[Médamoud : monument, fragment de talatat décoré d'une représentation de porte et de table d'offrandes]

Numérisé par le partenaireAppartient à l’ensemble documentaire : BbLevt0Numérisé par le partenair

Multiple regression analysis for plasma leptin concentration.

<p>CSA, cross sectional area; BW, body weight; HDL, high density lipoprotein; HbA1c, hemoglobin A1c; HOMA, homeostatic model assessment; hs-CRP, high-sensitivity C-reactive protein; WBCs, white blood cells.</p

Body mass index, thigh muscle cross-sectional area (CSA) and plasma leptin levels in sarcopenic, overweight, and sarcopenic overweight subjects.

<p>Corrected for age and body weight. Values are mean ± standard error. *p<.05 vs. normal, †p<.05 vs. sarcopenic, ‡p<.05 vs. overweight subjects.</p

Thigh muscle CT (top) at the mid-thigh level and abdominal CT (bottom) at umbilicus level.

<p>Thigh muscle cross-sectional area (CAS) and visceral fat area (Vis) were obtained.</p

Visceral fat area, thigh muscle cross-sectional area (CSA) and plasma levels of leptin in subjects with sarcopenia, visceral obesity, and sarcopenic visceral obesity.

<p>Corrected for age and body weight. Values are mean ± standard error. *p<.05 vs. normal, †p<.05 vs. sarcopenic, ‡p<.05 vs. visceral obesity.</p

Plasma leptin levels in tertiles of visceral fat area and thigh muscle cross-sectional area (CSA).

<p>Multiple regression analysis was performed for plasma leptin concentration with the following parameters in each sex: age, body weight, body height, tertiles of visceral fat area, tertiles of thigh muscle CSA, and interaction and interaction between visceral fat and thigh muscle tertiles. All values are mean values. <b>Men</b>: Visceral fat area tertile: F = 5.1, p = 0.007. Thigh muscle CSA tertile: F = 8.5, p = 0.0003. Interaction: F = 1.5, p = 0.33. <b>Women</b>: Visceral fat area tertile: F = 7.6, p = 0.0006. Thigh muscle CSA tertile: F = 5.2, p = 0.006. Interaction: F = 1.1, p = 0.34.</p

A double-blind, placebo-controlled, randomised clinical study of the effect of pork collagen peptide supplementation on atherosclerosis in healthy older individuals

<p>We examined whether baPWV could be affected by pork collagen peptide (CP) ingestion. Seventy subjects were randomized into two groups (2.5 g/day CP and 2.5 g/day placebo). A significant reduction in baPWV was observed in the CP group compared to the placebo group. This study demonstrated that pork CP may contribute to the prevention of atherosclerosis in elderly.</p

T2D prediction, glycemic genetic score.

<p>Forest plot of association between glycemic genetic score with incident T2D over a decade-long follow-up period, by ancestry. MESA (European and Asian ancestry) and the <i>G6PD</i> variant (rs1050828) in ARIC (European and African American) were not included in the discovery GWAS analysis. Effect estimates were combined in a fixed effects meta-analysis. Overall effect estimate: 1.05, 95% CI 1.04–1.06, <i>p</i> = 2.5 × 10⁻²⁹. ARIC, Atherosclerosis Risk in Communities Study; ES, Effect Size; FHS, Framingham Heart Study; GWAS, genome-wide association study; G6PD, glucose-6-phosphate dehydrogenase; I-Squared, Higgin's I-squared statistic, a measure of heterogeneity; MESA, Multiethnic Study of Atherosclerosis; SCHS, Singapore Chinese Health Study; T2D, type 2 diabetes.</p

Manhattan plot of HbA1c associated variants.

<p>Manhattan plot of the transethnic meta-analysis results in MANTRA. The dashed grey line indicates log₁₀BF = 6. Grey and green points denote known/novel loci, respectively. The lead HbA1c-associated variants identified through the ancestry-specific/transethnic analyses are circled in purple (the <i>G6PD</i> variant was not included in the MANTRA analysis, but the locus on the X-chromosome is indicated in the figure). Lines joining the plot & SNP number denote known loci (black), novel loci (green), and loci with a secondary distinct signal (red). MANTRA, Meta-Analysis of Transethnic Association.</p

Table of HbA1c associated variants.

<p>Table with results and classification of the 60 HbA1c-associated variants. SNP number corresponds to number in <a href="http://www.plosmedicine.org/article/info:doi/10.1371/journal.pmed.1002383#pmed.1002383.g001" target="_blank">Fig 1</a>.</p