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  • 1
    In: Acta Paediatrica, Wiley, Vol. 95, No. 12 ( 2006-12-1), p. 1625-1634
    Type of Medium: Online Resource
    ISSN: 0803-5253
    Language: Unknown
    Publisher: Wiley
    Publication Date: 2006
    detail.hit.zdb_id: 1492629-5
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  • 2
    In: Clinical Endocrinology, Wiley, Vol. 72, No. 3 ( 2010-03), p. 364-370
    Type of Medium: Online Resource
    ISSN: 0300-0664 , 1365-2265
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2010
    detail.hit.zdb_id: 2004597-9
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  • 3
    In: International Journal of Laboratory Hematology, Wiley, Vol. 42, No. 6 ( 2020-12), p. 750-760
    Abstract: Hematology laboratory parameters are among the most routinely ordered tests in support of adult and pediatric care. However, appropriate interpretation of test results has been a challenge in pediatrics since accurate and up‐to‐date reference intervals that reflect the dynamic physiological changes associated with growth and development have not been available. Critical gaps continue to exist in pediatric hematology reference intervals for modern laboratory platforms. To address this gap, this study establishes age‐ and sex‐specific reference intervals for 25 hematology parameters in the CALIPER cohort of healthy children and adolescents using a common platform, the Sysmex XN‐3000 analytical system. Methods Fresh whole blood samples collected from a total of 641 healthy children and adolescents (birth to 〈 21 years) with informed consent were analyzed for 25 hematological parameters on the Sysmex XN‐3000 Hematology Analyzer. Age‐ and sex‐specific reference standards were calculated based on Clinical and Laboratory Standards Institute guidelines. Results Of the 25 analytes assessed, 19 required age‐partitioning and seven required sex‐partitioning (ie, red blood cell count, hemoglobin, hematocrit, mean corpuscular volume, red blood cell distribution width—SD, red blood cell distribution width—CV, and monocyte percentage). Age‐ and sex‐specific differences mostly coincided with the onset of puberty. Conclusion This study establishes a comprehensive database of pediatric reference intervals for hematology parameters in the CALIPER cohort using the widely used Sysmex XN‐3000 analytical platform. These data highlight the dynamic hematological profile observed in healthy children and adolescents and the need for reference interval stratification by age and sex.
    Type of Medium: Online Resource
    ISSN: 1751-5521 , 1751-553X
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2268600-9
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  • 4
    In: International Journal of Laboratory Hematology, Wiley, Vol. 45, No. 4 ( 2023-08), p. 469-480
    Abstract: Hematological parameters vary significantly throughout growth and development due to physiological processes such as fetal‐to‐adult erythropoiesis and puberty. Pediatric age‐ and sex‐specific reference intervals (RIs) are thus essential for appropriate clinical decision‐making. The current study aimed to establish RIs for both common and novel hematology parameters on the Mindray BC‐6800Plus system. Methods Six hundred and eighty‐seven healthy children and adolescents (30 days to 18 years) were enrolled. Participants were recruited as part of the Canadian Laboratory Initiative on Pediatric Reference Intervals Program upon informed consent or identified from apparently healthy outpatient clinics. Whole blood was collected and assayed for 79 hematology parameters on the BC‐6800Plus system (Mindray). Age‐ and sex‐specific RIs were established as per Clinical and Laboratory Standards Institute EP28‐A3c guidelines. Results Dynamic reference value distributions were observed for several hematology parameters, including erythrocytes, leukocytes, platelets, reticulocytes, and research‐use‐only markers. Age partitioning was required for 52 parameters, demonstrating changes in infancy and puberty. Sex partitioning was required for 11 erythrocyte parameters (i.e., red blood cell (RBC), hemoglobin, hematocrit, mean corpuscular volume, mean corpuscular hemoglobin concentration, RBC distribution width coefficient of variation, hemoglobin distribution width, macrocyte count, macrocyte percentage, RBC (optical), and reticulocyte production index). Few parameters had undetectable levels in our healthy cohort (i.e., nucleated RBC count and immature granulocyte count). Conclusions The current study completed hematological profiling for 79 parameters on the BC‐6800Plus system in a healthy cohort of Canadian children and adolescents. These data emphasize the complex biological patterns of hematology parameters in childhood, particularly at the onset of puberty, and support the need for age‐ and sex‐specific RIs for clinical interpretation.
