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采用基于家系的关联方法对超重和肥胖意大利儿童的 CART 基因进行分子分析。

Molecular analysis of the CART gene in overweight and obese Italian children using family-based association methods.

机构信息

Department of Pediatrics, University Hospital, Messina, Italy.

出版信息

Acta Paediatr. 2010 May;99(5):722-726. doi: 10.1111/j.1651-2227.2010.01709.x. Epub 2010 Feb 11.

Abstract

AIM

In our study, we evaluated if CART gene A1475G and DeltaA1457 polymorphisms could be associated with obesity.

PATIENTS AND METHODS

We recruited 133 Italian trios from among 103 (50 males and 53 females) overweight children (mean age 10.5 years, range 6-14 years; mean BMI 26.1 +/- 3.2 kg/m(2)), and 30 (16 males and 14 females) obese children (mean age 9.0 years, range 6-11 years; mean BMI 32.3 +/- 2.0 kg/m(2)). We also selected 187 non-obese unrelated controls.

RESULTS

The allele frequencies of the A1475G single nucleotide polymorphism (SNP) were significantly higher in overweight children (0.07) than in control children (0.02) (p = 0.03) and control adults (0.02) (p = 0.02). Moreover, the allele frequencies were significantly different between obese children (0.08) and control children (0.02) (p = 0.03), and between obese children (0.08) and control adults (0.02) (p = 0.02). The DeltaA1457 SNP showed no significant association with overweight/obesity. TDT statistic revealed a preferential transmission of the 1475G allele from heterozygous parents to overweight children (p < 0.01) and to obese children (p < 0.05). No statistically significant excess transmission of the DeltaA1457 allele was found.

CONCLUSION

Our results supported the hypothesis that inherited variations of the CART gene could influence the development of obesity also in Italian children.

摘要

目的

在我们的研究中,我们评估了 CART 基因 A1475G 和 DeltaA1457 多态性是否与肥胖有关。

患者和方法

我们招募了 133 名来自意大利的三核苷酸,其中包括 103 名(50 名男性和 53 名女性)超重儿童(平均年龄 10.5 岁,范围 6-14 岁;平均 BMI 26.1 +/- 3.2 kg/m(2))和 30 名(16 名男性和 14 名女性)肥胖儿童(平均年龄 9.0 岁,范围 6-11 岁;平均 BMI 32.3 +/- 2.0 kg/m(2))。我们还选择了 187 名非肥胖的无关对照。

结果

A1475G 单核苷酸多态性(SNP)的等位基因频率在超重儿童(0.07)中明显高于对照组儿童(0.02)(p = 0.03)和对照组成人(0.02)(p = 0.02)。此外,肥胖儿童(0.08)与对照组儿童(0.02)(p = 0.03)和肥胖儿童(0.08)与对照组成人(0.02)(p = 0.02)之间的等位基因频率差异显著。DeltaA1457 SNP 与超重/肥胖无明显关联。TDT 统计显示,杂合父母的 1475G 等位基因优先传递给超重儿童(p < 0.01)和肥胖儿童(p < 0.05)。未发现 DeltaA1457 等位基因的过度传递有统计学意义。

结论

我们的结果支持了这样的假设,即 CART 基因的遗传变异可能影响意大利儿童肥胖的发展。

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