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Histogramm zur Alters- und Geschlechtsverteilung der Referenzpopulation aus der LIFE Child Kohorte zum Erstbesuch (Gesamt: n=1779, Jungen: n=903, Mädchen: n=876).

Histogramm zur Alters- und Geschlechtsverteilung der Referenzpopulation aus der LIFE Child Kohorte zum Erstbesuch (Gesamt: n=1779, Jungen: n=903, Mädchen: n=876).

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Zusammenfassung Einleitung: Es werden pädiatrische Referenzintervalle zu eisenabhängigen Parametern kontinuierlich über das Alter unter Anwendung des, in der Laboratoriumsmedizin noch wenig bekannten, R-Pakets GAMLSS aus einer hoch standardisierten Probenpopulation ermittelt. Methoden: 2778 Blutproben von LIFE Child-Probanden im Alter von 2,5 bis 1...

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Objectives The ‘Thomas plot’ is a very helpful diagnostic tool for evaluation, monitoring and therapy of the iron status and on the hemoglobinization of the reticulocytes of patients. In 2021 Roche Diagnostics launched a second generation assay for determination of the soluble transferrin receptor (sTfR). Here we compare the old and the new assay f...

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... Additionally, two findings of our study stand out: First, age groups can only roughly approximate the dynamics in children's laboratory test results, and second, the dynamics in the first months of life require particular attention. The arguments for (and against) continuous representations of pediatric reference intervals have been discussed extensively by the former International Federation of Clinical Chemistry and Laboratory Medicine (IFCC)'s Task Force on Pediatric Laboratory Medicine's chair Michael Metz [3,4,18], CALIPER [6,19], HAPPI Kids [7,20], the German LIFE study [21,22], and us [10][11][12][13]. There is general agreement that continuous approaches enable a more accurate representation of pediatric dynamics, although challenges to their integration into laboratory information systems remain, and no consensus exists whether continuous reference intervals are warranted for all analytes and age groups or only for those analytes that exhibit the most complex dynamics. ...
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Objectives: Assessment of children's laboratory test results requires consideration of the extensive changes that occur during physiological development and result in pronounced sex- and age-specific dynamics in many biochemical analytes. Pediatric reference intervals have to account for these dynamics, but ethical and practical challenges limit the availability of appropriate pediatric reference intervals that cover children from birth to adulthood. We have therefore initiated the multi-center data-driven PEDREF project (Next-Generation Pediatric Reference Intervals) to create pediatric reference intervals using data from laboratory information systems. Methods: We analyzed laboratory test results from 638,683 patients (217,883-982,548 samples per analyte, a median of 603,745 test results per analyte, and 10,298,067 test results in total) performed during patient care in 13 German centers. Test results from children with repeat measurements were discarded, and we estimated the distribution of physiological test results using a validated statistical approach (kosmic). Results: We report continuous pediatric reference intervals and percentile charts for alanine transaminase, aspartate transaminase, lactate dehydrogenase, alkaline phosphatase, γ-glutamyl-transferase, total protein, albumin, creatinine, urea, sodium, potassium, calcium, chloride, anorganic phosphate, and magnesium. Reference intervals are provided as tables and fractional polynomial functions (i.e., mathematical equations) that can be integrated into laboratory information systems. Additionally, Z-scores and percentiles enable the normalization of test results by age and sex to facilitate their interpretation across age groups. Conclusions: The provided reference intervals and percentile charts enable precise assessment of laboratory test results in children from birth to adulthood. Our findings highlight the pronounced dynamics in many biochemical analytes in neonates, which require particular consideration in reference intervals to support clinical decision making most effectively.
... As part of the Leipzig Research Centre for Civilization Diseases (LIFE), the population-based cohort study LIFE Child has started recruiting urban, primarily healthy infants, children, and adolescents in Leipzig (Germany) in 2011. This large population-based cohort has already been used to establish reference intervals for serum lipids [26], liver enzymes [27], and iron-related blood parameters [28] in children. The examinations take place in the LIFE Child study center and are carried out by trained medical staff using highly standardized procedures [29,30]. ...
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Background This study aims to establish age- and gender-specific cystatin C (CysC) reference values for healthy infants, children, and adolescents and to relate them to pubertal stage, height, weight, and body mass index (BMI). Methods Serum CysC and creatinine levels of 6217 fasting, morning venous blood samples from 2803 healthy participants of the LIFE Child study (age 3 months to 18 years) were analyzed by an immunoassay. Recruitment started in 2011; 1636 participants provided at least one follow-up measurement. Percentiles for CysC were calculated. Age- and gender-related effects of height, weight, BMI, and puberty status were assessed through linear regression models. Results Over the first 2 years of life, median CysC levels decrease depending on height (ß = − 0.010 mg/l/cm, p < 0.001) and weight (ß = − 0.033 mg/l/kg, p < 0.001) from 1.06 to 0.88 mg/l for males and from 1.04 to 0.87 mg/l for females. Following the second year of age, the levels remain stable for eight years. From 11 to 14 years of age, there is an increase of median CysC levels in males to 0.98 mg/l and a decrease in females to 0.86 mg/l. The change is associated with puberty (ß = 0.105 mg/l/Tanner stage, p < 0.001 in males and ß = − 0.093 mg/l/Tanner stage, p < 0.01 in females) and in males with height (ß = 0.003 mg/l/cm, p < 0.001). Conclusions CysC levels depend on age, gender, and height, especially during infancy and puberty. We recommend the use of age- and gender-specific reference values for CysC serum levels for estimating kidney function in clinical practice.
... (20) Estimation of parameters as continuous functions of age seems to be a more appropriate approach to reflect the physiological development of laboratory analytes. (9,21) Because LIFE Child has a longitudinal study design and recruits families participated with more than one child, our sampled data contain multiple measurements per child as well as measurements of siblings. Therefore, percentile calculations had to follow an adapted approach. ...
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