    Type of Medium: Online Resource
    ISSN: 1751-5521 , 1751-553X
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 2268600-9
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  • 5
    Online Resource
    Online Resource
    Wiley ; 1990
    In:  FEBS Letters Vol. 263, No. 2 ( 1990-04-24), p. 345-348
    In: FEBS Letters, Wiley, Vol. 263, No. 2 ( 1990-04-24), p. 345-348
    Abstract: We have developed a defined medium which can maintain efficient growth of HepG2 cells sustaining the synthesis of a variety of plasma proteins including apolipoprotein B. This defined system was used to investigate long‐term effects of insulin, estrogen, triiodothyronine, cholesterol, and oleate on the growth pattern of HepG2 cells and secretion rate of apolipoprotein B. Oleate and triiodothyronine caused significant increases in secretion of apolipoprotein B. The stimulatory effect of triiodothyronine was only observed after long (6 days) exposure of cells to the hormone. In contrast, insulin caused up to a 4‐fold decrease in the secretion rate of apolipoprotein B during the early growth periods. This inhibitory effect appeared to be partially abolished after 6 days. Our data suggest that some important questions on regulation of apolipoprotein B expression can be addressed by the long‐term culture of HepG2 cells in defined medium.
    Type of Medium: Online Resource
    ISSN: 0014-5793 , 1873-3468
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 1990
    detail.hit.zdb_id: 1460391-3
    SSG: 12
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  • 6
    In: International Journal of Laboratory Hematology, Wiley, Vol. 45, No. 6 ( 2023-12), p. 845-852
    Abstract: Defining accurate age‐ and sex‐specific reference intervals (RIs) for hematology parameters, especially for the pediatric population, is important for making an appropriate clinical diagnosis. To address gaps, we established age‐specific RIs for 11 hematologic parameters in Iranian children younger than 30 months for the first time. Methods Fresh whole blood samples collected from a total of 344 participants (males: 158 and females: 186) ages 3 days to 30 months, with a mean age of 12.91 ± 7.15 months, were recruited from healthcare centers in Mashhad, Iran. Hematologic parameters, including complete blood count (CBC), were analyzed on the Sysmex auto‐analyzer system (KX‐21 N). RIs were calculated with 90% confidence intervals using the direct method based on CLSI Ep28‐A3 and C28‐A3 guidelines. Results None of the CBC parameters required sex partitioning. Of 11 CBC parameters, six required age partitions of 3 days– 〈 4 months, 4– 〈 10, 10– 〈 15, and 4– 〈 30 months. Five parameters (i.e., white blood cell count, mean corpuscular hemoglobin concentration, mean platelet volume, red cell distribution width, and platelet distribution width) did not demonstrate age‐specific changes. RIs of red blood cell count and hematocrit, as well as hemoglobin, increased with age, while mean corpuscular volume, mean corpuscular hemoglobin, and platelet count, decreased with age. Conclusion In this study, we established RIs for 11 hematology parameters in young children. Age partitioning was required for six parameters demonstrating marked changes during the early period of growth and development and necessitating the use of pediatric‐specific reference standards.
    Type of Medium: Online Resource
    ISSN: 1751-5521 , 1751-553X
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 2268600-9
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  • 7
    Online Resource
    Online Resource
    Wiley ; 2007
    In:  Paediatric and Perinatal Epidemiology Vol. 21, No. 6 ( 2007-11), p. 518-524
    In: Paediatric and Perinatal Epidemiology, Wiley, Vol. 21, No. 6 ( 2007-11), p. 518-524
    Abstract: The cord blood lipid profile may be associated with lifelong changes in the metabolic functions of the individual. The aim of the present study was for the first time in Iran to assess the cord blood lipid profile of neonates, as well as some of its environmental influencing factors. The subjects were 442 (218 boys and 224 girls) normal vaginal delivery newborns. Overall, 14.4% of neonates were preterm and the rest were full‐term. In total, 9.2% ( n  = 35) of the full‐term newborns were small‐for‐gestational‐age (SGA), of which 16 had a ponderal index (PI) below the 10th percentile (SGA I) and 19 had a PI above the 10th percentile (SGA II), 5.5% ( n  = 21) were large‐for‐gestational‐age (LGA), and the remainder were appropriate‐for‐gestational‐age (AGA).Before becoming pregnant, 6.9% of mothers were underweight, 49.3% had normal body mass index (BMI), 39.4% were overweight and 4.4% were obese. Total and high‐density lipoprotein cholesterol (HDL‐C) in girls were significantly higher than in boys (80.3 ± 33.3 and 31.1 ± 9.9 vs. 73.3 ± 23.1 and 28.8 ± 8.7 mg/dL, respectively, P   〈  0.05). The mean apolipoprotein A (apoA) of neonates with underweight mothers was significantly lower, and the mean apoB level of those with overweight mothers was significantly higher than other neonates. The mean low‐density lipoprotein cholesterol (LDL‐C), HDL‐C and apoA of the LGA newborns were significantly lower, and their apoB was significantly higher compared with AGA and SGA neonates. The SGA I neonates had significantly lower total cholesterol, LDL‐C, HDL‐C and apoA, as well as higher triglycerides, lipoprotein a and apoB than the SGA II group. The mean cord blood triglycerides of full‐term neonates was significantly higher than preterm neonates (69.4 ± 11.9 vs. 61.4 ± 12.7 mg/dL, respectively, P  = 0.04). A preconception maternal BMI of ≥25 kg/m 2 correlated significantly with the cord triglycerides (OR = 1.3, [95% CI 1.07, 1.5]) and with apoB (OR = 1.4, [95% CI 1.1, 1.5] ). The BMI 〈 18 of mothers before pregnancy correlated with low HDL‐C (OR = 1.3, [95% CI 1.04, 1.7]). Birthweight correlated with high cord triglyceride level (SGA: OR = 1.4, [95% CI 1.1, 1.7] ; LGA: OR = 1.6, [95% CI 1.3, 1.7] compared with AGA). These associations remained significant even after adjusting for the preconception BMI of mothers. Our findings reflect the possible interaction of environmental factors and fetal growth and the in utero lipid metabolism. Long‐term longitudinal studies in different ethnicities would help to elucidate the relationship.
