Department and Clinic of Endocrinology, Diabetes and Isotope Therapy, Wroclaw Medical University, Wybrzeże Pasteura 4, 50-367 Wrocław, Poland.
Int J Mol Sci. 2023 Jun 30;24(13):10974. doi: 10.3390/ijms241310974.
The major causes of both morbidity and mortality in patients with acromegaly are cardiovascular diseases (CVDs). The polymorphisms of the fat mass and obesity-associated gene ( are associated with obesity, as well as with an increased risk of CVDs. The aim of the study was to determine the relationship of risk alleles of four gene polymorphisms with selected parameters of lipid and glucose metabolism as well as with IGF-1 and GH levels in the group of patients with acromegaly compared to the control group. The study group consisted of 104 patients with acromegaly and 64 healthy subjects constituting the control group. In the whole acromegaly group, the data reveal that the homozygous for risk allele carriers (rs1421085, rs9930506, rs9939609) as well as carriers of only one risk allele have lower IGF-1 concentrations. In the well-controlled acromegaly group, the homozygous for three risk allele carriers of gene polymorphisms have lower HDL cholesterol concentration (rs1121980, rs1421085, rs993609). In the cured acromegaly group, homozygous risk allele carriers rs9930506 tend to have higher levels of total cholesterol and LDL cholesterol. These associations are not observed in the control group. Conclusion: there is an association between gene polymorphisms and the metabolism of lipids, suggesting that the gene may be associated with higher CVD risk in patients with acromegaly. In addition, there is an association between gene polymorphisms and IGF-1, implying that gene may influence/modify IGF-1 synthesis. Further investigation on a larger scale is required to provide more precise evidence.
肢端肥大症患者的发病率和死亡率的主要原因是心血管疾病(CVD)。脂肪量和肥胖相关基因(的多态性与肥胖有关,并且与 CVD 风险增加有关。本研究的目的是确定四个 基因多态性的风险等位基因与选定的脂类和葡萄糖代谢参数以及 IGF-1 和 GH 水平在肢端肥大症患者组与对照组之间的关系。研究组包括 104 例肢端肥大症患者和 64 例健康受试者作为对照组。在整个肢端肥大症组中,数据显示,风险等位基因纯合子携带者(rs1421085、rs9930506、rs9939609)以及仅携带一个风险等位基因的携带者 IGF-1 浓度较低。在控制良好的肢端肥大症组中,基因多态性的三个风险等位基因纯合子携带者 rs1121980、rs1421085、rs993609 的 HDL 胆固醇浓度较低。在治愈的肢端肥大症组中,rs9930506 的纯合风险等位基因携带者总胆固醇和 LDL 胆固醇水平较高。这些关联在对照组中没有观察到。结论:基因多态性与脂质代谢之间存在关联,表明 基因可能与肢端肥大症患者的 CVD 风险增加有关。此外,基因多态性与 IGF-1 之间存在关联,这表明 基因可能影响/修饰 IGF-1 的合成。需要进行更大规模的进一步研究,以提供更准确的证据。