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生长激素缺乏症患者的瘦素表达和瘦素受体基因多态性。

Leptin expression and leptin receptor gene polymorphisms in growth hormone deficiency patients.

机构信息

Division of Genetics, Department of Pediatrics, Chung Shan Medical University Hospital, No. 110 Chien-Kuo N. Road, Sec. 1, 402, Taichung, Taiwan.

出版信息

Hum Genet. 2011 Apr;129(4):455-62. doi: 10.1007/s00439-010-0941-1. Epub 2011 Jan 5.

Abstract

Growth hormone deficiency (GHD) patients have lower weight, height, bone age, insulin-like growth factor 1 (IGF-1) levels, GH levels, fat metabolism and skeletal growth. The association of leptin with GHD characteristics and the effect of gene variants of leptin on GHD are unknown. Our aim was to examine the association of circulating leptin levels and common genetic variants in leptin (LEP) and leptin receptor (LEPR) genes with anthropometric measures, circulating hormone concentrations and GHD. A case control study of 125 GHD cases and 159 control subjects were characterized for bone age, body mass index (BMI), height, weight, leptin, IGF-1, GH and their genotype at the leptin promoter G-2548A, and LEPR variants, K109R and Q223R, at Chung Shan Medical University Hospital. Leptin levels were significantly associated with lower bone age, weight and BMI in GHD patients. Leptin levels were also significantly associated with reduced IGF-1 levels in girls but not boys in both groups. The frequency of LEPR223 [A/G or A/A] genotype was significantly higher than the LEPR223 G/G genotype in the GHD group. The LEPR223 [A/G or A/A] genotype was significantly associated with increased weight and BMI in the control group, but not in the GHD group. In conclusion, the GHD group carried a significantly higher frequency of the LEPR [G/A or A/A] genotype and of the A allele (LEPR223R). The LEPR223R polymorphism affected weight and BMI in control, but not in GHD patients, suggesting that the effect of LEPR223 [A/G or A/A] genotype was counteracted by other factor(s) in GHD patients.

摘要

生长激素缺乏症(GHD)患者的体重、身高、骨龄、胰岛素样生长因子 1(IGF-1)水平、生长激素水平、脂肪代谢和骨骼生长均较低。瘦素与 GHD 特征的相关性以及瘦素基因变异对 GHD 的影响尚不清楚。我们的目的是研究循环瘦素水平与瘦素(LEP)和瘦素受体(LEPR)基因常见遗传变异与人体测量指标、循环激素浓度和 GHD 的相关性。我们在中山东方医院对 125 例 GHD 患者和 159 例对照进行了病例对照研究,对骨龄、体重指数(BMI)、身高、体重、瘦素、IGF-1、生长激素及其在瘦素启动子 G-2548A 的基因型、LEPR 变异体 K109R 和 Q223R 进行了特征分析。瘦素水平与 GHD 患者的骨龄、体重和 BMI 降低显著相关。瘦素水平与两组女孩的 IGF-1 水平降低显著相关,但与男孩无关。LEPR223[A/G 或 A/A]基因型的频率在 GHD 组中明显高于 LEPR223G/G 基因型。在对照组中,LEPR223[A/G 或 A/A]基因型与体重和 BMI 的增加显著相关,但在 GHD 组中则无相关性。结论,GHD 组携带 LEPR[G/A 或 A/A]基因型和 A 等位基因(LEPR223R)的频率明显较高。LEPR223R 多态性影响了对照组的体重和 BMI,但对 GHD 患者则无影响,提示 LEPR223[A/G 或 A/A]基因型的作用在 GHD 患者中受到其他因素的抵消。

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