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1. |
Editorial |
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Clinical Chemistry and Laboratory Medicine,
Volume 36,
Issue 1,
1998,
Page 1-1
Gérard Siest,
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ISSN:1434-6621
DOI:10.1515/CCLM.1998.001
出版商:Walter de Gruyter
年代:1998
数据来源: Degruyter
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2. |
Predictive Medicine |
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Clinical Chemistry and Laboratory Medicine,
Volume 36,
Issue 1,
1998,
Page 3-3
Jean Dausset,
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ISSN:1434-6621
DOI:10.1515/CCLM.1998.002
出版商:Walter de Gruyter
年代:1998
数据来源: Degruyter
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3. |
Standardization and Clinical Management of Lipoprotein(a) Measurements |
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Clinical Chemistry and Laboratory Medicine,
Volume 36,
Issue 1,
1998,
Page 5-16
Giuseppe Lippi,
Giancesare Guidi,
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摘要:
AbstractThe present article proposes personal suggestions to improve determinations and clinical interpretation of results of lipoprotein(a) assays. Methods and procedures for sampling and quantification of the various isoforms of lipoprotein(a) in serum, plasma and urine are reviewed with the aim of improving the reliability and reproducibility of results and reinforcing the clinical utility of lipoprotein(a) measurements.
ISSN:1434-6621
DOI:10.1515/CCLM.1998.003
出版商:Walter de Gruyter
年代:1998
数据来源: Degruyter
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4. |
Evaluation of the Iron Status of the Newborn by Soluble Transferrin Receptors in Serum |
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Clinical Chemistry and Laboratory Medicine,
Volume 36,
Issue 1,
1998,
Page 17-22
Kramer Kuiper,
Wim Baerts,
Reinout Bakker,
Jim van Eyck,
Jan van Raan,
Henk G. van Eijk,
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摘要:
AbstractThe concentration of soluble transferrin receptors in serum has proven to be a reliable predictor of iron status in adults. Its high sensitivity for iron deficiency combined with a small sample size (10 μl) makes it an interesting parameter for the assessment of iron stores in newborn infants.In the present study we investigated the usefulness of the concentration of soluble transferrin receptors in serum in the assessment of iron metabolism in the newborn. Infants born after an uncomplicated labour were compared to infants in the intensive care unit. The concentration of soluble transferrin receptors in serum was found to be elevated compared to normal adults and independently of iron metabolism. The concentration of soluble transferrin receptors did not correlate with serum iron and ferritin concentrations. In contrast to what was found in other studies, no relationship could be demonstrated between soluble transferrin receptors and birth weight or gestational age. The results of this study have shown that care has to be taken in the interpretation of the concentration of soluble transferrin receptors in serum in newborn infants. It seems to be a parameter which is independent of iron metabolism at least during the first days of life.
ISSN:1434-6621
DOI:10.1515/CCLM.1998.004
出版商:Walter de Gruyter
年代:1998
数据来源: Degruyter
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5. |
Quantitation of IgG and IgM Human Anti-Mouse Antibodies (HAMA) Interference in CA 125 Measurements Using Affinity Chromatography |
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Clinical Chemistry and Laboratory Medicine,
Volume 36,
Issue 1,
1998,
Page 23-28
Norbert P. Koper,
Chris M. G. Thomas,
Leon F. A. G. Massuger,
Martin F. G. Segers,
André J. Olthaar,
André L. M. Verbeek,
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摘要:
AbstractCurrently no available immunoassay system offers complete protection against spuriously elevated or lowered results due to interference by Human Anti-Mouse Antibodies (HAMA). Although routine use of chromatography procedures is not an acceptable option because of the extra cost and workload involved, such a procedure would be highly desirable to ensure accurate immunoassay results. The present report describes a relatively simple affinity chromatography procedure using a HiTrap Protein G column to isolate immunoglobulin G (IgG) HAMA, followed by a HiTrap N-hydroxy-succinimide(NHS)-activated column coupled to goat-anti human immunoglobulin M (IgM) to bind IgM HAMA. To examine the usefulness of this purification procedure we determined CA 125 in forty serum samples prior to and following chromatography. Pre- and post-injection samples were obtained from 20 patients injected with 1 mg of 111In-Iabelled murine OC 125 F(ab′)2fragments in an immunoscintigraphy study.It is shown that this analytical procedure provides a technique to determine the extent and the nature of the existing HAMA interference in samples of patients afterin vivouse of monoclonal antibodies for diagnostic or therapeutic purposes. The procedure can also contribute to the clarification of clinically discordant CA 125 results. Finally, the availability of such a procedure in the clinical laboratory provides an opportunity to test the robustness of newly developed immunoassay systems towards HAMA interference.
