肢端肥大症患者Betatrophin, Chemerin和Kisspeptin水平的评估。

IF 2
Dondu Aysegul Cayan, Senay Topsakal, Esin Avci
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引用次数: 0

摘要

背景:肢端肥大症是一种慢性疾病,其特征是垂体生长激素(GH)分泌过多,导致代谢并发症和发病率增加。生长激素和胰岛素样生长因子1 (IGF-1)水平升高导致各种代谢和形态异常。Betatrophin在肝脏和脂肪组织中产生,在调节葡萄糖和脂质代谢中起重要作用。趋化素,一种脂肪因子,影响胰岛素敏感性、脂质代谢和炎症。此外,kisspeptin是一种神经肽,通过下丘脑-垂体-性腺轴刺激促黄体生成素(LH)和促卵泡激素(FSH)的分泌。目的:探讨肢端肥大症患者的betatrophin、chemerin和kisspeptin水平及其与血脂异常和糖尿病的潜在关系。方法:本研究包括40例肢端肥大症患者和40例健康对照。测定生长激素和IGF-1水平,并用ELISA法分析静脉血样本中的betatrophin、chemerin和kisspeptin水平。结果:分析显示肢端肥大症患者与对照组间betatrophin水平差异无统计学意义(p < 0.05)。然而,在肢端肥大症患者中观察到的chemerin和kisspeptin水平显著降低(结论:本研究强调了肢端肥大症患者中chemerin和kisspeptin水平的改变,表明它们参与了与该疾病相关的代谢失调。进一步研究IGF-1和kisspeptin之间的相关性可以为开发靶向治疗策略提供见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Betatrophin, Chemerin, and Kisspeptin Levels in Acromegaly Patients.

Background: Acromegaly is a chronic disorder characterized by excessive growth hormone (GH) secretion from pituitary somatotroph cells, resulting in metabolic complications and increased morbidity. Elevated levels of GH and insulin-like growth factor 1 (IGF-1) contribute to various metabolic and morphological abnormalities. Betatrophin, produced in the liver and adipose tissue, plays a significant role in regulating glucose and lipid metabolism. Chemerin, an adipokine, influences insulin sensitivity, lipid metabolism, and inflammation. Additionally, kisspeptin, a neuropeptide, stimulates the secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) through the hypothalamic-pituitary-gonadal axis.

Objective: This study aimed to investigate the levels of betatrophin, chemerin, and kisspeptin in acromegaly patients and their potential relationship with dyslipidemia and diabetes.

Methods: This study included 40 patients diagnosed with acromegaly and 40 healthy controls. GH and IGF-1 levels were measured, and venous blood samples were analyzed for betatrophin, chemerin, and kisspeptin levels using ELISA.

Results: The analysis revealed no significant difference in betatrophin levels between acromegaly patients and controls (p>0.05). However, significantly lower levels of chemerin and kisspeptin were observed in patients with acromegaly (p<0.001). Furthermore, a significant correlation was identified between IGF-1 and kisspeptin levels, indicating a potential pathway for future research in diagnostics and therapy.

Conclusion: This study highlights the altered levels of chemerin and kisspeptin in acromegaly patients, suggesting their involvement in metabolic dysregulation associated with the condition. Further investigation into the correlation between IGF-1 and kisspeptin could provide insights into developing targeted therapeutic strategies.

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