Parent-Offspring Transmission of Adipocytokine Levels and Their Associations with Metabolic TraitsReport as inadecuate

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Adipose tissue secreted cytokines adipocytokines have significant effects on the physiology and pathology of human metabolism relevant to diabetes and cardiovascular disease. We determined the relationship of the pattern of these circulating hormones with obesity-related phenotypes and whether such pattern is transmitted from parent to offspring. A combined total of 403 individuals from 156 consenting Saudi families divided into initial 119 families with 123 adults and 131 children and replication 37 families with 58 adults and 91 children cohorts were randomly selected from the RIYADH Cohort study. Anthropometrics were evaluated and metabolic measures such as fasting serum glucose, lipid profiles, insulin, leptin, adiponectin, resistin, tumor necrosis factor alpha TNFα, activated plasminogen activator inhibitor 1 aPAI1, high sensitivity C-reactive protein hsCRP and angiotensin II were also assessed. Parent-offspring regressions revealed that with the exception of hsCRP, all hormones measured showed evidence for significant inheritance. Principal component PC analysis of standardized hormone levels demonstrated surprising heritability of the three most common axes of variation. PC1, which explained 21% of the variation, was most strongly loaded on levels of leptin, TNFα, insulin, and aPAI1, and inversely with adiponectin. It was significantly associated with body mass index BMI and phenotypically stronger in children, and showed a heritability of ∼50%, after adjustment for age, gender and generational effects. We conclude that adipocytokines are highly heritable and their pattern of co-variation significantly influences BMI as early as the pre-teen years. Investigation at the genomic scale is required to determine the variants affecting the regulation of the hormones studied.

Author: Nasser M. Al-Daghri , Omar S. Al-Attas, Majed S. Alokail, Khalid M. Alkharfy, Sobhy M. Yakout, Shaun B. Sabico, Greg C. Gibson, G



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