ISSN:1434-6621
DOI:10.1515/CCLM.1998.005
出版商:Walter de Gruyter
年代:1998
数据来源: Degruyter
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6. |
Neopterin Plasma Concentrations Predict the Course of Severe Acute Pancreatitis |
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Clinical Chemistry and Laboratory Medicine,
Volume 36,
Issue 1,
1998,
Page 29-34
Peter Kaufmann,
Gernot P. Tilz,
Ulrike Demel,
Helmut Wachter,
Günter J. Kreijs,
Dietmar Fuchs,
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摘要:
AbstractIn a prospective, descriptive study in 25 patients with acute pancreatitis neopterin plasma concentrations were found to be associated with the severity of the disease, which was assessed using weights of the worst 17 physiological abnormalities of the APACHE-III score over a 24 h period after hospital admission. Neopterin concentrations were higher in severe pancreatitis (n = 10) compared to mild disease, and there existed a positive exponential correlation between neopterin and the Acute Physiology Score (r = 0.66). Higher neopterin concentrations were associated with the development of multiple organ failure (p = 0.012) and death (p = 0.019). At a cut-off concentration of 12 nmol/l the sensitivity (80 %) and specificity (100 %) of neopterin for the discrimination between mild and severe clinical course of pancreatitis was more accurate than C-reactive protein at a risk threshold of 1.2 g/l (70 % and 87 %). Development of pancreatic necrosis was associated with higher neopterin concentrations than edematous pancreatitis (p<0.001).
ISSN:1434-6621
DOI:10.1515/CCLM.1998.006
出版商:Walter de Gruyter
年代:1998
数据来源: Degruyter
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7. |
Objectives, Design and Recruitment of a Familial and Longitudinal Cohort for Studying Gene-Environment Interactions in the Field of Cardiovascular Risk: The Stanislas Cohort |
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Clinical Chemistry and Laboratory Medicine,
Volume 36,
Issue 1,
1998,
Page 35-42
Gérard Siest,
Sophie Visvikis,
Bernard Herbeth,
René Gueguen,
Viry Vincent,
Catherine Sass,
Brigitte Beaud,
Edith Lecomte,
Josiane Steinmetz,
Jean Locuty,
Philippe Chevrier,
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摘要:
AbstractThe main objective of the Stanislas cohort is to study the role and the contribution of genetic and environmental factors to cardiovascular status. We plan:a)to describe the degree of association of a large number of cardiovascular risk indicators with cardiovascular endpoints,b)to evaluate the contribution of genetic and that of environmental factors to this association,c)to follow the evolution of these risk indicators during a period of at least ten years,d)to search for the determinants influencing this evolution.The principal variables studied are:a)to describe the degree of association of a large number of cardiovascular risk indicators with cardiovascular endpoints,b)to evaluate the contribution of genetic and that of environmental factors to this association,c)to follow the evolution of these risk indicators during a period of at least ten years,d)to search for the determinants influencing this evolution.a)blood pressure, cardiac mass, and wall thickness of carotid and femoral arteries,b)obesity and fat mass,c)indicators of lipid metabolism,d)genetic polymorphisms of several cardiovascular risk candidate genes,e)food, tobacco and alcohol consumption,f)consumption of drugs and anti-oxidant vitamins.Between September 1993 and August 1995, 1006 families consisting of the two biological parents with at least two children were recruited totalling 4295 individuals. This cohort will be followed up until 2004. There will be two health examinations five and ten years after the initial examination. A bank of blood samples (serum and plasma) in liquid nitrogen and DNA (−80 °C) has been established.
ISSN:1434-6621
DOI:10.1515/CCLM.1998.007
出版商:Walter de Gruyter
年代:1998
数据来源: Degruyter
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8. |
Total Carbon Dioxide Measured by the Vitros Enzymatic Method |
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Clinical Chemistry and Laboratory Medicine,
Volume 36,
Issue 1,
1998,
Page 43-46
Annarita Frezzotti,
Anna Maria Margarucci Gambini,
Gilberto Coppa,
Giuseppina De Sio,
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摘要:
AbstractWe evaluated the performance of an enzymatic method using dry chemistry for serum total carbon dioxide (tCO2) determination using a Vitros 500 analyser. Imprecision results were acceptable and the linearity was verified for concentrations within a range of 5.5–39.2 mmol/l, i.e. ymeasured= 0.93 xcalculated+1.32, r = 0.99. The Vitros tCO2method was unaffected by haemoglobin at all concentrations tested. Significant interference was caused by bilirubin at concentrations higher than 30 μmol/l; the addition of bilirubin lowered the apparent values for tCO2dose-dependently. Serum tCO2results were practically the same as those for plasma. The reference interval for venous tCO2concentrations in a healthy population was: 22.4–34.2 mmol/l (mean: 28.3 mmol/l). Comparison of venous serum tCO2results assayed using the Vitros method with bicarbonate (HCO3−) values calculated by blood gas determination of pCO2and pH in arterial blood samples gave poor agreement, r = 0.58. The data revealed a mean difference of 5.48 ± 3.09 mmol/l between the tCO2measurements and calculated bicarbonate. This was statistically (p = 0.01) and clinically significant. We conclude that the Vitros method provides reliable tCO2results in venous serum but this method must not be used as an interchangeable alternative to calculated arterial bicarbonate in order to avoid confusion, misinterpretation of results and erroneous therapeutic decisions.
