Estimated net endogenous acid production and intake of bone health-related nutrients in Hong Kong Chinese adolescents.

BACKGROUND/OBJECTIVES: To examine the daily intake of bone health-related nutrients and to explore the association between diet composition and estimated net endogenous acid production (estimated NEAP) in Hong Kong Chinese adolescents. SUBJECT/METHODS: In total, 171 boys and 180 girls aged 10-12 years of Chinese origin from nine primary schools from the Hong Kong Adolescent Bone Health Cohort Study. The study design used food frequency questionnaire. Mean daily intakes of foods and selected nutrients were estimated. Mean percentage of nutrient intake contributed by different food groups was presented. Frassetto's method was used to calculate the estimated NEAP from the diet's protein to potassium ratio. RESULTS: There was no significant difference in the energy-adjusted intakes of most nutrients between boys and girls, except for intakes of vitamins C and D. Mean protein, sodium and potassium intakes were higher than the Chinese dietary reference intake (DRI), whereas mean intakes of magnesium, calcium and vitamin D were lower than the DRI. Boys had significantly higher estimated NEAP than girls (P=0.0051). Estimated NEAP was significantly positively correlated with meat intake and negatively associated with the consumption of fruits, vegetables, legumes, beverages and dairy products. CONCLUSIONS: The results highlight the importance of considering whole diet quality when interpreting the effects of single nutrient or diet's net acid load on bone. The effect on high protein intake and low fruit and vegetable intake on the long-term bone health of Hong Kong Chinese adolescents warrants attention.

Relationship between grip strength and bone mineral density in healthy Hong Kong adolescents.

UNLABELLED: This study evaluated the magnitude of the correlations among grip strength, bone mineral density (BMD) and bone mineral content (BMC), after controlling for weight, height, pubertal development, weight-bearing activities and calcium intake. The results lead to the conclusion that grip strength is an independent predictor of bone mass in both sexes. The relationship between muscle strength and bone mass is systemic. INTRODUCTION: Previous studies had shown a site-specific relationship between muscle strength and bone in pubertal children. This study evaluated the magnitude of the correlations among grip strength, bone mineral density (BMD) and bone mineral content (BMC) at distant bone. METHODS: Cross-sectional data of 169 11- to 12-year-old boys and 173 10- to 11-year-old girls came from the baseline result of a cohort study. Grip strength, BMD, BMC, weight, height, pubertal development, weight-bearing activities and calcium intake were measured. Pearson correlations and multiple regressions were used to calculate univariate and adjusted associations among grip strength and bone mass at distant bone. RESULTS: Significant correlations were shown between grip strength and bone mass at hip, spine and whole body (boys: BMC:0.72-0.74, BMD:0.38-0.60; girls: BMC:0.71-0.72, BMD:0.44-0.63; p<0.0001). Multiple regressions with all covariates showed that about 70% and 50%, respectively, of the variations in BMC and BMD could be explained but not for whole body BMD. Grip strength was an independent predictor of bone mass, except hip BMD in boys and whole body BMD in girls. Stepwise regression showed that grip strength was a robust predictor in both sexes. Prediction models by grip strength and weight explained about 60% and 40% of the variations in BMC of different sites and in BMD of hip and spine, respectively. CONCLUSIONS: We found that grip strength is an independent predictor of bone mass in both sexes. The relationship between muscle strength and bone mass is systemic.

Assessment of the fundamental accuracy of the Jendrassik-Gróf total and direct bilirubin assays.

Using unconjugated bilirubin (Bu) and authentic human disconjugated bilirubin (dBc) supplemented in low-bilirubin serum pools, we have directly verified for the first time that the Jendrassik-Gróf total bilirubin assay modified after Doumas et al. (Clin. Chem. 19: 984-993, 1973) detects Bu and dBc quantitatively, in Bu-equivalent concentrations relative to gravimetric concentration assignment reinforced with quantification by nuclear magnetic resonance (Wu et al., Clin. Chem. 26: 1323-1335, 1980). By contrast, the Jendrassik-Gróf direct bilirubin assay (also modified after Doumas) quantifies only 70 +/- 5% of the gravimetrically determined dBc as Bu equivalents. By using Bu and dBc (instead of Bu only, as is routinely done) to calibrate the responses of the total and direct bilirubin assays, the analyses of Bu and dBc become much more quantitative. We mathematically explored the meanings of the conventional terms total, direct, and indirect bilirubins. The clinical and diagnostic implications of our observations are discussed.

The Kodak Ektachem clinical chemistry slide for measurement of bilirubin in newborns: principles and performance.

In this slide, unconjugated bilirubin and its sugar conjugates interact with a cationic polymeric mordant to form spectrally enhanced complexes having similar absorptivities at approximately 400 nm. With reflection densitometry and appropriate mathematical transformation, readings at this wavelength are linearly related to bilirubin concentrations up to 260 mg/L. The slide requires 10 microL of serum, is precise (total CV less than 2% determined over 20 days for the analyte range 39-184 mg/L), gives results that correlate well with the Doumas et al. modification of the Jendrassik-Gróf method (slope 0.95, intercept 0.3, Sy . x 3.4, r = 0.991), and is relatively interference free. Also, the slide measures less loss of bilirubin after in vitro illumination of serum specimens than do diazo tests. An intermediate layer in the slide minimizes the spectral interference from hemoglobin and prevents the detection of the strongly protein-linked ("delta") bilirubin found in many jaundiced adults. The method is recommended for newborns (less than or equal to 14 days), in whom the incidence of delta bilirubin is negligible.

Automated approach to radioimmunoassays of somatotropin (human growth hormone) and insulin.

The adaptation of human somatotropin and insulin assays to the automated Centria radioimmunoassay system [Clin. Chem. 21, 1305 (1975)] is reported. For the somatotropin assay, reaction conditions include a borate/bovine serum albumin buffer (pH 8.4) AND 20-H Incubation at 4 degrees C. Assay results for clinical samples compared favorably (correlation coefficient = 0.930) with values obtained from a reference laboratory. The means determined for 92 patients' samples were 4.3 mug/liter (reference laboratory) and 5.1 mug/liter (Centria). Intra- and inter-run precision ranged from 3.2 to 15.9%. For the insulin assay, a phosphate/bovine serum albumin buffer (pH 7.4) is used, with a 20-h incubation at 4 degrees C. Previously analyzed insulin samples from a reference laboratory were determined by the Centria analyzer with excellent correlation (r = 0.965). Means for patients' samples were 43.0 milli (USP) units of insulin per liter (reference laboratory) and 47.5 milliunits of insulin per liter (Centria). In both assays an anionicexchange gel is used in the separation step. The criterion of parallelism, an indication of the validity of a radioimmunoassay, was satisfied in both assays. The Centria radioimmunoassay system offers the advantage of automating all the critical steps of these radioimmunoassays.