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Bivariate linkage confirms genetic contribution to fetal origins of childhood growth and cardiovascular disease risk in Hispanic children.

机译:双变量连锁证实了西班牙裔儿童对胎儿来源的童年成长和心血管疾病风险的遗传贡献。

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Birth weight has been shown to be associated with obesity and metabolic diseases in adulthood, however, the genetic contribution is still controversial. The objective of this analysis is to explore the genetic contribution to the relationship between birth weight and later risk for obesity and metabolic diseases in Hispanic children. Subjects were 1,030 Hispanic children in the Viva La Familia Study. Phenotypes included body size, body composition, blood pressure, fasting glucose, insulin, lipids, and liver enzymes. Birth weights were obtained from Texas birth certificates. Quantitative genetic analyses were conducted using SOLAR software. Birth weight was highly heritable, as were all other phenotypes. Phenotypically, birth weight was positively correlated to childhood body size parameters. Decomposition of these phenotypic correlations into genetic and environmental components revealed significant genetic correlations, ranging from 0.30 to 0.59. Negative genetic correlations were seen between birth weight and lipids. The genome scan of birth weight mapped to a region near marker D10S537 (LOD = 2.6). The bivariate genome-wide scan of birth weight and childhood weight or total cholesterol, improved the LOD score to 3.09 and 2.85, respectively. Chromosome 10q22 harbors genes influencing both birth weight and childhood body size and cardiovascular disease risk in Hispanic children.
机译:已证明出生体重与成年后的肥胖和代谢性疾病有关,但是,遗传贡献仍然存在争议。该分析的目的是探讨遗传因素对西班牙裔儿童出生体重与以后肥胖和代谢疾病风险之间关系的影响。 Viva La Familia研究的对象是1,030名西班牙裔儿童。表型包括体重,身体组成,血压,空腹血糖,胰岛素,脂质和肝酶。出生体重来自德克萨斯州的出生证明。使用SOLAR软件进行定量遗传分析。与其他所有表型一样,出生体重具有很高的遗传性。从表型上看,出生体重与儿童体重参数呈正相关。这些表型相关分解为遗传和环境成分揭示了显着的遗传相关,范围从0.30到0.59。出生体重和血脂之间存在负的遗传相关性。出生体重的基因组扫描定位到标记D10S537附近的区域(LOD = 2.6)。出生体重和儿童体重或总胆固醇的双变量全基因组扫描将LOD评分分别提高到3.09和2.85。染色体10q22包含影响西班牙裔儿童的出生体重,儿童体重和心血管疾病风险的基因。

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