ISSN:1434-6621
DOI:10.1515/CCLM.1998.008
出版商:Walter de Gruyter
年代:1998
数据来源: Degruyter
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9. |
Evaluation of Glucocard Memory 2 and Accutrend®Sensor Blood Glucose Meters |
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Clinical Chemistry and Laboratory Medicine,
Volume 36,
Issue 1,
1998,
Page 47-52
Sofie Arens,
Veronique Moons,
Paul Meuleman,
Frank Struyf,
Zahur Zaman,
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摘要:
AbstractThe performance and practicability of 2 blood glucose meters (Glucocard Memory 2 and Accutrendr sensor) were evaluated. Both glucose meters produced acceptably precise results in the hyper- and normoglycaemic concentration ranges. In the hypoglycaemic concentration range, the imprecision of Accutrend®sensor was much higher than recommended by the American Diabetes Association. Within-run coefficients of variation for Glucocard Memory 2 were 6.3 %, 3.9 % and 2.4 % at glucose concentrations of 1.7 mmol/l, 5.8 mmol/l and 11.7 mmol/l, respectively; for Accutrend®sensor these were 15.2 %, 5.0 % and 1.2% at respective concentrations of 0.9 mmol/l, 4.2 mmol/l and 19.6 mmol/l. Between-day coefficients of variation for Glucocard Memory 2 were 4.8 % and 3.5 % at glucose concentrations of 3.9 mmol/l and 17.2 mmol/l, respectively and for Accutrend®sensor they were 3.8 % and 2.9 % at glucose concentrations of 3.8 mmol/land 18.7 mmol/l, respectively. Results were linear over a range of 1.6 mmol/l–29.7 mmol/l for Glucocard Memory 2 and 1.6 mmol/l–33.3 mmol/l for Accutrend®sensor. Results of both blood glucose meters correlated closely with the hexokinase/glucose-6-phosphate dehydrogenase laboratory method. Ninety-eight percent of both Glucocard Memory 2 and Accutrend®sensor results were within 20 % of the comparison method values. Ninety-three percent of the Glucocard Memory 2 and 96 % of the Accutrend®sensor results were within 15 % of the comparison method results. An inverse relation between the glucose readings and haematocrit values was observed for both blood glucose meters in the hyperglycaemic range and this effect was more pronounced for Accutrend r sensor. In the normo- and hypoglycaemic ranges the effect was insignificant and absent, respectively. Minimum sample volume for Glucocard Memory 2 was 3 μl and for Accutrend®sensor it was 9 μl. Lower sample volumes gave erroneous results. Presenting more than the required volume had no effect on results.
ISSN:1434-6621
DOI:10.1515/CCLM.1998.009
出版商:Walter de Gruyter
年代:1998
数据来源: Degruyter
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10. |
Evaluation of Circulating Type I Procollagen Propeptides in Patients with Paget's Disease of Bone |
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Clinical Chemistry and Laboratory Medicine,
Volume 36,
Issue 1,
1998,
Page 53-55
Maria R. Bonnin,
Carmen Moragues,
Juan M. Nolla,
Francisco J. Lirón,
Escofet Roig,
Miguel A. Navarro,
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摘要:
AbstractWe evaluated circulating aminoterminal and carboxyterminal propeptides of type I procollagen and total alkaline phosphatase levels in eighty consecutive patients affected by Paget's disease of bone. We compared the biochemical data with the extent of bone disease calculated on the basis of the bone scintigraphic indices.Serum aminoterminal propeptide of type I procollagen levels were high in 77% of patients, serum carboxyterminal propeptide of type I procollagen levels in 22% and serum total alkaline phosphatase levels in 76%. We found significant correlations between the three markers studied. The three biochemical markers correlated significantly with the bone scintigraphic activity indices, but the highest correlation coefficient was between the aminoterminal propeptide and total alkaline phosphatase.We conclude that there is a discrepancy between serum levels of the propeptides studied in relation to Paget's disease of bone. The sensitivity of the carboxyterminal propeptide of type I procollagen in this disease is low. In contrast the aminoterminal propeptide may be as sensitive a marker for the evaluation of this disorder as total alkaline phosphatase, and in addition may be more specific.
ISSN:1434-6621
DOI:10.1515/CCLM.1998.010
出版商:Walter de Gruyter
年代:1998
数据来源: Degruyter
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