    Type of Medium: Online Resource
    ISSN: 0269-5022 , 1365-3016
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2007
    detail.hit.zdb_id: 2008566-7
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  • 8
    In: Pediatric Anesthesia, Wiley, Vol. 18, No. 3 ( 2008-03), p. 235-239
    Abstract: Background:  A previously published pharmacokinetic simulation suggested a simple manual infusion regimen to achieve propofol plasma concentrations of 3 μg·ml −1 . This study investigated if a simple variation in propofol infusion rates is able to achieve distinct propofol plasma concentrations and whether these are close to the propofol plasma concentrations predicted by the Kataria model. Methods:  With Research Ethics Board approval and written parental consent, a total of 17 healthy children requiring general anaesthesia were enrolled. Following inhalational induction of anaesthesia, a propofol bolus of 5 mg·kg −1 was given and anaesthesia maintained using an adaptation of the McFarlan continuous propofol infusion regimen to achieve three distinct depths of propofol anaesthesia. Weight and propofol infusion data were used to calculate simulated propofol concentrations using the Kataria dataset and the tiva ® simulation program. The performance of the infusion regimen was assessed by calculating the median performance error, median absolute performance error, wobble, and divergence. Results:  Measured propofol concentrations were (mean ±  sd ) 7.15 ± 1.4, 4.3 ± 0.85, and 2.85 ± 0.53 μg·ml −1 against simulation values of 6.6, 4.1, and 2.8 μg·ml −1 , respectively, at 30, 50, and 70 min using the Kataria dataset. These differences were not significant. Formal assessment of the infusion regimen’s performance was acceptable. Conclusion:  The manual propofol infusion regimen achieved three distinct depths of propofol anaesthesia. The manual infusion regimen produced higher plasma propofol concentrations than predicted during the early part of the infusion period but was more accurate for later time points.
    Type of Medium: Online Resource
    ISSN: 1155-5645 , 1460-9592
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2008
    detail.hit.zdb_id: 2008564-3
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  • 9
    In: Arthritis & Rheumatism, Wiley, Vol. 54, No. 4 ( 2006-04), p. 1283-1290
    Type of Medium: Online Resource
    ISSN: 0004-3591 , 1529-0131
    URL: Issue
    RVK:
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2006
    detail.hit.zdb_id: 2014367-9
    detail.hit.zdb_id: 2754614-7
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  • 10
    In: Lipids, Wiley, Vol. 45, No. 3 ( 2010-03), p. 237-244
    Abstract: Insulin resistance is the central defect in type 2 diabetes and obesity. During the development of insulin resistance a lipid accumulation is accompanied by increased PTP‐1B expression in the muscle. The aim of this study was to examine the effects of PTP‐1B knockdown on insulin signaling and insulin resistance in the presence or absence of palmitate in C2C12 skeletal muscle cells. A stable C2C12 cell line was established using short hairpin RNA (shRNA) to knockdown protein expression of PTP1B. Analysis of PTP‐1B protein expression and phosphorylation and protein levels of IRS‐1 and Akt were detected by western blot. The effects of PTP‐1B knockdown on the glucose uptake was also measured in C2C12 cells. The stable C2C12 cell line harboring the PTP‐1B shRNA showed 62% decrease in the PTP‐1B protein levels. 0.5 mM palmitate significantly induced insulin resistance in both control (26%) and PTP‐1B knockdown cells (16.5%) compared to the untreated cells. Under treatment with palmitate, insulin stimulated phosphorylation of IRS‐1 (Tyr632) and Akt (Ser473) in knockdown cells was significantly 1.55‐ and 1.86‐fold, respectively, greater than the controls. In the presence of palmitate, insulin dependent glucose uptake was significantly about 3‐fold higher in PTP‐1B knockdown stable C2C12 cells compared to the control cells. Our data showed that decreasing the PTP‐1B protein level by shRNA can enhance the activity of important elements of insulin signaling. The improvement in insulin action persisted even in palmitate treated insulin resistant myotubes.
    Type of Medium: Online Resource
    ISSN: 0024-4201 , 1558-9307
    Language: English
    Publisher: Wiley
    Publication Date: 2010
    detail.hit.zdb_id: 2030265-4
    SSG: 12
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