml), von Willebrand factor antigen, (1.9 U/ml, range 0.85–5.1 U/ml vs. 0.55 U/ml, range 0.3–1.57 U/ml), white cell count (WBC, 14.5×109/l, range 7.8–43.1 109/l vs. 8.9 109/l, range 5.7–10.8 109/l) and neutrophil count (PMN, 10.1×109/l, range 4.3–26.5 109/l vs. 4.3 109/l, range 3.7–6.6 109/l), allP〈0.005, and sICAM-1 was reduced (230 ng/ml, range 130–340 ng/ml vs. 400 ng/ml, range 260–690 ng/ml),P〈0.05. Within the acute D+HUS group there was a significant correlation between sICAM-1 and PMN (r=0.56,P〈0.01). There was no correlation between any adhesion molecule and plasma creatinine or von Willebrand factor. Comparing the acute HUS group with children with chronic renal failure, WBC (P〈0.001), PMN (P〈0.01) and sVCAM-1 (P〈0.01) were significantly elevated, but there was no difference between the von Willebrand factor (P=0.08) or the sICAM-1 (P〉0.1). sVCAM-1 is elevated and sICAM-1 decreased in acute D+HUS. This pattern of altered adhesion molecule concentration is unlike that in adults with vasculitis and suggests that different endothelial regulatory factors are at play.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-198X
    Keywords: Blood group P1 ; Haemolytic uraemic syndrome ; Verotoxin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Blood group P1 expression was scored by direct agglutination in 32 patients who had previously developed post-enteropathic haemolytic uraemic syndrome (HUS). Sixty-six children of similar ages undergoing venepuncture for other renal disorders acted as controls. The expression of P1 in controls was that expected from the normal caucasian population, 23% being negative. By contrast, there was an excess of HUS patients with weak or absent expression of P1 (χ2 for linear trend 5.45,P〈0.02), and this was particularly evident in those with a poor outcome. Verotoxin (VT), which is associated with HUS, requires the terminal disaccharide of the P1 antigen to bind to cells, and after internalization disrupts the transcription of ribonucleic acid. Mature erythrocytes do not synthesize protein and may be toxin resistant. We postulate that strong expression of P1 antigen may promote the binding of VT to red cells and thus reduce the dose to vulnerable nucleated cleated endothelial cells. P1 positivity may be protective, and P1 negativity a risk factor in HUS.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-5052
    Keywords: Beta diversity ; Bioregions ; Endemism ; Hotspots ; Plant Diversity ; Reserve design
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The Succulent Karoo biome is home to the world's richest succulent flora. It has approximately 1954 endemic plant species, and is the only semi-arid region to qualify as a hotspot of global significance. Despite its importance, only 2% of the biome is currently protected. Based on its flora, the biome can be divided into 12 bioregions, reflecting its high compositional turnover in relation to environmental and geographical gradients. Only three of these bioregions (the Gariep Centre, the Namaqualand Rocky Hills and the Tanqua Karoo) contain National Parks, and three contain large (over 10 000 ha) provincial reserves (the Gariep Centre, the Namaqualand Rocky Hills and the Little Karoo). The current reserve system does little to conserve biodiversity, with only one reserve significantly conserving Red Data Book (RDB) plant diversity. Using a RDB plant species database of 3874 records at a quarter degree scale (QDS = 15′×15′), we used hotspot analyses and iterative reserve selection algorithms to identify possible locations for future reserves. The hotspot analysis and iterative analyses yielded similar results for the top 11 QDS, mainly due to very high local endemism. Also because of the local endemism and the high species turnover within the biome, the real-world iterative algorithm (starting with the seven already reserved QDS) selected a very large total number of QDS (59% of the total in the biome) to conserve all RDB species. As a possible alternative to conservation planning based on QDS, we also assessed priorities at the scale of bioregions, but showed that representation at this geographic level misses important areas defined at a finer scale. We suggest that if the objective is to maximise the retention of RDB species in the landscape (to pre-empt extinction by scheduling the allocation of limited conservation resources), at least the top 5% of QDS (n=11) selected by the iterative procedure, and identified as the core conservation sequence by analysis of endemicity and threat, should be given priority for reservation. Less extensive and, in some cases, less formal conservation action can be applied to QDS later in the sequence, based on species-specific monitoring and action plans. Of the 11 core areas, four fall in a node centred on the Vanrhynsdorp Centre, two fall in a node centred on the Kamiesberg, and the remaining five are isolated. With existing reserves, the core areas capture 50% of the RDB flora in 8% of the biome.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    International journal of anthropology 14 (1999), S. 31-46 
    ISSN: 1824-3096
    Keywords: Total cholesterol ; high density lipoprotein cholesterol ; low density lipoprotein cholesterol ; blood pressure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract This paper examines the distribution and prevalence of risk factors for coronary heart disease in a sample of 165 men and 202 women over 40 years of age who had earlier participated in a coronary prevention trial from a general practice in Cambridge, UK. No significant differences were observed in total cholesterol levels between men and women, and a quarter of the sample had concentrations above 6.5 mmol/l which is 250 mg/dl. There were significant sex differences in a number of risk factors with males having significantly higher prevalence of low high density lipoprotein, systolic and diastolic blood pressures, obesity, and smoking than women. About 8% of men and women were obese (as defined by a body mass index 〉 30), while 47% of men and 35% of women were mildly overweight (body mass index 〉 25). Two or more risk factors for coronary heart disease (high total cholesterol and/or hypertension and/or obesity) were present in 4% and 9% of older men and women respectively. Furthermore, about half the subjects had more than one risk factor for coronary heart disease.
    Type of Medium: Electronic Resource
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