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黄体生成素β基因多态性在健康男孩青春期启动及进展中的作用。

The role of luteinizing hormone-beta gene polymorphism in the onset and progression of puberty in healthy boys.

作者信息

Raivio T, Huhtaniemi I, Anttila R, Siimes M A, Hagenäs L, Nilsson C, Pettersson K, Dunkel L

机构信息

Children's Hospital, University of Helsinki, Finland.

出版信息

J Clin Endocrinol Metab. 1996 Sep;81(9):3278-82. doi: 10.1210/jcem.81.9.8784083.

Abstract

An immunologically anomalous LH with two point mutations in its beta-subunit gene (Trp8Arg and Ile15Thr) has recently been described. This polymorphism is common in Finland; 28% of the population are homo- or heterozygous for the variant allele. To assess the effect of the LH variant on LH action, we correlated its presence in a group of 49 healthy boys with the onset and progression of puberty. This group was followed-up longitudinally from a mean age of 11.7 +/- 0.1 yr for 3 yr at 3-month intervals. In addition, we studied the prevalence of the variant LH in boys with constitutional pubertal delay (testicular volume < or = 4 mL after 13.5 yr of age). The LH beta gene status of each subject in this study was judged from a single venous blood sample using two immunofluorometric LH assays with different combinations of monoclonal antibodies: one detecting both the variant and wild-type LH, and the other detecting only wild-type hormone. Of the boys with pubertal onset at a normal age, 36 (74%) were homozygous for the wild-type LH beta allele, 12 (24%) were heterozygous, and 1 (2%) was homozygous for the variant LH beta allele. Clear differences in pubertal parameters were found between the boys with normal and mutated (homo- or heterozygous) LH genotypes. During the follow-up, the boys with the mutated genotype had smaller testicular volumes (P < 0.03), were shorter (P < 0.02), had slower growth rates (P < 0.04), and had lower serum insulin-like growth factor I-binding protein-3 levels (P < 0.03) than the boys with the normal LH genotype. In the boys with delayed onset of puberty, the frequency of the variant LH beta allele did not differ from that in the reference population, indicating that the variant LH is not associated with conditions due to disturbed control of the reactivation of GnRH secretion. We conclude that during the progression of puberty, the variant LH may be less active in stimulating testicular growth than wild-type LH. Thus, the gene may affect tempo, contributing to the wide normal variation in pubertal progression in healthy boys. Our results also suggest that the variant LH not only affects the course of puberty, but is already involved in the regulation of the GH-insulin-like growth factor I axis during childhood.

摘要

最近报道了一种在其β亚基基因中有两个点突变(Trp8Arg和Ile15Thr)的免疫异常促黄体生成素(LH)。这种多态性在芬兰很常见;28%的人口是变异等位基因的纯合子或杂合子。为了评估LH变异体对LH作用的影响,我们将其在一组49名健康男孩中的存在情况与青春期的开始和进展进行了关联。该组从平均年龄11.7±0.1岁开始纵向随访3年,每隔3个月进行一次。此外,我们研究了体质性青春期延迟男孩(13.5岁后睾丸体积≤4 mL)中变异LH的患病率。本研究中每个受试者的LHβ基因状态通过使用两种具有不同单克隆抗体组合的免疫荧光法LH检测从单个静脉血样本中判断:一种检测变异型和野生型LH,另一种仅检测野生型激素。在正常年龄开始青春期的男孩中,36名(74%)是野生型LHβ等位基因的纯合子,12名(24%)是杂合子,1名(2%)是变异型LHβ等位基因的纯合子。在具有正常和突变(纯合或杂合)LH基因型的男孩之间发现了青春期参数的明显差异。在随访期间,与具有正常LH基因型的男孩相比,具有突变基因型的男孩睾丸体积较小(P<0.03)、身高较矮(P<0.02)、生长速度较慢(P<0.04)且血清胰岛素样生长因子I结合蛋白-3水平较低(P<0.03)。在青春期延迟开始的男孩中,变异LHβ等位基因的频率与参考人群中的频率没有差异,这表明变异LH与由于GnRH分泌再激活控制紊乱导致的情况无关。我们得出结论,在青春期进展过程中,变异LH在刺激睾丸生长方面可能比野生型LH活性更低。因此,该基因可能影响节奏,导致健康男孩青春期进展存在广泛的正常变异。我们的结果还表明,变异LH不仅影响青春期进程,而且在儿童期就已经参与了生长激素-胰岛素样生长因子I轴的调节。

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