功能丧失的GHSR变体与矮身和低IGF-I相关
Lauren D Punt1, Sander Kooijman2,3, Noa J M Mutsters4
1Division of Pediatric Endocrinology, Department of Pediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Centre, 2333 ZA Leiden, the Netherlands.
The Journal of clinical endocrinology and metabolism
|January 9, 2025
概括
在儿童中生长激素分泌剂受体 (GHSR) 的哈普洛缺陷导致身材矮小. 这些患者在生长激素 (GH) 治疗后表现出显著的身高增加,支持GHSR在GH分泌中的作用.
科学领域:
- 内分泌学 在内分泌学.
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
背景情况:
- 增长激素 (GH) 分泌受体 (GHSR) 对于来自垂体腺的GH分泌至关重要.
- GHSR变种可能导致GH分泌受损,但它们对矮身的临床意义尚不清楚.
研究的目的:
- 在矮小的儿童中调查GHSR哈普隆缺陷的表型.
- 评估这些患者对GH治疗的生长反应.
主要方法:
- 一个26名患者的病例系列,具有矮身和异合的GHSR变体.
- 在体外功能研究中评估了受体活性和蛋白质水平.
- 临床数据包括身高,IGF-I水平和对GH治疗的反应.
主要成果:
- 确定了10种GHSR变异,其中6种是新型,具有部分或完全功能丧失.
- 患者呈现出相对矮小的身材,无法壮成长,食欲低下.
- 在两年内,GH治疗导致了显著的身高增长.
结论:
- GHSR哈普洛缺陷与儿童的矮身有关.
- 这些患者对GH治疗表现出强烈的反应.
- 这些发现加强了GHSR在调节GH分泌中的作用.
相关概念视频
Nature and Nurture
20.4K
Many human characteristics, like height, are shaped by both nature—in other words, by our genes—and by nurture, or our environment. For example, chronic stress during childhood inhibits the production of growth hormones and consequently reduces bone growth and height. Scientists estimate that 70-90% of variation in height is due to genetic differences among individuals, and 10-30% of variation in height is due to differences in the environments that individuals experience,...
20.4K
Pleiotropy
39.7K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
39.7K
Genome-wide Association Studies-GWAS
12.4K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
12.4K
TGF - β Signaling Pathway
7.2K
The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors...
7.2K
Hedgehog Signaling Pathway
7.3K
The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
7.3K
Signs of Puberty
235
Puberty is a critical phase, typically beginning between the ages of 8 and 13 in girls and 9 and 14 in boys, though timing can vary based on genetics, environmental factors, and overall health. This period is characterized by the development of secondary sexual characteristics and the attainment of reproductive potential. Endocrine changes underpin puberty, with hormonal surges of Luteinizing Hormone (LH) and Follicle-Stimulating Hormone (FSH) instigated by Gonadotropin-Releasing Hormone (GnRH)...
235


